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Volumn 43, Issue 34, 2002, Pages 5989-5991

Proton-catalysed E-Z isomerisation and Pd(II) assisted carbon-carbon cleavage on 3-phenyl-4-(2,4,6-trimethoxyphenyl)methyleneisoxazolin-5-one

Author keywords

E Z isomerisation; Pd(II) assisted C C sp2 exocyclic cleavage; Proton catalysis

Indexed keywords

3 PHENYL 4 (2,4,6 TRIMETHOXYPHENYL)METHYLENEISOXAZOLIN 5 ONE; CARBON; ISOXAZOLINE DERIVATIVE; PALLADIUM; PROTON; UNCLASSIFIED DRUG;

EID: 0037136183     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01258-3     Document Type: Article
Times cited : (5)

References (23)
  • 11
    • 0009908957 scopus 로고    scopus 로고
    • 3), δ=6.06 (s, 2H, Ar).
  • 17
    • 0009935774 scopus 로고    scopus 로고
    • 3 of 2). Corrections for the relaxation rate, calculated by the residual relative intensity of the 3.40 ppm resonance after long selective irradiation at 3.82 ppm, went from 5 to 18%. The ionic strength was maintained constant at μ=0.5 by addition of anhydrous LiCl.
  • 18
    • 0009906143 scopus 로고    scopus 로고
    • 2 were added to the solutions. Pseudo-first-order rates of 11 formation from the acid mixtures of 1-2 at equilibrium were obtained by periodic monitoring of the trimethoxy-benzene resonance intensity at 3.75 ppm. The ionic strength was maintained constant at μ=0.5 by addition of anhydrous LiCl.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.