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Volumn 9, Issue 16, 2007, Pages 3117-3119

Design of a novel inherently chiral calix[4]arene for chiral molecular recognition

Author keywords

[No Author keywords available]

Indexed keywords

CALIX(4)ARENE; CALIXARENE; MANDELIC ACID; MANDELIC ACID DERIVATIVE; PHENOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34547942528     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071249p     Document Type: Article
Times cited : (101)

References (60)
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  • 7
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    • For representative reviews on calixarenes, see: a, Stoddart, J. F, Ed, The Royal Society of Chemistry: Cambridge, U.K
    • For representative reviews on calixarenes, see: (a) Gutsche, C. D. Calixarenes; Monographs in Supramolecular Chemistry; Stoddart, J. F., Ed.; The Royal Society of Chemistry: Cambridge, U.K., 1989.
    • (1989) Calixarenes; Monographs in Supramolecular Chemistry
    • Gutsche, C.D.1
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    • Gutsche, C. D. Caixarenes Revisited; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry, 2; The Royal Society of Chemistry: Cambridge, U.K., 1998.
    • (g) Gutsche, C. D. Caixarenes Revisited; Stoddart, J. F., Ed.; Monographs in Supramolecular Chemistry, Vol. 2; The Royal Society of Chemistry: Cambridge, U.K., 1998.
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    • Mandolini, L, Ungaro, R, Eds, Imperial College Press: London, U.K
    • (h) Calixarenes in Action; Mandolini, L., Ungaro, R., Eds.; Imperial College Press: London, U.K., 2000.
    • (2000) Calixarenes in Action
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    • Asfari, Z, Böhmer, V, Harrowfield, J, Vicens, J, Eds, Kluwer: Dordrecht, The Netherlands
    • (i) Calixarenes 2001; Asfari, Z., Böhmer, V., Harrowfield, J., Vicens, J., Eds.; Kluwer: Dordrecht, The Netherlands, 2001.
    • (2001) Calixarenes 2001
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    • 0029785123 scopus 로고    scopus 로고
    • For representative examples, see: a
    • For representative examples, see: (a) Kubo, Y.; Maeda, S.; Tokita, S.; Kubo, M. Nature 1996, 382, 522-524.
    • (1996) Nature , vol.382 , pp. 522-524
    • Kubo, Y.1    Maeda, S.2    Tokita, S.3    Kubo, M.4
  • 44
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    • Chiral HPLC analysis of 1 was performed by SUMICHIRAL OA-4800 column with hexane/i-PrOH/MeOH/TFA (90/5/5/0.3) as the eluent.
    • Chiral HPLC analysis of 1 was performed by SUMICHIRAL OA-4800 column with hexane/i-PrOH/MeOH/TFA (90/5/5/0.3) as the eluent.
  • 45
    • 0036015094 scopus 로고    scopus 로고
    • Inherently chiral calix[4]arene phosphoric acids with chiral amines were separated into diasteromeric forms by the achiral HPLC in analytical level: Tairov, M. A.; Vysotsky, M. O.; Kalchenko, O. I.; Pirozhenko, V. V.; Kalchenko, V. I. J. Chem. Soc., Perkin Trans. 1 2002, 1405-1411.
    • Inherently chiral calix[4]arene phosphoric acids with chiral amines were separated into diasteromeric forms by the achiral HPLC in analytical level: Tairov, M. A.; Vysotsky, M. O.; Kalchenko, O. I.; Pirozhenko, V. V.; Kalchenko, V. I. J. Chem. Soc., Perkin Trans. 1 2002, 1405-1411.
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    • 295-1, respectively.
    • 295-1, respectively.
  • 47
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    • For enantiomeric recognition of mandelic acid by artificial chiral receptors, see: a
    • For enantiomeric recognition of mandelic acid by artificial chiral receptors, see: (a) Takahashi, I.; Odashima, K.; Koga, K. Tetrahedron Lett. 1984, 25, 973-976.
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    • Takahashi, I.1    Odashima, K.2    Koga, K.3
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    • For representative reviews on organocatalyst, see: a
    • For representative reviews on organocatalyst, see: (a) Dalko, P. I.; Moisan, L. Angew. Chem., Int. Ed. 2004, 43, 5138-5175.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 5138-5175
    • Dalko, P.I.1    Moisan, L.2
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    • For chiral calixarenes as chiral catalyst, see: (a) Arnott, G.; Heaney, H.; Hunter, R.; Page, P. C. B. Eur. J. Org. Chem. 2004, 5126-5134.
    • For chiral calixarenes as chiral catalyst, see: (a) Arnott, G.; Heaney, H.; Hunter, R.; Page, P. C. B. Eur. J. Org. Chem. 2004, 5126-5134.
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    • Arnott, G.; Hunter, R. Tetrahedron 2006, 62, 992-1000. See also ref. 6a.
    • (c) Arnott, G.; Hunter, R. Tetrahedron 2006, 62, 992-1000. See also ref. 6a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.