{"id":2875,"date":"2022-09-12T11:26:13","date_gmt":"2022-09-12T02:26:13","guid":{"rendered":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/?page_id=2875"},"modified":"2023-10-30T13:23:16","modified_gmt":"2023-10-30T04:23:16","slug":"publication-list-prof-asano","status":"publish","type":"page","link":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/member\/cv-prof-asano\/publication-list-prof-asano\/","title":{"rendered":"Publication List -Prof. Asano-"},"content":{"rendered":"\n<h2>\u539f\u8457\u8ad6\u6587<\/h2>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>202<\/strong>3<\/h3>\n\n\n\n<div class=\"wp-container-3 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-1 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbOrganocatalytic Access to Tetrasubstituted Chiral Carbons Integrating Functional Groups<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.; Matsubara, S.<br>\u3000<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/tcr.202200200\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chem. Rec.<\/em>\u00a0<strong>2023<\/strong>, <em>23<\/em>, e202200200.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-2 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large is-resized\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min.png\"><img loading=\"lazy\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-1024x362.png\" alt=\"\" class=\"wp-image-2928\" width=\"512\" height=\"181\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-1024x362.png 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-300x106.png 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-768x272.png 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-1536x544.png 1536w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/ChemRec2022-min-2048x725.png 2048w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2022<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-6 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-4 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbNon-Enzymatic Catalytic Asymmetric Cyanation of Acylsilanes<\/strong><\/p>\n\n\n\n<p>\u3000Nagano, T.; Matsumoto, A.; Yoshizaki, R.; Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/www.nature.com\/articles\/s42004-022-00662-y\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Commun. Chem.<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>5<\/em>, 45.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-5 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large is-resized\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min.png\"><img loading=\"lazy\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-1024x362.png\" alt=\"\" class=\"wp-image-2929\" width=\"512\" height=\"181\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-1024x362.png 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-300x106.png 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-768x272.png 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-1536x543.png 1536w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/CommunChem2022_Nagano-min-2048x725.png 2048w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2021<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-9 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-7 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbCatalytic Asymmetric Cycloetherification via Intramolecular Oxy-Michael Addition of Enols<\/strong><\/p>\n\n\n\n<p>\u3000Murata, R.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a rel=\"noreferrer noopener\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402021006372\" target=\"_blank\"><em>Tetrahedron<\/em>&nbsp;<strong>2021<\/strong>,&nbsp;<em>97<\/em>, 132381.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in <a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2023\/09January.shtm\" target=\"_blank\" rel=\"noreferrer noopener\">Organic Chemistry Highlights in Organic Chemistry Portal<\/a>.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-8 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large is-resized\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021.jpg\"><img loading=\"lazy\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021-1024x590.jpg\" alt=\"\" class=\"wp-image-2931\" width=\"512\" height=\"295\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021-1024x590.jpg 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021-300x173.jpg 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021-768x442.jpg 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021-1536x885.jpg 1536w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Tetrahedron2021.jpg 1538w\" sizes=\"(max-width: 512px) 100vw, 512px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-13 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-10 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\">\n<p>\u30fb<strong>Multipoint Recognition of Molecular Conformations with Organocatalysts for Asymmetric Synthetic Reactions<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.<br>\u3000<a rel=\"noreferrer noopener\" href=\"https:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/bcsj.20200343\" target=\"_blank\"><em>Bull. Chem. Soc. Jpn.<\/em>&nbsp;<strong>2021<\/strong>,&nbsp;<em>94<\/em>, 694\u2013712.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Selected as&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.journal.csj.jp\/do\/10.5555\/1641fdbd-8ef1-47e1-8c3e-3865c5721eca\/abs\/\" target=\"_blank\">the inside cover<\/a>.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-11 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min.png\"><img loading=\"lazy\" width=\"1024\" height=\"430\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-1024x430.png\" alt=\"\" class=\"wp-image-2926\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-1024x430.png 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-300x126.png 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-768x322.png 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-1536x645.png 1536w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/BCSJ2020_Asano-min-2048x860.png 2048w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/a><\/figure><\/div><\/div>\n\n\n\n<div class=\"wp-container-12 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:20%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"alignright size-medium\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min.jpg\"><img loading=\"lazy\" width=\"223\" height=\"300\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min-223x300.jpg\" alt=\"\" class=\"wp-image-2927\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min-223x300.jpg 223w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min-760x1024.jpg 760w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min-768x1035.jpg 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min-1140x1536.jpg 1140w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/10\/Bull.-Chem.-Soc.-Jpn.-2021_Asano_Inside-Cover-min.jpg 1241w\" sizes=\"(max-width: 223px) 100vw, 223px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2020<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-17 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-14 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\">\n<p><strong>\u30fbDesymmetrization of&nbsp;<em>gem<\/em>-Diols via Water-Assisted Organocatalytic Enantio- and Diastereoselective Cycloetherification<\/strong><\/p>\n\n\n\n<p>\u3000Murata, R.; Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc05509c#!divAbstract\" target=\"_blank\"><em>Chem. Commun.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>56<\/em>, 12335\u201312338.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Selected as<a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/cc\/d0cc90450c#!divAbstract\" target=\"_blank\">&nbsp;the inside back cover<\/a>.<br>\u3000Highlighted in <a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-0040-1706378\" target=\"_blank\"><em>Synfacts<\/em> <strong>2020<\/strong>, <em>16<\/em>, 1276<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-15 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun2020.jpg\"><img loading=\"lazy\" width=\"517\" height=\"261\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun2020.jpg\" alt=\"\" class=\"wp-image-2949\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun2020.jpg 517w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun2020-300x151.jpg 300w\" sizes=\"(max-width: 517px) 100vw, 517px\" \/><\/a><\/figure><\/div><\/div>\n\n\n\n<div class=\"wp-container-16 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:20%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synfacts_InsideBackCover_2020.jpg\"><img loading=\"lazy\" width=\"206\" height=\"267\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synfacts_InsideBackCover_2020.jpg\" alt=\"\" class=\"wp-image-2950\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-21 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-18 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\">\n<p><strong>\u30fb<em>trans<\/em>-Cyclooctenes as Chiral Ligands in Rhodium-Catalyzed Asymmetric 1,4-Additions<\/strong><\/p>\n\n\n\n<p>\u3000Nagano, T.; Einaru, S.; Shitamichi, K.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.202000956\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Eur. J. Org. Chem.<\/em>&nbsp;<strong>2020<\/strong>, 7131\u20137133.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Selected as the Very Important Paper (VIP).<br>\u3000Selected as&nbsp;<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.202001293\" target=\"_blank\" rel=\"noreferrer noopener\">the Front Cover<\/a>.<br>\u3000Highlighted in <a href=\"https:\/\/www.chemistryviews.org\/details\/ezine\/11265818\/Trans-Cyclooctenes_as_Chiral_Ligands.html\" target=\"_blank\" rel=\"noreferrer noopener\">Chemistry Views<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-19 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_2020.jpg\"><img loading=\"lazy\" width=\"669\" height=\"149\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_2020.jpg\" alt=\"\" class=\"wp-image-2960\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_2020.jpg 669w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_2020-300x67.jpg 300w\" sizes=\"(max-width: 669px) 100vw, 669px\" \/><\/a><\/figure><\/div><\/div>\n\n\n\n<div class=\"wp-container-20 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:20%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-medium\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_FrontCover_2020.jpg\"><img loading=\"lazy\" width=\"225\" height=\"300\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_FrontCover_2020-225x300.jpg\" alt=\"\" class=\"wp-image-2961\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_FrontCover_2020-225x300.jpg 225w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/EJOC_FrontCover_2020.jpg 500w\" sizes=\"(max-width: 225px) 100vw, 225px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-24 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-22 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbEnantio- and Diastereoselective Construction of Contiguous Tetrasubstituted Chiral Carbons in Organocatalytic Oxadecalin Synthesis<\/strong><\/p>\n\n\n\n<p>\u3000Wada, Y.; Murata, R.; Fujii, Y.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c01501\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>22<\/em>, 4710\u20134715.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2020\/21December.shtm\" target=\"_blank\">Organic Chemistry Highlights in Organic Chemistry Portal<\/a>.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-23 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2020.jpg\"><img loading=\"lazy\" width=\"533\" height=\"202\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2020.jpg\" alt=\"\" class=\"wp-image-2963\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2020.jpg 533w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2020-300x114.jpg 300w\" sizes=\"(max-width: 533px) 100vw, 533px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2019<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-27 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-25 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbEnantioselective Bromination of Axially Chiral Cyanoarenes in the Presence of Bifunctional Organocatalysts<\/strong><\/p>\n\n\n\n<p>\u3000Wada, Y.; Matsumoto, A.; Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/ra\/c9ra05532k#!divAbstract\" target=\"_blank\" rel=\"noreferrer noopener\"><em>RSC Adv<\/em>.&nbsp;<strong>2019<\/strong>,&nbsp;<em>9<\/em>, 31654\u201331658<em>.<\/em><\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-26 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/RSCAdv_2019.jpg\"><img loading=\"lazy\" width=\"518\" height=\"275\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/RSCAdv_2019.jpg\" alt=\"\" class=\"wp-image-2966\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/RSCAdv_2019.jpg 518w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/RSCAdv_2019-300x159.jpg 300w\" sizes=\"(max-width: 518px) 100vw, 518px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-30 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-28 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric&nbsp;<em>syn<\/em>-1,3-Dioxane Construction via Kinetic Resolution of Secondary Alcohols Using Chiral Phosphoric Acid Catalysts<\/strong><\/p>\n\n\n\n<p>\u3000Matsumoto, A.; Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/ajoc.201900239\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Asian J. Org. Chem.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>8<\/em>, 814\u2013818.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-29 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/AJOC_2019.jpg\"><img loading=\"lazy\" width=\"748\" height=\"294\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/AJOC_2019.jpg\" alt=\"\" class=\"wp-image-2967\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/AJOC_2019.jpg 748w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/AJOC_2019-300x118.jpg 300w\" sizes=\"(max-width: 748px) 100vw, 748px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-33 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-31 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fb<\/strong><strong>Organocatalytic Enantio- and Diastereoselective Construction of&nbsp;<em>syn<\/em>-1,3-Diol Motifs via Dynamic Kinetic Resolution of In Situ Generated Chiral Cyanohydrins<\/strong><\/p>\n\n\n\n<p>\u3000Matsumoto, A.; Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b00677\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Org. Lett.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>21<\/em>, 2688\u20132692.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-32 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2688.jpg\"><img loading=\"lazy\" width=\"530\" height=\"210\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2688.jpg\" alt=\"\" class=\"wp-image-2971\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2688.jpg 530w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2688-300x119.jpg 300w\" sizes=\"(max-width: 530px) 100vw, 530px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-36 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-34 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers<\/strong><\/p>\n\n\n\n<p>\u3000Kurimoto, Y.; Nasu, T.; Fujii, Y.; Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b00462\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Org. Lett.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>21<\/em>, 2156\u20132160.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-35 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2156.jpg\"><img loading=\"lazy\" width=\"535\" height=\"217\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2156.jpg\" alt=\"\" class=\"wp-image-2972\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2156.jpg 535w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2019_2156-300x122.jpg 300w\" sizes=\"(max-width: 535px) 100vw, 535px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-40 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-37 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\">\n<p><strong>\u30fbKinetic Resolution of Acylsilane Cyanohydrins via Organocatalytic Cycloetherification<\/strong><\/p>\n\n\n\n<p>\u3000Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/asia.201801600\" target=\"_blank\" rel=\"noreferrer noopener\"><em><em>Chem.\u2014Asian J.<\/em>&nbsp;<\/em><strong>2019<\/strong><em>,&nbsp;<em>14<\/em>, <\/em>116\u2013120<em>.<\/em><\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Selected&nbsp;as&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201801786\" target=\"_blank\">the Cover Feature<\/a>.<br>\u3000Selected as&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/e8100653-1e20-43e6-a3d3-0887c97a5130.filesusr.com\/ugd\/2ee17f_1bac88019ff14e89a2ea699adab2dde3.pdf\" target=\"_blank\">the top 10% most downloaded paper<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-38 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019.jpg\"><img loading=\"lazy\" width=\"556\" height=\"284\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019.jpg\" alt=\"\" class=\"wp-image-2975\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019.jpg 556w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019-300x153.jpg 300w\" sizes=\"(max-width: 556px) 100vw, 556px\" \/><\/a><\/figure><\/div><\/div>\n\n\n\n<div class=\"wp-container-39 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:20%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover.jpg\"><img loading=\"lazy\" width=\"770\" height=\"1024\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover-770x1024.jpg\" alt=\"\" class=\"wp-image-2976\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover-770x1024.jpg 770w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover-226x300.jpg 226w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover-768x1021.jpg 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemAsianJ_2019_FrontCover.jpg 826w\" sizes=\"(max-width: 770px) 100vw, 770px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2018<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-43 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-41 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fb<em>trans<\/em>-Cyclooctenes as Halolactonization Catalysts<\/strong><\/p>\n\n\n\n<p>\u3000Einaru, S.; Shitamichi, K.; Nagano, T.;&nbsp;Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201808320\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Angew. Chem., Int. Ed.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>57<\/em>, 13863\u201313867.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0037-1611047\" target=\"_blank\"><em>Synfacts<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>14<\/em>, 1198<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-42 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2018.jpg\"><img loading=\"lazy\" width=\"528\" height=\"250\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2018.jpg\" alt=\"\" class=\"wp-image-2979\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2018.jpg 528w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2018-300x142.jpg 300w\" sizes=\"(max-width: 528px) 100vw, 528px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-46 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-44 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Cycloetherification by Bifunctional Organocatalyst<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1591592\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Synthesis<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>50<\/em>, 4243\u20134253.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-45 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synthesis_2018.gif\"><img loading=\"lazy\" width=\"550\" height=\"325\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synthesis_2018.gif\" alt=\"\" class=\"wp-image-2985\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-49 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-47 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbCatalytic Approaches to Optically Active 1,5-Benzothiazepines<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.; Matsubara, S.<br>\u3000<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.8b00908\" target=\"_blank\" rel=\"noreferrer noopener\"><em><em>ACS Catal.<\/em>&nbsp;<\/em><strong>2018<\/strong><em>,&nbsp;<em>8<\/em>, <\/em>6273\u20136282<em>.<\/em><\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-48 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ACSCatal_2018.gif\"><img loading=\"lazy\" width=\"500\" height=\"203\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ACSCatal_2018.gif\" alt=\"\" class=\"wp-image-2986\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2017<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-52 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-50 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fb<strong>Organocatalytic Enantio- and Diastereoselective Cycloetherification via Dynamic Kinetic Resolution of Chiral Cyanohydrins<\/strong><\/strong><\/p>\n\n\n\n<p>\u3000Yoneda, N.; Fujii, Y.; Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/www.nature.com\/articles\/s41467-017-01099-x\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Nat. Commun.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>8<\/em>, 1397.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/www.kyoto-u.ac.jp\/ja\/research\/research_results\/2017\/171110_1.html\" target=\"_blank\">Press release on Kyoto University website<\/a>.<br>\u3000Highlighted in Newspapers (<a rel=\"noreferrer noopener\" href=\"https:\/\/www.nikkei.com\/article\/DGXLRSP463239_U7A111C1000000\/\" target=\"_blank\">Nikkei Shinbun<\/a>&nbsp;&amp;&nbsp;<a href=\"https:\/\/smatsubara.wixsite.com\/matsubara-kyoto-u\/kagaku-kogyo-nippo-2017-11-jp\">Kagaku Kogyo Nippo<\/a>).<br>\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme.de\/en\/thieme-chemistry\/organocatalytic-enantio-and-diastereoselective-cycloetherification-122814.htm\" target=\"_blank\"><em>Synform<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>3<\/em>, A33<\/a>.<br>\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"http:\/\/www.organic-chemistry.org\/Highlights\/2018\/09April.shtm\" target=\"_blank\">Organic Chemistry Highlights in Organic Chemistry Portal<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-51 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min.png\"><img loading=\"lazy\" width=\"1024\" height=\"543\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-1024x543.png\" alt=\"\" class=\"wp-image-2987\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-1024x543.png 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-300x159.png 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-768x407.png 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-1536x814.png 1536w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/NatCommun2017-min-2048x1086.png 2048w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-55 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-53 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Net Cycloaddition for Access to Diverse Substituted 1,5-Benzothiazepines<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Yao, K.; Miyaji, R.;&nbsp;Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.7b02451\" target=\"_blank\" rel=\"noreferrer noopener\"><em>J. Org. Chem.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>82<\/em>, 12655\u201312668.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.organic-chemistry.org\/abstracts\/lit6\/121.shtm\" target=\"_blank\">Abstracts in Organic Chemistry Portal<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-54 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JOC_2017.gif\"><img loading=\"lazy\" width=\"500\" height=\"197\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JOC_2017.gif\" alt=\"\" class=\"wp-image-2992\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-58 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-56 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbBifunctional Organocatalysts for the Asymmetric Synthesis of Axially Chiral Benzamides<\/strong><\/p>\n\n\n\n<p>\u3000Miyaji, R.; Wada, Y.; Matsumoto, A.;&nbsp;Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/www.beilstein-journals.org\/bjoc\/articles\/13\/151\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Beilstein J. Org. Chem.<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>13<\/em>, 1518\u20131523.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-57 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/BeilsteinJOC_2017.jpg\"><img loading=\"lazy\" width=\"528\" height=\"244\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/BeilsteinJOC_2017.jpg\" alt=\"\" class=\"wp-image-2994\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/BeilsteinJOC_2017.jpg 528w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/BeilsteinJOC_2017-300x139.jpg 300w\" sizes=\"(max-width: 528px) 100vw, 528px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-62 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-59 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\">\n<p><strong>\u30fb<strong>Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts<\/strong><\/strong><\/p>\n\n\n\n<p>\u3000Miyaji, R.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201701707\/full\" target=\"_blank\" rel=\"noreferrer noopener\"><em><em>Chem.\u2014Eur. J.<\/em>&nbsp;<\/em><strong>2017<\/strong><em>,&nbsp;<em>23<\/em>, <\/em>9996\u201310000.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Selected as&nbsp;<a rel=\"noreferrer noopener\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201702325\/abstract\" target=\"_blank\">the Inside Cover<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-60 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:40%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017.jpg\"><img loading=\"lazy\" width=\"789\" height=\"172\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017.jpg\" alt=\"\" class=\"wp-image-2997\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017.jpg 789w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017-300x65.jpg 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017-768x167.jpg 768w\" sizes=\"(max-width: 789px) 100vw, 789px\" \/><\/a><\/figure><\/div><\/div>\n\n\n\n<div class=\"wp-container-61 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:20%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover.jpg\"><img loading=\"lazy\" width=\"770\" height=\"1024\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover-770x1024.jpg\" alt=\"\" class=\"wp-image-2998\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover-770x1024.jpg 770w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover-226x300.jpg 226w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover-768x1021.jpg 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemEurJ_2017_InsideCover.jpg 826w\" sizes=\"(max-width: 770px) 100vw, 770px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2016<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-65 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-63 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fb\u7a4f\u548c\u306a\u6709\u6a5f\u89e6\u5a92\u304c\u3082\u305f\u3089\u3059\u7cbe\u5bc6\u4e0d\u6589\u5408\u6210<\/strong><\/p>\n\n\n\n<p>\u3000&nbsp;Asano, K.<br><em>\u3000<\/em><a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/74\/12\/74_1194\/_article\/-char\/ja\/\" target=\"_blank\" rel=\"noreferrer noopener\">\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c&nbsp;<strong>2016<\/strong>,&nbsp;<em>74<\/em>, 1194\u20131205.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-64 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Yugoka_2016.jpg\"><img loading=\"lazy\" width=\"529\" height=\"273\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Yugoka_2016.jpg\" alt=\"\" class=\"wp-image-3001\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Yugoka_2016.jpg 529w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Yugoka_2016-300x155.jpg 300w\" sizes=\"(max-width: 529px) 100vw, 529px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-68 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-66 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Cycloetherification via the Kinetic Resolution of Alcohols Using Chiral Phosphoric Acid Catalysts<\/strong><\/p>\n\n\n\n<p>\u3000&nbsp;Yoneda, N.; Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.160727\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chem. Lett.<\/em>&nbsp;<strong>2016<\/strong>,&nbsp;<em>45<\/em>, 1300\u20131303.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-67 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-large\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016.jpeg\"><img loading=\"lazy\" width=\"1024\" height=\"388\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016-1024x388.jpeg\" alt=\"\" class=\"wp-image-3002\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016-1024x388.jpeg 1024w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016-300x114.jpeg 300w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016-768x291.jpeg 768w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemLett_2016.jpeg 1048w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2015<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-71 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-69 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Synthesis of Spiroketals with Aminothiourea Catalysts<\/strong><\/p>\n\n\n\n<p>\u3000Yoneda, N.; Fukata, Y.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201508405\/full\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Angew. Chem., Int. Ed.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>54<\/em>, 15497\u201315500.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1561067\" target=\"_blank\"><em>Synfacts<\/em>&nbsp;<strong>2016<\/strong>,&nbsp;<em>12<\/em>, 89<\/a>.<br><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-70 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2015.jpg\"><img loading=\"lazy\" width=\"533\" height=\"143\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2015.jpg\" alt=\"\" class=\"wp-image-3004\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2015.jpg 533w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Angew_2015-300x80.jpg 300w\" sizes=\"(max-width: 533px) 100vw, 533px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-73 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-72 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:100%\">\n<p><strong>\u30fb\u7a4f\u3084\u304b\u306a\u89e6\u5a92\u304c\u3082\u305f\u3089\u3059\u7cbe\u5bc6\u6709\u6a5f\u5408\u6210<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.<br><em>\u3000<\/em><a href=\"http:\/\/www.chemistry.or.jp\/journal\/doc\/ci1509.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">\u5316\u5b66\u3068\u5de5\u696d&nbsp;<strong>2015<\/strong>,&nbsp;<em>68<\/em>, 832\u2013833.<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-76 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-74 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbDiastereoselective Reduction of \u03b2-(1,3-Dioxan-4-yl)ketones<\/strong><\/p>\n\n\n\n<p>\u3000Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0034-1378725\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Synlett<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>26<\/em>, 1872\u20131874.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-75 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synlett_2015.gif\"><img loading=\"lazy\" width=\"470\" height=\"136\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synlett_2015.gif\" alt=\"\" class=\"wp-image-3003\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-79 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-77 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbA Chiral Phosphoric Acid Catalyst for Asymmetric Construction of 1,3-Dioxanes<\/strong><\/p>\n\n\n\n<p>\u3000Matsumoto, A.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/cc\/c5cc04124d#!divAbstract\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chem.&nbsp;Commun.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>51<\/em>, 11693\u201311696.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-78 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2015.jpg\"><img loading=\"lazy\" width=\"522\" height=\"209\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2015.jpg\" alt=\"\" class=\"wp-image-3005\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2015.jpg 522w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2015-300x120.jpg 300w\" sizes=\"(max-width: 522px) 100vw, 522px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-82 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-80 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbBifunctional Organocatalysts for the Enantioselective Synthesis of Axially Chiral Isoquinoline&nbsp;<em>N<\/em>-Oxides<\/strong><\/p>\n\n\n\n<p>\u3000Miyaji, R.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.5b04151?journalCode=jacsat&amp;quickLinkVolume=137&amp;quickLinkPage=6766&amp;selectedTab=citation&amp;volume=137\" target=\"_blank\" rel=\"noreferrer noopener\"><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>137<\/em>,&nbsp;6766\u20136769.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-81 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015.jpg\"><img loading=\"lazy\" width=\"529\" height=\"222\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015.jpg\" alt=\"\" class=\"wp-image-3006\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015.jpg 529w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015-300x126.jpg 300w\" sizes=\"(max-width: 529px) 100vw, 529px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-85 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-83 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fb<\/strong><strong>Facile Net Cycloaddition Approach to Optically Active 1,5\u2011Benzothiazepines<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Asano, K.; Matsubara, S.<br><em>\u3000<\/em><a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/jacs.5b02537?journalCode=jacsat&amp;quickLinkVolume=137&amp;quickLinkPage=5320&amp;selectedTab=citation&amp;volume=137\" target=\"_blank\" rel=\"noreferrer noopener\"><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>137<\/em>,&nbsp;5320\u20135323.<\/a><\/p>\n\n\n\n<p class=\"has-vk-color-custom-5-color has-text-color\">\u3000Highlighted in&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0034-1380968\" target=\"_blank\"><em>Synfacts<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>11<\/em>, 770<\/a>.<br>\u3000Highlighted in&nbsp;<em>J.&nbsp;Synth. Org. Chem., Jpn.<\/em>&nbsp;<strong>2015<\/strong>,&nbsp;<em>73<\/em>, 1162.<\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-84 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015_5320.jpg\"><img loading=\"lazy\" width=\"517\" height=\"241\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015_5320.jpg\" alt=\"\" class=\"wp-image-3007\" srcset=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015_5320.jpg 517w, https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2015_5320-300x140.jpg 300w\" sizes=\"(max-width: 517px) 100vw, 517px\" \/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2014<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-88 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-86 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Oxy-Michael Addition to \u03b3-Hydroxy-\u03b1,\u03b2-Unsaturated Carbonyls Using Formaldehyde as an Oxygen-Centered Nucleophile<\/strong><\/p>\n\n\n\n<p>\u3000Yoneda, N.; Hotta, A.;&nbsp;Asano, K.; Matsubara, S.&nbsp;<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol503104b?journalCode=orlef7&amp;quickLinkVolume=16&amp;quickLinkPage=6264&amp;selectedTab=citation&amp;volume=16\" target=\"_blank\"><em>Org. Lett.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>16<\/em>, 6264\u20136266.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-87 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2014_6264.gif\"><img loading=\"lazy\" width=\"500\" height=\"189\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2014_6264.gif\" alt=\"\" class=\"wp-image-3017\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-91 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-89 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Isomerization of \u03c9-Hydroxy-\u03b1,\u03b2-Unsaturated Thioesters into \u03b2-Mercaptolactones by a Bifunctional Aminothiourea Catalyst<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Okamura, T.;&nbsp;Asano, K.;&nbsp;Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol500637x?journalCode=orlef7&amp;quickLinkVolume=16&amp;quickLinkPage=2184&amp;selectedTab=citation&amp;volume=16\" target=\"_blank\"><em>Org. Lett.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>16<\/em>, 2184\u20132187.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-90 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2014_2184.gif\"><img loading=\"lazy\" width=\"500\" height=\"171\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2014_2184.gif\" alt=\"\" class=\"wp-image-3018\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-94 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-92 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric chroman synthesis&nbsp;<em>via<\/em>&nbsp;an intramolecular oxy-Michael addition by bifunctional organocatalysts<\/strong><\/p>\n\n\n\n<p>\u3000Miyaji, R.; Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/ob\/c3ob41938j#!divAbstract\" target=\"_blank\"><em>Org. Biomol. Chem.<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>12<\/em>, 119\u2013122.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-93 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OrgBilmolChem_2014.gif\"><img loading=\"lazy\" width=\"378\" height=\"186\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OrgBilmolChem_2014.gif\" alt=\"\" class=\"wp-image-3019\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2013<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-97 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-95 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbProcedure-Controlled Enantioselectivity Switch in Organocatalytic 2-Oxazolidinone Synthesis<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Asano, K.;&nbsp;Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja407027e?journalCode=jacsat&amp;quickLinkVolume=135&amp;quickLinkPage=12160&amp;selectedTab=citation&amp;volume=135\" target=\"_blank\"><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>135<\/em>, 12160\u201312163.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-96 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2013_12160.gif\"><img loading=\"lazy\" width=\"500\" height=\"213\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2013_12160.gif\" alt=\"\" class=\"wp-image-3020\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-100 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-98 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Indoline Synthesis via Intramolecular Aza-Michael Addition Mediated by Bifunctional Organocatalysts<\/strong><\/p>\n\n\n\n<p>\u3000Miyaji, R.; Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol401538b?journalCode=orlef7&amp;quickLinkVolume=15&amp;quickLinkPage=3658&amp;selectedTab=citation&amp;volume=15\" target=\"_blank\"><em>Org. Lett.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>15<\/em>, 3658\u20133661.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-99 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2013_3658.gif\"><img loading=\"lazy\" width=\"500\" height=\"209\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2013_3658.gif\" alt=\"\" class=\"wp-image-3021\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-103 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-101 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Cycloetherifications by Bifunctional Aminothiourea Catalysts: The Importance of Hydrogen Bonding<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Miyaji, R.; Okamura, T.; Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0032-1316920\" target=\"_blank\"><em>Synthesis<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>45<\/em>, 1627\u20131634.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-102 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synthesis_2013_1627.gif\"><img loading=\"lazy\" width=\"359\" height=\"204\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/Synthesis_2013_1627.gif\" alt=\"\" class=\"wp-image-3022\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-106 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-104 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Synthesis of 1,3-Oxazolidines via Intramolecular Aza-Michael Addition by Bifunctional Organocatalysts<\/strong><\/p>\n\n\n\n<p>\u3000Fukata, Y.; Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.121245\" target=\"_blank\"><em>Chem. Lett.<\/em>&nbsp;<strong>2013<\/strong>,&nbsp;<em>42<\/em>, 355\u2013357.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-105 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/CL_2013_355.gif\"><img loading=\"lazy\" width=\"399\" height=\"189\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/CL_2013_355.gif\" alt=\"\" class=\"wp-image-3023\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2012<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-109 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-107 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbOrganocatalytic asymmetric oxy-Michael addition to a \u03b3-hydroxy-\u03b1,\u03b2-unsaturated thioester<em>via <\/em>hemiacetal intermediates<\/strong><\/p>\n\n\n\n<p>\u3000Okamura, T.; Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/cc\/c2cc31602a#!divAbstract\" target=\"_blank\"><em>Chem. Commun.<\/em>&nbsp;<strong>2012<\/strong>,&nbsp;<em>48<\/em>, 5076\u20135078.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-108 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2012.gif\"><img loading=\"lazy\" width=\"378\" height=\"186\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/ChemCommun_2012.gif\" alt=\"\" class=\"wp-image-3024\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<div class=\"wp-container-112 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-110 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Synthesis of 1,3-Dioxolanes by Organocatalytic Formal [3 + 2] Cycloaddition via Hemiacetal Intermediates<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol3003755?journalCode=orlef7&amp;quickLinkVolume=14&amp;quickLinkPage=1620&amp;selectedTab=citation&amp;volume=14\" target=\"_blank\"><em>Org. Lett.<\/em>&nbsp;<strong>2012<\/strong>,&nbsp;<em>14<\/em>, 1620\u20131623.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-111 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2012_1620.gif\"><img loading=\"lazy\" width=\"500\" height=\"189\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/OL_2012_1620.gif\" alt=\"\" class=\"wp-image-3025\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n\n\n\n<h3 class=\"has-large-font-size\"><strong>2011<\/strong><\/h3>\n\n\n\n<div class=\"wp-container-115 wp-block-columns are-vertically-aligned-center\">\n<div class=\"wp-container-113 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\">\n<p><strong>\u30fbAsymmetric Catalytic Cycloetherification Mediated by Bifunctional Organocatalysts<\/strong><\/p>\n\n\n\n<p>\u3000Asano, K.; Matsubara, S.<br>\u3000<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja207322d?journalCode=jacsat&amp;quickLinkVolume=133&amp;quickLinkPage=16711&amp;selectedTab=citation&amp;volume=133\" target=\"_blank\"><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2011<\/strong>,&nbsp;<em>133<\/em>, 16711\u201316713.<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-container-114 wp-block-column is-vertically-aligned-center\" style=\"flex-basis:50%\"><div class=\"wp-block-image is-style-vk-image-shadow\">\n<figure class=\"aligncenter size-full\"><a href=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2011_16711.gif\"><img loading=\"lazy\" width=\"500\" height=\"194\" src=\"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-content\/uploads\/2022\/11\/JACS_2011_16711.gif\" alt=\"\" class=\"wp-image-3026\"\/><\/a><\/figure><\/div><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>\u539f\u8457\u8ad6\u6587 2023 \u30fbOrganocatalytic Access to Tetrasubstituted Chiral Carbons Integrating Functional Groups \u3000Asano, K.; [&hellip;]<\/p>\n","protected":false},"author":8,"featured_media":0,"parent":2520,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_lightning_design_setting":{"layout":"default","header_trans":"default","section_base":"default"},"vkexunit_cta_each_option":""},"_links":{"self":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2875"}],"collection":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/comments?post=2875"}],"version-history":[{"count":38,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2875\/revisions"}],"predecessor-version":[{"id":3095,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2875\/revisions\/3095"}],"up":[{"embeddable":true,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2520"}],"wp:attachment":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/media?parent=2875"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}