메뉴 건너뛰기




Volumn 76, Issue 4, 2003, Pages 709-719

Copper(I) ion mediated self-assembly of triple-stranded helicates from oligo(2-ethynylpyridines): Synthesis, structure, and properties

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL REACTIONS; COPPER; SELF ASSEMBLY; SOLUTIONS;

EID: 0037660482     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.76.709     Document Type: Article
Times cited : (8)

References (40)
  • 9
    • 0001336237 scopus 로고
    • 2,6-Bis(2-pyridylethynyl)pyridine derivatives, which possess three pyridine rings, are still very rare. a) K. T. Potts, C. P. Horwitz, A. Fessak, M. Keshavarz-K, K. E. Nash, and P. J. Toscano, J. Am. Chem. Soc., 115, 10444 (1993). b) M. Inouye, J. Chiba, and H. Nakazumi, J. Org. Chem., 64, 8170 (1999). c) M. Inouye, K. Takahashi, and H. Nakazumi, J. Am. Chem. Soc., 121, 341 (1999). d) M. Inouye, T. Miyake, M. Furusyo, and H. Nakazumi, J. Am. Chem. Soc., 117, 12416 (1995).
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10444
    • Potts, K.T.1    Horwitz, C.P.2    Fessak, A.3    Keshavarz-K, M.4    Nash, K.E.5    Toscano, P.J.6
  • 10
    • 0033615518 scopus 로고    scopus 로고
    • 2,6-Bis(2-pyridylethynyl)pyridine derivatives, which possess three pyridine rings, are still very rare. a) K. T. Potts, C. P. Horwitz, A. Fessak, M. Keshavarz-K, K. E. Nash, and P. J. Toscano, J. Am. Chem. Soc., 115, 10444 (1993). b) M. Inouye, J. Chiba, and H. Nakazumi, J. Org. Chem., 64, 8170 (1999). c) M. Inouye, K. Takahashi, and H. Nakazumi, J. Am. Chem. Soc., 121, 341 (1999). d) M. Inouye, T. Miyake, M. Furusyo, and H. Nakazumi, J. Am. Chem. Soc., 117, 12416 (1995).
    • (1999) J. Org. Chem. , vol.64 , pp. 8170
    • Inouye, M.1    Chiba, J.2    Nakazumi, H.3
  • 11
    • 0033585613 scopus 로고    scopus 로고
    • 2,6-Bis(2-pyridylethynyl)pyridine derivatives, which possess three pyridine rings, are still very rare. a) K. T. Potts, C. P. Horwitz, A. Fessak, M. Keshavarz-K, K. E. Nash, and P. J. Toscano, J. Am. Chem. Soc., 115, 10444 (1993). b) M. Inouye, J. Chiba, and H. Nakazumi, J. Org. Chem., 64, 8170 (1999). c) M. Inouye, K. Takahashi, and H. Nakazumi, J. Am. Chem. Soc., 121, 341 (1999). d) M. Inouye, T. Miyake, M. Furusyo, and H. Nakazumi, J. Am. Chem. Soc., 117, 12416 (1995).
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 341
    • Inouye, M.1    Takahashi, K.2    Nakazumi, H.3
  • 12
    • 0029550884 scopus 로고
    • 2,6-Bis(2-pyridylethynyl)pyridine derivatives, which possess three pyridine rings, are still very rare. a) K. T. Potts, C. P. Horwitz, A. Fessak, M. Keshavarz-K, K. E. Nash, and P. J. Toscano, J. Am. Chem. Soc., 115, 10444 (1993). b) M. Inouye, J. Chiba, and H. Nakazumi, J. Org. Chem., 64, 8170 (1999). c) M. Inouye, K. Takahashi, and H. Nakazumi, J. Am. Chem. Soc., 121, 341 (1999). d) M. Inouye, T. Miyake, M. Furusyo, and H. Nakazumi, J. Am. Chem. Soc., 117, 12416 (1995).
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 12416
    • Inouye, M.1    Miyake, T.2    Furusyo, M.3    Nakazumi, H.4
  • 34
    • 0000119469 scopus 로고    scopus 로고
    • Many reports on the inversion of chiral helicate were documented in the literature. For example, see: a) M. Albrecht and M. Schneider, Chem. Commun., 1997, 137. b) B. Kersting, M. Meyer, R. E. Powers, and K. N. Raymond, J. Am. Chem. Soc., 118, 7221 (1996). c) R. F. Carina, A. F. Williams, and C. Piguet, Helv. Chim. Acta, 81, 548 (1998).
    • (1997) Chem. Commun. , pp. 137
    • Albrecht, M.1    Schneider, M.2
  • 35
    • 0029760749 scopus 로고    scopus 로고
    • Many reports on the inversion of chiral helicate were documented in the literature. For example, see: a) M. Albrecht and M. Schneider, Chem. Commun., 1997, 137. b) B. Kersting, M. Meyer, R. E. Powers, and K. N. Raymond, J. Am. Chem. Soc., 118, 7221 (1996). c) R. F. Carina, A. F. Williams, and C. Piguet, Helv. Chim. Acta, 81, 548 (1998).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7221
    • Kersting, B.1    Meyer, M.2    Powers, R.E.3    Raymond, K.N.4
  • 36
    • 0000866847 scopus 로고    scopus 로고
    • Many reports on the inversion of chiral helicate were documented in the literature. For example, see: a) M. Albrecht and M. Schneider, Chem. Commun., 1997, 137. b) B. Kersting, M. Meyer, R. E. Powers, and K. N. Raymond, J. Am. Chem. Soc., 118, 7221 (1996). c) R. F. Carina, A. F. Williams, and C. Piguet, Helv. Chim. Acta, 81, 548 (1998).
    • (1998) Helv. Chim. Acta , vol.81 , pp. 548
    • Carina, R.F.1    Williams, A.F.2    Piguet, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.