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Volumn 131, Issue 44, 2009, Pages 16006-16007

Diels-Alder reactivity of polycyclic aromatic hydrocarbon bay regions: Implications for metal-free growth of single-chirality carbon nanotubes

Author keywords

[No Author keywords available]

Indexed keywords

BIANTHRONE; CHEMICAL EQUATIONS; CYCLOADDUCTS; DENSITY-FUNCTIONAL CALCULATIONS; DIELS-ALDER; DIELS-ALDER CYCLOADDITIONS; DIELS-ALDER REACTION; DIENOPHILES; DIETHYL ACETYLENEDICARBOXYLATE; HYDROCARBON TEMPLATES; METAL CATALYSIS; PERYLENES; STRUCTURE ACTIVITY RELATIONSHIPS;

EID: 70450187433     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja907802g     Document Type: Article
Times cited : (218)

References (20)
  • 3
  • 4
    • 67749099629 scopus 로고    scopus 로고
    • For thermal [4+2] cycloaddition and cycloreversion reactions of dihydrogen, see: and references cited therein
    • For thermal [4+2] cycloaddition and cycloreversion reactions of dihydrogen, see: (a) Hayden, A. E.; Houk, K. N. J. Am. Chem. Soc. 2009, 131, 4084-4089, and references cited therein.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4084-4089
    • Hayden, A.E.1    Houk, K.N.2
  • 11
    • 55649087990 scopus 로고    scopus 로고
    • For recent calculations on the ground states of periacenes, see
    • For recent calculations on the ground states of periacenes, see: Jiang, D.- e.; Dai, S. Chem. Phys. Lett. 2008, 466, 72-75.
    • (2008) Chem. Phys. Lett. , vol.466 , pp. 72-75
    • Jiang, D.-.E.1    Dai, S.2
  • 12
    • 3142702625 scopus 로고
    • Modeled after the synthesis of 4,11-diphenylbisanthene by See SI
    • Modeled after the synthesis of 4,11-diphenylbisanthene by Maulding, D. R. J. Org. Chem. 1970, 35, 1221-1223. See SI.
    • (1970) J. Org. Chem. , vol.35 , pp. 1221-1223
    • Maulding, D.R.1
  • 13
    • 70450216277 scopus 로고    scopus 로고
    • Calculations predict a slower second addition. See SI
    • Calculations predict a slower second addition. See SI.
  • 14
    • 34250646053 scopus 로고    scopus 로고
    • Under more forcing conditions, 2:1 Diels-Alder adducts of perylene can be prepared
    • Under more forcing conditions, 2:1 Diels-Alder adducts of perylene can be prepared: (a) Alibert-Fouet, S.; Seguy, I.; Bobo, J.-F.; Destruel, P.; Bock, H. Chem.-Eur. J. 2007, 13, 1746-1753.
    • (2007) Chem.-Eur. J. , vol.13 , pp. 1746-1753
    • Alibert-Fouet, S.1    Seguy, I.2    Bobo, J.-F.3    Destruel, P.4    Bock, H.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.