Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Yuri Yu. Morzherin"'
Publikováno v:
ARKIVOC, Vol 2008, Iss 17, Pp 306-317 (2009)
Externí odkaz:
https://doaj.org/article/a9a81bf4876d4907b8fb117c80720e94
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:
Konstantin L. Obydennov, Tatiana V. Glukhareva, Aleksei N. Galushchinskiy, Yuri Yu. Morzherin, M. F. Kosterina
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:622-625
It was shown that 2-(1,3-thiazolidin-2-ylidene)acetamides can be used as 2-enamides in cyclocondensation reactions with oxalyl chloride, leading to the formation of new heterocyclic assemblies – 4-(4-oxo-1,3-thiazolidin-2-ylidene)pyrrolidine-2,3,5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::559c18f8ea5e1b4804d906b8f67d8032
https://doi.org/10.1007/s10593-017-2102-0
https://doi.org/10.1007/s10593-017-2102-0
Autor:
Yuri Yu. Morzherin, Vadim A. Shevyrin, Tatiana O. Kolesnikova, Allan V. Kalueff, Sergey L. Khatsko
Publikováno v:
Neurotoxicology and Teratology. 59:62-67
Tiletamine is a non-competitive N-methyl-d-aspartate (NMDA) receptor antagonist chemically related to ketamine and phencyclidine. A common veterinary anesthetic drug, tiletamine is currently a Schedule III controlled substance in USA. This compound e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcbe8d5dfe40aa767f1a7a52cdcbb953
https://doi.org/10.1016/j.ntt.2016.11.009
https://doi.org/10.1016/j.ntt.2016.11.009
Autor:
Yuri Yu. Morzherin, Vadim A. Shevyrin, Olga V. Kupriyanova, Albert T. Lebedev, Oleg S. Eltsov, Yuri Shafran, Vladimir Melkozerov, Raziya Sadykova
Publikováno v:
Journal of Mass Spectrometry. 51:969-979
Emergence of new psychoactive substances, hallucinogenic phenethylamines in particular, in illicit market is a serious threat to human health in global scale. We have detected and identified N-(2-methoxybenzyl)-2-(2,4,6-trimethoxyphenyl)ethanamine (2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c22921ff19b0b686012be53d0002cd7d
https://doi.org/10.1002/jms.3808
https://doi.org/10.1002/jms.3808
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:716-720
1-Benzyl-N-tolyl-1,2,3-triazole-4-carboxamide was accessed via rearrangement of N-benzyl-1-tolyl-1,2,3-triazole-4-carboxamide. It is shown that by boiling in various solvents an equilibrium between isomeric triazoles and diazomalondiamides is establi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45b3546afe5345f05fee248bfc11886a
https://doi.org/10.1007/s10593-016-1953-0
https://doi.org/10.1007/s10593-016-1953-0
Publikováno v:
Forensic Science International. 259:95-100
We were the first to detect 3-benzyl-5-[1-(2-pyrrolidin-1-ylethyl)-1 H -indol-3-yl]-1,2,4-oxadiazole (given name BzODZ-EPyr ) as a new synthetic cannabinoid, in illegal market of new psychoactive compounds (NPS). The compound was known only from phar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3893da65d0b66c739226862143a7279
https://doi.org/10.1016/j.forsciint.2015.12.019
https://doi.org/10.1016/j.forsciint.2015.12.019
Autor:
T. A. Kalinina, O. A. Vysokova, Tatiana A. Pospelova, Tatiana V. Glukhareva, Yuri Yu. Morzherin, Marina A. Tokareva
Publikováno v:
Chemistry of Heterocyclic Compounds. 53:236-238
A method is proposed for the synthesis of ethyl 5-(3-aryl-4-formyl-1H-pyrazol-1-yl)-1,2,3-thiadiazole-4-carboxylates by a reaction of acetophenone (4-ethoxycarbonyl-1,2,3-thiadiazol-5-yl)hydrazones with a Vilsmeier–Haack complex. The obtained heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8036593014d8df78e86a614282dc5fcb
https://doi.org/10.1007/s10593-017-2045-5
https://doi.org/10.1007/s10593-017-2045-5
Autor:
Svetlana A. Shatunova, Mariya F. Kosterina, Konstantin L. Obydennov, T. A. Kalinina, Zhijin Fan, L. A. Khamidullina, Tatiana V. Glukhareva, Alexey N. Galushchinskiy, Yuri Yu. Morzherin
Publikováno v:
Journal of agricultural and food chemistry. 66(24)
Synthesis, isomerism, and fungicidal activity against potato diseases of new (5Z)-[2-(2,4,5-trioxopyrrolidin-3-ylidene)-4-oxo-1,3-thiazolidin-5-ylidene]acetate derivatives with 1,3-thiazolidine-4-one and pyrrolidine-2,3,5-trione moieties linked by an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::561e061500f561f73f8a1e1add7cdf0f
https://pubmed.ncbi.nlm.nih.gov/29807429
https://pubmed.ncbi.nlm.nih.gov/29807429
Publikováno v:
Journal of Heterocyclic Chemistry. 54:137-146
The transformation of 1,2,3-thiadiazolyl hydrazones of aldehydes and ketones including Dimroth rearrangement giving 1-alkylidenamino-5-mercapto-1,2,3-triazoles, alkylation of mercapto group of these heterocyclic compounds by α-bromoacetophenones and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f88718a2e966b5011ab6582db4750aa0
https://doi.org/10.1002/jhet.2554
https://doi.org/10.1002/jhet.2554