메뉴 건너뛰기




Volumn 26, Issue 11-12, 2007, Pages 1165-1174

Rotaxanes and catenanes by click chemistry

Author keywords

Catenanes; Click chemistry; Interlocked molecules; Rotaxanes; Self assembly; Surface chemistry

Indexed keywords

CATALYSIS; COPPER COMPOUNDS; CRYSTAL STRUCTURE; CYCLOADDITION; HYDROCARBONS; MOLECULAR ELECTRONICS; SUPRAMOLECULAR CHEMISTRY; SURFACE REACTIONS; SYNTHESIS (CHEMICAL);

EID: 37549032702     PISSN: 1611020X     EISSN: 16110218     Source Type: Journal    
DOI: 10.1002/qsar.200740070     Document Type: Short Survey
Times cited : (70)

References (70)
  • 9
    • 34247237682 scopus 로고    scopus 로고
    • For a recent Minireview, see: a
    • For a recent Minireview, see: a) J. F. Lutz. Angew. Chem. Int. Ed. 2007, 46, 1018-1025.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 1018-1025
    • Lutz, J.F.1
  • 10
    • 23844451374 scopus 로고    scopus 로고
    • See also: b
    • See also: b) C. J. Hawker, K. L. Wooley, Science 2005, 309, 1200-1205;
    • (2005) Science , vol.309 , pp. 1200-1205
    • Hawker, C.J.1    Wooley, K.L.2
  • 11
  • 12
    • 34547179800 scopus 로고    scopus 로고
    • For some very recent applications of the CuAAC reaction in polymer chemistry and materials science, see: a
    • For some very recent applications of the CuAAC reaction in polymer chemistry and materials science, see: a) N. V. Tsarevsky, S. A. Bencherif, K. Matyjaszewski, Macromolecules 2007, 40, 4439-4445;
    • (2007) Macromolecules , vol.40 , pp. 4439-4445
    • Tsarevsky, N.V.1    Bencherif, S.A.2    Matyjaszewski, K.3
  • 30
    • 85192684475 scopus 로고    scopus 로고
    • It is worthwhile mentioning that the uncatalyzed Huisgen's 1,3-dipolar cycloaddition between azides and alkynes has been used to prepare interlocked molecules based on dialkylammonium-crown ether recognition motif. For the most recent example, see: a J. D. Badjić, V. Balzani, A. Credi, J. N. Lowe, S. Silvi, J. F. Stoddart, Chem. - Eur. J. 2004, 10, 1926-1935.
    • It is worthwhile mentioning that the uncatalyzed Huisgen's 1,3-dipolar cycloaddition between azides and alkynes has been used to prepare interlocked molecules based on dialkylammonium-crown ether recognition motif. For the most recent example, see: a) J. D. Badjić, V. Balzani, A. Credi, J. N. Lowe, S. Silvi, J. F. Stoddart, Chem. - Eur. J. 2004, 10, 1926-1935.
  • 32
    • 85192672017 scopus 로고    scopus 로고
    • The ability of cucurbituril to catalyze 1,3-dipolar cycloaddition between azides and alkynes has been used to construct rotaxanes and semirotaxanes: c D. Tuncel, J. H. G. Steinke, Chem. Commun. 2002, 496-497.
    • The ability of cucurbituril to catalyze 1,3-dipolar cycloaddition between azides and alkynes has been used to construct rotaxanes and semirotaxanes: c) D. Tuncel, J. H. G. Steinke, Chem. Commun. 2002, 496-497.
  • 33
    • 0003542983 scopus 로고    scopus 로고
    • J.-P. Sauvage, C. Dietrich-Buchecker Eds, Sauvage, Wiley-VCH, Weinheim
    • J.-P. Sauvage, C. Dietrich-Buchecker (Eds.) Molecular Catenanes, Rotaxanes and Knots, Sauvage, Wiley-VCH, Weinheim 1999.
    • (1999) Molecular Catenanes, Rotaxanes and Knots
  • 34
    • 33746911942 scopus 로고    scopus 로고
    • For the sake of brevity, this Minireview will not discuss the preparation of cucurbituril-based polypseudorotaxanes using the CuAAC reaction. See
    • For the sake of brevity, this Minireview will not discuss the preparation of cucurbituril-based polypseudorotaxanes using the CuAAC reaction. See: T. Ooya, D. Inoue, H. S. Choi, Y. Kobayashi, S. Loethen, D. H. Thompson, Y. H. Ko, K. Kim, N. Yui, Org. Lett. 2006, 8, 3159-3162.
    • (2006) Org. Lett , vol.8 , pp. 3159-3162
    • Ooya, T.1    Inoue, D.2    Choi, H.S.3    Kobayashi, Y.4    Loethen, S.5    Thompson, D.H.6    Ko, Y.H.7    Kim, K.8    Yui, N.9
  • 51
    • 33846503504 scopus 로고    scopus 로고
    • P. Ball, Nature 2007, 445, 362-363.
    • (2007) Nature , vol.445 , pp. 362-363
    • Ball, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.