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Issue 18, 2012
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Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

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Abstract

A concise and practical enantioselective synthesis of (+)-galbulin has been achieved using organocatalytic domino Michael–Michael–aldol condensation and organocatalytic kinetic resolution as the key steps.

Graphical abstract: Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

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Article information


Submitted
28 Oct 2011
Accepted
29 Nov 2011
First published
01 Dec 2011

Chem. Commun., 2012,48, 2385-2387
Article type
Communication

Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

B. Hong, C. Hsu and G. Lee, Chem. Commun., 2012, 48, 2385
DOI: 10.1039/C2CC16682H

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