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Org Lett ; 12(5): 1012-4, 2010 Mar 05.
Article in English | MEDLINE | ID: mdl-20143842

ABSTRACT

When gamma,delta-epoxy-alpha,beta-unsaturated esters or amides were treated with 2 equiv of Grignard reagents in the presence of 10-24 mol % FeCl(2), regio- and stereoselective substitution of the epoxide moiety with the Grignard reagent occurred to give exclusively delta-hydroxy-gamma-alkyl or aryl-alpha,beta-unsaturated esters or amides in good yields.


Subject(s)
Amides/chemistry , Esters/chemistry , Iron/chemistry , Alcohols/chemistry , Catalysis , Indicators and Reagents/chemistry , Stereoisomerism , Substrate Specificity
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