Issue 35, 2005

A total synthesis of guanacastepene C

Abstract

A total synthesis of the structure corresponding to the novel tricyclic diterpene guanacastepene C has been realized in which a Knoevenagel cyclization serves as a key step to annulate the six-membered C-ring on a stereochemically secured bicyclic hydroazulene precursor.

Graphical abstract: A total synthesis of guanacastepene C

Supplementary files

Article information

Article type
Communication
Submitted
17 May 2005
Accepted
04 Jul 2005
First published
29 Jul 2005

Chem. Commun., 2005, 4456-4458

A total synthesis of guanacastepene C

G. Mehta, K. Pallavi and J. D. Umarye, Chem. Commun., 2005, 4456 DOI: 10.1039/B506931A

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