Sciact
  • EN
  • RU

Synthetic transformations of higher terpenoids: X. Intramolecular cyclization of N-allyl- and N-propargyl-16-dialkylammoniomethyl-12-furfuryl-13,14,15,16-tetranorlabdanoid bromides Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2005, Volume: 41, Number: 8, Pages: 1145-1157 Pages count : 13 DOI: 10.1007/s11178-005-0307-7
Authors Kharitonov YV 1 , Shults EE 1 , Shakirov MM 1 , Tolstikov GA 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Quaternary ammonium salts obtained by quaternization of lambertian acid 16-dialkylaminomethyl derivatives effected by allyl halides or proparglbromide undergo intramolecular [4+2]-cycloaddition resulting in diterpenoids of labdane type containing a heterocyclic fragment of 10-oxa-3-azatricyclo[5.2.1.0(1,5)]decene or 10oxa-3-azatricyclo[5.2.1.0(1,5)]deca-6,8-diene.
Cite: Kharitonov Y. , Shults E. , Shakirov M. , Tolstikov G.
Synthetic transformations of higher terpenoids: X. Intramolecular cyclization of N-allyl- and N-propargyl-16-dialkylammoniomethyl-12-furfuryl-13,14,15,16-tetranorlabdanoid bromides
Russian Journal of Organic Chemistry. 2005. V.41. N8. P.1145-1157. DOI: 10.1007/s11178-005-0307-7 WOS Scopus РИНЦ OpenAlex
Original: Харитонов Ю.В. , Шульц Э.Э. , Шакиров М.М. , Толстиков Г.А.
Синтетические трансформации высших терпеноидов. x. внутримолекулярная циклизация бромидов n-аллил-и n-пропаргил-16-диалкиламмониометил-12-фурфурил-13.14.15.16-тетранорлабданоилов
Журнал органической химии (RUSS J ORG CHEM+). 2005. Т.41. №8. С.1167-1179. РИНЦ
Dates:
Published print: Aug 1, 2005
Identifiers:
Web of science: WOS:000232963000006
Scopus: 2-s2.0-27744436051
Elibrary: 13478619
OpenAlex: W2951788220
Citing:
DB Citing
Web of science 7
Scopus 6
Elibrary 6
OpenAlex 8
Altmetrics: