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Volumn 72, Issue 22, 2007, Pages 8402-8415

Syntheses and reactivity of meso-unsubstituted azuliporphyrins derived from 6-tert-butyl- and 6-phenylazulene

Author keywords

[No Author keywords available]

Indexed keywords

AZULENES; AZULIPORPHYRINS; DIPOLAR RESONANCE; DOWNFIELD SHIFTS;

EID: 35548980026     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo701523s     Document Type: Article
Times cited : (64)

References (49)
  • 3
    • 0001004194 scopus 로고    scopus 로고
    • Kadish, K. M, Smith, K. M, Guilard, R, Eds, Academic Press: San Diego
    • Lash, T. D. In The Porphyrin Handbook; Kadish, K. M., Smith, K. M., Guilard, R., Eds.; Academic Press: San Diego, 2000; Vol. 2, pp 125-199.
    • (2000) The Porphyrin Handbook , vol.2 , pp. 125-199
    • Lash, T.D.1
  • 11
    • 10044247395 scopus 로고    scopus 로고
    • For an example of an azulisapphyrin, see
    • For an example of an azulisapphyrin, see: Richter, D. T.; Lash, T. D. J. Org. Chem. 2004, 69, 8842-8850.
    • (2004) J. Org. Chem , vol.69 , pp. 8842-8850
    • Richter, D.T.1    Lash, T.D.2
  • 23
    • 35549001788 scopus 로고    scopus 로고
    • These results were presented, in part, at the following meeting: 229th National American Chemical Society Meeting, San Diego, California, March 2005 (El-Beck, J. A.; Lash, T. D. Book of Abstracts; American Chemical Society: Washington, DC, 2005; CHED 546).
    • These results were presented, in part, at the following meeting: 229th National American Chemical Society Meeting, San Diego, California, March 2005 (El-Beck, J. A.; Lash, T. D. Book of Abstracts; American Chemical Society: Washington, DC, 2005; CHED 546).
  • 26
    • 0013075396 scopus 로고    scopus 로고
    • These procedues were adapted from a previously reported synthesis of 6-methylazulene: Rudolf, K.; Robinette, D.; Koenig, T. J. Org. Chem. 1987, 52, 641-647.
    • These procedues were adapted from a previously reported synthesis of 6-methylazulene: Rudolf, K.; Robinette, D.; Koenig, T. J. Org. Chem. 1987, 52, 641-647.
  • 34
    • 35548998762 scopus 로고    scopus 로고
    • 2, nonaromatic) returned an average 1.48 ± 0.02 Å distance for over 500 hits.
    • 2, nonaromatic) returned an average 1.48 ± 0.02 Å distance for over 500 hits.
  • 40
    • 35548989708 scopus 로고    scopus 로고
    • Bruker SMART CCD software package, version 5.630; Bruker Advanced X-ray Solutions: Madison, WI, 1997-2002
    • (a) Bruker SMART CCD software package, version 5.630; Bruker Advanced X-ray Solutions: Madison, WI, 1997-2002.
  • 41
    • 35549010654 scopus 로고    scopus 로고
    • Bruker SAINT+ Integration Software for Single Crystal Data frames, h,k,l, intensity, version 6.45; Bruker Advanced X-ray Solutions: Madison, WI, 2003
    • (b) Bruker SAINT+ Integration Software for Single Crystal Data frames - h,k,l, intensity, version 6.45; Bruker Advanced X-ray Solutions: Madison, WI, 2003.
  • 48
    • 35548997866 scopus 로고    scopus 로고
    • Persistence of Vision Team
    • Persistence of Vision Team, 2006, www.povray.org.
    • (2006)
  • 49
    • 35548979963 scopus 로고    scopus 로고
    • Crystallographic data (excluding structure factors) for 16a has been deposited with the Cambridge Crystallographic Data Center as supplementary publication number CCDC 650546. Copies of this data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 IEZ, UK [fax: +44 (0)12233 336033 or e-mail: deposit@ccdc.cam.ac.uk].
    • Crystallographic data (excluding structure factors) for 16a has been deposited with the Cambridge Crystallographic Data Center as supplementary publication number CCDC 650546. Copies of this data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 IEZ, UK [fax: +44 (0)12233 336033 or e-mail: deposit@ccdc.cam.ac.uk].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.