First chemoenzymatic synthesis of organoselenium amines and amides


Autoria(s): ANDRADE, Leandro H.; SILVA, Alexandre V.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

A series of organoselenium amines have been synthesized and submitted to the enzymatic kinetic resolution by acetylation mediated by CAL-B (Novozym 435) to give the corresponding chiral amides in an enantiomerically pure form. After evaluating the appropriate lipase, solvent, temperature,and lipase/substrate ratio in the kinetic resolution, the chiral organoselenium amides were obtained with enantiomeric excess of up to 99%. (C) 2008 Elsevier Ltd. All rights reserved.

Identificador

TETRAHEDRON-ASYMMETRY, v.19, n.10, p.1175-1181, 2008

0957-4166

http://producao.usp.br/handle/BDPI/31300

10.1016/j.tetasy.2008.04.026

http://dx.doi.org/10.1016/j.tetasy.2008.04.026

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Tetrahedron-asymmetry

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #ASYMMETRIC ALLYLIC ALKYLATION #ENANTIOSELECTIVE SYNTHESIS #ENZYMATIC RESOLUTION #DERIVATIVES #LIGANDS #LIPASE #DISELENIDES #COMPLEXES #REAGENTS #CELLS #Chemistry, Inorganic & Nuclear #Chemistry, Organic #Chemistry, Physical
Tipo

article

original article

publishedVersion