Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent


Autoria(s): Lv GH; Jin RH; Mai WP; Gao LX
Data(s)

2008

Resumo

A series Of pyrrolidine-triazole based dendritic catalysts have been synthesized and applied directly in the asymmetric Michael addition of ketones to nitroolefins without the use of an organic solvent. Good yields (up to 99%), and high diastereoselectivities (up to syn/anti = 45:1) and enantioselectivities (up to 95% ee) have been obtained. Furthermore. the third generation catalyst can be reused at least five times without significant loss of catalytic activity. (C) 2008 Elsevier Ltd. All rights reserved.

Identificador

http://ir.ciac.jl.cn/handle/322003/10785

http://www.irgrid.ac.cn/handle/1471x/147635

Idioma(s)

英语

Fonte

Lv GH;Jin RH;Mai WP;Gao LX.Highly efficient and recoverable dendritic organocatalyst from click chemistry for the asymmetric michael addition of ketones to nitroolefins without the use of organic solvent,TETRAHEDRON-ASYMMETRY,2008,19(22):2568-2572

Palavras-Chave #CHIRAL IONIC LIQUID #DIELS-ALDER REACTIONS #ALDOL REACTION #RECYCLABLE ORGANOCATALYST #SUPPORTED ORGANOCATALYST #L-PROLINE #PYRROLIDINE SULFONAMIDE #ENANTIOSELECTIVE ALDOL #WATER #ALDEHYDES
Tipo

期刊论文