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The stereospecificity and stereoselectivity of hydrogen transfer in photochemical reactions
Authors:EL Ghisalberti  PR Jefferies  MA Sefton
Institution:Department of Organic Chemistry, University of Western Australia, Nedlands, Western Australia 6009
Abstract:The photolysis of methyl ent-19-acetoxy-3-oxo-beyer-15-en-17-oate (3) occurs with retention of configuration of C-4 to give the 4S-3,4-seco acid. In the phototransformation of 3-ketobeyeranes to 3,4-seco acids the C-2 axial hydrogen is transferred preferentially to C-4.
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