83734-38-7Relevant articles and documents
Sm-Catalyzed Synthesis and Biological Activity of Acyclic and Cyclic Azadiperoxides
Makhmudiyarova,Rakhimov, R. Sh.,Tyumkina,Meshcheryakova,Ibragimov,Dzhemilev
, p. 620 - 632 (2019/07/17)
Acyclic diaminodiperoxides and cyclic azadiperoxides are synthesized by the reaction of 1,1-bis-(hydroperoxy)cycloalkanes with formaldehyde and primary arylamines in the presence of Sm-containing catalysts [SmCl3·6H2O, Sm(NO3/s
Task-specific ionic liquid-mediated facile synthesis of 1,3,5 triaryltriazines by cyclotrimerization of imines and their biological evaluation
Dandia, Anshu,Jain, Anuj K.,Sharma, Sonam
supporting information, p. 521 - 523 (2014/04/17)
A highly efficient method for the synthesis of fluorinated 1,3,5-triaryltriazine derivatives is developed by the condensation reaction of aromatic amines and formaldehyde followed by spontaneous cyclotrimerization using task-specific 1,1,3,3-tetramethylguanidine trifluoroacetate [TMG][Tfa] ionic liquid as a environmentally benign solvent in excellent yields at room temperature. The synthesized compounds were subjected for in vitro antitubercular activity against Mycobacterium tuberculosis H37Rv strain using the LoewensteinJensen medium.
Conformations of 1,3,5-Triaryl-1,3,5-triazacyclohexanes: Comparison of the o-, m-, and p-Fluorophenyl Compounds
Bouchemma, Ahcene,McCabe, Peter H.,Sim, George A.
, p. 583 - 588 (2007/10/02)
Crystallographic studies of 1,3,5-tris-(o-, m-, and p-fluorophenyl)-1,3,5-triazacyclohexane disclose examples of diaxial-equatorial chair conformations for 1,3,5-triaryl-1,3,5-triazacyclohexanes.The repulsion between axial aryl groups is relieved by the N
