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Volumn 14, Issue 7, 2008, Pages 2067-2074

Antiaromaticity and reactivity of a planar cyclooctatetraene fully annelated with bicyclo[2.1.1]hexane units

Author keywords

Antiaromaticity; Bicyclo 2.1.1 hexene; Cyclooctatetraene; Reduction; X ray diffraction

Indexed keywords

ELECTRONIC STRUCTURE; HEXANE;

EID: 53849118166     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200701405     Document Type: Article
Times cited : (33)

References (48)
  • 35
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    • The same method was applied for adding artificial strain to benzene and COT nuclei: see a
    • The same method was applied for adding artificial strain to benzene and COT nuclei: see a) A. Stanger, J. Am. Chem. Soc. 1991, 113, 8277;
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 8277
    • Stanger, A.1
  • 40
    • 53849132302 scopus 로고    scopus 로고
    • exo = 1.364 Å) by the DFT calculations at the B3LYP/6-31G(d) level.
    • exo = 1.364 Å) by the DFT calculations at the B3LYP/6-31G(d) level.
  • 47
    • 53849106426 scopus 로고    scopus 로고
    • M. J. Frisch et al., Gaussian 98, revision A.5, Gaussian, Inc., Pittsburgh, PA, 1998.
    • M. J. Frisch et al., Gaussian 98, revision A.5, Gaussian, Inc., Pittsburgh, PA, 1998.
  • 48
    • 53849138649 scopus 로고    scopus 로고
    • 13C NMR spectra, and Catesian coordinates of the optimized structures for all the compounds in this study are available in the Supporting Information.
    • 13C NMR spectra, and Catesian coordinates of the optimized structures for all the compounds in this study are available in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.