메뉴 건너뛰기




Volumn 6, Issue 3, 2009, Pages 219-238

Transition metal-catalyzed [2+2] cycloaddition reactions between bicyclic alkenes and alkynes

Author keywords

Alkyne; Bicyclic alkene; Cycloaddition; Cyclobutene; Transition metal

Indexed keywords


EID: 70350099473     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017909788921907     Document Type: Article
Times cited : (30)

References (102)
  • 2
    • 0004136903 scopus 로고
    • Vols. JAI Press: Greenwich, 1999
    • Advances in Cycloaddition; Vols. 1-6, JAI Press: Greenwich, 1988-1999.
    • (1988) Advances in Cycloaddition , vol.1-6
  • 3
    • 0002110351 scopus 로고    scopus 로고
    • For reviews on transition metal-catalyzed cycloadditions, see:
    • For reviews on transition metal-catalyzed cycloadditions, see: (a) Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49
    • (1996) Chem. Rev. , vol.96 , pp. 49
    • Lautens, M.1    Klute, W.2    Tam, W.3
  • 9
    • 0001216151 scopus 로고    scopus 로고
    • Jabosen, E. N.; Pfaltz, A.; Yamamoto, H., Springer-Verlag: Berlin
    • Buchwald, S. L.; Hicks, F. A. In: Jabosen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Comprehensive Asymmetric Catalysis I-III, Springer-Verlag: Berlin, 1999, Vol. 2, pp. 491-510
    • (1999) Comprehensive Asymmetric Catalysis I-III , vol.2 , pp. 491-510
    • Buchwald, S.L.1    Hicks, F.A.2
  • 27
    • 0001218192 scopus 로고
    • For selected examples of metal-catalyzed [2+2] cycloadditions of a bicyclic alkene and an alkene for the formation of cyclobutane rings (Scheme 1, path b), see:
    • For selected examples of metal-catalyzed [2+2] cycloadditions of a bicyclic alkene and an alkene for the formation of cyclobutane rings (Scheme 1, path b), see: (a) Noyori, R.; Ishigumi, T.; Hayashi, N.; Takaya, H. J. Am. Chem. Soc. 1973, 95, 1674
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 1674
    • Noyori, R.1    Ishigumi, T.2    Hayashi, N.3    Takaya, H.4
  • 30
    • 0007626692 scopus 로고
    • For example of metal-catalyzed [2+2] dimerization of norbornadiene (Scheme 1, path c), see:
    • For example of metal-catalyzed [2+2] dimerization of norbornadiene (Scheme 1, path c), see: (a) Schrauzer, G.N.; Bastian, B.N.; Fosselius, G.A. J. Am. Chem. Soc. 1966, 88, 4890
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 4890
    • Schrauzer, G.N.1    Bastian, B.N.2    Fosselius, G.A.3
  • 33
    • 37049132250 scopus 로고
    • For selected examples of metal-catalyzed Pauson-Khand [2+2+1] cycloadditions of norbornadienes (Scheme 1, path d), see: (a)
    • For selected examples of metal-catalyzed Pauson-Khand [2+2+1] cycloadditions of norbornadienes (Scheme 1, path d), see: (a) Khand, I. U.; Knox, G. R.; Pauson, P. L.; Watts, W. E.; Foreman, M. I. J. Chem. Soc. Perkin Trans. 1, 1973, 977
    • (1973) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 977
    • Khand, I.U.1    Knox, G.R.2    Pauson, P.L.3    Watts, W.E.4    Foreman, M.I.5
  • 36
    • 0000142305 scopus 로고
    • For selected examples of metal-catalyzed [3+2] cycloadditions of norbornadienes (Scheme 1, path e), see:
    • For selected examples of metal-catalyzed [3+2] cycloadditions of norbornadienes (Scheme 1, path e), see: (a) Trost, B. M.; Chan, D. M. T. J. Am. Chem. Soc.,1983, 105, 2315
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 2315
    • Trost, B.M.1    Chan, D.M.T.2
  • 38
    • 0025886856 scopus 로고
    • For selected examples of Co-catalyzed [2+2+2] Homo-diels-Alder reaction of norbornadienes (Scheme 1, path f), see:
    • For selected examples of Co-catalyzed [2+2+2] Homo-diels-Alder reaction of norbornadienes (Scheme 1, path f), see: (a) Duan, I. F.; Cheng, C. H.; Shaw, J. S.; Cheng, S. S.; Liou, K. F. Chem. Soc. Chem. Commun. 1991, 1347
    • (1991) Chem. Soc. Chem. Commun. , pp. 1347
    • Duan, I.F.1    Cheng, C.H.2    Shaw, J.S.3    Cheng, S.S.4    Liou, K.F.5
  • 40
    • 0000435481 scopus 로고
    • For an example of Ni-catalyzed [2+2+2] Homo-diels-Alder reaction of norbornadienes (Scheme 1, path g), see:, and references cited therein
    • For an example of Ni-catalyzed [2+2+2] Homo-diels-Alder reaction of norbornadienes (Scheme 1, path g), see: Lautens, M.; Edwards, L. G.; Tam, W.; Lough, A. J. J. Am. Chem. Soc.,1995, 117, 10276 and references cited therein.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10276
    • Lautens, M.1    Edwards, L.G.2    Tam, W.3    Lough, A.J.4
  • 41
    • 0001675970 scopus 로고
    • For an examples of a Ni-catalyzed [2+2+2] cycloadditions of nor-bornadienes (Scheme 1, path i), see: (a) see:
    • For an examples of a Ni-catalyzed [2+2+2] cycloadditions of nor-bornadienes (Scheme 1, path i), see: (a) see: Schrauzer, G.N.; Glockner, P. Chem. Ber. 1964, 97, 2451.
    • (1964) Chem. Ber. , vol.97 , pp. 2451
    • Schrauzer, G.N.1    Glockner, P.2
  • 42
    • 70350102389 scopus 로고    scopus 로고
    • For an example of a Ni-catalyzed [2+2+2+2] cycloaddition of norbornadiene (Scheme 1, path i), see
    • For an example of a Ni-catalyzed [2+2+2+2] cycloaddition of norbornadiene (Scheme 1, path i), see: Schrauzer, G. N.; Glockner, P. Chem. Ber. 1964, 97, 2451.
    • (2451) Chem. Ber. , vol.1964 , pp. 97
    • Schrauzer, G.N.1    Glockner, P.2
  • 43
    • 0000123583 scopus 로고
    • For an example of a Ti-catalyzed [6+2+2] cycloaddition of norbornadiene (Scheme 1, path j), see
    • For an example of a Ti-catalyzed [6+2+2] cycloaddition of norbornadiene (Scheme 1, path j), see: Turecek, F.; Mach, K.; Antropiusova, H.; Petrusova, L.; Hanus, V.; Sedmera, P. Tetrahedron, 1984, 40, 3295.
    • (1984) Tetrahedron , vol.40 , pp. 3295
    • Turecek, F.1    Mach, K.2    Antropiusova, H.3    Petrusova, L.4    Hanus, V.5    Sedmera, P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.