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Transition-Metal-Free Regiospecific Aroylation of Nitroarenes Using Ethyl Arylacetates at Room Temperature.
Kumar, Promod; Sharma, Anup Kumar; Guntreddi, Tirumaleswararao; Singh, Rahul; Singh, Krishna Nand.
Afiliação
  • Kumar P; Department of Chemistry (Centre of Advanced Study), Institute of Science, Banaras Hindu University , Varanasi-221005, India.
  • Sharma AK; Department of Chemistry (Centre of Advanced Study), Institute of Science, Banaras Hindu University , Varanasi-221005, India.
  • Guntreddi T; Department of Chemistry (Centre of Advanced Study), Institute of Science, Banaras Hindu University , Varanasi-221005, India.
  • Singh R; Department of Chemistry (Centre of Advanced Study), Institute of Science, Banaras Hindu University , Varanasi-221005, India.
  • Singh KN; Department of Chemistry (Centre of Advanced Study), Institute of Science, Banaras Hindu University , Varanasi-221005, India.
Org Lett ; 20(3): 744-747, 2018 02 02.
Article em En | MEDLINE | ID: mdl-29345475
A novel regiospecific C(sp3)-C(sp2) coupling between ethyl arylacetates and nitroarenes has been developed to deliver biaryl ketones in excellent yields. The protocol is metal-free, mild, and compatible with a number of functional groups on both of the reacting partners.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Índia