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Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent Full article

Journal Journal of Molecular Structure
ISSN: 0022-2860 , E-ISSN: 1872-8014
Output data Year: 2022, Volume: 1247, Article number : 131373, Pages count : DOI: 10.1016/j.molstruc.2021.131373
Tags Cross-coupling reaction; Eudesmane-type methylene lactones; Isoalantolactone; Isoquinoline; Quinoline; X-ray structure
Authors Stepanova V.A. 1 , Patrushev S.S. 1,2 , Rybalova T.V. 1 , Shults E.E. 1
Affiliations
1 N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Lavrentyev Ave, 9Novosibirsk 630090, Russian Federation
2 Novosibirsk State University, Pirogova St. 2Novosibirsk 630090, Russian Federation

Abstract: An efficient and simple protocol for the Heck reaction of accessible natural eudesmane-type methylene lactone isoalantolactone or its derivatives - 4,15-epoxyisoalantolactone, and 3-hydroxyisoalantolactone, with halosubstituted quinolines and isoquinolines using Pd(OAc)2 as the catalyst is presented. The reactions proceed well in dimethylformamide and TBAB in the absence of phosphine ligands. The structures of isoalantolactone-quinoline and isoalantolactone-isoquinoline hybrids were analyzed by mass spectrum, elemental analysis and NMR spectral studies. The crystal structure of new compounds was determined from single crystal X-ray diffraction data. © 2021 Elsevier B.V.
Cite: Stepanova V.A. , Patrushev S.S. , Rybalova T.V. , Shults E.E.
Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent
Journal of Molecular Structure. 2022. V.1247. 131373 . DOI: 10.1016/j.molstruc.2021.131373 WOS Scopus РИНЦ OpenAlex
Identifiers:
Web of science: WOS:000704359900017
Scopus: 2-s2.0-85114128429
Elibrary: 47051095
OpenAlex: W3196402499
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Scopus 2
Elibrary 1
Web of science 2
OpenAlex 2
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