1123636-91-8Relevant academic research and scientific papers
Intramolecular cascade C-S bond formation: Regioselective synthesis of substituted benzothiazoles
Bose, D. Subhas,Idrees, Mohd.
, p. 1983 - 1988 (2010)
Carbon-fluorine bond fission has been coupled with C-S bond formation under metal-free conditions, which is seldom reported in the literature. The intramolecular C-S bond formation reaction takes place by fission of the carbon-fluorine bond in situ, and is believed to proceed through an S NAr mechanism. The approach represents a practical and atom-economical approach for regioselective and metal-free cascade synthesis of substituted benzothiazoles. This one-pot, environmentally benign protocol involves 2-fluoroanilines, benzoyl chlorides and Lawessons reagent under microwave irradiation (5 min) or conventional thermal conditions (3h). Georg Thieme Verlag Stuttgart.
Hybrids of privileged structures benzothiazoles and pyrrolo[2,1-c] [1,4]benzodiazepin-5-one, and diversity-oriented synthesis of benzothiazoles
Subhas Bose,Idrees, Mohd.,Todewale, Ismail K.,Jakka,Venkateswara Rao
, p. 27 - 38 (2012/07/01)
Privileged structures like Benzothiazole and Pyrrolobenzodiazepine offer wonderful opportunity to explore in anti-cancer drug discovery as a mean to counter drug-resistance problem. BT-PBD hybrids and diverse BT derivatives have been synthesized and their in vitro cytotoxic activities were screened against five cancer cell lines have been discussed. The novel compounds showed promising results as compared with the marketed drug etoposide and could well be used in future anti-cancer drug development studies.
