Facile stereoselective synthesis of the C12-C24 fragnent of macrolactin A

Yadav, Jhillu S. ; Gupta, Manoj K. ; Prathap, I. (2007) Facile stereoselective synthesis of the C12-C24 fragnent of macrolactin A Synthesis, 2007 (9). pp. 1343-1348. ISSN 0039-7881

Full text not available from this repository.

Official URL: https://www.thieme-connect.com/ejournals/abstract/...

Related URL: http://dx.doi.org/10.1055/s-2007-966010

Abstract

A simple and efficient stereoselective synthesis of the C12-C24 fragment of the natural product macrolactin-A was achieved from D-glucose as the starting material and with use of the Wittig and modified Julia olefination reactions as key steps.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:D-glucose; Raney Nickel; Wittig Reaction; Modified Julia Olefination
ID Code:63208
Deposited On:28 Sep 2011 03:34
Last Modified:28 Sep 2011 03:34

Repository Staff Only: item control page