Nucleophilic addition of potassium organotrifluoroborates to chiral cyclic N-acyliminium ions: stereoselective synthesis of functionalized N-heterocycles


Autoria(s): VIEIRA, Adriano S.; FERREIRA, Fernando P.; FIORANTE, Pedro F.; GUADAGNIN, Rafael C.; STEFANI, Helia A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

The stereoselective nucleophilic addition of potassium aryl- and alkynyltrifluoroborates to cyclic N-acyliminium ion derivatives from N-benzyl-3,4,5-triacetoxy-2-pyrrolidinone, affording the respective 5-substituted 2-pyrrolidinone is described. The products were obtained in moderate to good yields and with preference for the syn diastereomer. (C) 2008 Elsevier Ltd. All rights reserved.

Identificador

TETRAHEDRON, v.64, n.15, p.3306-3314, 2008

0040-4020

http://producao.usp.br/handle/BDPI/19723

10.1016/j.tet.2008.02.006

http://dx.doi.org/10.1016/j.tet.2008.02.006

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Tetrahedron

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #ALPHA-METHOXY AMIDES #COMPLEX-CATALYZED ALLYLATION #ASYMMETRIC-SYNTHESIS #ELECTROORGANIC CHEMISTRY #SUBSTITUTION-REACTIONS #COUPLING REACTIONS #3,4-DIHYDROXYGLUTAMIC ACIDS #STEREOCONTROLLED SYNTHESIS #PYRROLIDINE DERIVATIVES #ORGANOCOPPER REAGENTS #Chemistry, Organic
Tipo

article

original article

publishedVersion