Chemistry Letters p. 163 - 166 (1980)
Update date:2022-08-04
Topics:
Takeda, Takeshi
Mukaiyama, Teruaki
An asymmetric total synthesis of indolmycin was achieved via a key intermediate, α-indolmycenic acid ester.The ester was obtained by oxygenation of methyl (S)-3-(3-indolyl)butanoate which was prepared by asymmetric synthesis utilizing (2R,3S)-3,4-dimethyl
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Doi:10.1248/cpb.28.1403
(1980)Doi:10.1016/S0008-6215(00)85378-1
(1980)Doi:10.1021/om2002238
(2011)Doi:10.1021/ja01863a076
(1940)Doi:10.1016/S0008-6215(00)84689-3
(1981)Doi:10.1021/jo01310a062
(1980)
