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Volumn 17, Issue 8, 2006, Pages 1258-1263

Synthesis and chiral recognition abilities of new calix[6]arenes bearing amino alcohol moieties

Author keywords

[No Author keywords available]

Indexed keywords

5,11,17,23,29,35 TERT BUTYL 37,38 DIMETHOXY 39,40,41,42 (4 TOSYLETHOXY)CALIX[6]ARENE; 5,11,17,23,29,35 TERT BUTYL 37,38 DIMETHOXY 39,40,41,42 (HYDROXYETHOXY)CALIX[6]ARENE; 5,11,17,23,29,35 TERT BUTYL 37,38 DIMETHOXY 39,40,41,42 (METHOXYCARBONYLMETHOXY)CALIX[6]ARENE; AMINOALCOHOL; CALIXARENE; PHENYLALANINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33646853502     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.04.013     Document Type: Article
Times cited : (20)

References (47)
  • 1
    • 0003894828 scopus 로고    scopus 로고
    • For general references on calixarenes, see:. Stoddart J.F. (Ed), The Royal Society of Chemistry, Cambridge, UK
    • For general references on calixarenes, see:. Gutsche C.D. In: Stoddart J.F. (Ed). Calixarenes Revisited, Monographs in Supramolecular Chemistry (1998), The Royal Society of Chemistry, Cambridge, UK
    • (1998) Calixarenes Revisited, Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
  • 2
    • 0004266535 scopus 로고    scopus 로고
    • Mandolini L., and Ungaro R. (Eds), Imperial College Press, London
    • In: Mandolini L., and Ungaro R. (Eds). Calixarenes in Action (2000), Imperial College Press, London
    • (2000) Calixarenes in Action
  • 3
    • 0004287470 scopus 로고    scopus 로고
    • Asfari Z., Bohmer V., Harrowfield J., and Vicens J. (Eds), Kluwer, Dordrecht
    • In: Asfari Z., Bohmer V., Harrowfield J., and Vicens J. (Eds). Calixarenes 2001 (2001), Kluwer, Dordrecht
    • (2001) Calixarenes 2001
  • 9
    • 0001595328 scopus 로고    scopus 로고
    • Gokel G.W. (Ed), Pergamon Press, New York, Oxford
    • Moyer B.A. In: Gokel G.W. (Ed). Molecular Recognition: Receptors for Cationic Guests. Comprehensive Supramolecular Chemistry Vol. 1 (1996), Pergamon Press, New York, Oxford 377-416
    • (1996) Comprehensive Supramolecular Chemistry , vol.1 , pp. 377-416
    • Moyer, B.A.1
  • 24
    • 2742595750 scopus 로고
    • Roberts S.M. (Ed), Royal Society of Chemistry, London Special Publication no. 78
    • In: Roberts S.M. (Ed). Molecular Recognition: Chemical and Biochemical Problems (1990), Royal Society of Chemistry, London Special Publication no. 78
    • (1990) Molecular Recognition: Chemical and Biochemical Problems
  • 30
    • 0036139996 scopus 로고    scopus 로고
    • The cavity of the more studied calix[4]arenes is not well adapted for the inclusion of organic molecules. Thus, they have mainly been used for the preorganization of a chiral binding site outside of the cavity. For recent leading references on chiral recognition with calix[4]arenes, see:
    • The cavity of the more studied calix[4]arenes is not well adapted for the inclusion of organic molecules. Thus, they have mainly been used for the preorganization of a chiral binding site outside of the cavity. For recent leading references on chiral recognition with calix[4]arenes, see:. Lynam C., Jennings K., Nolan K., Kane P., Anthony McKervey M., and Diamond D. Anal. Chem. 74 (2002) 59-66
    • (2002) Anal. Chem. , vol.74 , pp. 59-66
    • Lynam, C.1    Jennings, K.2    Nolan, K.3    Kane, P.4    Anthony McKervey, M.5    Diamond, D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.