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Volumn 9, Issue 11, 2014, Pages 3084-3088

Dramatic mechanistic change in acid-catalyzed arylation of azafulleroids depending on their ambident N/C basicity: Formation of cyclopentene centered pentakisadduct

Author keywords

Arylation; Fullerenes; Homogeneous catalysis; Nucleophilic substitution; Protonation

Indexed keywords

AROMATIC COMPOUNDS; FULLERENES; PROTONATION; REACTION KINETICS;

EID: 84915745690     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201402728     Document Type: Article
Times cited : (7)

References (42)
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    • note
    • Proton Affinity calculations were carried out with Gaussian 09. Optimized structures of pentakisadducts were with Spartan '08. Their full citations are given in the Supporting Information.
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    • note
    • CrystalStructure 3.8: Crystal Structure Analysis Package, Rigaku and Rigaku Americas (2000-2007). 9009 New Trails Dr. The Woodlands TX 77381 USA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.