Journal of the Chemical Society. Chemical communications p. 1310 - 1311 (1990)
Update date:2022-09-26
Topics:
Takanami, Toshikatsu
Abe, Akie
Suda, Kohji
Ohmori, Hidenobu
Electrochemical oxidation of triphenylphosphine in the presence of cyclic enol silyl ethers or enol esters gave 2-oxocycloalkyltriphenylphosphonium salts, which underwent the Wittig reaction with aldehydes to afford (E)-2-alkylidenecycloalkan-1-ones.
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Doi:10.1021/cm201424a
(2011)Doi:10.1016/S0040-4039(00)97094-1
(1990)Doi:10.1016/0223-5234(91)90129-B
(1991)Doi:10.1021/ja00180a081
(1990)Doi:10.1021/acs.orglett.0c00529
(2020)Doi:10.3987/COM-90-5563
(1990)
