Synthesis of alpha,beta-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides

Stefani, Helio A.; Pena, Jesus M.; Gueogjian, Kemilla; Petragnani, Nicola; Vaz, Boniek G.; Eberlin, Marcos N.

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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Synthesis of alpha,beta-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides

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Author(s):	Stefani, Helio A. ^{[1, 2]} ; Pena, Jesus M. ^[2] ; Gueogjian, Kemilla ^[2] ; Petragnani, Nicola ^[3] ; Vaz, Boniek G. ^[4] ; Eberlin, Marcos N. ^[4] Total Authors: 6
Affiliation:	^[1] Univ Fed Sao Paulo, Dept Biofis, Sao Paulo - Brazil ^[2] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo - Brazil ^[3] Univ Sao Paulo, Inst Quim, Sao Paulo - Brazil ^[4] Univ Estadual Campinas, Inst Quim, Lab ThoMSon Espectrometria Massas, BR-13084971 Campinas, SP - Brazil Total Affiliations: 4
Document type:	Journal article
Source:	Tetrahedron Letters; v. 50, n. 40, p. 5589-5595, OCT 7 2009.
Web of Science Citations:	13
Abstract
A variety of alpha,beta-unsaturated aryl esters were prepared by the direct reaction of unsymmetrical aryltellurides and ethyl acrylate, catalyzed by PdCl(2) via a Heck cross-coupling reaction. (C) 2009 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process:	03/09931-5 - Development and study of functional and structured materials: a view from complexity
Grantee:	Marcos Nogueira Eberlin
Support Opportunities:	PRONEX Research - Thematic Grants

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