Logo image
Sign in
Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization)
Journal article   Peer reviewed

Cyclosulfamide as a chiral auxiliary: application to efficient asymmetric synthesis (alkylation/aldolization)

Fabien Fécourt, Gérald Lopez, Arie van Der Lee, Jean Martinez and Georges Dewynter
Tetrahedron: Asymmetry, Vol.21, pp.2361-2366
07/10/2010

Abstract

The chiral cyclosulfamide (S)-2-benzyl-4-isopropyl-1,2,5-thiadiazolidine 1,1-dioxide was designed as a chimera of Evans and Oppolzer chiral auxiliaries. The N-propionyl derivative appeared to be very powerful for the stereocontrolled synthesis of chiral building blocks through asymmetric aldolization and alkylation reactions.
url
Find in HALView

Metrics

1 Record Views

Details

Logo image