Literature DB >> 21877737

Tandem reactions of 1,2-allenic ketones leading to substituted benzenes and α,β-unsaturated nitriles.

Xinying Zhang1, Xuefei Jia, Liangliang Fang, Nan Liu, Jianji Wang, Xuesen Fan.   

Abstract

One-pot double Michael addition/intramolecular aldol reaction/decarboxylation of 1,2-allenic ketones with cyanoacetate offers an efficient and convenient approach to highly functionalized benzenes. With 2-substituted cyanoacetates, the reaction proceeds via a different tandem process to afford α,β-unsaturated nitriles effectively.
© 2011 American Chemical Society

Entities:  

Year:  2011        PMID: 21877737     DOI: 10.1021/ol201789z

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  3-(4-Chloro-benzo-yl)-6-(4-chloro-phen-yl)-2,4-dimethyl-benzonitrile.

Authors:  Xin Wang; Yi-Min Zhang; Xue-Fei Jia
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-08-25

2.  5,6-Dimethyl-4-phenyl-2H-pyran-2-one.

Authors:  Hai-Yun Xu; Sheng-Hai Guo; Kun Li; Xue-Sen Fan
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-03-21
  2 in total

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