One-step synthesis of optically active benzyl N-trityl-L-aziridine-2-carboxylic esters

Tetrahedron Letters

Volumn 33, Issue 21, 1992, Pages 3013-3016

  Kuyl Yeheskiely, E ^a   Lodder, M ^a   van der Marel, G A ^a   van Boom, J H ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; SYNTHESIS;

EID: 0026650692     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)79586-4     Document Type: Article

References (18)

1. An expeditious in situ preparation of benzyl (S)-2-aziridinecarboxylate
2. Perkin communications. Asymmetric amino acid synthesis: preparation of the ? anion derived from aspartic acid
3. A model study directed towards the preparation of nucleopeptidesviaH-phosphonate intermediates
4. Studies on Aziridine-2-carboxylic Acid. I. Synthesis of the Optically Active L-Aziridine-2-carboxylic Acid and Its Derivatives
5. Synthesis of threo-3-methylcysteine from threonine.
6. STUDIES ON HYDROXY AMINO ACIDS V. SYNTHESIS AND N-ACYLATION OF 3-METHYL-L-AZYLYLGLYCINE BENZYL ESTER