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Volumn 27, Issue 7, 2008, Pages 1645-1648

Nickel-catalyzed coupling of alkyne-tethered vinylcyclopropanes and allyl chloride

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHEMICAL BONDS; REACTION KINETICS; STEREOSELECTIVITY;

EID: 42449155887     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om7012524     Document Type: Article
Times cited : (13)

References (42)
  • 3
    • 4544385916 scopus 로고    scopus 로고
    • Reactions with VCPs (Y = C): (a) Zuo, G.; Louie, J. Angew. Chem., Int. Ed. 2004, 43, 2277.
    • Reactions with VCPs (Y = C): (a) Zuo, G.; Louie, J. Angew. Chem., Int. Ed. 2004, 43, 2277.
  • 7
    • 33646463634 scopus 로고    scopus 로고
    • Reaction with cyclopropyl ketones and imines (Y = O, N): (a) Liu, L.; Montgomery, J. J. Am. Chem. Soc. 2006, 128, 5348.
    • Reaction with cyclopropyl ketones and imines (Y = O, N): (a) Liu, L.; Montgomery, J. J. Am. Chem. Soc. 2006, 128, 5348.
  • 23
    • 11844273927 scopus 로고    scopus 로고
    • and references therein. For a recent review on the catalytic cleavage of a carbon-carbon bond, including β-carbon eliminations, see
    • For a recent review on the catalytic cleavage of a carbon-carbon bond, including β-carbon eliminations, see: Jun, C.-H. Chem. Soc. Rev. 2004, 33, 610 and references therein.
    • (2004) Chem. Soc. Rev , vol.33 , pp. 610
    • Jun, C.-H.1
  • 24
    • 4143056958 scopus 로고    scopus 로고
    • For other examples of the nickel-catalyzed reactions, including the β-carbon elimination process, see: a
    • For other examples of the nickel-catalyzed reactions, including the β-carbon elimination process, see: (a) Necas, D.; Tursky, M.; Kotora, M. J. Am. Chem. Soc. 2004, 126, 10222.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 10222
    • Necas, D.1    Tursky, M.2    Kotora, M.3
  • 41
    • 32944471300 scopus 로고    scopus 로고
    • o species by Zn powder. The nickel hydride species would catalyze the cycloisomerization of 1,6-enynes; see: Ikeda, S.; Daimon, N.; Sanuki, R.; Odashima, K. Chem. Eur. J. 2006, 12, 1797.
    • o species by Zn powder. The nickel hydride species would catalyze the cycloisomerization of 1,6-enynes; see: Ikeda, S.; Daimon, N.; Sanuki, R.; Odashima, K. Chem. Eur. J. 2006, 12, 1797.
  • 42
    • 0002941081 scopus 로고
    • On the other hand, 2 did not react with Zn powder in MeCN at room temperature to generate the allylzinc chloride
    • Furukawa, J.; Kawabata, N. Adv. Organomet. Chem. 1974, 12, 83. On the other hand, 2 did not react with Zn powder in MeCN at room temperature to generate the allylzinc chloride.
    • (1974) Adv. Organomet. Chem , vol.12 , pp. 83
    • Furukawa, J.1    Kawabata, N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.