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SnCl4-promoted rearrangement of 2,3-epoxy alcohol derivatives: stereochemical control of the reaction
Authors:Yasuyuki Kita  Satoshi Matsuda  Ryoko Inoguchi  Jnaneshwara K. Ganesh  Hiromichi Fujioka
Affiliation:Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka 565-0871, Japan
Abstract:The SnCl4-promoted rearrangement of 2,2,3,3-tetrasubstituted-2,3-epoxy-1-alcohol derivatives proceeded in a regio- and stereo-controlled manner to selectively give two types of rearranged products from a single isomer by changing the protecting group of the alcohol.
Keywords:SnCl4-promoted rearrangement   Tetrasubstituted-2,3-epoxy alcohol   Stereocontrol   α-Alkoxy ketone   β-Hydroxy ketone
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