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.
Keywords: Acetal, Pauson-Khand, anti-HIV, total synthesis, natural products
Letters in Organic Chemistry
Title: Stereoselective Synthesis of the Core of Naturally Occurring Anti-HIV Isolitseane B
Volume: 4 Issue: 4
Author(s): Paul Bremond, Elodie Girardeau, Yoann Coquerel and Jean Rodriguez
Affiliation:
Keywords: Acetal, Pauson-Khand, anti-HIV, total synthesis, natural products
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.
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Cite this article as:
Paul Bremond , Elodie Girardeau , Yoann Coquerel and Jean Rodriguez , Stereoselective Synthesis of the Core of Naturally Occurring Anti-HIV Isolitseane B, Letters in Organic Chemistry 2007; 4 (4) . https://dx.doi.org/10.2174/157017807781024237
DOI https://dx.doi.org/10.2174/157017807781024237 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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