Issue 13, 2010

Chiral primary amine mediated conjugate addition of branched aldehydes to vinyl sulfone: asymmetric generation of quaternary carbon centers

Abstract

Novel L-threonine-derived bifunctional organic catalysts containing primary amine and sulfonamide groups were utilized to promote asymmetric conjugate addition of α,α-disubstitued aldehydes to 1,1-bis(benzenesulfonyl)ethylene. The adducts with quaternary stereogenic centers adjacent to an aldehyde group were obtained in high yield and with good enantioselectivity.

Graphical abstract: Chiral primary amine mediated conjugate addition of branched aldehydes to vinyl sulfone: asymmetric generation of quaternary carbon centers

Supplementary files

Article information

Article type
Communication
Submitted
18 Sep 2009
Accepted
22 Dec 2009
First published
21 Jan 2010

Chem. Commun., 2010,46, 2235-2237

Chiral primary amine mediated conjugate addition of branched aldehydes to vinyl sulfone: asymmetric generation of quaternary carbon centers

Q. Zhu and Y. Lu, Chem. Commun., 2010, 46, 2235 DOI: 10.1039/B919549A

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