Eco-friendly strategy: design and synthesis of biologically potent benzimidazole–amine hybrids via visible-light generated oxidative C–H arylamylation of analenic amidines
摘要:
An operationally simple visible light mediated intramolecular cyclization of benzimidazole to 2-amino benzimidazole hybrid. The disclosed procedure is rapid and the convenient synthesis of benzimidazole-amine hybrids from easily available substituted cyclic, acyclic amines, and benzimidazole under neat conditions in the presence of catalyst tris(2,2-bipyridine)ruthenium(II) chloride. Indubitably this methodology gives a facile and straightforward pathway to construct benzimidazole-amine hybrid derivatives in an eco-friendly fashion. The reaction proved to be economical interims of product yield, low loading of catalyst under solvent free condition. The solvent free method has supreme importance in industrial research. The scope and efficiency of this new green method is significantly better than the existing methods. (C) 2015 Published by Elsevier Ltd.
NONAQUEOUS ELECTROLYTE AND NONAQUEOUS SECONDARY BATTERY
申请人:Asahi Kasei Kabushiki Kaisha
公开号:EP3279997A1
公开(公告)日:2018-02-07
The purpose of the present invention is to provide a nonaqueous electrolyte that contains acetonitrile having an excellent balance between viscosity and the dielectric constant and a fluorine-containing inorganic lithium salt, wherein the generation of complex cations comprising a transition metal and acetonitrile is suppressed, excellent load characteristics are exhibited, and increases in internal resistance upon repeated charge/discharge cycles are suppressed; a further purpose of the present invention is to provide a nonaqueous secondary battery. The present invention relates to a nonaqueous electrolyte which contains: a nonaqueous solvent comprising acetonitrile; a fluorine-containing inorganic lithium salt; and a specific nitrogenous cyclic compound typified by benzotriazole.
Eco-friendly strategy: design and synthesis of biologically potent benzimidazole–amine hybrids via visible-light generated oxidative C–H arylamylation of analenic amidines
作者:I.R. Siddiqui、Farah Ibad、Afshan Ibad、Malik Abdul Waseem、Geeta Watal
DOI:10.1016/j.tetlet.2015.10.042
日期:2016.1
An operationally simple visible light mediated intramolecular cyclization of benzimidazole to 2-amino benzimidazole hybrid. The disclosed procedure is rapid and the convenient synthesis of benzimidazole-amine hybrids from easily available substituted cyclic, acyclic amines, and benzimidazole under neat conditions in the presence of catalyst tris(2,2-bipyridine)ruthenium(II) chloride. Indubitably this methodology gives a facile and straightforward pathway to construct benzimidazole-amine hybrid derivatives in an eco-friendly fashion. The reaction proved to be economical interims of product yield, low loading of catalyst under solvent free condition. The solvent free method has supreme importance in industrial research. The scope and efficiency of this new green method is significantly better than the existing methods. (C) 2015 Published by Elsevier Ltd.
<i>N</i>-Heterocyclic Carbenes as a Robust Platform for Surface-Enhanced Raman Spectroscopy
作者:Joseph F. DeJesus、Michael J. Trujillo、Jon P. Camden、David M. Jenkins
DOI:10.1021/jacs.7b12779
日期:2018.1.31
commercial and fundamental applications. SERS often relies on ligands, usually thiols, bound to a noble metal surface. The difficulty of straightforward thiol synthesis combined with their instability on surfaces highlights the need for alternative ligand design. We present the first example of SERS utilizing N-heterocycliccarbene ligands. A general three step synthesis is presented for functionalized NHC-CO2