Issue 9, 2005

Memory of chirality in intramolecular conjugate addition of enolates: a novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters

Abstract

Nitrogen heterocycles with contiguous quaternary and tertiary stereocenters have been prepared in high enantiomeric purity by intramolecular conjugate addition of enolates generated from α-amino acid derivatives via memory of chirality.

Graphical abstract: Memory of chirality in intramolecular conjugate addition of enolates: a novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters

Supplementary files

Article information

Article type
Communication
Submitted
29 Oct 2004
Accepted
11 Mar 2005
First published
30 Mar 2005

Org. Biomol. Chem., 2005,3, 1609-1611

Memory of chirality in intramolecular conjugate addition of enolates: a novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters

T. Kawabata, S. Majumdar, K. Tsubaki and D. Monguchi, Org. Biomol. Chem., 2005, 3, 1609 DOI: 10.1039/B416535G

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