First chemoenzymatic synthesis of organoselenium amines and amides
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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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 |
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 |