Stereoselective routes for the total synthesis of (+)-cryptocarya diacetate

Sabitha, Gowravaram ; Reddy, Nandyala M. ; Prasad, Muddala N. ; Yadav, Jhillu S. (2009) Stereoselective routes for the total synthesis of (+)-cryptocarya diacetate Helvetica Chimica Acta, 92 (5). pp. 967-976. ISSN 0018-019X

Full text not available from this repository.

Official URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.20...

Related URL: http://dx.doi.org/10.1002/hlca.200800355

Abstract

A stereoselective total synthesis of (+)-cryptocarya diacetate (1) was achieved by two different routes (Schemes 2 and 3). The sequences involve LiAlH4/LiI reduction, ring-closing metathesis, Prins cyclization, Wacker oxidation, and Wittig olefination reactions as key steps.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Stereoselective Synthesis; Cryptocarya Diacetate; Prins Cyclization; Wacker Oxidation; Wittig Olefination
ID Code:62955
Deposited On:24 Sep 2011 05:00
Last Modified:24 Sep 2011 05:00

Repository Staff Only: item control page