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Volumn 132, Issue 26, 2010, Pages 8878-8879

Rhodium-catalyzed arylzincation of terminal allenes providing allylzinc reagents and its application to versatile three-component coupling reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALLENES; ELECTROPHILES; FUNCTIONALIZED; REGIO-SELECTIVE; RHODIUM-CATALYZED; THREE-COMPONENT COUPLING REACTION;

EID: 77954289640     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja102303s     Document Type: Article
Times cited : (25)

References (41)
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    • Catalytic three-component couplings involving allenes, aryl halides, and carbonyls in the presence of In metal
  • 13
    • 77954247683 scopus 로고    scopus 로고
    • Catalytic two-component allene-carbonyl reductive coupling via hydrogenation for diversity-oriented efficient synthesis of homoallyl alchohols:
    • Catalytic two-component allene-carbonyl reductive coupling via hydrogenation for diversity-oriented efficient synthesis of homoallyl alchohols:
  • 18
    • 77954255868 scopus 로고    scopus 로고
    • Recent examples of transition-metal-catalyzed carbozincation of alkynes: Ni
    • Recent examples of transition-metal-catalyzed carbozincation of alkynes: Ni
  • 31
    • 33644650016 scopus 로고    scopus 로고
    • Rhodium-catalyzed hydroarylation of allenes with arylboronic acids proceeds via direct protonation of the resulting allylrhodium without transmetalation between the allylrhodium and arylboronic acid
    • Rhodium-catalyzed hydroarylation of allenes with arylboronic acids proceeds via direct protonation of the resulting allylrhodium without transmetalation between the allylrhodium and arylboronic acid: Nishimura, T., Hirabayashi, S., Yasuhara, Y., and Hayashi, T. J. Am. Chem. Soc. 2006, 128, 2556
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 2556
    • Nishimura, T.1    Hirabayashi, S.2    Yasuhara, Y.3    Hayashi, T.4
  • 32
    • 34250882833 scopus 로고    scopus 로고
    • Copper-catalyzed conjugate addition of organozinc reagents to reactive allenic esters providing zinc dienolates
    • Copper-catalyzed conjugate addition of organozinc reagents to reactive allenic esters providing zinc dienolates: Oisaki, K., Zhao, D., Kanai, M., and Shibasaki, M. J. Am. Chem. Soc. 2007, 129, 7439
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 7439
    • Oisaki, K.1    Zhao, D.2    Kanai, M.3    Shibasaki, M.4
  • 33
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    • Addition to allenes bearing a directing hydroxy group providing allylzincs
    • Addition to allenes bearing a directing hydroxy group providing allylzincs: Richey, H. G., Jr. and Szucs, S. S. Tetrahedron Lett. 1971, 41, 3785
    • (1971) Tetrahedron Lett. , vol.41 , pp. 3785
    • Richey Jr., H.G.1    Szucs, S.S.2
  • 34
    • 33845799176 scopus 로고    scopus 로고
    • Efficient three-component coupling of allenes, Grignard reagents, and chlorosilanes or alkyl halides was reported. However, precise mechanistic investigations of the reactions showed that generation of allylmagnesium intermediates might not be a major pathway
    • Efficient three-component coupling of allenes, Grignard reagents, and chlorosilanes or alkyl halides was reported. However, precise mechanistic investigations of the reactions showed that generation of allylmagnesium intermediates might not be a major pathway: Fujii, Y., Terao, J., Kuniyasu, H., and Kambe, N. J. Organomet. Chem. 2007, 692, 375
    • (2007) J. Organomet. Chem. , vol.692 , pp. 375
    • Fujii, Y.1    Terao, J.2    Kuniyasu, H.3    Kambe, N.4
  • 37
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    • The regioselectivity of the allylic substitution reaction with allylic copper reagents is known to heavily depend on substrates and reagents used. See
    • The regioselectivity of the allylic substitution reaction with allylic copper reagents is known to heavily depend on substrates and reagents used. See: Liepins, V. and Bäckvall, J.-E. Eur. J. Org. Chem. 2002, 3527
    • (2002) Eur. J. Org. Chem. , pp. 3527
    • Liepins, V.1    Bäckvall, J.-E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.