1220125-56-3Relevant academic research and scientific papers
An Expedient, Direct, Three-Component Approach for the Synthesis of 4-Thioarylpyrroles
Anandan, Sambandam,Neelamegam, Chinnaraj,Rajeshkumar, Venkatachalam
supporting information, p. 4023 - 4033 (2019/10/28)
A three-component strategy for the synthesis of 4-thioarylpyrroles from 1,4-enediones, thiols, and ammonium formate in one-pot has been developed. The reaction proceeds through the sequential thiol-Michael/Paal-Knorr reaction of 1,4-enediones with the for
Heterogeneous synthesis of 1,4-enediones and 1,4-diketones with manganese oxide molecular sieves OMS-2 as a recyclable catalyst
Meng, Xu,Zhang, Jinqi,Chen, Gexin,Chen, Baohua,Zhao, Peiqing
, p. 239 - 242 (2015/07/27)
An efficient manganese oxide octahedral molecular sieves OMS-2-catalyzed chemoselective synthesis of 1,4-enediones and 1,4-diketones from 1,3-dicarbonyls and α-iodoacetophenones is described. The present catalytic system can be applied in one-pot, three-c
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
Gao, Meng,Yang, Yan,Wu, Yan-Dong,Deng, Cong,Cao, Li-Ping,Meng, Xiang-Gao,Wu, An-Xin
supporting information; experimental part, p. 1856 - 1859 (2010/10/03)
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.
