Issue 68, 2013

Asymmetric anti-aldol addition of achiral ketonesvia chiral N-amino cyclic carbamate hydrazones

Abstract

The asymmetric anti-aldol addition of ketone-derived donors and aldehyde acceptors is described. Asymmetric induction is achieved through the use of chiral N-amino cyclic carbamate (ACC) auxiliaries. The transformation exhibits essentially perfect anti-diastereoselectivity and enantioselectivity, and has the unusual feature of proceeding via thermodynamic, rather than kinetic control.

Graphical abstract: Asymmetric anti-aldol addition of achiral ketones via chiral N-amino cyclic carbamate hydrazones

Supplementary files

Article information

Article type
Communication
Submitted
23 Jun 2013
Accepted
02 Jul 2013
First published
04 Jul 2013

Chem. Commun., 2013,49, 7495-7497

Asymmetric anti-aldol addition of achiral ketones via chiral N-amino cyclic carbamate hydrazones

J. D. Knight and D. M. Coltart, Chem. Commun., 2013, 49, 7495 DOI: 10.1039/C3CC44716B

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