Synthetic transformations of higher terpenoids: XIV. Heterocyclization reactions of 15,16,18-ricarboxylabdadiene. New nitrogen-containing diterpenoids Full article
Journal |
Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
||
---|---|---|---|
Output data | Year: 2006, Volume: 42, Number: 5, Pages: 707-718 Pages count : DOI: 10.1134/S1070428006050113 | ||
Authors |
|
||
Affiliations |
|
Abstract:
The oxidation of methyl lambertianate with Jones' reagent formed the corresponding anhydride which reacted with amines to form N-substituted terpenoid maleimides. New maleimides demonstrated high activity and stereoselectivity in the Diels-Alder reaction with cyclopentadiene. The condensation of the diterpenoid anhydride with hydrazines led to the formation of derivatives of 3,6-dioxo-1,2,3,6-tetrahydropyridazines of labdane type.
Cite:
Kharitonov Y.V.
, Shul'ts E.E.
, Shakirov M.M.
, Tolstikov G.A.
Synthetic transformations of higher terpenoids: XIV. Heterocyclization reactions of 15,16,18-ricarboxylabdadiene. New nitrogen-containing diterpenoids
Russian Journal of Organic Chemistry. 2006. V.42. N5. P.707-718. DOI: 10.1134/S1070428006050113 WOS Scopus РИНЦ
Synthetic transformations of higher terpenoids: XIV. Heterocyclization reactions of 15,16,18-ricarboxylabdadiene. New nitrogen-containing diterpenoids
Russian Journal of Organic Chemistry. 2006. V.42. N5. P.707-718. DOI: 10.1134/S1070428006050113 WOS Scopus РИНЦ
ArticleLinkType.TRANSLATED_TO_ORIGINAL:
Харитонов Ю.В.
, Шульц Э.Э.
, Шакиров М.М.
, Толстиков Г.А.
Синтетические трансформации высших терпеноидов. xiii. реакции гете-роциклизации 15,16,18-трикарбокси-лабдадиена. новые азотсодержащие дитерпеноиды
Журнал органической химии (RUSS J ORG CHEM+). 2006. Т.42. №5. С.725-735. РИНЦ
Синтетические трансформации высших терпеноидов. xiii. реакции гете-роциклизации 15,16,18-трикарбокси-лабдадиена. новые азотсодержащие дитерпеноиды
Журнал органической химии (RUSS J ORG CHEM+). 2006. Т.42. №5. С.725-735. РИНЦ
Dates:
Published print: | May 1, 2006 |
Identifiers:
Web of science | WOS:000238334600011 |
Scopus | 2-s2.0-33745909372 |
Elibrary | 13521652 |
OpenAlex | W2949700668 |