Literature DB >> 18834133

Organocatalytic Michael addition of aldehydes to vinyl sulfones: enantioselective alpha-alkylations of aldehydes and their derivatives.

Qiang Zhu1, Yixin Lu.   

Abstract

Organocatalytic asymmetric Michael reaction of unmodified aldehydes to vinyl sulfones catalyzed by silylated biarylprolinol afforded the desired Michael products with exceptional enantioselectivity. The described enantioselective addition to vinyl sulfones, in combination with desulfonation, offers a unique, asymmetric entry to alpha-alkylated aldehydes and their derivatives.

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Year:  2008        PMID: 18834133     DOI: 10.1021/ol8019296

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


  2 in total

1.  N-heterocyclic carbene-catalyzed rearrangements of vinyl sulfones.

Authors:  Roxanne L Atienza; Howard S Roth; Karl A Scheidt
Journal:  Chem Sci       Date:  2011-06-10       Impact factor: 9.825

2.  N-Heterocyclic Carbene-Promoted Rauhut]Currier Reactions between Vinyl Sulfones and α,β-Unsaturated Aldehydes.

Authors:  Roxanne L Atienza; Karl A Scheidt
Journal:  Aust J Chem       Date:  2011-08-19       Impact factor: 1.321

  2 in total

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