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Volumn , Issue 5, 2006, Pages 1185-1192

Effect of the leaving group on the rate and mechanism of the palladium-catalyzed isomerization of cyclic allylic benzoates in allylic substitutions

Author keywords

Allylic benzoates; Allylic complexes; Isomerization; Kinetics; Mechanism; Palladium

Indexed keywords


EID: 33644798263     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200500708     Document Type: Article
Times cited : (33)

References (43)
  • 1
    • 0003417469 scopus 로고
    • (Eds: B. M. Trost, I. Pflemming, M. F Semmelhack) Pergamon, Oxford
    • a) S. A. Godleski, in: Comprehensive Organic Synthesis, vol. 4 (Eds: B. M. Trost, I. Pflemming, M. F Semmelhack) Pergamon, Oxford, 1991;
    • (1991) Comprehensive Organic Synthesis, Vol. 4 , vol.4
    • Godleski, S.A.1
  • 29
    • 33644790374 scopus 로고    scopus 로고
    • note
    • [7a,7b]
  • 30
    • 33644813353 scopus 로고    scopus 로고
    • note
    • a) The straight line does not go through zero due to an S-shaped curve at short time (see Figure 1, b);
  • 31
    • 33644800114 scopus 로고    scopus 로고
    • note
    • -5 M (DMF, 25°C, Scheme 5);
  • 32
    • 33644815264 scopus 로고    scopus 로고
    • note
    • -1 (25°C);
  • 33
    • 33644791388 scopus 로고    scopus 로고
    • note
    • -1.
  • 35
    • 0038271730 scopus 로고    scopus 로고
    • For the use of conductivity measurements for the determination of mechanisms, see: A. Jutand, Eur. J. Inorg. Chem. 2003, 2017.
    • (2003) Eur. J. Inorg. Chem. , pp. 2017
    • Jutand, A.1
  • 40
    • 33644788587 scopus 로고    scopus 로고
    • note
    • 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.