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Volumn 128, Issue 32, 2006, Pages 10388-10390

Efficient templated synthesis of donor - Acceptor rotaxanes using click chemistry

Author keywords

[No Author keywords available]

Indexed keywords

ROTAXANE;

EID: 33747624198     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja063127i     Document Type: Article
Times cited : (175)

References (65)
  • 5
    • 0037124873 scopus 로고    scopus 로고
    • (e) Luo, Y.; et al. ChemPhysChem 2002, 3, 519.
    • (2002) ChemPhysChem , vol.3 , pp. 519
    • Luo, Y.1
  • 41
    • 23844451374 scopus 로고    scopus 로고
    • For examples of the click reaction for the synthesis of linear and diblock polymers, see: (a) Hawker, C. J.; Wooley, K. L. Science 2005, 309, 1200.
    • (2005) Science , vol.309 , pp. 1200
    • Hawker, C.J.1    Wooley, K.L.2
  • 60
    • 0001603015 scopus 로고    scopus 로고
    • (b) Previously, [2]- and [3]rotaxanes have been self-assembled from secondary dialkylammonium salts and crown ethers by using uncatalyzed Huisgen 1,3-dipolar cycloadditions to attach stoppers to the ends of the threads of [2]- and [3]pseudorotaxanes. See: Ashton, P. R.; Glink, P. T.; Stoddart, J. F.; Tasker, P. A.; White, A. J. P.; Williams, D. J. Chem.-Eur. J. 1996, 2, 729.
    • (1996) Chem.-Eur. J. , vol.2 , pp. 729
    • Ashton, P.R.1    Glink, P.T.2    Stoddart, J.F.3    Tasker, P.A.4    White, A.J.P.5    Williams, D.J.6
  • 62
    • 33747598165 scopus 로고    scopus 로고
    • note
    • 6, is sensitive to bases and nucleophilic conditions typically used in the synthesis of rotaxane dumbbells.
  • 64
    • 33747593431 scopus 로고    scopus 로고
    • note
    • We anticipate that the production of bistable [3]rotaxanes will proceed equally smoothly simply by incorporating a second recognition site into the azide containing a half-dumbbell component.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.