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Cu(II)-Catalyzed 6π-Photocyclization of Dienynes.
Jin, Ruiwen; Chen, Jinjin; Chen, Yiyong; Liu, Wangsheng; Xu, Dawen; Li, Yawei; Ding, Aishun; Guo, Hao.
Afiliação
  • Jin R; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Chen J; Department of Child Health Care, Shanghai Children's Hospital Affiliated to Shanghai Jiao Tong University , 1400 Beijing Xi Road, Shanghai 200040, P. R. China.
  • Chen Y; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Liu W; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Xu D; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Li Y; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Ding A; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
  • Guo H; Department of Chemistry, Fudan University , 220 Handan Road, Shanghai 200433, P. R. China.
J Org Chem ; 81(24): 12553-12558, 2016 12 16.
Article em En | MEDLINE | ID: mdl-27978759
ABSTRACT
The first 6π-photocyclization of dienynes was developed, which provides a new and effective protocol for the synthesis of the phenyl ring in excellent yields with nice functional group tolerance. In this transformation, the Cu(OTf)2 catalyst plays a key role in the conversion of alkyne moiety into an alkene-type moiety, which means that the dienyne reactant is converted into a triene-type substrate. Thus, this reaction proceeds via a Cu(II)-catalyzed 6π-photocyclization of triene-type derivatives.
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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