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Chemoselective Reduction of Trichloromethyl Compounds to gem-Dichloromethyl Groups Following Appel's Reaction Protocol.
Romero-Reyes, Moises A; Zaragoza-Galicia, Ivann; Olivo, Horacio F; Romero-Ortega, Moises.
Afiliação
  • Romero-Reyes MA; Departamento de Quimica Organica, Facultad de Quimica, Universidad Autonoma del Estado de Mexico , Paseo Colon/Paseo Tollocan, Toluca, Estado de Mexico, Mexico.
  • Zaragoza-Galicia I; Departamento de Quimica Organica, Facultad de Quimica, Universidad Autonoma del Estado de Mexico , Paseo Colon/Paseo Tollocan, Toluca, Estado de Mexico, Mexico.
  • Olivo HF; Division of Medicinal and Natural Products Chemistry, The University of Iowa , Iowa City, Iowa 52246, United States.
  • Romero-Ortega M; Departamento de Quimica Organica, Facultad de Quimica, Universidad Autonoma del Estado de Mexico , Paseo Colon/Paseo Tollocan, Toluca, Estado de Mexico, Mexico.
J Org Chem ; 81(19): 9515-9519, 2016 10 07.
Article em En | MEDLINE | ID: mdl-27622837
A simple and easy reduction of trichloroacetyl compounds following the modification of Appel's reaction protocol, using triphenylphosphine and methanol, afforded the corresponding dichloroacetyl compounds, with the exception of trichloroacetylmorpholine, in yields of 80-98% under very mild experimental conditions. Likewise, when trichloromethyl heterocyclic compounds contain another reactive functional group, the reaction is highly chemoselective giving the dichloromethyl derivative.
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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