Zobrazeno 1 - 9
of 9
pro vyhledávání: '"N. S. Kaverina"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 6:715-718
The IR absorption spectra in 3800-1400 cm−1 region of 1-propyl-, 1-carboxy-, 1-carboxy-1-methyl-, and 1-benzyl-1-carboxy-6-hydroxy-1,-tetrahydro-Β-carbolines, their O-methyl derivatives, and their hydrochlorides are discussed. An assignment of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c858a919d29504288ea522209300147f
https://doi.org/10.1007/bf00470525
https://doi.org/10.1007/bf00470525
Publikováno v:
Chemistry of Heterocyclic Compounds. 7:991-993
Some 3-substituted 5-hydroxyindoles are smoothly hydrogenated in acid media in the presence of a palladium catalyst to the corresponding indolines, which in turn are readily oxidized by air oxygen in aqueous solutions at pH 10 to the corresponding 5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d90ee57a4b73b352e1cc84f08abf248
https://doi.org/10.1007/bf00477380
https://doi.org/10.1007/bf00477380
Publikováno v:
Chemischer Informationsdienst. 3
Die Indolinderivate (I) liefern bei der Oxidation mit Kaliumdichromat in 0,001 Schwefelsaure die sehr instabilen Chinonimine (II), aus denen durch Behandlung mit Sauren die Indole (III) entstehen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d0b366807631edad351cac83f25e970
https://doi.org/10.1002/chin.197249212
https://doi.org/10.1002/chin.197249212
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40af10a4e4f25d8e59a7e4afebf2b13a
https://doi.org/10.1002/chin.197206243
https://doi.org/10.1002/chin.197206243
Autor:
M F, Petrova, P N, Kibal'chich, Iu K, Man'ko, N S, Kaverina, G P, Men'shikov, E Ch, Pukhal'skaia
Publikováno v:
Voprosy onkologii. 14(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::080bbf5b2107811c8c911b4e09154c5d
https://pubmed.ncbi.nlm.nih.gov/5722200
https://pubmed.ncbi.nlm.nih.gov/5722200
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49f107550667f70171da436ba7451fbf
https://doi.org/10.1002/chin.197044084
https://doi.org/10.1002/chin.197044084
Publikováno v:
Chemistry of Heterocyclic Compounds. 8:914-915
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bb6d4018dc3b36a909437f9f36ba8d
https://doi.org/10.1007/bf00475235
https://doi.org/10.1007/bf00475235
Publikováno v:
Pharmaceutical Chemistry Journal. 1:471-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f0a027ef2a1121a4ec530d4f99dd2da
https://doi.org/10.1007/bf00766098
https://doi.org/10.1007/bf00766098
Publikováno v:
Chemistry of Heterocyclic Compounds. 3:684-685
A study has been made of the condensation of serotonin with aldehydes to give the corresponding β-carboline derivatives. In most cases the reaction was run under biological conditions (pH 5. 4, 36‡). The following aldehydes were reacted: acetaldeh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::799244dfb0d3fc65a69282fd4b2d2f0e
https://doi.org/10.1007/bf00468345
https://doi.org/10.1007/bf00468345