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Volumn 92, Issue 22, 1970, Pages 6630-6635

The Palladium Chloride Catalyzed Cyclodimerization of 1-Methylcyclopropene

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EID: 33947297312     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00725a041     Document Type: Article
Times cited : (56)

References (37)
  • 3
    • 84981887315 scopus 로고
    • For a review, see
    • For a review, see G. N. Schrauzer, Advan. Catal., 18, 377 (1968).
    • (1968) Advan. Catal. , vol.18 , pp. 377
    • Schrauzer, G.N.1
  • 5
    • 0003019335 scopus 로고
    • For a review of transition metal-acetylene chemistry, see
    • For a review of transition metal-acetylene chemistry, see F. L. Bowden and A. B. P. Lever, Organometal. Chem. Rec., 3, 227 (1968).
    • (1968) Organometal. Chem. Rec. , vol.3 , pp. 227
    • Bowden, F.L.1    Lever, A.B.P.2
  • 11
    • 49849125100 scopus 로고
    • Octamethyl-.y-tncyclo[4.2.0.02′6]octa-3,7-diene
    • Octamethyl-.y-tncyclo[4.2.0.02′6]octa-3,7-diene, H. Hart and L. R. Lerner, Tetrahedron, 25, 813 (1969);
    • (1969) Tetrahedron , vol.25 , pp. 813
    • Hart, H.1    Lerner, L.R.2
  • 16
    • 48249112048 scopus 로고
    • have recently reported the ene dimerization of cyclopropene itself
    • P. Dowd and A. Gold have recently reported the ene dimerization of cyclopropene itself: Tetrahedron Lett., 85 (1969);
    • (1969) Tetrahedron Lett. , pp. 85
    • Dowd, P.1    Gold, A.2
  • 17
    • 84981808066 scopus 로고
    • for a recent review of the ene reaction, see
    • for a recent review of the ene reaction, see H. M. R. Hoffmann, Angew. Chem., Int. Ed. Engl., 8, 556 (1969).
    • (1969) Angew. Chem., Int. Ed. Engl. , vol.8 , pp. 556
    • Hoffmann, H.M.R.1
  • 23
    • 37049050303 scopus 로고
    • Although the trimerization of 2-butyne by dichlorobis(benzonitrile)paUadium(II) is described as catalytic1 there is no evidence for more than one “catalyst cycle.”
    • Although the trimerization of 2-butyne by dichlorobis(benzonitrile)paUadium(II) is described as catalytic1 (W. I. Dent, R. Long, and A. J. Wilkinson, J. Chem. Soc. 1585 (1964)), there is no evidence for more than one “catalyst cycle.”
    • (1964) J. Chem. Soc. , pp. 1585
    • Dent, W.I.1    Long, R.2    Wilkinson, A.J.3
  • 34
    • 33947298707 scopus 로고
    • For an intramolecular example of this type of a reaction, see
    • For an intramolecular example of this type of a reaction, see T. J. Katz and S. A. Cerefice, J. Amer. Chem. Soc., 91, 6519 (1969).
    • (1969) J. Amer. Chem. Soc. , vol.91 , pp. 6519
    • Katz, T.J.1    Cerefice, S.A.2
  • 36
    • 85022715906 scopus 로고    scopus 로고
    • See ref 18
    • See Dent, et al., ref 18.
    • Dent1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.