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Volumn , Issue 12, 1997, Pages 2451-2469

Polyhalogenated cyclopentadienes in [4+2] cycloadditions: Preparative aspects

Author keywords

1,2,4 Triazoline 3,5 diones; Cycloadditions; Cyclopentadienes; Structure elucidation; Through space interactions

Indexed keywords


EID: 2742588417     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719971208     Document Type: Article
Times cited : (7)

References (100)
  • 1
    • 42749088179 scopus 로고
    • Polyfluorinated cyclopentadienes (X = F): e.g., R = H or F: [1a] G. Paprott, S. Lehmann, K. Seppelt, Chem. Ber. 1988, 121, 727-733.
    • (1988) Chem. Ber. , vol.121 , pp. 727-733
    • Paprott, G.1    Lehmann, S.2    Seppelt, K.3
  • 6
    • 33749029558 scopus 로고
    • Ph. D. Dissertation, Universität Regensburg
    • 2Ar:
    • (1993)
    • Steiner, A.1
  • 9
    • 33749008919 scopus 로고
    • [Chem. Abstr. 1989, 111, 174189u]. - R = OMe (1d):
    • (1989) Chem. Abstr. , vol.111
  • 13
    • 0001881504 scopus 로고
    • [1l] K. Mackenzie, J. Chem. Soc. 1964, 5710-5716. - 1,2,4-Trichloro-3,5,5-trimethoxycyclopentadiene (1h):
    • (1964) J. Chem. Soc. , pp. 5710-5716
    • Mackenzie, K.1
  • 16
    • 0012528844 scopus 로고
    • [1o] R. G. Pews, C. W. Roberts, C. R. Hand, Tetrahedron 1970, 26, 1711-1717. - "Heterocyclopentadienes", e.g. 1,2,3,4-tetrachloro-5-oxacyclopenta-1,3-diene:
    • (1970) Tetrahedron , vol.26 , pp. 1711-1717
    • Pews, R.G.1    Roberts, C.W.2    Hand, C.R.3
  • 17
    • 33749033540 scopus 로고
    • [1p] H. Krzikalla, H. Linge, Chem. Ber. 1963, 96, 1751-1753. - 2,3,4,5,5-pentachloro-1-azacyclopenta-1,3-diene (1I):
    • (1963) Chem. Ber. , vol.96 , pp. 1751-1753
    • Krzikalla, H.1    Linge, H.2
  • 21
    • 33748988633 scopus 로고    scopus 로고
    • Chem. Abstr. 1996, 124, 8576-8577.
    • (1996) Chem. Abstr. , vol.124 , pp. 8576-8577
  • 30
    • 33847804900 scopus 로고
    • [8a] V. Mark, J. Org. Chem. 1974, 39, 3179-3181.
    • (1974) J. Org. Chem. , vol.39 , pp. 3179-3181
    • Mark, V.1
  • 39
    • 33749027947 scopus 로고
    • Diplomarbeit, Universität Bochum
    • H. J. Figge, Diplomarbeit, Universität Bochum, 1982. 1c: commercially available (Merck).
    • (1982)
    • Figge, H.J.1
  • 63
  • 65
    • 33749000498 scopus 로고
    • Ph. D. Dissertation, Universität Regensburg
    • B. Prantl, Ph. D. Dissertation, Universität Regensburg, 1982.
    • (1982)
    • Prantl, B.1
  • 66
    • 33749000187 scopus 로고    scopus 로고
    • unpublished results
    • J. Sauer, H. M. Schuhbauer, unpublished results. AM1 and PM3 semiempirical calculations using proquantum™ software (V 1.33, Oxford Molecular Ltd., Oxford OX 446A) and silicon graphics™ hardware give evidence that dienes 1a, 1d, and 1e have the highest lying HOMOs amongst the dienes.
    • Sauer, J.1    Schuhbauer, H.M.2
  • 75
    • 33749012872 scopus 로고
    • Ph. D. Dissertation, University of Louisville
    • P. H. Daniels, Ph. D. Dissertation, University of Louisville 1979.
    • (1979)
    • Daniels, P.H.1
  • 92
    • 85051305389 scopus 로고
    • [40e] Velsicol Corp., EP 614931, 1948 [Chem. Abstr. 1949, 43, 4693c];
    • (1949) Chem. Abstr. , vol.43
  • 93
    • 33748993319 scopus 로고
    • Velsicol Chem. Corp., U.S. 2901510, 1960 [Chem. Abstr. 1960, 54, 1451h];
    • (1960) Chem. Abstr. , vol.54
  • 94
    • 84943869597 scopus 로고
    • Universal Oil Prod. Co., U.S. 2860161 [Chem. Abstr. 1960, 54, 1364c].
    • (1960) Chem. Abstr. , vol.54
  • 96
    • 33749002436 scopus 로고
    • Ph. D. Dissertation, Universität München
    • [41b] H. Wiest, Ph. D. Dissertation, Universität München 1963.
    • (1963)
    • Wiest, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.