Synthetic studies on a marine natural product, palmerolide A: synthesis of C1-C9 and C15-C21 fragments

Kaliappan, Krishna P. ; Gowrisankar, Parthasarathy (2007) Synthetic studies on a marine natural product, palmerolide A: synthesis of C1-C9 and C15-C21 fragments Synlett, 2007 (10). pp. 1537-1540. ISSN 0936-5214

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Official URL: https://www.thieme-connect.de/products/ejournals/a...

Related URL: http://dx.doi.org/10.1055/s-2007-982539

Abstract

An efficient cross metathesis and Pd-catalyzed allylic rearrangement have been successfully used to construct the northern hemisphere of a cytotoxic marine natural product, palmerolide A.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers Inc.
Keywords:Grubbs’ Catalyst; Cross Metathesis; Pd(II)-Catalyzed; Allylic Rearrangement; Marine Natural Product; Mitsunobu Reaction
ID Code:104962
Deposited On:23 May 2017 05:27
Last Modified:23 May 2017 05:27

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