Zobrazeno 1 - 10
of 138
pro vyhledávání: '"Vnira R. Akhmetova"'
Autor:
Vnira R. Akhmetova, Regina R. Khairullina, Ivan S. Bushmarinov, Tat’yana V. Tyumkina, Vasiliy M. Yanybin
Publikováno v:
ARKIVOC, Vol 2011, Iss 8, Pp 149-162 (2011)
Externí odkaz:
https://doaj.org/article/b7ba2275922d45d6a0df796dac29531f
Autor:
Zalifa T. Niatshina, Natal’ya N. Murzakova, Inna V. Vasilieva, Elena B. Rakhimova, Vnira R. Akhmetova, Askhat G. Ibragimov
Publikováno v:
ARKIVOC, Vol 2011, Iss 8, Pp 141-148 (2011)
Externí odkaz:
https://doaj.org/article/c5d90478f2b9411ea75ea15eb5ebef01
Autor:
Keshav Lalit Ameta, Ahanthem Priyanca Devi, Andrea Penoni, Vnira R. Akhmetova, Rajendra P. Pawar, Is Fatimah
Publikováno v:
Mini-Reviews in Organic Chemistry. 20:455-482
Abstract: Heterocycles are the largest family of organic compounds due to their wide applications as therapeutic agents, synthetic intermediates, scaffolds, building blocks or fine chemicals. Heterocyclic compounds are continuously used in material s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c61a748982f4af8b778c091cade608e
https://doi.org/10.2174/1570193x19666220615095645
https://doi.org/10.2174/1570193x19666220615095645
Publikováno v:
Chemistry of Heterocyclic Compounds. 59:5-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::751d52e58ad576449fb31ff23964eca6
https://doi.org/10.1007/s10593-023-03156-4
https://doi.org/10.1007/s10593-023-03156-4
Publikováno v:
Russian Journal of General Chemistry. 91:1453-1458
An approach to the synthesis of 1,3,5-dithiazinanes and 1,3,5-thiadiazinanes was developed based on the cyclothiomethylation of aliphatic amines with 9-aqueous Na2S and CH2O. Linear aliphatic primary amines form predominantly 1,3,5-thiadiazinanes, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0b709cb6cb443b4f23826f3c377bcdf
https://doi.org/10.1134/s1070363221080053
https://doi.org/10.1134/s1070363221080053
Autor:
Nail S. Akhmadiev, Vnira R. Akhmetova, V. R. Khairullina, Askhat G. Ibragimov, Ekaterina S. Mescheryakova
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:473-481
A selective method was developed for the synthesis of acyclic sulfanyl derivatives of ampyrone by thiomethylation reaction of 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one with formaldehyde and thiols in aqueous medium under various conditions (roo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27de4cc606a666a61cfac0a5d5e2c474
https://doi.org/10.1007/s10593-020-02683-8
https://doi.org/10.1007/s10593-020-02683-8
Publikováno v:
N-Heterocycles ISBN: 9789811908316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a31f4d1113f2e9018bfd317b21adc05
https://doi.org/10.1007/978-981-19-0832-3_5
https://doi.org/10.1007/978-981-19-0832-3_5
Publikováno v:
N-Heterocycles ISBN: 9789811908316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07687dbfb0e7b6c3555b84d93a035156
https://doi.org/10.1007/978-981-19-0832-3_7
https://doi.org/10.1007/978-981-19-0832-3_7
Publikováno v:
Russian Journal of General Chemistry. 89:1760-1764
A series of bi- and trinuclear pyrrole derivatives was prepared by the 5 mol % ZrOCl2 ·8H2O-catalyzed CH-sp2-aminomethylation reaction of pyrrole with bis(1,3-oxazacycloalk-3-yl)methanes. The reaction proceeds at the positions 2, 5 or 2 of pyrrole d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2695d8eaef04840fe4f5a1ab47bf7560
https://doi.org/10.1134/s1070363219090056
https://doi.org/10.1134/s1070363219090056
Metal-free multicomponent synthesis of novel macrocyclic tetrathiadienes with cyano and amino groups
Publikováno v:
RSC advances. 11(31)
The first synthesis of 5,12-diamino-7,14-bis(aryl)-1,4,8,11-tetrathiacyclotetradeca-5,12-diene-6,13-dicarbonitriles was performed as a multicomponent macroheterocyclization of malononitrile, aryl aldehydes, and 1,2-ethanedithiol in the presence of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e32ac4fc6dc7ea50784e0b6319578fbf
https://pubmed.ncbi.nlm.nih.gov/35478647
https://pubmed.ncbi.nlm.nih.gov/35478647