83734-38-7Relevant academic research and scientific papers
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
Synthesis, molecular structure, conformation and biological activity of Ad-substituted N-aryl-tetraoxaspiroalkanes
Tyumkina, Tatyana V.,Makhmudiyarova, Nataliya N.,Kiyamutdinova, Guzeliya M.,Meshcheryakova, Ekaterina S.,Bikmukhametov, Kamil Sh.,Abdullin, Marat F.,Khalilov, Leonard M.,Ibragimov, Askhat G.,Dzhemilev, Usein M.
, p. 1749 - 1758 (2018/03/07)
An efficient method has been developed for the synthesis of 7′-arylspiro{adamantane-[2,3′]-(1′,2′,4′,5′,7′-tetraoxazocanes)} by the ring transformation reaction of spiro{adamantane-[2,3’]-(1′,2′,4′,5′,7′-pentaoxacane)} with arylamines in the presence of 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.
Green chemical synthesis of fluorinated 1,3,5-triaryl-s-triazines in aqueous medium under microwaves as potential antifungal agents
Dandia, Anshu,Arya, Kapil,Sati, Meha,Sarawgi, Pritima
, p. 1273 - 1277 (2007/10/03)
Reasonable pure fluorinated s-triazines were synthesized in quantitative yield (96-99%) in 2-3 min in aqueous medium under microwaves, by reaction of fluorinated anilines and aqueous formaldehyde. All synthesized compounds have been screened in vitro for
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
Revisitation of Formaldehyde Aniline Condensation. VII. 1,3,5-Triarylhexahydro-sym-triazines and 1,3,5,7-Tetraaryl-1,3,5,7-tetrazocines from Aromatic Amines and Paraformaldehyde
Giumanini, Angelo G.,Verardo, Giancarlo,Zangrando, Ennio,Lassiani, Lucia
, p. 1087 - 1103 (2007/10/02)
A product study of the reaction between a number of aromatic amines substituted with widely different groups and paraformaldehyde in inert solvents was performed and found to yield 1,3,5-triaryl-1,3,5-hexahydrotriazines, 1,3,5,7-tetraaryl-1,3,5,7-tetrazocines and formaminals.It was not possible to correlate the product outcomes with the actual structure of the amine substrate.The X-ray diffraction structural determination of 1,3,5-tri-(t-butylphenyl)- (1b) and 1,3,5-tri-(m-fluorophenyl)-1,3,5-hexahydrotriazine (1c) showed the diaxial arrangement of the N-substituents.
