Issue 12, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Chemistry of zamoranic acid. Part 10. Homochiral hemisynthesis of pereniporin A

Julio G. Urones,   David Díez,   Patricio M. Gómez,   Isidro S. Marcos,   Pilar Basabe  and  Rosalina F. Moro  

Abstract

The synthetic versatility of 12-acetoxydrima-7,9(11)-diene 1 obtained from 15-hydroxylabda-7,13-dien-17-oic acid (zamoranic acid), as a key intermediate in the homochiral semisynthesis of highly functionalized drimanes such as pereniporin A 3, an important antibiotic, through the carbonate 2, is highlighted.

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Article information

DOI
https://doi.org/10.1039/A700377C
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 1815-1818

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Chemistry of zamoranic acid. Part 10. Homochiral hemisynthesis of pereniporin A

J. G. Urones, D. Díez, P. M. Gómez, I. S. Marcos, P. Basabe and R. F. Moro, J. Chem. Soc., Perkin Trans. 1, 1997, 1815 DOI: 10.1039/A700377C

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