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First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.0(4,16)]hexadeca-1,12-diene Научная публикация

Журнал Mendeleev Communications
ISSN: 0959-9436
Вых. Данные Год: 2009, Том: 19, Номер: 5, Страницы: 246-247 Страниц : DOI: 10.1016/j.mencom.2009.09.003
Авторы Agafontsev Alexander M. 1 , Rybalova Tatyana V. 1 , Gatilov Yurii V. 1 , Tkachev Alexey V. 1,2
Организации
1 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

Реферат: A simple synthetic derivative of natural diterpene cembrene [(1S,2E,4S,7E, 11E)-4-morpholin-4-ylcembra-2,7,11-trien-5-one E-oxime] was found to be highly sensitive to acids (sulfuric and trifluoroacetic), and it is transformed under acidic conditions to a tricyclic bridged system with the 5,6-dihydro-4H-1,2-oxazine moiety.
Библиографическая ссылка: Agafontsev A.M. , Rybalova T.V. , Gatilov Y.V. , Tkachev A.V.
First stereoselective cyclisation in the cembrane series: X-ray structure of (+)-(4R,8R,11S,12E,14S,16R)-11-isopropyl-4,8,14-trimethyl-14-morpholin-4-yl-3-oxa-2-azatricyclo[6.6.2.0(4,16)]hexadeca-1,12-diene
Mendeleev Communications. 2009. V.19. N5. P.246-247. DOI: 10.1016/j.mencom.2009.09.003 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 сент. 2009 г.
Идентификаторы БД:
Web of science: WOS:000271368800003
Scopus: 2-s2.0-70349339516
РИНЦ: 15300097
OpenAlex: W2952304214
Цитирование в БД:
БД Цитирований
Scopus 1
OpenAlex 2
Альметрики: