Zobrazeno 1 - 10 of 10 pro vyhledávání: '"I. A. Stazharova"'
1
Chemical reactions of 4,5,6,7-tetrahydro-4,5,7-trimethylpyrrolo[3,2-c]pyridine and its 2-formyl derivative
Autor: A. A. Sinitsyna, Tatiana N. Borisova, Alexey V. Varlamov, E. A. Sakhnova, I. A. Stazharova, Ae Aliev
Publikováno v: Chemistry of Heterocyclic Compounds. 29:582-587
N-Alkyl substituted tetrahydropyrrolo[3,2-c]pyridines have been obtained by alkylation of 4,5,6,7-tetrahydro-4,-5, 7-trimethylpyrrolo[3,2-c]pyridine and its 2-formyl derivative chloroalkyldimethylamines, acrylonitrile, methyl acetylenedicarboxylate a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2973833359385d93bf916091276a767d
https://doi.org/10.1007/bf00534474
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2
Study of the stereochemistry of N-H and N-vinyl-4,5,7-trimethyi-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines and their nitro derivatives by the method of 1H and 13C NMR
Autor: A. A. Sinitsyna, N. S. Prostakov, Ae Aliev, T. N. Borisova, Alexey V. Varlamov, I. A. Stazharova
Publikováno v: Chemistry of Heterocyclic Compounds. 29:65-70
The configurations and conformational features of N-H and N-vinyl-4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines and their nitro derivatives were established by the method of 1H and 13C NMR spectroscopy. It was shown that the conformationa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e292202c920526ece516b892133ba95b
https://doi.org/10.1007/bf00528638
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5
ChemInform Abstract: Synthesis and Nitration of NH- and N-Vinyl-4,5,7-trimethyl-4,5,6,7- tetrahydropyrrolo(3,2-c)pyridines
Autor: N. S. Prostakov, Tatiana N. Borisova, I. A. Stazharova, Alexey V. Varlamov, Abil E. Aliev
Publikováno v: ChemInform. 24
It has been shown that the most efficient catalysts for the synthesis of 4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine from 1,2,5-trimethylpyridin-4-one and acetylene under Trofimov conditions are rubidium and potassium hydroxides. Use of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6a03046ddb9aa8c28b0a138bb19f416f
https://doi.org/10.1002/chin.199314198
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7
Synthesis, structure, and tautomerism of 3a,7-dimethyl-4,6-diphenyl-2-ethynyl-7a-hydroxyperhydropyrrolo[3,2-c]pyridine
Autor: I. A. Stazharova, N. S. Prostakov, Alexey V. Varlamov, Abil E. Aliev, A. A. Sinitsyna, Mikaya Anzor I, Tatiana N. Borisova
Publikováno v: Chemistry of Heterocyclic Compounds. 28:750-760
Isomeric [with respect to the fusion of the piperidine and pyrrolidine rings, as well as with respect to the mutual orientation of the substituents attached to the C(2) and C(3a) carbon atoms] 3a, 7-dimethyl-4,6-diphenyl2-ethynyl-7a-hydroxyperhydropy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5a72b76e8b7bd71f4eb37f7b56d3c7bb
https://doi.org/10.1007/bf00474487
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8
Synthesis and nitration of NH- and N-vinyl-4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines
Autor: N. S. Prostakov, Alexey V. Varlamov, Abil E. Aliev, I. A. Stazharova, Tatiana N. Borisova
Publikováno v: Chemistry of Heterocyclic Compounds. 27:1105-1109
It has been shown that the most efficient catalysts for the synthesis of 4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine from 1,2,5-trimethylpyridin-4-one and acetylene under Trofimov conditions are rubidium and potassium hydroxides. Use of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::da1aec907a1ad59ad14993567e458a80
https://doi.org/10.1007/bf00486807
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9
9-(2-Oxo-1-azetidinyl)-10,10-dimethyl-9,10-dihydro-10-sila-2-azaanthracenes
Autor: I. A. Stazharova, Ae Aliev, Alexey V. Varlamov, P. Kandzhi, N. S. Prostakov
Publikováno v: Chemistry of Heterocyclic Compounds. 27:447-450
9-(3-Methyl-3-bromo-2-oxo-1-azetidinyl)-10,10-dimethyl-9,10-dihydro-10-sila-2-azaanthracene was obtained in the form of a mixture of two diastereomers by intramolecular cyclization of the corresponding 9-(α,Β-dibromoisobutyrylamino)dihydrosilaazaan
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2dec49c27c1691a171f0c4c45d336320
https://doi.org/10.1007/bf00480849
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