Stereoselective total synthesis of (-)-colletol by Prins cyclisation

Yadav, Jhillu S. ; Mallikarjuna Reddy, N. ; Adi Narayana Reddy, P. ; Ather, Hissana ; Prasad, Attaluri R. (2010) Stereoselective total synthesis of (-)-colletol by Prins cyclisation Synthesis, 2010 (9). pp. 1473-1478. ISSN 0039-7881

Full text not available from this repository.

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

Related URL: http://dx.doi.org/10.1055/s-0029-1218679

Abstract

A simple and efficient asymmetric total synthesis of the bis-macrolactone (-)-colletol was accomplished, proving the versatility of the Prins cyclisation in natural product synthesis. The synthesis mainly relies upon reductive opening of a pyran ring, Mitsunobu inversion, the Wittig reaction, and Yamaguchi macrolactonisation as the key steps.

Item Type:Article
Source:Copyright of this article belongs to Thieme Medical Publishers.
Keywords:Natural Products; Prins Cyclization; Mitsunobu Reaction; Macrolactonization; Lactones
ID Code:63115
Deposited On:28 Sep 2011 03:46
Last Modified:28 Sep 2011 03:46

Repository Staff Only: item control page