Chiral Sulfinamides as Highly Enantioselective Organocatalysts

ChemCatChemVolume 6, Issue 11 p. 3063-3066 Highlight Chiral Sulfinamides as Highly Enantioselective Organocatalysts Dr. Peter Dinér, Corresponding Author Dr. Peter Dinér diner@kth.se Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this authorDr. Arghya Sadhukhan, Dr. Arghya Sadhukhan Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this authorBjörn Blomkvist, Björn Blomkvist Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this author Dr. Peter Dinér, Corresponding Author Dr. Peter Dinér diner@kth.se Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this authorDr. Arghya Sadhukhan, Dr. Arghya Sadhukhan Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this authorBjörn Blomkvist, Björn Blomkvist Department of Chemistry, KTH-Royal Institute of Technology, Teknikringen 30, SE-10044 Stockholm (Sweden), Fax: (+46) 8-7912333, Homepage: www.kth.se/en/che/divisions/orgkem/research/diner/Search for more papers by this author First published: 11 September 2014 https://doi.org/10.1002/cctc.201402558Citations: 17Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Abstract From auxiliary to catalyst: Chiral sulfinamides have emerged as versatile organocatalysts showing both Lewis base and Lewis acid activation modes. The reactions highlighted here involve several highly enantioselective transformations, such as reduction of imines, CC-bond forming reactions, enantioselective protonation, [4+2] cycloadditions etc. Citing Literature Volume6, Issue11November 2014Pages 3063-3066 RelatedInformation