Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations Научная публикация
Журнал |
Journal of Inclusion Phenomena and Macrocyclic Chemistry
ISSN: 0923-0750 , E-ISSN: 1573-1111 |
||||
---|---|---|---|---|---|
Вых. Данные | Год: 2020, Том: 96, Номер: 3-4, Страницы: 245-250 Страниц : 6 DOI: 10.1007/s10847-019-00965-z | ||||
Ключевые слова | Macroheterocycles; Diterpenoids; Furanolabdanoid dialkynes; Diazides; CuAAC reaction; Zinc ion | ||||
Авторы |
|
||||
Организации |
|
Реферат:
The design and the preparation of a small library of optically active polyazamacrocyclic compounds with a furan bridge, connected by (4-(methylaminomethyl)-1,2,3-triazole) rings with methylene, ethyloxyethyl or ethylethoxyethyl units from natural labdanoid lambertianic acid is reported. The synthesis of the key 15,16-bis((tert-butoxycarbonyl(prop-2-ynyl)amino)methyl)labda-8(9),13,15-labdatriene from the plant diterpenoid lambertianic acid is also described. CuAAC reaction of this compounds with various diazides in the presence of Cu(II)/sodium ascorbate in methylene chloride/water reaction medium led to the mentioned chiral macrocyclic compounds with a furan bridge binding Zn2+ ions in solution. [GRAPHICS]
Библиографическая ссылка:
Brusentzeva O.I.
, Kharitonov Y.V.
, Fadeev D.S.
, Shults E.E.
Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020. V.96. N3-4. P.245-250. DOI: 10.1007/s10847-019-00965-z WOS Scopus
Synthesis and spectroscopic studies of furan-bridged polyazamacrocycles through 15,16-bis((prop-2-ynylamino)methyl)labdatriene transformations
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 2020. V.96. N3-4. P.245-250. DOI: 10.1007/s10847-019-00965-z WOS Scopus
Даты:
Опубликована online: | 22 нояб. 2019 г. |
Опубликована в печати: | 1 апр. 2020 г. |
Идентификаторы:
Web of science | WOS:000498020800001 |
Scopus | 2-s2.0-85075348240 |
OpenAlex | W2990704197 |