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Volumn 39, Issue 25, 1998, Pages 4417-4420

Effect of carbenoid structure on the reactivity of rhodium-stabilized carbenoids

Author keywords

[No Author keywords available]

Indexed keywords

CARBENOID; PHENYLDIAZOACETATE DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG; VINYLDIAZOACETATE DERIVATIVE;

EID: 0032543492     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00836-3     Document Type: Article
Times cited : (45)

References (25)
  • 1
    • 0000180645 scopus 로고    scopus 로고
    • (1) For representative examples of vinylcarbenoid transformations, see: (a) Davies, H. M. L. Aldrichimica Acta 1997, 30, 107.
    • (1997) Aldrichimica Acta , vol.30 , pp. 107
    • Davies, H.M.L.1
  • 8
    • 84987014061 scopus 로고
    • (d) Paulini, K.; Reissig. H. -U. J. Prakt. Chem. 1995, 337, 55. Aller, E.; Cox, G. G.; Miller, D. J.; Moody, C. J. Tetrahedron Lett. 1994, 35, 5949.
    • (1995) J. Prakt. Chem. , vol.337 , pp. 55
    • Paulini, K.1    Reissig, H.-U.2
  • 20
    • 0000709206 scopus 로고
    • (7) For recent reviews that discuss the status of intermolecular C-H insertions, see: (a) Ye, T.; McKervey, M. A. Chem. Rev. 1994, 94, 1091.
    • (1994) Chem. Rev. , vol.94 , pp. 1091
    • Ye, T.1    McKervey, M.A.2
  • 22
    • 84920311374 scopus 로고    scopus 로고
    • note
    • 1H-decoupling experiments). Furthermore, irradiation of one of the C(4) protons (2.60 ppm) results in an nOe enhancement of the C(5) proton (5.81 ppm); irradiation of this C(5) proton results in enhancement of the same C(4) proton resonance. Additional nOe enhancements were observed between the C(3) and the C(4) protons, the C(5) and one of the C(6) protons, and the C(8) and one of the C(9) protons. (equation presented)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.