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Volumn 46, Issue 10, 2010, Pages 1637-1639

Self-folding cavitands: Structural characterization of the induced-fit model

Author keywords

[No Author keywords available]

Indexed keywords

2 PYRROLIDONE DERIVATIVE; AMIDE; CAVITANDS; CHEMICAL COMPOUND; POLYCYCLIC AROMATIC HYDROCARBON; RESORCINOL; UNCLASSIFIED DRUG;

EID: 77249173980     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b927031k     Document Type: Article
Times cited : (18)

References (31)
  • 24
    • 42649084352 scopus 로고    scopus 로고
    • Conversion of the nitro function to a simple secondary anilide would lead to a cavitand that exists as a mixture of cyclodiastereoisomers (with clockwise and counterclockwise arrangement of the hydrogen bond seam). These conformations on an intrinsically chiral cavitand would lead to NMR spectra too difficult to interpret unambiguously
    • S. R. Shenoy F. R. Pinacho Crisóstomo T. Iwasawa J. Rebek J. Am. Chem. Soc. 2008 130 5658
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 5658
    • Shenoy, S.R.1    Pinacho Crisóstomo, F.R.2    Iwasawa, T.3    Rebek, J.4
  • 26
    • 0001304511 scopus 로고
    • The upfield signatures of the NMR spectra indicate that the guest keeps the same "upright" orientation inside the four different hosts
    • C. L. Perrin T. J. Dwyer Chem. Rev. 1990 90 935
    • (1990) Chem. Rev. , vol.90 , pp. 935
    • Perrin, C.L.1    Dwyer, T.J.2
  • 27
    • 61349159909 scopus 로고    scopus 로고
    • Related half-open conformations have been detected in covalently-stabilized cavitands:
    • R. J. Hooley S. R. Shenoy J. Rebek, Jr. Org. Lett. 2008 10 5397
    • (2008) Org. Lett. , vol.10 , pp. 5397
    • Hooley, R.J.1    Shenoy, S.R.2    Rebek Jr., J.3
  • 31
    • 77249152291 scopus 로고    scopus 로고
    • 1H NMR integration, the estimated error is 10%
    • 1H NMR integration, the estimated error is 10%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.