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Volumn 9, Issue 17, 2007, Pages 3263-3266

Are antiaromatic rings stacked face-to-face aromatic?

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Indexed keywords


EID: 34548162137     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071183y     Document Type: Article
Times cited : (59)

References (72)
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    • Cyclophanes I and II
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    • Cf.: Greenberg, A.; Liebman, J. F. Strained Organic Molecules; Academic Press: New York, 1978; p 170.
    • Cf.: Greenberg, A.; Liebman, J. F. Strained Organic Molecules; Academic Press: New York, 1978; p 170.
  • 59
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    • According to our unpublished computations.
    • According to our unpublished computations.
  • 61
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    • Gaussian, Inc, Wallingford, CT, Full reference given in Supporting Information
    • Frisch, M. J. et al. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004. Full reference given in Supporting Information.
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    • For a review of Möbius aromaticity, see
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    • + triplet state has the lowest energy. See: Gogonea, V.; Schleyer, P. v. R.; Schreiner, P. R. Angew. Chem., Int. Ed., 1998, 37, 1945-1948.
    • + triplet state has the lowest energy. See: Gogonea, V.; Schleyer, P. v. R.; Schreiner, P. R. Angew. Chem., Int. Ed., 1998, 37, 1945-1948.
  • 72
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    • For a review of antiaromatic annulenes and triplet aromaticity, see
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.