140635-67-2Relevant academic research and scientific papers
Self-Assembled Multilayer Iron(0) Nanoparticle Catalyst for Ligand-Free Carbon-Carbon/Carbon-Nitrogen Bond-Forming Reactions
Akiyama, Toshiki,Arisawa, Mitsuhiro,Haneoka, Hitoshi,Harada, Kazuo,Hasegawa, Jun-Ya,Honma, Tetsuo,Mashima, Kazushi,Sato, Yoshihiro,Shimoda, Shuhei,Shio, Yasunori,Suzuki, Takeyuki,Tamenori, Yusuke,Tsurugi, Hayato,Tsuruta, Kazuki,Wada, Yuki,Yamada, Makito
, p. 7244 - 7249 (2020)
Self-assembled multilayer iron(0) nanoparticles (NPs, 6-10 nm), namely, sulfur-modified Au-supported Fe(0) [SAFe(0)], were developed for ligand-free one-pot carbon-carbon/carbon-nitrogen bond-forming reactions. SAFe(0) was successfully prepared using a well-established metal-nanoparticle catalyst preparative protocol by simultaneous in situ metal NP and nanospace organization (PSSO) with 1,4-bis(trimethylsilyl)-1,4-dihydropyrazine (Si-DHP) as a strong reducing agent. SAFe(0) was easy to handle in air and could be recycled with a low iron-leaching rate in reaction cycles.
Intramolecular Carbonylative C–H Functionalization of 1,2,3- Triazoles for the Synthesis of Triazolo[1,5-a]indolones
Veryser, Cedrick,Steurs, Gert,Van Meervelt, Luc,De Borggraeve, Wim M.
supporting information, p. 1271 - 1276 (2017/04/18)
This study presents a synthesis of 4H-[1,2,3]triazolo[1,5-a]indol-4-ones. The key step in the synthesis of this new heterocyclic scaffold is an intramolecular cyclization via an unprecedented carbonylative C–H functionalization of 1-(2-bromoaryl)-1,2,3-tr
Iron-catalyzed bromination of aryl azides by N-bromosuccinimide: Efficient method for the synthesis of brominated aryl azides
Jin, Hui,Huang, Zhen Dong,Kuang, Chun Xiang,Wang, Xiao Kun
experimental part, p. 310 - 313 (2012/01/14)
An efficient and mild protocol for bromination of aryl azides with N-bromosuccinimide (NBS) under FeCl3 catalysis in 1,2-dichloroethane was developed. It is proved to be an efficient method for obtaining brominated aryl azides.
A PRACTICAL SYNTHESIS OF ISOTOPICALLY LABELLED 1-(4-ISOTHIOCYANATOPHENYL)-4-(t-BUTYL)-2,6,7-TRIOXABICYCLOOCTANE, A PROBE FOR THE BENZODIAZEPINE RECEPTOR-COUPLED CHLORIDE IONOPHORE
Costa, Brian R. de,Lewin, Anita,Schoenheimer, Joyce A.,Skolnick, Phil,Rice, Kenner C.
, p. 2343 - 2355 (2007/10/02)
An efficient synthesis of high specific activity 1-(4-isothiocyanato-3,5-ditritiophenyl)-4-(t-butyl)-2,6,7-trioxabicyclooctane (-1), an affinity ligand for the benzodiazepine (BZ)-coupled γ-aminobutyric acid (GABA)-gated chloride channel, w
