Stereoselective formal synthesis of (-)-salicylihalamides A and B via prins cyclisation

Yadav, J. S. ; Venkateswar Rao, N. ; Puroshothama Rao, P. ; Sridhar Reddy, M. ; Preasad, A. R. (2010) Stereoselective formal synthesis of (-)-salicylihalamides A and B via prins cyclisation Letters in Organic Chemistry, 7 (6). pp. 457-460. ISSN 1570-1786

Full text not available from this repository.

Official URL: http://www.ingentaconnect.com/content/ben/loc/2010...

Related URL: http://dx.doi.org/10.2174/157017810791824856

Abstract

A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our recently developed strategy for the construction of polyketide precursors via Prins cyclisation. The approach mainly relies upon reductive opening of 1-iodomethyl cyclic ethers, Mitsunobu inversion and ring closing metathesis along with Prins cyclisation.

Item Type:Article
Source:Copyright of this article belongs to Bentham Science Publishers.
ID Code:63144
Deposited On:28 Sep 2011 03:49
Last Modified:28 Sep 2011 03:49

Repository Staff Only: item control page