Efficient synthesis of selenol esters from acid chlorides mediated by indium metal
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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Resumo |
This article describes an efficient and easy one-pot route for the synthesis of a wide range of selenol esters from acyl chloride with diselenides in the presence of indium metal. A variety of functional groups can be tolerated within the diorgano diselenide and the acyl chloride coupling partner. (C) 2009 Elsevier Ltd. All rights reserved. CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) CNPq FAPESP Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FINEP (Brazil) Financiadora de Estudos e Projetos (FINEP) |
Identificador |
TETRAHEDRON, v.65, n.23, p.4614-4618, 2009 0040-4020 http://producao.usp.br/handle/BDPI/31511 10.1016/j.tet.2009.03.069 |
Idioma(s) |
eng |
Publicador |
PERGAMON-ELSEVIER SCIENCE LTD |
Relação |
Tetrahedron |
Direitos |
restrictedAccess Copyright PERGAMON-ELSEVIER SCIENCE LTD |
Palavras-Chave | #CHIRAL ORGANOSELENIUM COMPOUNDS #ASYMMETRIC ALLYLIC ALKYLATION #LIQUID-CRYSTAL COMPOUNDS #RING-OPENING REACTION #DIORGANYL SELENIDES #ORGANIC-SYNTHESIS #TELLUROL ESTERS #ACYL RADICALS #SELENOCYSTEINE DERIVATIVES #STRAIGHTFORWARD SYNTHESIS #Chemistry, Organic |
Tipo |
article original article publishedVersion |