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Reactivity of a-Oxophosphonium Ylides: A Contribution to the Mechanistics

Melo, Teresa M. Pinho e; Gonsalves, António M. d'A. Rocha; Carrapato, Sara M.; Taborda, Ana M.

Ylides 1f and 1g react with chlorine, with bromine and with N-chlorosuccinimide in the presence of a range of nucleophiles. The 2,3-disubstitutedbutenedioates obtained in this way allow us to gather more information about the mechanism involved. Ylide 1c was also studied showing similar reactivity and leading to the highly selective synthesis of 2,3- disubstituted-3-phenylpropenoates


Intramolecular Cycloaddition of Imines of Cysteine Derivatives

Cabral, Ana M. T. D. P. V.; Gonsalves, António M. d'A. Rocha; Melo, Teresa M. Pinho e

Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield


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Fundação para a Ciência e a Tecnologia Universidade do Minho   Governo Português Ministério da Educação e Ciência Programa Operacional da Sociedade do Conhecimento União Europeia