Výsledky vyhledávání - "B N, Anisimov"

Indolopyridines with an angular heteroatom. 11. Synthesis of 12-arylidenindolo-[2,1-a]isoquinolinium salts

Autor: Kh. A. R. Alarkon, N. I. Golovtsov, Anatoly T. Soldatenkov, Svetlana A. Soldatova, Zh. Ntaganda, B. N. Anisimov

Publikováno v: Chemistry of Heterocyclic Compounds. 35:699-702

The condensation of aromatic aldehydes with indolo[2,1-a]isoquinoline in a solution of trifluoroacetic acid yielded a series of 12-arylidenindolo[2,1-a]isoquinolinium trifluoroacetates. Analogous quaternary salts are formed with trichloroacetic and a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eb006f3f3263d665b7aca2082ddf98be
https://doi.org/10.1007/bf02251629

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9-(β-pyridylmethylene)-4-azafluorene synthesis of the Z- and E-isomers of its methiodides and reduction of the Z-isomer

Autor: N. S. Prostakov, B. N. Anisimov, Anatoly T. Soldatenkov, N. M. Kolyadina, Siako Soro Siako Soro

Publikováno v: Chemistry of Heterocyclic Compounds. 34:1066-1069

The 9-(β-pyridylmethylene)-4-azafluorene was obtained as the mixture of the Z- and E-isomers. Condensation of 4-azafluorene with methiodides of 3-formylpyridine afforded the methiodides of these isomers which were isolated in discrete form. Their co

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https://doi.org/10.1007/bf02251552

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Synthesis, structure, and biological activity of [2.2]paracyclophanes. 6. Synthesis of 2-([2.2]paracyclophan-4-yl)(benzo[g])indoles

Autor: Anatoly T. Soldatenkov, T. P. Khristoforova, B. N. Anisimov, Svetlana A. Soldatova, L. I. Kryvenko

Publikováno v: Chemistry of Heterocyclic Compounds. 33:929-932

Cyclocondensation of 2-([2.2]paracyclophan-4-yl)-2-oxoethyltriethylammonium bromide with aniline and α-naphthylamine gives 2-(paracyclophan-4-yl)indoles and benzo[g]indole respectively.

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https://doi.org/10.1007/bf02253163

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Synthesis, structure, and biological activity of derivatives of [2,2]-para-cyclophane

Autor: Anatoly T. Soldatenkov, Zh. A. Mamyrbekova, Siako Soro Siako Soro, B. N. Anisimov, D. Lozinskaya

Publikováno v: Pharmaceutical Chemistry Journal. 28:267-270

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5c2ba39241d2b99cad82a17d3358f2b4
https://doi.org/10.1007/bf02219800

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Indolopyridines with a hetero atom at a position of fusion. 7. Electrophilic substitution in 5,6-dihydroindolo-[2,1-a]isoquinoline

Autor: G. Ntaganda, S. A. Soldatova, Anatoly T. Soldatenkov, J. A. R. Alarcon, B. N. Anisimov

Publikováno v: Chemistry of Heterocyclic Compounds. 30:196-199

Halogenation, acylation, azo coupling, and alkylaminomethylation of 5,6-dihydroindoto[2,I-alisoguinoline were carried out at the C(11) position (pyrrole fragment). In dibromination, the second bromine atom was introduced into the C(9) position (indol

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https://doi.org/10.1007/bf01165011

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