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.

	PDF Enantioselective.pdf - Published Version Restricted to Registered users only Download (837kB) | Request a copy
	PDF Supporting_information.pdf - Published Supplemental Material Restricted to Registered users only Download (5MB) | Request a copy

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
Publication:	Organic Letters
Publisher:	American Chemical Society
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.ac.in/id/eprint/40447

Actions (login required)

View Item