92192-08-0Relevant academic research and scientific papers
Iron(III) phthalocyanine-chloride-catalyzed synthesis of sulfones from sulfonylhydrazones
Zhao, Jun-Long,Guo, Shi-Huan,Qiu, Jun,Gou, Xiao-Feng,Hua, Cheng-Wen,Chen, Bang
supporting information, p. 2375 - 2378 (2016/05/19)
In this study, sulfones are synthesized from sulfonylhydrazones catalyzed by iron(III) phthalocyanine chloride. This reaction offers broad substrate scope, occurs under mild conditions, utilized readily available reactants, and forms products in good-to-h
Efficient synthesis of 1,5-disubstituted carbohydrazones using K 2CO3 as a carbonyl donor
Wen, Jun,Yang, Chu-Ting,Jiang, Tao,Hu, Sheng,Yang, Tong-Zai,Wang, Xiao-Lin
supporting information, p. 2398 - 2401 (2014/05/20)
A novel reaction that generates 1,5-disubstituted carbohydrazones via the carbonylation of tosylhydrazones has been developed. For the first time, the inexpensive, readily available, environmentally friendly, and nongaseous potassium carbonate is used as
Chemoselective preparation of oximes, semicarbazones, and tosylhydrazones without catalyst and solvent
Bandgar, Babasaheb P.,Sadavarte, Vaibhav S.,Uppalla, Lav S.,Govande, Rahul
, p. 403 - 406 (2007/10/03)
A simple and versatile method for the synthesis of oximes, semicarbazones, and tosylhydrazones of aldehydes in the presence of ketones without catalyst and solvent is presented.
