Studies on 2-Aziridinecarboxylic Acid. X. Simple Stereospecific Synthesis of Optically Active Cystine andthreo-3,3′-Dimethylcystine
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/56/5/56_5_1565/_pdf
Reference7 articles.
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4. AZLACTONES
5. Preparation of the enantiomers of threo-and erythro-2-amino-3-mercaptobutyric acid
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1. The regioselectivity of the ring opening of 1-activated or nonactivated 2-alkoxycarbonyl or 2-cyanoaziridines by carbanions of the dicarbonyl compounds;Journal of Heterocyclic Chemistry;2009-03-11
2. Simple and efficient synthesis of allo- and threo-3,3′-dimethylcystine derivatives in enantiomerically pure form;Tetrahedron: Asymmetry;2008-06
3. Versatile and Stereoselective Syntheses of Orthogonally Protected β-Methylcysteine and β-Methyllanthionine;Organic Letters;2005-05-20
4. Triphenylphosphonium salts bearing an l-alanyl substituent: short synthesis and enantiomeric analysis by NMR;Tetrahedron Letters;2001-06
5. Use of (S)-N-tert-butoxycarbonylaziridine-2-carboxylate derivatives for α-amino acid synthesis;Tetrahedron Letters;1996-05
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