Zobrazeno 1 - 10
of 90
pro vyhledávání: '"V. S. SHKLYAEV"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:602-610
Reactions of alkyl-substituted 3,4-dihydroisoquinolines, with 2-acetylcyclopentane-1,3-dione were used to prepare 3,4-dihydroisoquinolinium 2-acetylcyclopentane-1, 3-dionates, which could not be converted into ABCD-tetracyclic derivatives of the 8-az
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e303f6a995f94f57eed51f79787cf7dc
https://doi.org/10.1007/bf02290946
https://doi.org/10.1007/bf02290946
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:211-215
The cyclic imines 3,3-dimethyl-, 3-spiro-3,4-dihydro-, and benzo[f]isoquinolines were synthesized, and their quaternary salts were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5648068aa650d040c70b68729b7d574a
https://doi.org/10.1007/bf02315187
https://doi.org/10.1007/bf02315187
Autor:
A. G. Mikhailovskii, V. S. Shklyaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 33:243-265
Published data on the synthesis of compounds containing the pyrrolo[2,1-a]isoquinoline system in their structure are reviewed. Examples of substances that have useful properties for practical purposes are given.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d0d3bddf5fb2fdbd99f66ac306ae7d6
https://doi.org/10.1007/bf02253103
https://doi.org/10.1007/bf02253103
Publikováno v:
Chemistry of Heterocyclic Compounds. 31:813-816
Reactions between 2,3-dioxopyrrolo[2,1-a]-isoquinolines and hydrazines and hydroxylamine afforded the corresponding hydrazones and oximes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfef19ccea7d64bff38704614a1af3a5
https://doi.org/10.1007/bf01170741
https://doi.org/10.1007/bf01170741
Autor:
A. G. Mikhailovskii, V. S. Shklyaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 31:573-576
The electronic absorption spectra of dioxo-compounds of the pyrroto[2,1-a]isoquinoline and pyrrolo[1,2-f]phenanthridine series and products of their condensation with o phenylenediamine were studied. The influence of substituents was demonstrated; ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac665c1b294246096751a970d8aa3086
https://doi.org/10.1007/bf01166332
https://doi.org/10.1007/bf01166332
Autor:
N. I. Vakhrina, N. A. Gornova, B. Ya. Syropyatov, V. S. Shklyaev, T. L. Malkova, V. I. Pantsurkin
Publikováno v:
Pharmaceutical Chemistry Journal. 28:660-663
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87f685147c9a6426c3d7ee7a539e40be
https://doi.org/10.1007/bf02219208
https://doi.org/10.1007/bf02219208
Autor:
A. G. Mikhailovskii, V. S. Shklyaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 30:818-821
Compounds of the 2,3-dioxopyrrolo[2, 1-a]isoquinoline and 2,3-dioxopyrrolo[1, 2-f]phenanthridine series were synthesized and the products of their condensation with o-phenylenediamine were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b512b0b429473d473035e744f70ee6be
https://doi.org/10.1007/bf01169639
https://doi.org/10.1007/bf01169639
Autor:
E. N. Glushkova, Yu. V. Shklyaev, B. B. Aleksandrov, B. A. Glushkov, A. A. Gorbunov, V. S. Shklyaev
Publikováno v:
Chemistry of Heterocyclic Compounds. 30:449-452
The reaction of 1-methylthio-3,3-dimethyl-6,7-di-R-dihydroisoquinolines with carboxylic acid hydrazides gives the corresponding hydrazides converted into derivatives of 1,2,4-triazolo[3,4-alisoquinoline. Reaction of these dihydroisoquinolines with hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fcd3501933cca2ab28d1252bc8f8ee2
https://doi.org/10.1007/bf01169940
https://doi.org/10.1007/bf01169940
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:1178-1181
We have synthesized secondary and tertiary enamines, derivatives of 1,2,3,4,4a,5,6,10b-octahydrophenanthridine, and we have considered the Z,E-isomerism of the enaminoesters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09717f93d883563967ea3b03ffb54b90
https://doi.org/10.1007/bf00538065
https://doi.org/10.1007/bf00538065
Autor:
V. S. Shklyaev, M. S. Gavrilov, N. D. Chkanikov, B. B. Aleksandrov, V. D. Sviridov, M. V. Galakhov
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4cd5b4bb895179b7f96d82822f1ca69
https://doi.org/10.1002/chin.199110184
https://doi.org/10.1002/chin.199110184