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Volumn 74, Issue 16, 2009, Pages 6253-6259

Regioselective intramolecular nucleophilic addition of alcohols to C 60: One-step formation of a cis-1 bicyclic-fused fullerene

Author keywords

[No Author keywords available]

Indexed keywords

[60] FULLERENE; CHEMICAL EQUATIONS; CYCLIZATION REACTIONS; DOUBLE BONDS; FULLERENE SURFACES; FURAN RING; HIGH TEMPERATURE; HIGH-ENERGY BARRIERS; HYDROXYL GROUPS; METHYL GROUP; NUCLEOPHILIC ADDITIONS; NUCLEOPHILIC ATTACK; ONE-STEP REACTIONS; ONIOM APPROACH; PENTAGONAL RINGS; PYRROLIDINE RINGS; PYRROLIDINES; PYRROLIDINOFULLERENES; REFLUXING; REGIO-SELECTIVE; SARCOSINE; STEP FORMATION; THEORETICAL CALCULATIONS;

EID: 70349123766     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901171r     Document Type: Article
Times cited : (32)

References (75)
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    • For a recent review on the nano-forms of carbon, see
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  • 2
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    • For some recent books, see: (a) Wiley-VCH: Weinheim, Germany
    • For some recent books, see: (a) Hirsch, A. The Chemistry of Fullerenes; Wiley-VCH: Weinheim, Germany, 2005.
    • (2005) The Chemistry of Fullerenes
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  • 3
    • 0038128851 scopus 로고    scopus 로고
    • Guldi, D. M.; Martín, N., Eds. Kluwer Academic Publishers: Dordrecht, The Netherlands
    • (b) Guldi, D. M.; Martín, N., Eds. Fullerenes: From Synthesis to Optoelectronic Properties; Kluwer Academic Publishers: Dordrecht, The Netherlands, 2002.
    • (2002) Fullerenes: from Synthesis to Optoelectronic Properties
  • 5
    • 37749023862 scopus 로고    scopus 로고
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    • (2006) Chem. Commun. , pp. 2093-2104
    • Martín, N.1
  • 12
    • 34250885713 scopus 로고    scopus 로고
    • and references cited therein
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  • 37
    • 29444440540 scopus 로고    scopus 로고
    • The retro-cycloaddition process has also recently been reported as a useful protection-deprotection protocol in fullerenes as well as in carbon nanotubes, see
    • The retro-cycloaddition process has also recently been reported as a useful protection-deprotection protocol in fullerenes as well as in carbon nanotubes, see: Martín, N.; Altable, M.; Filippone, S.; Martín-Domenech, A.; Echegoyen, L.; Cardona, C. M. Angew. Chem., Int. Ed. 2006, 45, 110-114.
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 110-114
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  • 44
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    • For a systematic and simple system to indicate the relative positional relationships of addends in fullerene derivatives, see
    • For a systematic and simple system to indicate the relative positional relationships of addends in fullerene derivatives, see: Hirsch, A.; Lamparth, I.; Karfunkel, H. R. Angew. Chem., Int. Ed. 1994, 33, 437-438.
    • (1994) Angew. Chem., Int. Ed. , vol.33 , pp. 437-438
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.