Zobrazeno 1 - 10
of 180
pro vyhledávání: '"A. F. Kirillov"'
Publikováno v:
Journal of Chemistry, Vol 2019 (2019)
Interaction of the Reformatsky reagents, prepared from methyl 1-bromocyclopentane-1-carboxylate or methyl 1-bromocyclohexane-1-carboxylate, with N,N′-bis(arylmethylidene)benzidines has given rise to a set of intermediates as a result of nucleophili
Externí odkaz:
https://doaj.org/article/58c32cc6dd464bf3b8df601ab10c41fd
Publikováno v:
Journal of Ichthyology. 61:701-708
Abstract In order to study the distribution of phylogenetic mtDNA lineages of Arctic charr Salvelinus alpinus in their contact zones in the north of East Siberia we analyzed nucleotide sequences of mtDNA control region of charr from 10 Arctic populat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7377034e3a4770c843cac8b21d0415f9
https://doi.org/10.1134/s0032945221050064
https://doi.org/10.1134/s0032945221050064
Publikováno v:
Russian Journal of Organic Chemistry. 57:1275-1280
2- and 4-(Arylmethylideneamino)phenols react with Reformatsky reagent, obtained from methyl 1-bromocyclohexanecarboxylate and zinc, to form 3-aryl-2-[2-(or 4-)hydroxyphenyl]-2-azaspiro[3.5]nonan-1-ones. The reaction involves the initial addition of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05f3382e265fb9fa592aac169511b9e9
https://doi.org/10.1134/s1070428021080066
https://doi.org/10.1134/s1070428021080066
Autor:
A M. Romanov, Nikolay F. Kirillov, E. A. Nikiforova, R. R. Makhmudov, A. A. Rudin, Maksim V. Dmitriev, D. V. Baibarodskikh, D. P. Zverev
Publikováno v:
Russian Journal of General Chemistry. 91:64-71
Depending on the ring size in the Reformatsky reagent and the nature of substituents in arylmethylidene fragment, the reactions of Reformatsky reagents obtained from methyl esters of 1-bromocycloalkanecarboxylic acids and zinc with N′-(arylmethylid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a82dbf39d049b0576caa45f07bd6e2cc
https://doi.org/10.1134/s1070363221010060
https://doi.org/10.1134/s1070363221010060
Publikováno v:
Russian Journal of Organic Chemistry. 56:2074-2078
1-Aryl-3-(2-hydroxy-5-R-phenyl)prop-2-en-1-ones reacted with the Reformatsky reagent derived from methyl 1-bromocyclohexanecarboxylate to give 4-(2-aryl-2-oxoethyl)-6-R-2H,4H-spiro[[1]benzopyran-3,1′-cyclohexan]-2-ones. The products are formed as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3106b2766b56b7d3b3a06809fa4f6a9d
https://doi.org/10.1134/s1070428020120040
https://doi.org/10.1134/s1070428020120040
Publikováno v:
Russian Journal of Organic Chemistry. 56:1029-1033
Reformatsky reagent prepared from methyl 1-bromocyclohexanecarboxylate reacted with N,N′-(1,4-phenylene)bis(1-arylmethanimines) to produce 2,2′-(1,4-phenylene)bis[3-aryl-2-azaspiro[3.5]nonan-1-ones] as a result of successive nucleophilic addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5512302b5bbd63b1da16adac5abd303
https://doi.org/10.1134/s107042802006010x
https://doi.org/10.1134/s107042802006010x
Autor:
E. A. Nikiforova, Nikolay F. Kirillov, Dmitry P. Zverev, Sergey N. Shurov, Maksim V. Dmitriev
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:92-94
The reactions of 1-benzoyl-2,4-diphenyl-2,3-dihydro-1H-1,5-benzodiazepine with methyl 1-bromocycloalkanecarboxylates and zinc, followed by hydrolysis of the reaction mixtures, resulted in the formation of spiro-δ-lactams bearing a 2-(N-benzoylamino)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15ec1f1ed65325d9e3d18b5fb94df87c
https://doi.org/10.1007/s10593-021-02872-z
https://doi.org/10.1007/s10593-021-02872-z
Autor:
E. A. Nikiforova, Nikolay F. Kirillov, Sergey N. Shurov, Maksim V. Dmitriev, D. V. Baibarodskikh
Publikováno v:
Russian Journal of Organic Chemistry. 55:339-344
Reformatsky reaction of methyl 1-bromocyclopentanecarboxylate with 1-aryl-3-(2-hydroxyphenyl)-prop-2-en-1-ones afforded 6-substituted 4-(2-aryl-2-oxoethyl)-2H,4H-spiro[chromene-3,1′-cyclopentan]-2-ones. A probable reaction mechanism was proposed on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f07e99e2065083325cd490061741c450
https://doi.org/10.1134/s1070428019030114
https://doi.org/10.1134/s1070428019030114
Autor:
L. S. Govorushkin, T. A. Zakharova, E. A. Nikiforova, Nikolay F. Kirillov, D. V. Baibarodskikh
Publikováno v:
Journal of Chemistry, Vol 2019 (2019)
Interaction of the Reformatsky reagents, prepared from methyl 1-bromocyclopentane-1-carboxylate or methyl 1-bromocyclohexane-1-carboxylate, with N,N′-bis(arylmethylidene)benzidines has given rise to a set of intermediates as a result of nucleophili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7f281196d3fe8b3693e24f95445dd1
https://doi.org/10.1155/2019/7496512
https://doi.org/10.1155/2019/7496512
Publikováno v:
Journal of Ichthyology. 58:808-818
In order to extend the geography of genetic studies at the broad circumpolar range of Arctic charr we analyzed sequence variation of mtDNA control region (537–547 b.p.) in 25 populations of the European part of Russia and Siberia. In most of them,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::835ba28ecb3dd1a37f7b1b44336a8607
https://doi.org/10.1134/s0032945218050089
https://doi.org/10.1134/s0032945218050089