Title of article
Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita–Baylis–Hillman adducts
Author/Authors
Bruno A. Sousa، نويسنده , , Arthur F. Keppler، نويسنده , , Rogério A. Gariani، نويسنده , , Jo?o V. Comasseto، نويسنده , , Alcindo A. Dos Santos، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
8
From page
10406
To page
10413
Abstract
Chalcogenolate mediated Michael-aldol cascade reactions consists of a very efficient route to multi-functionalized γ-hydroxichalcogenides. Although, when selenolates are employed, these γ-hydroxichalcogenides can be readily converted into the corresponding Morita–Baylis–Hillman adducts by oxidative elimination of the selenium moiety. In this context, herein we present a complete study on the scope and limitations of this reaction.
Keywords
Michael-aldol , cascade reaction , chalcogens , Organometallics , Morita–Baylis–Hillman
Journal title
Tetrahedron
Serial Year
2012
Journal title
Tetrahedron
Record number
1105226
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