154558-92-6Relevant articles and documents
Metal-Free Synthesis of 2-Arylbenzothiazoles from Aldehydes, Amines, and Thiocyanate
Dey, Amrita,Hajra, Alakananda
supporting information, p. 1686 - 1689 (2019/03/11)
A highly efficient method for the synthesis of 2-arylbenzothiazoles has been developed using readily available aromatic amines, benzaldehydes, and NH4SCN as a sulfur source. A library of 2-arylbenzothiazoles with wide functional group compatibility has been synthesized in good yields through iodine-mediated oxidative annulation.
Synthesis, anticancer activity and docking of some substituted benzothiazoles as tyrosine kinase inhibitors
Bhuva, Hemal A.,Kini, Suvarna G.
experimental part, p. 32 - 37 (2011/10/09)
Protein tyrosine kinases occupy a central position in the control of cellular proliferation and its inactivation might lead to the discovery of a new generation anticancer compounds. Substituted benzothiazoles have been found to mimic the ATP-competitive
3-H-1,2,3-Benzodithiazole-2-oxides as synthons for the synthesis of five- and six-membered heterocycles containing sulphur and nitrogen
Sawhney, S N,Sharma, P. K.,Bajaj, K,Gupta, A
, p. 280 - 284 (2007/10/02)
The reaction of 6-substituted-1,2,3-benzodithiazole-2-oxides (2) with aromatic aldehydes, carboxylic acids and acid chlorides in the presence of an organic base such as triethylamine and N,N-dimethylaniline lead to the formation of 6-substituted-2-arylben
