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The stereochemistry of the Grignard reaction of steroidal 4,5-epoxy-3-ketones
Authors:Uyanik Cavit  Malay Aslihan  Ayna Azra S  Hanson James R  Hitchcock Peter B
Institution:Department of Chemistry, Kocaeli University, Izmit 41300, Kocaeli, Turkey. cuyanik@kou.edu.tr
Abstract:The stereochemistry of the addition of methylmagnesium bromide to a steroidal 4,5-epoxy-3-ketone has been shown to be determined by the stereochemistry of the epoxide. The epoxidation to the corresponding 3-alkyl-3-hydroxy-4-enes by per-acid was determined by the stereochemistry of the allylic alcohol.
Keywords:Grignard reagents  Per-acid  Steroids  Epoxides  Enes  Crystal structure
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