142913-02-8Relevant academic research and scientific papers
An odorless, one-pot synthesis of nitroaryl thioethers via SNAr reactions through the in situ generation of S-alkylisothiouronium salts
Lu, Guo-Ping,Cai, Chun
, p. 59990 - 59996 (2015/02/19)
A newly developed C-S bond formation nucleophilic aromatic substitution (SNAr) reaction in aqueous Triton X-100 (TX100) micelles has been disclosed. This chemistry, in which odorless, cheap and stable thiourea in place of thiols is used as the sulfur reagent, provides an efficient approach for the generation of nitroaryl thioethers, which are useful structural units of many bioactive molecules, rendering this methodology attractive to both synthetic and medicinal chemistry.
Synthesis, crystal structures, spectral studies and reactivity of square planar copper(II) complexes containing Schiff base ligand
Pattanayak, Poulami,Pratihar, Jahar Lal,Patra, Debprasad,Lin, Chia-Her,Brandao, Paula,Mal, Dasarath,Felix, Vitor
, p. 568 - 579 (2013/06/26)
The reactions of HL1 [2-((2-(benzylthio)phenylimino)methyl) phenol] and HL2 [3-((2-(benzylthio)phenylimino)methyl)-2-hydroxy-5- methylbenzaldehyde] separately with Cu(OAc)2·H2O afforded new Cu(II) complexes [Cu(
