17223-18-6Relevant articles and documents
Synthesis of poly(m-phenyleneisophthalamide) by solid-state polycondensation of isophthalic acid with m-phenylenediamine
Zhang, Cenyao,Shoji, Yu,Higashihara, Tomoya,Tsukuda, Akimitsu,Ochi, Takashi,Ueda, Mitsuru
, p. 4725 - 4728 (2011)
The synthesis of poly(m-phenyleneisophthalamide) was performed by thermal solid-phase polymerization from isophthalic acid and m-phenylenediamine without using any solvents or condensation agents. The two-stage heating process was conducted. The oligo(m-p
Synthesis of New Bulky Bis(amidine) with the Conformationally Rigid meta-Phenylene Bridge and Its Dilithium Derivative [1,3-C6H4{NC(Ph)N(2,6-iso-Pr2C6H3)}2]Li2(TMEDA)2
Tolpygin,Cherkasov,Fukin,Trifonov
, p. 288 - 294 (2019)
Abstract: The reaction of 2,6-diisopropylaniline with m-phenylenedibenzimidoyl chloride 1,3-C6H4{N=C(Ph)Cl}2 in the presence of triethylamine in a toluene solution affords bis(amidine) 1,3-C6H4{NC(Ph)
Synthesis of 2-Amino-1,3-dienes from Propargyl Carbonates via Palladium-Catalyzed Carbon-Nitrogen Bond Formation
O'Broin, Calvin Q.,Guiry, Patrick J.
supporting information, p. 879 - 883 (2020/02/04)
A catalytic method to synthesize 1,3,-dienes from propargylic precursors is reported. This palladium-catalyzed carbon-nitrogen bond-forming reaction furnishes 2-amino-1,3-dienes in excellent yields (up to 98%) and shows a broad tolerance to functional group diversity. The reaction has been demonstrated for over 30 amine substrates, including anilines and indoles, and proceeds under mild neutral conditions. The resulting 1,3-dienes are of great synthetic interest because of their further reaction potential.
Design, synthesis and structure-activity relationship studies of novel sirtuin 2 (SIRT2) inhibitors with a benzamide skeleton
Sakai, Taki,Matsumoto, Yotaro,Ishikawa, Minoru,Sugita, Kazuyuki,Hashimoto, Yuichi,Wakai, Nobuhiko,Kitao, Akio,Morishita, Era,Toyoshima, Chikashi,Hayashi, Tomoatsu,Akiyama, Tetsu
, p. 328 - 339 (2015/03/03)
Human sirtuin 2 (SIRT2) is an attractive target molecule for development of drugs to treat neurodegenerative diseases and cancer, because SIRT2 inhibitors have a protective effect against neurodegeneration and an anti-proliferative effect on cancer stem c