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Volumn 61, Issue 6, 1996, Pages 2051-2055

Molecular recognition and phase transfer of underivatized amino acids by a foldable artificial host

Author keywords

[No Author keywords available]

Indexed keywords

BINDING MOIETIES; CHARGED AMINO ACIDS; ENANTIOSELECTION; EXTRACTION PROCESS; GUANIDINIUM; PHASE TRANSFER; SILYL ETHERS; SIMILAR DESIGN;

EID: 0346496062     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951436d     Document Type: Article
Times cited : (130)

References (47)
  • 15
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    • Cram, D. J. Angew. Chem. 1988, 100, 1041-1052.
    • (1988) Angew. Chem , vol.100 , pp. 1041-1052
    • Cram, D.J.1
  • 18
    • 76049100668 scopus 로고    scopus 로고
    • In terms of scope of applicability it seems more desirable to design molecular hosts that recognize a defined set of functional groups in a guest molecule than to strive for utmost selectivity in binding one particular guest species
    • In terms of scope of applicability it seems more desirable to design molecular hosts that recognize a defined set of functional groups in a guest molecule than to strive for utmost selectivity in binding one particular guest species.
  • 24
    • 76049107805 scopus 로고
    • (b) 1988, 110, 4076-4077.
    • (1988) , vol.4076-4077 , Issue.110
  • 29
    • 7744228798 scopus 로고
    • (b) J. Inclusion Phenom. 1987, 5, 161-164.
    • (1987) J. Inclusion Phenom , vol.5 , pp. 161-164
  • 30
    • 0023317465 scopus 로고
    • (c) Z. Naturforsch. 1987, 42C, 476-485.
    • (1987) Z. Naturforsch , vol.42 C , pp. 476-485
  • 32
    • 0001111152 scopus 로고
    • For the synthesis of chiral guanidinium anchor groups see: a
    • For the synthesis of chiral guanidinium anchor groups see: (a) Kurzmeier, H.; Schmidtchen, F. P. J. Org. Chem. 1990, 55, 3749-3755.
    • (1990) J. Org. Chem , vol.55 , pp. 3749-3755
    • Kurzmeier, H.1    Schmidtchen, F.P.2
  • 39
    • 76049121839 scopus 로고    scopus 로고
    • Experimentally, this aza-crown ether ring shows a marked preference of primary ammonium versus alkali metal cation binding. This is why the selection of this anchor group was done though the origin of this effect is debatable (see, e.g.: Kuleshova, L. N.; Zorkii, P. M. Acta Crystallogr. 1981, B37, 1363).
    • Experimentally, this aza-crown ether ring shows a marked preference of primary ammonium versus alkali metal cation binding. This is why the selection of this anchor group was done though the origin of this effect is debatable (see, e.g.: Kuleshova, L. N.; Zorkii, P. M. Acta Crystallogr. 1981, B37, 1363).
  • 44
    • 76049099428 scopus 로고    scopus 로고
    • The estimates given are based on recalculations of the original data. In ref 8 CHCl3 is taken as the organic solvent for distribution instead of CH2Cl2. This difference should be of minor influence. The relation of extraction efficiencies to another amino acid host (cf. ref 2a) has not been possible.
    • The estimates given are based on recalculations of the original data. In ref 8 CHCl3 is taken as the organic solvent for distribution instead of CH2Cl2. This difference should be of minor influence. The relation of extraction efficiencies to another amino acid host (cf. ref 2a) has not been possible.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.