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One-Step Trimethylstannylation of Benzyl and Alkyl Halides.
Jiang, Jianbing; Crabtree, Robert H; Brudvig, Gary W.
Afiliação
  • Jiang J; Department of Chemistry, Yale University , New Haven, Connecticut 06520, United States.
  • Crabtree RH; Energy Sciences Institute, Yale University , West Haven, Connecticut 06516, United States.
  • Brudvig GW; Department of Chemistry, Yale University , New Haven, Connecticut 06520, United States.
J Org Chem ; 81(19): 9483-9488, 2016 10 07.
Article em En | MEDLINE | ID: mdl-27643532
ABSTRACT
Trialkylstannanes are good leaving groups that have been used for the formation of carbon-metal bonds to electrode surfaces for analyses of single-molecule conductivity. Here, we report the multistep synthesis of two amide-containing compounds that are of interest in studies of molecular rectifiers. Each molecule has two trimethylstannyl units, one linked by a methylene and the other by an ethylene group. To account for the very different reactivities of the parent halides, a new methodology for one-step trimethylstannylation was developed and optimized.
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article