Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations Научная публикация
| Журнал |
Macroheterocycles
ISSN: 1998-9539 |
||||
|---|---|---|---|---|---|
| Вых. Данные | Год: 2021, Том: 14, Номер: 1, Страницы: 105-111 Страниц : 7 DOI: 10.6060/mhc200817s | ||||
| Ключевые слова | CuAAC-reaction; Dialkynes; Diazides; Diterpenoids; Isopimaric acid; Macrocycles | ||||
| Авторы |
|
||||
| Организации |
|
Реферат:
The first macrocyclic pimarane type diterpenoids containing fragments of 1,2,3-triazole and tricyclic diterpenoid isopimaric acid moieties were synthesized. The key step was the CuAAC reaction of various diazides with the dialkyne derivative obtained from 16-(carboxyphenyl)isopimaric acid. The molecular structure of the macrocyclic compound with 1,5-diazopentane unit was determined by single crystal X-ray diffraction analysis.
Библиографическая ссылка:
Gromova M.A.
, Kharitonov Y.V.
, Rybalova T.V.
, Shults E.E.
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations
Macroheterocycles. 2021.
V.14. N1. P.105-111. DOI: 10.6060/mhc200817s
WOS
Scopus
РИНЦ
OpenAlex
Click synthesis of triazole-linked polyazamacrocycles through selective isopimaric acid transformations
Macroheterocycles. 2021.
V.14. N1. P.105-111. DOI: 10.6060/mhc200817s
WOS
Scopus
РИНЦ
OpenAlex
Файлы:
Полный текст от издателя
Идентификаторы БД:
| Web of science: | WOS:000659682000012 |
| Scopus: | 2-s2.0-85108643262 |
| РИНЦ: | 46155970 |
| OpenAlex: | W3174085912 |