REGIOSELECTIVE OPENING OF 3-SUBSTITUTED N-ETHOXYCARBONYL AZIRIDINE-2-CARBOXYLATE WITH METAL-HALIDES TOWARD THE PREPARATION OF ALPHA-AMINO AND BETA-AMINO ACIDS

Authors
RIGHI G DACHILLE R BONINI C
Citation
G. Righi et al., REGIOSELECTIVE OPENING OF 3-SUBSTITUTED N-ETHOXYCARBONYL AZIRIDINE-2-CARBOXYLATE WITH METAL-HALIDES TOWARD THE PREPARATION OF ALPHA-AMINO AND BETA-AMINO ACIDS, Tetrahedron letters, 37(38), 1996, pp. 6893-6896
Citations number
16
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
37
Issue
38
Year of publication
1996
Pages
6893 - 6896
Database
ISI
SICI code
0040-4039(1996)37:38<6893:ROO3NA>2.0.ZU;2-N
Abstract
3-Substituted N-Ethoxy carbonyl aziridine-2-carboxylates are opened in a regio and stereoselective fashion whether in C-2 position by NaX (X = I, Br) or in C-B by MgBr2. Copyright (C) 1996 Published by Elsevier Science Ltd