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