Journal of the Chemical Society. Perkin transactions I p. 2677 - 2680 (1990)
Update date:2022-08-22
Topics:
Honda, Toshio
Imai, Minako
Keino, Katsuyuki
Tsubuki, Masayoshi
Enantioselective synthesis of (-)-malyngolide (1) was accomplished by employing diastereoselective addition of nonylmagnesium bromide to the 2-acylfuran derivative (4), followed by a ring transformation of the resulting optically active 2-furylalcohol (5) to give the pyranone derivative (7) as key step.
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