Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Andrey V. Kachanov"'
Autor:
Maxim E. Zhidkov, Maria A. Sidorova, Polina A. Smirnova, Oleg A. Tryapkin, Andrey V. Kachanov, Alexey V. Kantemirov, Lyubov G. Dezhenkova, Natalia E. Grammatikova, Elena B. Isakova, Andrey E. Shchekotikhin, Marina A. Pak, Olga N. Styshova, Anna A. Klimovich, Aleksandr M. Popov
Publikováno v:
Marine Drugs, Vol 22, Iss 2, p 53 (2024)
Based on the results of our own preliminary studies, the derivative of the marine alkaloid fascaplysin containing a phenyl substituent at C-9 was selected to evaluate the therapeutic potential in vivo and in vitro. It was shown that this compound has
Externí odkaz:
https://doaj.org/article/a3843695dc414199a26dc76a21fa30e7
Autor:
Andrey V. Gerasimenko, Andrey V. Kachanov, Andrey V. Zamaraev, Oleg Yu. Slabko, Konstantin V. Maslov, V. A. Kaminskii
Publikováno v:
Synlett. 29:2035-2038
New cyano-group-containing 1,3-oxaselenoles were obtained by the treatment of aroylacetonitriles with selenium(IV) oxide. The resulting products were shown to react with ammonia, hydrazine, or primary amines; this reaction was accompanied by aryl rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bffd5b902d08037a3934deeaff31826
https://doi.org/10.1055/s-0037-1609939
https://doi.org/10.1055/s-0037-1609939
Publikováno v:
Russian Journal of Organic Chemistry. 53:462-464
A simple laboratory procedure has been proposed for the synthesis of tetracyanoethylene in up to 54% yield by oxidative dimerization of malononitrile in the presence of selenium(IV) oxide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b93a4690d597c7848a34b0dcfe70d1c1
https://doi.org/10.1134/s1070428017030253
https://doi.org/10.1134/s1070428017030253
Publikováno v:
Journal of Heterocyclic Chemistry. 52:688-691
Salts of 5-amino-4-cyano-3-dicyanomethylene-2-pyrrolinone are formed by action of dilute aqueous solutions of alkalis on pentacyanopropenide-anion salts. These cyclic salts are transformed to 2,6-diamino-3,5-dicyanoisonicotinates by subsequent action
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d32545aeda4253271c9accf96bd3c06a
https://doi.org/10.1002/jhet.2157
https://doi.org/10.1002/jhet.2157
Publikováno v:
Russian Journal of Organic Chemistry. 48:1180-1186
Reactions of some 1,5-diketones with 2-aminobenzyl alcohol and 2-aminomethylaniline follow double cyclization scheme with formation of pyridobenzoxazine and pyridoquinazoline derivatives, respectively. Oxidative coupling of the cyclization products w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03ccf1a874b02252a2d8053d33e836d3
https://doi.org/10.1134/s1070428012090059
https://doi.org/10.1134/s1070428012090059
Publikováno v:
Synthetic Communications. 42:2464-2470
The thio- and selenocyanation of quinone monoimines of pyrido[1,2-a]benzimidazole series with the participation of dithiocyanogen and triselenodicyanide in mild reaction conditions results in forma...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ca5efb49c3bd04fe3a8ac8ac8d0a564
https://doi.org/10.1080/00397911.2011.560743
https://doi.org/10.1080/00397911.2011.560743
Publikováno v:
ChemInform. 46
Action of dilute aqueous solutions of alkalis on pentacyanopropenide salts affords pyrrolinone salts (II), which are transformed into isonicotinates [cf.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48be213ef5abfe415a148353ac85505d
https://doi.org/10.1002/chin.201535030
https://doi.org/10.1002/chin.201535030
Publikováno v:
ChemInform. 44
Reactions of 2-aminobenzyl alcohol (Ia) or related diamine (Ib) with diketones (II), (IV), (VI), or (VIII) follow double cyclization scheme with formation of pyridobenzoxazines, cf.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85c8e229849f04970d300f30e1d3264d
https://doi.org/10.1002/chin.201310185
https://doi.org/10.1002/chin.201310185
Publikováno v:
ChemInform. 43
A new, simple and efficient method for the electrophilic substitution of hydrogen in title quinoid structures by use of in situ formed triselenodicyanide or thiocyanogen is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a382db8f9d9e218658c568c37119ad5
https://doi.org/10.1002/chin.201247151
https://doi.org/10.1002/chin.201247151
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f574d7e6cbe2bd19dd69efc24b21b211
https://doi.org/10.1002/chin.200642141
https://doi.org/10.1002/chin.200642141