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Volumn 119, Issue 11, 1997, Pages 2614-2627

Structure-reactivity relationship in interlocked molecular compounds and in their supramolecular model complexes

Author keywords

[No Author keywords available]

Indexed keywords

MACROCYCLIC COMPOUND; POLYCYCLIC HYDROCARBON;

EID: 0030972332     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja962937z     Document Type: Article
Times cited : (44)

References (38)
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    • 4.
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    • 4+, the carbonyl oxygen atoms sustain intra-pseudorotaxane hydrogen bonding interactions with the hydrogen atpms Hα.
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    • note
    • 6. Presumably, the intramolecular hydrogen bonding interactions responsible for the enhanced reactivity of the ester function in solution are over-ruled in the solid state by more favorable intermolecular hydrogen bonding interactions.
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    • 0030134511 scopus 로고    scopus 로고
    • For a discussion on the conformational analysis of 1,2-dimethoxyethane in the gas and solution phases, see: Williams, D. J.; Hall, K. B. J. Phys. Chem. 1996, 100, 8224-8229.
    • (1996) J. Phys. Chem. , vol.100 , pp. 8224-8229
    • Williams, D.J.1    Hall, K.B.2
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    • This effect is reminicent of the different basicity observed for syn and anti lone pairs of carboxylates, see: (a) Zimmerman, S. C.; Cramer, K. D. J. Am. Chem. Soc. 1988, 110, 5906-5908. (b) Huff, J. B.; Askew, B.; Duff, R. J.; Rebek, J., Jr. J. Am. Chem. Soc. 1988, 110, 5908-5909. (c) Li, Y.; Houk, K. N. J. Am. Chem. Soc. 1989, 111, 4505-4507. (d) Huff, J. B.; Tadayoni, B. M.; Rebek, J., Jr. J. Am. Chem. Soc. 1991, 113, 2247-2253.
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    • Zimmerman, S.C.1    Cramer, K.D.2
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    • This effect is reminicent of the different basicity observed for syn and anti lone pairs of carboxylates, see: (a) Zimmerman, S. C.; Cramer, K. D. J. Am. Chem. Soc. 1988, 110, 5906-5908. (b) Huff, J. B.; Askew, B.; Duff, R. J.; Rebek, J., Jr. J. Am. Chem. Soc. 1988, 110, 5908-5909. (c) Li, Y.; Houk, K. N. J. Am. Chem. Soc. 1989, 111, 4505-4507. (d) Huff, J. B.; Tadayoni, B. M.; Rebek, J., Jr. J. Am. Chem. Soc. 1991, 113, 2247-2253.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5908-5909
    • Huff, J.B.1    Askew, B.2    Duff, R.J.3    Rebek Jr., J.4
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    • 0001193005 scopus 로고
    • This effect is reminicent of the different basicity observed for syn and anti lone pairs of carboxylates, see: (a) Zimmerman, S. C.; Cramer, K. D. J. Am. Chem. Soc. 1988, 110, 5906-5908. (b) Huff, J. B.; Askew, B.; Duff, R. J.; Rebek, J., Jr. J. Am. Chem. Soc. 1988, 110, 5908-5909. (c) Li, Y.; Houk, K. N. J. Am. Chem. Soc. 1989, 111, 4505-4507. (d) Huff, J. B.; Tadayoni, B. M.; Rebek, J., Jr. J. Am. Chem. Soc. 1991, 113, 2247-2253.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4505-4507
    • Li, Y.1    Houk, K.N.2
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    • This effect is reminicent of the different basicity observed for syn and anti lone pairs of carboxylates, see: (a) Zimmerman, S. C.; Cramer, K. D. J. Am. Chem. Soc. 1988, 110, 5906-5908. (b) Huff, J. B.; Askew, B.; Duff, R. J.; Rebek, J., Jr. J. Am. Chem. Soc. 1988, 110, 5908-5909. (c) Li, Y.; Houk, K. N. J. Am. Chem. Soc. 1989, 111, 4505-4507. (d) Huff, J. B.; Tadayoni, B. M.; Rebek, J., Jr. J. Am. Chem. Soc. 1991, 113, 2247-2253.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 2247-2253
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    • Laidler, K.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.