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Volumn 16, Issue 39, 2010, Pages 11876-11889

Electrochemical synthesis and characterisation of alternating tripyridyl-dipyrrole molecular strands with multiple nitrogen-based donor-acceptor binding sites

Author keywords

copper; electrochemistry; N ligands; nitrogen heterocycles; ring contraction

Indexed keywords

BINDING SITES; CHLORINE COMPOUNDS; CHROMOPHORES; COPPER; COPPER COMPOUNDS; ELECTROCHEMISTRY; ELECTROLYTIC REDUCTION; ISOMERS; NITROGEN; PYRIDINE; SYNTHESIS (CHEMICAL); ZINC COMPOUNDS;

EID: 78249275198     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201000859     Document Type: Article
Times cited : (17)

References (65)
  • 7
    • 0035898520 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 2591 - 2611
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2591-2611
  • 36
  • 48
    • 78249270881 scopus 로고    scopus 로고
    • Halogenopyridazines 10a - c were synthesized through Negishi cross-coupling between the 3-chloro-6-iodopyridazine and the appropriate pyridyl zinc reagents 12a - c
    • Halogenopyridazines 10a - c were synthesized through Negishi cross-coupling between the 3-chloro-6-iodopyridazine and the appropriate pyridyl zinc reagents 12a - c.
  • 50
    • 0036193456 scopus 로고    scopus 로고
    • Stannyl pyridines 10a - c were prepared by following the Lehn procedure from the corresponding bromopyridine
    • Stannyl pyridines 10a - c were prepared by following the Lehn procedure from the corresponding bromopyridine (, H. Nierengarten, J. Rojo, E. Leize, J. M. Lehn, A. Van Dorsselaer, Eur. J. Inorg. Chem. 2002, 573 - 579).
    • (2002) Eur. J. Inorg. Chem. , pp. 573-579
    • Nierengarten, H.1    Rojo, J.2    Leize, E.3    Lehn, J.M.4    Van Dorsselaer, A.5
  • 51
    • 0001186779 scopus 로고    scopus 로고
    • 2-Bromopyridine and 2-bromo-6-methylpyridine are commercially available, and 2-bromo-4,6-dimethylpryridine was synthesized from 2-amino-4,6- dimethylpryridine according to the Schubert protocol
    • 2-Bromopyridine and 2-bromo-6-methylpyridine are commercially available, and 2-bromo-4,6-dimethylpryridine was synthesized from 2-amino-4,6- dimethylpryridine according to the Schubert protocol (, U. S. Schubert, C. Eschbaumer, M. Heller, Org. Lett. 2000, 2, 3373 - 3376).
    • (2000) Org. Lett. , vol.2 , pp. 3373-3376
    • Schubert, U.S.1    Eschbaumer, C.2    Heller, M.3
  • 58
    • 0029938816 scopus 로고    scopus 로고
    • Contrary to 1b and 1c, 1a was produced in very low yields (<5%) and purified with great difficulty, so our procedure is not better than another Paal-Knoor approach proposed by Jones et al. for compound 1a. However, the tricky preparation of the 1,4-diketo precursor (15% yield) from 2,6-diacetylpyridine appeared inadequate for our purpose
    • Contrary to 1b and 1c, 1a was produced in very low yields (<5%) and purified with great difficulty, so our procedure is not better than another Paal-Knoor approach proposed by Jones et al. for compound 1a. However, the tricky preparation of the 1,4-diketo precursor (15% yield) from 2,6-diacetylpyridine appeared inadequate for our purpose:, R. A. Jones, M. Karatza, T. N. Toro, P. U. Civcir, A. Franck, O. Ozturk, J. P. Seaman, A. P. Whitmore, D. J. Williamson, Tetrahedron 1996, 52, 8707 - 8724.
    • (1996) Tetrahedron , vol.52 , pp. 8707-8724
    • Jones, R.A.1    Karatza, M.2    Toro, T.N.3    Civcir, P.U.4    Franck, A.5    Ozturk, O.6    Seaman, J.P.7    Whitmore, A.P.8    Williamson, D.J.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.