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Volumn 61, Issue 18, 1996, Pages 6462-6464

Cyclopropene: A new simple synthesis and Diels-Alder reactions with cyclopentadiene and 1,3-diphenylisobenzofuran

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EID: 0001399489     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo960728r     Document Type: Article
Times cited : (56)

References (37)
  • 1
    • 36749118248 scopus 로고
    • Stigliani, W. M.; Laurie, V. W.; Li, J. C. J. Chem. Phys. 1975, 62, 1890. Kasai, P. H.; Myers, R. J.; Eggers, D. F. Jr.; Wiberg, K. B. J. Chem. Phys. 1959,30, 512. Dunitz, J. D.; Feldman, H. G.; Schomaker, V. J. Chem. Phys. 1952, 20, 1708.
    • (1975) J. Chem. Phys. , vol.62 , pp. 1890
    • Stigliani, W.M.1    Laurie, V.W.2    Li, J.C.3
  • 2
    • 36849117236 scopus 로고
    • Stigliani, W. M.; Laurie, V. W.; Li, J. C. J. Chem. Phys. 1975, 62, 1890. Kasai, P. H.; Myers, R. J.; Eggers, D. F. Jr.; Wiberg, K. B. J. Chem. Phys. 1959,30, 512. Dunitz, J. D.; Feldman, H. G.; Schomaker, V. J. Chem. Phys. 1952, 20, 1708.
    • (1959) J. Chem. Phys. , vol.30 , pp. 512
    • Kasai, P.H.1    Myers, R.J.2    Eggers Jr., D.F.3    Wiberg, K.B.4
  • 3
    • 2342655790 scopus 로고
    • Stigliani, W. M.; Laurie, V. W.; Li, J. C. J. Chem. Phys. 1975, 62, 1890. Kasai, P. H.; Myers, R. J.; Eggers, D. F. Jr.; Wiberg, K. B. J. Chem. Phys. 1959,30, 512. Dunitz, J. D.; Feldman, H. G.; Schomaker, V. J. Chem. Phys. 1952, 20, 1708.
    • (1952) J. Chem. Phys. , vol.20 , pp. 1708
    • Dunitz, J.D.1    Feldman, H.G.2    Schomaker, V.3
  • 9
    • 3643076440 scopus 로고
    • Houben-Weyl, Thieme: Stuttgart
    • (d) Wendisch, D. In Houben-Weyl, Methoden der Organischen Chemie, 1971; Thieme: Stuttgart, Vol. 4/3, pp 679.
    • (1971) Methoden der Organischen Chemie , vol.4 , Issue.3 , pp. 679
    • Wendisch, D.1
  • 10
  • 14
    • 84987110619 scopus 로고
    • (b) Dijachenko, A. I.; Agre, S. A.; Rudashevskaya, T. Y.; Shafran, R. M.; Nefedov, O. M. Izv. Akad. Nauk. SSSR, 1984, 2820; Engl. Transl. 1984, 33, 2585.
    • (1984) Engl. Transl. , vol.33 , pp. 2585
  • 15
    • 85033822536 scopus 로고    scopus 로고
    • unpublished results
    • Binger, P., unpublished results.
    • Binger, P.1
  • 23
    • 84953492347 scopus 로고
    • Sodium bis(trimethylsilyl)amide was prepared according to the following references: (a) Wannagat, U.; Niederprüm, H. Chem. Ber. 1961, 94, 1540. (b) Krüger, C.; Rochow, E. G.; Wannagat, U. Chem. Ber. 1963, 96, 2132.
    • (1961) Chem. Ber. , vol.94 , pp. 1540
    • Wannagat, U.1    Niederprüm, H.2
  • 24
    • 84857445436 scopus 로고
    • Sodium bis(trimethylsilyl)amide was prepared according to the following references: (a) Wannagat, U.; Niederprüm, H. Chem. Ber. 1961, 94, 1540. (b) Krüger, C.; Rochow, E. G.; Wannagat, U. Chem. Ber. 1963, 96, 2132.
    • (1963) Chem. Ber. , vol.96 , pp. 2132
    • Krüger, C.1    Rochow, E.G.2    Wannagat, U.3
  • 31
    • 3643052272 scopus 로고
    • Battiste, M. A.; Sprouse, C. T., Jr. Tetrahedron Lett. 1970, 4661; Tetrahedron Lett. 1969, 3165.
    • (1969) Tetrahedron Lett. , pp. 3165
  • 33
    • 85033808497 scopus 로고    scopus 로고
    • note
    • The authors have deposited atomic coordinates for this structure with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystalographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK.
  • 37
    • 85033805349 scopus 로고    scopus 로고
    • unpublished
    • According to AM1 calculations, exo-adduct 3 is 3.1 kcal/mol more stable than endo-adduct 4. Rosenberg, M. G.; Brinker, U. H., unpublished.
    • Rosenberg, M.G.1    Brinker, U.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.