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Volumn 8, Issue 25, 2006, Pages 5829-5832

Palladium-catalyzed oxidative activation of arylcyclopropanes

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; CYCLOPROPANE DERIVATIVE; HETEROCYCLIC COMPOUND; LACTAM; PALLADIUM;

EID: 33846334815     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol062476e     Document Type: Article
Times cited : (59)

References (40)
  • 2
    • 33846328880 scopus 로고
    • The Chemistry of the Cyclopropyl Group;, Ed, Wiley: Chichester, UK
    • The Chemistry of the Cyclopropyl Group; Rappoport, Z., Ed.; Wiley: Chichester, UK, 1987; Vol. 1.
    • (1987) Rappoport, Z , vol.1
  • 5
    • 33846323064 scopus 로고    scopus 로고
    • In this paper, the term electroneutral refers to the cyclopropanes that do not have carbon- or heteroatom-containing electron-withdrawing and/or electron-donating substituents
    • In this paper, the term "electroneutral" refers to the cyclopropanes that do not have carbon- or heteroatom-containing electron-withdrawing and/or electron-donating substituents.
  • 26
    • 33846325268 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 27
    • 29344449953 scopus 로고    scopus 로고
    • For a recent example of β-alkoxy elimination in Wacker chemistry, see
    • (a) For a recent example of β-alkoxy elimination in Wacker chemistry, see: Trend, R. M.; Ramtohul, Y. K.; Stoltz, B. M. J. Am. Chem. Soc. 2005, 127, 17778.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 17778
    • Trend, R.M.1    Ramtohul, Y.K.2    Stoltz, B.M.3
  • 28
    • 0038640197 scopus 로고    scopus 로고
    • For a detailed molecular orbital discussion of phenylcyclopropane derivatives, see
    • (b) For a detailed molecular orbital discussion of phenylcyclopropane derivatives, see: Rademacher, P. Chem. Rev. 2003, 103, 933-975.
    • (2003) Chem. Rev , vol.103 , pp. 933-975
    • Rademacher, P.1
  • 29
    • 33846311195 scopus 로고    scopus 로고
    • No deuterium incorporation into the ring-opened product was detected in the case of the deuterated (COOD) derivative of acid 3a
    • No deuterium incorporation into the ring-opened product was detected in the case of the deuterated (COOD) derivative of acid 3a.
  • 30
    • 33846320631 scopus 로고
    • For the formation of π-allyl complexes during metal-promoted cyclopropane activation, see: a
    • For the formation of π-allyl complexes during metal-promoted cyclopropane activation, see: (a) Tulip, T. H.; Ibers, J. A. J. Am. Chem. Soc. 1979, 101, 9283.
    • (1979) J. Am. Chem. Soc , vol.101 , pp. 9283
    • Tulip, T.H.1    Ibers, J.A.2
  • 32
    • 33847085179 scopus 로고
    • For nucleophilic attack on the central carbon of π-allyl palladium complexes, see: a
    • For nucleophilic attack on the central carbon of π-allyl palladium complexes, see: (a) Hegedus, L. S.; Darlington, W. H.; Russell, C. E. J. Org. Chem. 1980, 45, 5193.
    • (1980) J. Org. Chem , vol.45 , pp. 5193
    • Hegedus, L.S.1    Darlington, W.H.2    Russell, C.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.