메뉴 건너뛰기




Volumn 50, Issue 3, 2009, Pages 350-353

Induced-fit recognition by p-carboxylatocalix[4]arene hosts

Author keywords

Calixarenes; DOSY experiments; Induced fit; NMR titrations; p Carboxylatocalixarenes; Paraquat

Indexed keywords

4 CARBOXYLATOCALIX[4]ARENE; CALIXARENE; PARAQUAT; UNCLASSIFIED DRUG;

EID: 57149127658     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.11.016     Document Type: Article
Times cited : (15)

References (45)
  • 4
    • 0041437436 scopus 로고    scopus 로고
    • Atwood J.L., and Steed J.W. (Eds), Dekker and references cited therein
    • Liu Y., Li L., and Zhang H.-Y. In: Atwood J.L., and Steed J.W. (Eds). Encyclopedia of Supramolecular Chemistry (2002), Dekker 717-726 and references cited therein
    • (2002) Encyclopedia of Supramolecular Chemistry , pp. 717-726
    • Liu, Y.1    Li, L.2    Zhang, H.-Y.3
  • 5
    • 33748539998 scopus 로고
    • For general reviews on calixarenes, see:
    • For general reviews on calixarenes, see:. Böhmer V. Angew. Chem., Int. Ed. Engl. 34 (1995) 713-745
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 713-745
    • Böhmer, V.1
  • 8
    • 0004287470 scopus 로고    scopus 로고
    • Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds), Kluwer, Dordrecht
    • In: Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer, Dordrecht
    • (2001) Calixarenes 2001
  • 9
    • 57149136058 scopus 로고    scopus 로고
    • Rappoport Z. (Ed), Wiley, Chichester, UK Chapter 19
    • Böhmer V. In: Rappoport Z. (Ed). The Chemistry of Phenols (2003), Wiley, Chichester, UK Chapter 19
    • (2003) The Chemistry of Phenols
    • Böhmer, V.1
  • 10
    • 84892021501 scopus 로고    scopus 로고
    • Vicens J., and Harrowfield J. (Eds), Springer, Dordrecht
    • In: Vicens J., and Harrowfield J. (Eds). Calixarenes in the Nanoworld (2007), Springer, Dordrecht
    • (2007) Calixarenes in the Nanoworld
  • 12
    • 21244492862 scopus 로고    scopus 로고
    • It is well known that the interconversion among these four calix[4]arene conformations is impeded when substituents larger than ethyl group are attached at the phenolic OH groups (Iwamoto, K.; Araki, K.; Shinkai, S. J. Org. Chem. 1991, 56, 4955-4962).
    • It is well known that the interconversion among these four calix[4]arene conformations is impeded when substituents larger than ethyl group are attached at the phenolic OH groups (Iwamoto, K.; Araki, K.; Shinkai, S. J. Org. Chem. 1991, 56, 4955-4962).
  • 13
    • 57149139278 scopus 로고    scopus 로고
    • Analogously, Rebek (Castellano, R. K.; Rudkevich, D. M.; Rebek, J., Jr.; J. Am. Chem. Soc. 1996, 118, 10002-10003) has reported that the conformational equilibrium of tetramethoxycalix[4]arene can be influenced through a self-assembly process.
    • Analogously, Rebek (Castellano, R. K.; Rudkevich, D. M.; Rebek, J., Jr.; J. Am. Chem. Soc. 1996, 118, 10002-10003) has reported that the conformational equilibrium of tetramethoxycalix[4]arene can be influenced through a self-assembly process.
  • 25
    • 0002480659 scopus 로고    scopus 로고
    • Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds), Kluwer, Dordrecht Chapter 24, and references cited therein
    • Casnati A., Sciotto D., and Arena G. In: Asfari Z., Böhmer V., Harrowfield J., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer, Dordrecht 440-456 Chapter 24, and references cited therein
    • (2001) Calixarenes 2001 , pp. 440-456
    • Casnati, A.1    Sciotto, D.2    Arena, G.3
  • 31
    • 57149129461 scopus 로고    scopus 로고
    • note
    • See the Supplementary data for additional details.
  • 34
    • 57149137205 scopus 로고    scopus 로고
    • note
    • 4
  • 35
    • 57149138442 scopus 로고    scopus 로고
    • Macromodel Version 9.0, Schrödinger, LLC, New York, NY, 2005.
    • Macromodel Version 9.0, Schrödinger, LLC, New York, NY, 2005.
  • 45
    • 0031101168 scopus 로고    scopus 로고
    • 1/3 (Waldeck, A. R.; Kuchel, P. W.; Lennon, A. J.; Chapman, B. E. Prog. Nucl. Magn. Reson. Spectrosc. 1997, 30, 39-68).
    • 1/3 (Waldeck, A. R.; Kuchel, P. W.; Lennon, A. J.; Chapman, B. E. Prog. Nucl. Magn. Reson. Spectrosc. 1997, 30, 39-68).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.