Zobrazeno 1 - 10
of 12
pro vyhledávání: '"B. Ya. Eryshev"'
Publikováno v:
Theoretical and Experimental Chemistry. 14:653-656
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6461c3fae325a57162a23e623263240
https://doi.org/10.1007/bf00519074
https://doi.org/10.1007/bf00519074
Autor:
M. D. Mashkovskii, P. I. Mushulov, B. Ya. Eryshev, V. S. Fedorova, N. N. Suvorov, V. G. Avramenko, I. A. Orlova, T. K. Trubitsyna
Publikováno v:
Pharmaceutical Chemistry Journal. 4:671-674
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e28da537daff9877e8a6d5d80935cb07
https://doi.org/10.1007/bf00758473
https://doi.org/10.1007/bf00758473
Autor:
B. Ya. Eryshev, N. N. Suvorov
Publikováno v:
Chemistry of Heterocyclic Compounds. 16:158-160
The alkylation of indole with the tridecanolide, pentadecanolide, and oxo lactones of ω-hydroxyethoxyundecanoic and ω-hydroxybutoxyundecanoic acids was investigated. Higher indolylalkanoic acids, viz., ω-(3-indolyl)undecanoic, ω-(3-indolyl)tride-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbd70c994083d2aa54f97a62f69b7d88
https://doi.org/10.1007/bf02401692
https://doi.org/10.1007/bf02401692
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:1313-1315
ω-(3-Indolyl)alkyl bromides, the structure of which was confirmed by alternative synthesis fromω-(3-indolyl)alkanols, were obtained by a modified Borodin-Hunsdiecker reaction from mercury salts ofω-(3-indolyl)alkanoie acids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a0f3855de4ecab0a36d3db635648d1e
https://doi.org/10.1007/bf01175086
https://doi.org/10.1007/bf01175086
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:433-435
The alkylation of indole by polyesters of ω-hydroxyalkanoic acids was studied. The optimum conditions and ratios of the reacting substances were found, and a number of ω-(3-indolyl)alkanoic acids were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52fbb81a3036c1680d203bc65db42673
https://doi.org/10.1007/bf00504405
https://doi.org/10.1007/bf00504405
Publikováno v:
Pharmaceutical Chemistry Journal. 9:569-571
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82e293f70df148291dc6a7502eb28531
https://doi.org/10.1007/bf00758851
https://doi.org/10.1007/bf00758851
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe393876dc3482d9f4e42e0d7eb34074
https://doi.org/10.1002/chin.197510240
https://doi.org/10.1002/chin.197510240
Autor:
N. N. Suvorov, B. Ya. Eryshev
Publikováno v:
Chemischer Informationsdienst. 11
The alkylation of indole with the tridecanolide, pentadecanolide, and oxo lactones of ω-hydroxyethoxyundecanoic and ω-hydroxybutoxyundecanoic acids was investigated. Higher indolylalkanoic acids, viz., ω-(3-indolyl)undecanoic, ω-(3-indolyl)tride-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d42294899e00521b83e6a2c05c489d5
https://doi.org/10.1002/chin.198025199
https://doi.org/10.1002/chin.198025199
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d30911f9367e79ec78189e409c56fa4
https://doi.org/10.1002/chin.198536178
https://doi.org/10.1002/chin.198536178
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c23d1601bd58f70a9ee17f4d982e883c
https://doi.org/10.1002/chin.197605173
https://doi.org/10.1002/chin.197605173