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Volumn 79, Issue 19, 2014, Pages 9222-9230

Regio- and stereoselective synthesis of 2,3,5-trienoates by palladium-catalyzed alkoxycarbonylation of conjugated enyne carbonates

Author keywords

[No Author keywords available]

Indexed keywords

CARBONATES; CARBONYLATION; CATALYSIS; STEREOCHEMISTRY; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 84907761944     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo5014993     Document Type: Article
Times cited : (20)

References (57)
  • 13
    • 22944485617 scopus 로고    scopus 로고
    • Ma, S. Chem. Rev. 2005, 105, 2829
    • (2005) Chem. Rev. , vol.105 , pp. 2829
    • Ma, S.1
  • 35
    • 79961038042 scopus 로고    scopus 로고
    • An extended version of the method involves the reaction of enyne carbonates and organoboronic acids, which yields aryl vinylallenes
    • An extended version of the method involves the reaction of enyne carbonates and organoboronic acids, which yields aryl vinylallenes: Üçüncü, M.; Karakuş, E.; Kuş, M.; Akpinar, G. E.; Aksin-Artok, Ö.; Krause, N.; Karaca, S.; Elmaci, N.; Artok, L. J. Org. Chem. 2011, 76, 5959
    • (2011) J. Org. Chem. , vol.76 , pp. 5959
    • Üçüncü, M.1    Karakuş, E.2    Kuş, M.3    Akpinar, G.E.4    Aksin-Artok Ö.5    Krause, N.6    Karaca, S.7    Elmaci, N.8    Artok, L.9
  • 43
    • 84907802247 scopus 로고    scopus 로고
    • Such a trend was also observed for the alkoxycarbonylation reactions of conjugated enyne oxiranes: Manuscript in preparation.
    • Such a trend was also observed for the alkoxycarbonylation reactions of conjugated enyne oxiranes: Kuş, M.; Artok, L. Manuscript in preparation.
    • Kuş, M.1    Artok, L.2
  • 44
    • 0034605866 scopus 로고    scopus 로고
    • Reactions of enantiopure 2-en-4-yne acetates and organocuprates is the only example of the 1,5-substitution type reaction of conjugated enyne systems hitherto reported in the literature
    • Reactions of enantiopure 2-en-4-yne acetates and organocuprates is the only example of the 1,5-substitution type reaction of conjugated enyne systems hitherto reported in the literature: Krause, N.; Hoffman-Röder, A. Angew. Chem., Int. Ed. 2000, 39, 4355
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 4355
    • Krause, N.1    Hoffman-Röder, A.2
  • 48
    • 0030861889 scopus 로고    scopus 로고
    • Similarly, a palladium-catalyzed carbonylative reaction of a phenyl-substituted secondary enynol in methanol was also shown to undergo allylic etherification
    • Similarly, a palladium-catalyzed carbonylative reaction of a phenyl-substituted secondary enynol in methanol was also shown to undergo allylic etherification: Gabriele, B.; Salerno, G.; De Pascali, F.; Sciano, G. T.; Costa, M.; Chiusoli, G. P. Tetrahedron Lett. 1997, 38, 6877
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6877
    • Gabriele, B.1    Salerno, G.2    De Pascali, F.3    Sciano, G.T.4    Costa, M.5    Chiusoli, G.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.