932-85-4Relevant articles and documents
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Fife
, p. 271 (1965)
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The complete stereochemistry of the enzymatic dehydration of 4-hydroxybutyryl coenzyme A to crotonyl coenzyme A
Friedrich, Peter,Darley, Daniel J.,Golding, Bernard T.,Buckel, Wolfgang
, p. 3254 - 3257 (2008/12/23)
(Chemical Equation Presented) The stereospecific action of the microbial enzyme 4-hydroxybutyryl-CoA dehydratase on the three prochiral centers of its substrate 4-hydroxybutyryl-CoA can now be described as anti elimination of the 2Re and 3Si hydrogen atoms with retention of configuration during the substitution of the hydroxy group by a hydrogen atom. The results confirm the relationship of the dehydratase to acyl-CoA dehydrogenases and the view that the Fe4S4 cluster acts as a Lewis acid.
THE TRANSFORMATION OF ALKENES INTO γ-LACTONES USING α-IODOESTERS
Kraus, George A.,Landgrebe, Kevin
, p. 3939 - 3942 (2007/10/02)
Iodostannyl esters react with alkenes in the presence of AIBN to afford γ-lactones.