Haughan, Alan F. and Sweeney, Joseph B. (1994) Diastereospecific hydroxyselenation of cyclohex-2-enyl phenylglycinates. Tetrahedron: Asymmetry, 5 (2). pp. 177-180. ISSN 0957-4166Metadata 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.
|Subjects:||Q Science > QD Chemistry|
|Schools:||School of Applied Sciences|
|Depositing User:||Joseph Sweeney|
|Date Deposited:||17 Oct 2012 12:58|
|Last Modified:||17 Oct 2012 12:58|
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