Literature DB >> 20307053

Formation of unsymmetrical 1,4-enediones via a focusing domino strategy: cross-coupling of 1,3-dicarbonyl compounds and methyl ketones or terminal aryl alkenes.

Meng Gao1, Yan Yang, Yan-Dong Wu, Cong Deng, Li-Ping Cao, Xiang-Gao Meng, An-Xin Wu.   

Abstract

A highly efficient synthesis of unsymmetrical 1,4-enediones from 1,3-dicarbonyl compounds and methyl ketones or terminal aryl alkenes has been developed via a focusing domino strategy. Simple and readily available starting materials, mild reaction conditions, and a very simple operation are advantages of the reaction, which allow straightforward synthesis of a variety of unsymmetrical 1,4-enediones.

Entities:  

Year:  2010        PMID: 20307053     DOI: 10.1021/ol100473f

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


  2 in total

1.  Isolation and Synthesis of Novel Meroterpenoids from Rhodomyrtus tomentosa: Investigation of a Reactive Enetrione Intermediate.

Authors:  Xu-Jie Qin; Tyler J Rauwolf; Pan-Pan Li; Hui Liu; James McNeely; Yan Hua; Hai-Yang Liu; John A Porco
Journal:  Angew Chem Int Ed Engl       Date:  2019-02-20       Impact factor: 15.336

2.  (E)-Ethyl 2-benzoyl-4-(naphthalen-2-yl)-4-oxobut-2-enoate.

Authors:  Liuming Wu; Cong Deng; Yan Yang
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-05-25
  2 in total

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