Issue 48, 2010

Enantioselective total synthesis of cytotoxic taiwaniaquinones A and F

Abstract

The first synthesis of cytotoxic (−)-taiwaniaquinone A and (−)-taiwaniaquinone F has been achieved through the intramolecular aldol condensation of a ketoaldehyde and the oxidative cleavage of an isopropylidene ketal.

Graphical abstract: Enantioselective total synthesis of cytotoxic taiwaniaquinones A and F

Supplementary files

Article information

Article type
Communication
Submitted
09 Sep 2010
Accepted
08 Oct 2010
First published
01 Nov 2010

Chem. Commun., 2010,46, 9244-9246

Enantioselective total synthesis of cytotoxic taiwaniaquinones A and F

E. Alvarez-Manzaneda, R. Chahboun, E. Alvarez, R. Tapia and R. Alvarez-Manzaneda, Chem. Commun., 2010, 46, 9244 DOI: 10.1039/C0CC03763J

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