en
Scientific article
English

Highly enantioselective organocascade intermolecular iminium/enamine Michael addition on enals

Published inChemical communications, vol. 47, no. 25, p. 7212-7214
Publication date2011
Abstract

An unprecedented intermolecular iminium/enamine Michael addition on enals has been developed by taking advantage of the high reactivity of vinyl sulfones. This powerful organocascade allows for the rapid construction of attractive synthons in high enantioselectivities (typically 99% ee).

Citation (ISO format)
QUINTARD, Adrien, ALEXAKIS, Alexandre. Highly enantioselective organocascade intermolecular iminium/enamine Michael addition on enals. In: Chemical communications, 2011, vol. 47, n° 25, p. 7212–7214. doi: 10.1039/c1cc11967b
Main files (1)
Article (Published version)
accessLevelRestricted
Identifiers
ISSN of the journal1359-7345
514views
0downloads

Technical informations

Creation06/20/2011 9:46:00 AM
First validation06/20/2011 9:46:00 AM
Update time03/14/2023 4:52:20 PM
Status update03/14/2023 4:52:20 PM
Last indexation01/15/2024 10:24:58 PM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack