Journal of the Chemical Society. Chemical communications p. 1452 - 1454 (1985)
Update date:2022-08-04
Topics:
Ibuka, Toshiro
Aoyagi, Takeshi
Yoneda, Fumio
Reaction of γ-acetoxy-α,β-enoates with lithium dibutylcuprate followed by alkyl halides results in the predominant or exclusive formation of α-alkyl-β,γ-enoates in high yields under mild conditions; a synthetic route to (+/-)-α-vetispirene is also present
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