6265-58-3Relevant academic research and scientific papers
Syntheses of 2-aryl benzothiazoles via photocatalyzed oxidative condensation of amines with 2-aminothiophenol in the presence of bodipy derivatives
Zhou, Zeyin,Yang, Weijun
supporting information, p. 3189 - 3198 (2015/10/06)
A simple, convenient, and efficient new method for synthesis of 2-aryl benzothiazoles under mild conditions with nonmetal catalyst has been developed. Boron-dipyrromethene (BODIPY) dyes were used as photocatalysts for aerobic oxidative reactions of amine with 2-aminothiophenol. The approach will be very useful for the synthesis of benzothiazole derivatives and the development of photocatalytic reactions.
Synthesis of 2-substituted benzothiazoles from 1-iodo-2-nitrobenzenes by a copper-catalyzed one-pot three-component reaction
Liu, Jidan,Gui, Qingwen,Yang, Zhiyong,Tan, Ze,Guo, Ruqing,Shi, Ji-Cheng
, p. 943 - 951 (2013/05/08)
A novel method was developed for synthesizing 2-substituted 1,3-benzothiazoles through a copper-catalyzed, one-pot, three-component reaction of a 1-iodo-2-nitrobenzene with sodium sulfide and an aldehyde. Georg Thieme Verlag Stuttgart - New York.
Synthesis of 2-aryl benzothiazoles via K2S2O 8-mediated oxidative condensation of benzothiazoles with aryl aldehydes
Yang, Zhiyong,Chen, Xiang,Wang, Sizhuo,Liu, Jidan,Xie, Kai,Wang, Anwei,Tan, Ze
experimental part, p. 7086 - 7091 (2012/10/18)
Nontransition metal-catalyzed synthesis of 2-aryl benzothiazoles was achieved through K2S2O8-mediated oxidative condensation of benzothiazoles with aryl aldehydes. The same transformation can also be effected when the aryl
Solid phase combinatorial synthesis of benzothiazoles and evaluation of topoisomerase II inhibitory activity
Choi, Suk-June,Park, Hyen Joo,Lee, Sang Kook,Kim, Sang Woong,Han, Gyoonhee,Choo, Hea-Young Park
, p. 1229 - 1235 (2007/10/03)
To investigate one possible mechanism of action of the cytotoxic activity of benzothiazoles, we synthesized 2-(substituted-phenyl)benzothiazoles and evaluated their ability to inhibit topoisomerase II activities. Solid phase combinatorial method using tri
Control of acarids using certain benzothiazoles or benzothiazolines
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, (2008/06/13)
Compounds having either of the structures SPC1 Have strong acaricidal activity, in which R is a phenyl or naphthyl group, or phenyl with certain designated substitution. Thus, mites may be controlled on such crops as cotton by applying such compounds as 2-(1-naphthyl)benzothiazoline or 2-(5-t-butyl-2-hydroxyphenyl)benzothiazole.
