Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Nikolay F. Kirillov"'
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:
Вестник Пермского университета. Серия «Химия» = Bulletin of Perm University. CHEMISTRY. 8:444-450
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4786f412d0ad1c901e4dc248cf8620b
https://doi.org/10.17072/2223-1838-2018-4-444-450
https://doi.org/10.17072/2223-1838-2018-4-444-450
Publikováno v:
Pharmaceutical Chemistry Journal. 52:408-410
Reformatsky reactions of dicarboxylic acid anhydrides formed monomethyl esters of oxodicarboxylic acids with antinociceptive and anti-inflammatory activity.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e2264424b6e5ad847e355c4a1a5af31
https://doi.org/10.1007/s11094-018-1831-4
https://doi.org/10.1007/s11094-018-1831-4
Publikováno v:
Russian Journal of Organic Chemistry. 55:1244-1245
The reaction of 3-(3-arylpropenoyl)-2H-chromen-2-ones with methyl 1-bromocyclopentane-1-carboxylate and zinc resulted in the isolation, after hydrolysis of the reaction mixture, adducts of the Reformatsky reagent across the double bond of the heteroc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d2893d205682661f1f1cd2a45991337
https://doi.org/10.1134/s1070428019080281
https://doi.org/10.1134/s1070428019080281