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Volumn 62, Issue 16, 1997, Pages 5354-5362

Synthesis, Structure, and Redox Behavior of the Dehydroannulenes Fused with Bicyclo[2.2.2]octene Frameworks

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EID: 0001654649     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9705531     Document Type: Article
Times cited : (35)

References (47)
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    • For example: (a) Bedard, T. C.; Moore, J. S. J. Am. Chem. Soc. 1995, 117, 10662. (b) Wu, Z.; Moore, J. S. Angew. Chem., Int. Ed. Engl. 1996, 35, 297. (c) Shetty, A. S.; Zhang, J.; Moore, J. S. J. Am. Chem. Soc. 1996, 118, 1019.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10662
    • Bedard, T.C.1    Moore, J.S.2
  • 3
    • 33746353789 scopus 로고    scopus 로고
    • For example: (a) Bedard, T. C.; Moore, J. S. J. Am. Chem. Soc. 1995, 117, 10662. (b) Wu, Z.; Moore, J. S. Angew. Chem., Int. Ed. Engl. 1996, 35, 297. (c) Shetty, A. S.; Zhang, J.; Moore, J. S. J. Am. Chem. Soc. 1996, 118, 1019.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 297
    • Wu, Z.1    Moore, J.S.2
  • 4
    • 0029935228 scopus 로고    scopus 로고
    • For example: (a) Bedard, T. C.; Moore, J. S. J. Am. Chem. Soc. 1995, 117, 10662. (b) Wu, Z.; Moore, J. S. Angew. Chem., Int. Ed. Engl. 1996, 35, 297. (c) Shetty, A. S.; Zhang, J.; Moore, J. S. J. Am. Chem. Soc. 1996, 118, 1019.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 1019
    • Shetty, A.S.1    Zhang, J.2    Moore, J.S.3
  • 10
  • 37
    • 0027740974 scopus 로고
    • A homocoupling reaction of terminal acetylenes under palladium-copper-catalyzed condition were reported: Crisp, G. T.; Flynn, B. L. J. Org. Chem. 1993, 58, 6614.
    • (1993) J. Org. Chem. , vol.58 , pp. 6614
    • Crisp, G.T.1    Flynn, B.L.2
  • 38
    • 0001255215 scopus 로고
    • For examples of the X-ray structure: (a) Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. J. Am. Chem. Soc. 1964, 86, 4725. (b) Bordner, J.; Parker, R. G.; Stanford, R. H., Jr. Acta Crystallogr. 1972, 28B, 1069. (c) Laird, B. B.; Davis, R. E. Acta Crystallogr., Sect. B 1982, B38, 678.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 4725
    • Pawley, G.S.1    Lipscomb, W.N.2    Freedman, H.H.3
  • 39
    • 0001255215 scopus 로고
    • For examples of the X-ray structure: (a) Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. J. Am. Chem. Soc. 1964, 86, 4725. (b) Bordner, J.; Parker, R. G.; Stanford, R. H., Jr. Acta Crystallogr. 1972, 28B, 1069. (c) Laird, B. B.; Davis, R. E. Acta Crystallogr., Sect. B 1982, B38, 678.
    • (1972) Acta Crystallogr. , vol.28 B , pp. 1069
    • Bordner, J.1    Parker, R.G.2    Stanford Jr., R.H.3
  • 40
    • 0001255215 scopus 로고
    • For examples of the X-ray structure: (a) Pawley, G. S.; Lipscomb, W. N.; Freedman, H. H. J. Am. Chem. Soc. 1964, 86, 4725. (b) Bordner, J.; Parker, R. G.; Stanford, R. H., Jr. Acta Crystallogr. 1972, 28B, 1069. (c) Laird, B. B.; Davis, R. E. Acta Crystallogr., Sect. B 1982, B38, 678.
    • (1982) Acta Crystallogr., Sect. B , vol.B38 , pp. 678
    • Laird, B.B.1    Davis, R.E.2
  • 43
    • 84961474198 scopus 로고
    • The transition state of ring inversion in cyclooctateraene was calculated to be a planar conformation: Paquette, L. A. Pure Appl. Chem. 1982, 54, 987.
    • (1982) Pure Appl. Chem. , vol.54 , pp. 987
    • Paquette, L.A.1
  • 47
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    • note
    • The authors have deposited atomic coordinates for these structures with the Cambridge Crystallographic Data Centre. The coordinates, bond distances, and angles can be obtained, on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 4E2, U.K.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.