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Enantioselective Formal Synthesis of Palmerolide A

Prasad, Kavirayani R and Pawar, Amit B (2011) Enantioselective Formal Synthesis of Palmerolide A. In: Organic Letters, 13 (16). pp. 4252-4255.

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Abstract

Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product, is described. Key strategies in the synthesis include the oxidative furan ring-opening of a chiral furyl carbinol for the installation of the 1,4-dienol core and a Jung nonaldol-aldol reaction for the dienamide core.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to American Chemical Society.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 15 Sep 2011 10:55
Last Modified: 15 Sep 2011 10:55
URI: http://eprints.iisc.ernet.in/id/eprint/40447

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