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Wiley-VCH Verlag, ChemInform, 52(38), 2007

DOI: 10.1002/chin.200752182

Bentham Science Publishers, Letters in Organic Chemistry, 4(4), p. 232-233

DOI: 10.2174/157017807781024237

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Stereoselective Synthesis of the Core of Naturally Occurring Anti-HIV Isolitseane B

Journal article published in 2007 by Bentham Science Publisher Paul Bremond, Bentham Science Publisher Yoann Coquerel, Bentham Science Publisher Paul Brémond, Bentham Science Publisher Elodie Girardeau, Elodie Girardeau, Jean Rodriguez, Bentham Science Publisher Yoann Coquerel ORCID, Bentham Science Publisher Jean Rodriguez
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

A key intermediate in the total synthesis of naturally occurring anti-HIV Isolitseane B has been prepared in five steps from propargyl alcohol, featuring a highly selective mono-transacetalization and a stereoselective Pauson-Khand cyclization.