Computing and Library Services - delivering an inspiring information environment

Diastereospecific hydroxyselenation of cyclohex-2-enyl phenylglycinates

Haughan, Alan F. and Sweeney, Joseph B. (1994) Diastereospecific hydroxyselenation of cyclohex-2-enyl phenylglycinates. Tetrahedron: Asymmetry, 5 (2). pp. 177-180. ISSN 0957-4166

Metadata only available from this repository.


Cyclohex-2-enyl esters of homochiral (R)-Z-phenylglycine undergo completely regio- and diastereospecific addition reactions with N-phenylselenophthalimide. The resulting selenoalcohols are separable by routine chromatography and may be converted into homochiral 1,3-cyclohexonediols in which the hydroxyl groups are differentiated.

Item Type: Article
Subjects: Q Science > QD Chemistry
Schools: School of Applied Sciences
Related URLs:
Depositing User: Joseph Sweeney
Date Deposited: 17 Oct 2012 11:58
Last Modified: 17 Oct 2012 11:58


Downloads per month over past year

Repository Staff Only: item control page

View Item View Item

University of Huddersfield, Queensgate, Huddersfield, HD1 3DH Copyright and Disclaimer All rights reserved ©