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Volumn 52, Issue 28, 2013, Pages 7314-7316

Stereoelectronic effect of curved aromatic structures: Favoring the unexpected endo conformation of benzylic-substituted sumanene

Author keywords

conformation analysis; density functional calculations; hyperconjugation; through bond interactions; through space interactions

Indexed keywords

AROMATIC STRUCTURES; BUCKYBOWLS; C-H BOND; CONFORMATION ANALYSIS; HYPERCONJUGATION; STEREOELECTRONIC EFFECT; THROUGH-BOND INTERACTIONS; THROUGH-SPACE INTERACTION;

EID: 84880176212     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201303134     Document Type: Article
Times cited : (35)

References (11)
  • 9
    • 0037031628 scopus 로고    scopus 로고
    • Conformational analysis of 1-alkyl-1,2-dihydrocorannulenes has been reported. Only strain energy and steric repulsion were discussed:, A. Sygula, R. Sygula, F. R. Fronczek, P. W. Rabideau, J. Org. Chem. 2002, 67, 6487-6492.
    • (2002) J. Org. Chem. , vol.67 , pp. 6487-6492
    • Sygula, A.1    Sygula, R.2    Fronczek, F.R.3    Rabideau, P.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.