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Volumn 134, Issue 9, 2012, Pages 4076-4079

Cyclo[m]pyridine[n]pyrroles: Hybrid macrocycles that display expanded π-conjugation upon protonation

Author keywords

[No Author keywords available]

Indexed keywords

MACROCYCLES; OPTICAL SPECTROSCOPIC; STRUCTURAL PARAMETER; STRUCTURAL STUDIES; SUZUKI COUPLINGS;

EID: 84863230536     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja211985k     Document Type: Article
Times cited : (75)

References (24)
  • 7
    • 33746146895 scopus 로고    scopus 로고
    • Such delocalization effects have previously been suggested in the case of pyridyl porphyrin analogues, albeit not studied in detail; cf.
    • Such delocalization effects have previously been suggested in the case of pyridyl porphyrin analogues, albeit not studied in detail; cf. (a) Mysliborski, R.; Latos-Grazynski, L.; Szterenberg, L. Eur. J. Org. Chem. 2006, 3064-3068.
    • (2006) Eur. J. Org. Chem. , pp. 3064-3068
    • Mysliborski, R.1    Latos-Grazynski, L.2    Szterenberg, L.3
  • 16
    • 79955032485 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see: (c) Osuka, A.; Saito, S. Chem. Commun. 2011, 47, 4330-4339.
    • (2011) Chem. Commun. , vol.47 , pp. 4330-4339
    • Osuka, A.1    Saito, S.2
  • 20
    • 84863291751 scopus 로고    scopus 로고
    • note
    • The NH protons of precursors 7 and 9 resonate in this range.
  • 21
    • 84863231800 scopus 로고    scopus 로고
    • note
    • In unsubstituted sexipyridine the corresponding resonance is found at 7.8-8.1 ppm. Cf. ref 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.