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Volumn 2, Issue 23, 2000, Pages 3723-3726

Synthesis of functionalized ethynylphenothiazine fluorophores

Author keywords

[No Author keywords available]

Indexed keywords

PHENOTHIAZINE DERIVATIVE;

EID: 0034676586     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0066328     Document Type: Article
Times cited : (94)

References (55)
  • 1
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    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Oxford, New York, Toronto, Sydney, Paris, Frankfurt
    • Sainsbury, M. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Oxford, New York, Toronto, Sydney, Paris, Frankfurt, 1984; Vol. 3, p 995.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 995
    • Sainsbury, M.1
  • 29
    • 23544440675 scopus 로고    scopus 로고
    • For applications of AFM and STM in chemistry, see, for example: (a) various authors, Chem. Rev. 1997, 97, issue 4.
    • (1997) Chem. Rev. , vol.97 , Issue.4
  • 30
    • 0002983668 scopus 로고
    • Petty, M. C., Bryce, M. R., Bloor, D., Eds.;, Oxford University Press: New York
    • For applications in molecular electronics, see, for example: (b) Rabe, J. P. In An Introduction to Molecular Electronics: Petty, M. C., Bryce, M. R., Bloor, D., Eds.;, Oxford University Press: New York. 1995; p 261.
    • (1995) An Introduction to Molecular Electronics , pp. 261
    • Rabe, J.P.1
  • 31
    • 0042801372 scopus 로고    scopus 로고
    • For nanoscale materials, see, for example: (c) various authors in Acc. Chem. Res. 1999, 32, issue 5.
    • (1999) Acc. Chem. Res. , vol.32 , Issue.5
  • 41
    • 85037498056 scopus 로고    scopus 로고
    • note
    • All new compounds have been characterized spectroscopically and by correct elemental analysis or HRMS (oils).
  • 46
    • 25344462527 scopus 로고
    • Bodea, C.; Terdic, M. Acad. Rep. Pop. Rom. 1962, 13, 81; Chem. Abstr. 1963, 59, 11477h.
    • (1963) Chem. Abstr. , vol.59
  • 47
    • 85037515029 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-149969 (7a). Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: + 44-1223/336-033. E-mail: deposit@ccdc.cam.ac.uk).
  • 48
    • 85037492896 scopus 로고    scopus 로고
    • note
    • 2 (319.4): C, 71.44; H, 4.10; N, 4.38; S, 20.07. Found: C. 71.20; H, 4.22; N, 4.26; S, 19.87.
  • 49
    • 85037516546 scopus 로고    scopus 로고
    • note
    • 20NSOBr (390.3): C, 58.46; H, 5.16; N, 3.59; S, 8.21; Br, 20.47. Found: C, 58.28; H, 5.23; N, 3.57; S, 8.02; Br, 20.40.
  • 51
    • 0000154678 scopus 로고
    • Stang, P. J., Diederich, F., Eds.; VCH: Weinheim
    • (b) Scott, L. T.; Cooney, M. J. In Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds.; VCH: Weinheim, 1995; p 321.
    • (1995) Modern Acetylene Chemistry , pp. 321
    • Scott, L.T.1    Cooney, M.J.2
  • 54
    • 85037518495 scopus 로고    scopus 로고
    • note
    • 15NSO (341.4): C, 77.39; H, 4.43; N, 4.10; S, 9.39. Found: C, 77.06; H, 4.43; N, 4.03; S, 9.37.
  • 55
    • 85037500038 scopus 로고    scopus 로고
    • note
    • 2 (528.6): C, 72.70; H, 3.81: N, 5.30; S, 12.13. Found: C, 72.66; H, 3.91; N, 5.42; S, 11.82.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.