6634-55-5Relevant articles and documents
Synthesis and characterization of six-membered pincer nickelacycles and application in alkylation of benzothiazole
Pandiri, Hanumanprasad,Sharma, Dipesh M,Gonnade, Rajesh G,Punji, Benudhar
, p. 1161 - 1169 (2017)
Six-membered pincer nickelacycle complexes have been synthesized and employed for the catalytic C–H bond alkylation of benzothiazole. The pincer nickelacycle, {κP, κC, κP- (2 - iPr 2POCH 2-
Catalytic C-H Bond Alkylation of Azoles with Alkyl Halides Mediated by Nickel(II) Complexes of Phenanthridine-Based N^ N-^ N Pincer Ligands
Braun, Jason D.,Herbert, David E.,Mandapati, Pavan,Sidhu, Baldeep K.,Wilson, Gabrielle
, p. 1989 - 1997 (2020/06/08)
Ni(II) complexes supported by tridentate N^N-^N diarylamido pincer-type ligands have been demonstrated to act as active catalysts in the carbon-carbon bond forming alkylation of azoles using unactivated alkyl halides. Here, we show that benzann
Controllable assembly of the benzothiazole framework using a CC triple bond as a one-carbon synthon
Huang, Yubing,Yan, Donghao,Wang, Xu,Zhou, Peiqi,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 1742 - 1745 (2018/02/21)
A concise and efficient protocol to assemble diverse benzothiazole derivatives in high yields was provided via copper catalyzed tandem cyclization with o-haloanilines, elemental sulfur and terminal alkynes as raw materials. In this protocol, C atoms on the CC triple bond were controllably involved in the construction of the benzothiazole framework and multiple carbon-heteroatom bonds through divergent routes.
