Literature DB >> 21714489

Catalytic asymmetric addition of thiols to nitrosoalkenes leading to chiral non-racemic α-sulfenyl ketones.

John M Hatcher1, Mark C Kohler, Don M Coltart.   

Abstract

The first asymmetric organocatalytic sulfenylation of in situ derived nitrosoalkenes leading to chiral nonracemic α-sulfenylated ketones is described. The transformation proceeds in an umpolung fashion, relative to enolate/azaenolate methods, and uses simple thiols, thereby obviating the need for electrophilic sulfur reagents.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21714489     DOI: 10.1021/ol2012633

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Stereochemical investigation of conjugate additions of carbon- and heteronucleophiles to ring-substituted nitrosocyclohexenes.

Authors:  Ritobroto Sengupta; Jason A Witek; Steven M Weinreb
Journal:  Tetrahedron       Date:  2011-10-28       Impact factor: 2.457

2.  Diastereoselective addition of Grignard reagents to α-epoxy N-sulfonyl hydrazones.

Authors:  Maulen M Uteuliyev; Thien T Nguyen; Don M Coltart
Journal:  Nat Chem       Date:  2015-10-19       Impact factor: 24.427

3.  Catalytic, enantioselective sulfenylation of ketone-derived enoxysilanes.

Authors:  Scott E Denmark; Sergio Rossi; Matthew P Webster; Hao Wang
Journal:  J Am Chem Soc       Date:  2014-09-05       Impact factor: 15.419

  3 in total

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