New Structural Modifications of Cotarnine Alkaloid Derivatives: Cotarnone and Dihydrocotarnine Full article
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Russian Journal of General Chemistry
ISSN: 1070-3632 , E-ISSN: 1608-3350 |
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| Output data | Year: 2020, Volume: 90, Number: 2, Pages: 238-243 Pages count : 6 DOI: 10.1134/s1070363220020127 | ||||||||
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Abstract:
Simplest derivatives of the cotarnine alkaloid, like cotarnone and 1,2-dihydrocotarnine, undergo electrophilic Einhorn acylamidomethylation (with 60–95% yield) and sulfochlorination with chlorosulfonic acid at position 5. At the same time cotarnone and its derivatives undergo additional O-protodemethylation. Using these and some other reactions, we synthesized a number of previously unknown derivatives of two substrates with 5-chloroacetamidomethyl, 5-arylaminomethyl, 5-aminomethyl and 5-sulfamide groups.
Cite:
Kartsev V.G.
, Zubenko A.A.
, Divaeva L.N.
, Morkovnik A.S.
, Baryshnikova T.K.
, Shirinian V.Z.
New Structural Modifications of Cotarnine Alkaloid Derivatives: Cotarnone and Dihydrocotarnine
Russian Journal of General Chemistry. 2020. V.90. N2. P.238-243. DOI: 10.1134/s1070363220020127 WOS Scopus OpenAlex
New Structural Modifications of Cotarnine Alkaloid Derivatives: Cotarnone and Dihydrocotarnine
Russian Journal of General Chemistry. 2020. V.90. N2. P.238-243. DOI: 10.1134/s1070363220020127 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000522647800012 |
| Scopus: | 2-s2.0-85083091180 |
| OpenAlex: | W3014881260 |