A novel preparation of chiral (Z[hair space])-O-alkyl enol ethers from alkenylselenonium salts

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Shin-ichi Watanabe, Keiichirou Yamamoto, Yukiko Itagaki and Tadashi Kataoka


Abstract

The reactions of alkenylselenonium salts with chiral secondary alkoxides afforded chiral (Z[hair space])-O-alkyl enol ethers in good yields and, especially in the case of sterically hindered secondary cyclic alcohols, the best results were obtained from reactions of dimethylalkenylselenonium salt 7b with alkoxides prepared from PhLi and the corresponding alcohols in THF at –78 °C.


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