An efficient homogeneous catalytic enantioselective synthesis of α-amino acid derivatives

Autor:	Francisca Delgado, Martin J. O'Donnell, Reinhard Schwesinger, Curt Hostettler
Rok vydání:	1998
Předmět:	chemistry.chemical_classification organic chemicals Organic Chemistry Imine Enantioselective synthesis Alkylation Biochemistry Catalysis Amino acid chemistry.chemical_compound chemistry Drug Discovery Benzophenone Organic chemistry heterocyclic compounds Alkyl Phosphazene
Zdroj:	Tetrahedron Letters. 39:8775-8778
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(98)01995-9
Popis:	The catalytic enantioselective alkylation of the benzophenone imine of glycine t-butyl ester is realized by an efficient homogeneous reaction with alkyl halides, the neutral, non-ionic phosphazene base (BEMP or BTPP), and chiral quaternary ammonium salts derived from thecinchona alkaloids.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::77e270c29b0660315fa8316b6951c58b https://doi.org/10.1016/s0040-4039(98)01995-9 Zobrazit plný text záznamu Full Text from ScienceDirect