Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Inna S. Khazhieva"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 10, Pp o798-o798 (2015)
The title compound, C11H12N4O2,was prepared via the transformation of sodium 4-acetyl-1-phenyl-1H-[1.2.3]triazolate under the action of methoxyamine hydrochloride. The dihedral angle between the triazole and phenyl rings is 25.12 (16)° and the C ato
Externí odkaz:
https://doaj.org/article/8c3bd9d71ba642f5b28d0de8dcbe8255
Autor:
Tatiana V. Glukhareva, Lai Chen, Yuri Yu. Morzherin, T. A. Kalinina, Oleg S. Eltsov, Zhijin Fan, Yulia I. Nein, Inna S. Khazhieva, Bin Zhao, Pavel M. Demkin
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:956-963
4-Acetyl-3-(2-aryl-2-oxoethyl)-1-phenyl-1Н-1,2,3-triazol-3-ium-5-olates, as well as 4-hydroxy-, 4-acetoxy-, and 4-amino derivatives of 2,6-diaryl-2H-[1,2,3]triazolо[1,5-а]pyridin-8-ium-3-olates were synthesized and tested for fungicidal activity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f2615827f6b312516d63f4e0ca42102
https://doi.org/10.1007/s10593-018-2380-1
https://doi.org/10.1007/s10593-018-2380-1
Autor:
Zhu Yujie, Nataliya P. Belskaya, Lai Chen, Inna S. Khazhieva, Guo Xiaofeng, Zhang Zhiming, Vasiliy A. Bakulev, Zhang Nailou, Zhijin Fan, Morzherin Y. Yurievich
Publikováno v:
RSC Advances
A series of 3,4-dichloroisothiazole based novel strobilurin analogs were designed and synthesized, and their structures were elucidated by NMR and HRMS, and the typical crystal structure was determined by X-ray diffraction for validation. Results fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be53fb910494d1addd522a4baada04fc
https://doi.org/10.1039/c6ra25520e
https://doi.org/10.1039/c6ra25520e
Autor:
Oleg S. Eltsov, A. A. Minin, Tatiana V. Glukhareva, Yu. Yu. Morzherin, V. A. Pozdina, M. V. Ulitko, Inna S. Khazhieva
Publikováno v:
Pharmaceutical Chemistry Journal. 49:296-300
A series of 1,2,3-triazole derivatives was prepared and their cytotoxic actions on glioma cell cultures were studied. Amethod for the synthesis of 1-R-5-methyl- 1 H-[1,2,3]triazole-4-carboxamides is presented, based on transformation of 4-acetyl-1-ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::924f2b15af46054f0ed4f75856bd3bf8
https://doi.org/10.1007/s11094-015-1273-1
https://doi.org/10.1007/s11094-015-1273-1
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:199-202
Alkylation of sodium 4-acetyl-1-phenyl-1,2,3-triazol-5-olate with α-bromoacetophenones was shown to occur at position 3 of the heterocycle, with the formation of 1,2,3-triazol-3-ium-5-olates. Intramolecular crotonic condensation of the latter led to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3278f5c52eb61d7a3ceed312ad3edd
https://doi.org/10.1007/s10593-015-1681-x
https://doi.org/10.1007/s10593-015-1681-x
Publikováno v:
ChemInform. 46
A general approach has been developed for the one-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles from secondary amides and hydrazides via triflic anhydride activation followed by microwave-induced cyclodehydration. In addition, the 1,2,4-triaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82f331f202a7dd6de99512b3c614ac79
https://doi.org/10.1002/chin.201529189
https://doi.org/10.1002/chin.201529189
Publikováno v:
Organic letters. 17(5)
A general approach has been developed for the one-pot synthesis of 3,4,5-trisubstituted 1,2,4-triazoles from secondary amides and hydrazides via triflic anhydride activation followed by microwave-induced cyclodehydration. In addition, the 1,2,4-triaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a37304e145dfd3ed17addf3ad4ee4d
https://pubmed.ncbi.nlm.nih.gov/25700199
https://pubmed.ncbi.nlm.nih.gov/25700199
Publikováno v:
Acta Crystallographica Section E-Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 10, Pp o798-o798 (2015)
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 10, Pp o798-o798 (2015)
The title compound,C11H12N4O2,was preparedviathe transformation of sodium 4-acetyl-1-phenyl-1H-[1.2.3]triazolate under the action of methoxyamine hydrochloride. The dihedral angle between the triazole and phenyl rings is 25.12 (16)° and the C atom o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186348f2b4f751bd890defc916e8170a
https://doi.org/10.1107/s2056989015017776
https://doi.org/10.1107/s2056989015017776