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Issue 9, 2005
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Memory of chirality in intramolecular conjugate addition of enolates: a novel access to nitrogen heterocycles with contiguous quaternary and tertiary stereocenters

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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

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Supplementary files

Article information


Submitted
29 Oct 2004
Accepted
11 Mar 2005
First published
30 Mar 2005

Org. Biomol. Chem., 2005,3, 1609-1611
Article type
Communication

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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