123685-60-9Relevant articles and documents
Stereoselective Synthesis of Hexahydroimidazo[1,2- a]quinolines via SN2-Type Ring-Opening Hydroarylation-Hydroamination Cascade Cyclization of Activated Aziridines with N-Propargylanilines
Bhattacharyya, Aditya,Chauhan, Navya,Ghorai, Manas K.,Pradhan, Sajan,Shahi, Chandan K.
, p. 7903 - 7908 (2020)
A novel synthetic approach for the construction of 1,2,3,3a,4,5-hexahydroimidazo[1,2-a]quinolines in good yields (up to 75%) with excellent stereoselectivity (dr up to 94:6, ee up to >99%) under one-pot domino ring-opening cyclization (DROC) conditions ha
Nucleophilicity of N-propargylanilines in the coordination to zinc tetraphenylporphyrin in chloroform
Andreev,Sobolev,Zaitsev,Vizer,Erzhanov,Tafeenko
, p. 1599 - 1607 (2014)
Thermodynamic parameters (ΔG 0and ΔS 0) of the isoenthalpic (except for 4-halo derivatives) coordination of (tetraphenylporphyrinato)zinc(II) with anilines in chloroform at 273-313 K linearly correlate with the shift of their electro
Synthesis and biological evaluation of coumarin-linked 4-anilinomethyl-1,2,3-triazoles as potent inhibitors of carbonic anhydrases ix and xiii involved in tumorigenesis
Thacker, Pavitra S.,Tiwari, Prerna L.,Angeli, Andrea,Srikanth, Danaboina,Swain, Baijayantimala,Arifuddin, Mohammed,Supuran, Claudiu T.
, (2021/04/22)
A series of coumarin-linked 4-anilinomethyl-1,2,3-triazoles (6a–t) was synthesized via a molecular hybridization approach, through carbon C-6 of the coumarin moiety. The synthesized compounds were evaluated for their inhibition of carbonic anhydrase (CA)