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Volumn 132, Issue 49, 2010, Pages 17635-17641

Synthesis of cyclododeciptycene quinones

Author keywords

[No Author keywords available]

Indexed keywords

INTRAMOLECULAR DIELS-ALDER REACTION; SINGLE CRYSTAL X-RAY ANALYSIS; SYNTHETIC SEQUENCE; TRIPTYCENES;

EID: 78650153392     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja1088309     Document Type: Article
Times cited : (21)

References (29)
  • 18
    • 78650160718 scopus 로고    scopus 로고
    • For a recent review, see
    • For a recent review, see
  • 24
    • 78650100366 scopus 로고    scopus 로고
    • The single-crystal X-ray structure of compound 2 has not been reported previously. The authors have deposited atomic coordinates for the structures, compound 2 and 1a with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 175022. The coordinates can be obtained on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K
    • The single-crystal X-ray structure of compound 2 has not been reported previously. The authors have deposited atomic coordinates for the structures, compound 2 and 1a with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 175022. The coordinates can be obtained on request, from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, U.K.
  • 28
    • 78650115694 scopus 로고    scopus 로고
    • 3, 400 MHz) of the assumed cyclododeciptycene hexaquinone (red solid) shows three set of signals, δ 7.33 (dd, J = 7.2, 2.8 Hz, 12 H), 7.16 (dd, J = 5.6, 2.8 Hz, 12 H), and 6.04 (s, 12 H) ppm
    • 3, 400 MHz) of the assumed cyclododeciptycene hexaquinone (red solid) shows three set of signals, δ 7.33 (dd, J = 7.2, 2.8 Hz, 12 H), 7.16 (dd, J = 5.6, 2.8 Hz, 12 H), and 6.04 (s, 12 H) ppm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.