Tetrahedron Letters p. 2463 - 2466 (1985)
Update date:2022-07-30
Topics:
Akiba, Kin-ya
Takasu, Yasuhito
Wada, Makoto
Ethyl α-chloro-α-phenylthioacetate reacted with 1-alkenes in CH2Cl2 at -78-0 deg C in the presence of SnCl4 to afford the ene reaction products (80-90percent), which were readily converted into the corresponding γ-butyrolactones.
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