Autor(es):
Gilchrist, Thomas L. 
; Lemos, A.
Data: 1993
Identificador Persistente: http://hdl.handle.net/10400.1/936
Origem: Sapientia - Universidade do Algarve
Assunto(s): Diels-Alder; Heterocycles; azoalkene
Detalhes do Documento
Reaction of pyrroles with ethyl 2-nitroso- and 2-azo-propenoates, and with ethy...
Descrição
The reaction of ethyl 2-nitrosopropenoate 2a with 1 -methylpyrrole, 2.5-dimethylpyrrole and 2.5- diphenylpyrrole has been investigated. In every case the products result from highly regioselective attack at C-2 of the pyrrole by the electrophile. The azopropenoate esters 2b and 2c react similarly with pyrroles, to the extent that even 1 -(triisopropylsilyl)pyrrole is attacked exclusively at the 2-position by the azo ester 2b. In contrast, the nitrile oxide ethyl cyanoformate N-oxide 12 reacts at the 3-position of 2.5- dimethyl- and of 2,5-diphenyl-pyrrole. The reactions of the nitroso and azo esters with pyrroles are interpreted as Diels-Alder cycloadditions with inverse electron demand.
The reaction of ethyl 2-nitrosopropenoate 2a with 1 -methylpyrrole, 2.5-dimethylpyrrole and 2.5- diphenylpyrrole has been investigated. In every case the products result from highly regioselective attack at C-2 of the pyrrole by the electrophile. The azopropenoate esters 2b and 2c react similarly with pyrroles, to the extent that even 1 -(triisopropylsilyl)pyrrole is attacked exclusively at the 2-position by the azo ester 2b. In contrast, the nitrile oxide ethyl cyanoformate N-oxide 12 reacts at the 3-position of 2.5- dimethyl- and of 2,5-diphenyl-pyrrole. The reactions of the nitroso and azo esters with pyrroles are interpreted as Diels-Alder cycloadditions with inverse electron demand.
Tipo de Documento
Artigo
Idioma Inglês
Idioma Inglês
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