Studies on 2-Aziridinecarboxylic Acid. IX. Convenient Synthesis of Optically Active S-Alkylcysteine, threo-S-Alkyl-β-methylcysteine, and Lanthionine Derivatives via the Ring-opening Reaction of Aziridine by Several Thiols

DOI: 10.1246/bcsj.56.520

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Bulletin of the Chemical Society of Japan p. 520 - 522 (1983)

Update date:2022-08-05

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Authors:

Nakajima, Kiichiro

Oda, Hitomi

Okawa, Kenji

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Article abstract of DOI:10.1246/bcsj.56.520

A convenient synthesis of optically active S-alkylcysteine, threo-S-alkyl-β-methylcysteine, and lanthionine derivatives has been investigated.Benzyl 1-benzyloxycarbonyl-(2S)-2-aziridinecarboxylate and benzyl (2S,3S)-1-benzyloxycarbonyl-3-methyl-2-aziridin

Full text of DOI:10.1246/bcsj.56.520

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