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Volumn , Issue 17, 2003, Pages 3372-3377

Oligo(1,4-phenylenepyrazole-3,5-diyl)s

Author keywords

Conjugation; Heterocycles; Oligomers; Regioselectivity; Ring closure

Indexed keywords

1H PYRAZOLE DERIVATIVE; 2 PYRAZOLINE DERIVATIVE; BENZENE DERIVATIVE; CHALCONE DERIVATIVE; METHYLHYDRAZINE; OLIGO(1,4 PHENYLENEPYRAZOLE 3,5 DIYL) DERIVATIVE; PYRAZOLE DERIVATIVE; PYRAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0043287135     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300221     Document Type: Article
Times cited : (7)

References (27)
  • 1
    • 0004139257 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1998) Electronic Materials: The Oligomer Approach
    • Müllen, K.1    Wegner, G.2
  • 2
    • 0000788915 scopus 로고    scopus 로고
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1999) Angew. Chem. , vol.111 , pp. 1440-1469
    • Martin, R.E.1    Diederich, F.2
  • 3
    • 17044396896 scopus 로고    scopus 로고
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 1350-1377
  • 4
    • 0000064020 scopus 로고    scopus 로고
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1998) Angew. Chem. , vol.110 , pp. 416-443
    • Kraft, A.1    Grimsdale, A.C.2    Holmes, A.B.3
  • 5
    • 0001531762 scopus 로고    scopus 로고
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 403-428
  • 6
    • 0028392622 scopus 로고
    • See for example: [1a] K. Müllen, G. Wegner, Electronic Materials: The Oligomer Approach; Wiley-VCH, Weinheim, 1998. [1b] R. E. Martin, F. Diederich, Angew. Chem. 1999, 111, 1440-1469; Angew. Chem. Int. Ed. 1999, 38, 1350-1377. [1c] A. Kraft, A. C. Grimsdale, A. B. Holmes, Angew. Chem. 1998, 110, 416-443; Angew. Chem. Int. Ed. 1998, 37, 403-428. [1d] J. M. Tour, Adv. Mater. 1994, 6, 190-198.
    • (1994) Adv. Mater. , vol.6 , pp. 190-198
    • Tour, J.M.1
  • 12
    • 84944033746 scopus 로고    scopus 로고
    • (Eds. A. R. Katritzky, C. W. Rees, E. F. Scriven), Pergamon, Oxford, and refs [8-19]
    • See for example: J. Elguero, in Comprehensive Heterocyclic Chemistry II (Eds.: A. R. Katritzky, C. W. Rees, E. F. Scriven), Pergamon, Oxford, 1996, vol. 3, p. 1-75, and refs. [8-19]
    • (1996) Comprehensive Heterocyclic Chemistry , vol.3 , pp. 1-75
    • Elguero, J.1
  • 27
    • 0042730801 scopus 로고    scopus 로고
    • note
    • 13C NMR spectroscopic data are summarized in Tables 1 and 2. TMS as internal standard; the numbering corresponds to the nomenclature.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.