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Volumn 122, Issue 15, 2000, Pages 3617-3627

Control of structural isomerism in noncovalent hydrogen-bonded assemblies using peripheral chiral information

Author keywords

[No Author keywords available]

Indexed keywords

BARBITURIC ACID DERIVATIVE; CALIXARENE; CYANURIC ACID; MELAMINE;

EID: 0034685439     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9936262     Document Type: Article
Times cited : (94)

References (52)
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    • (1997) Chem. Rev. , vol.97 , pp. 1669-1680
    • Linton, B.1    Hamilton, A.D.2
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    • For reviews, see: (a) Conn, M. M.; Rebek, J., Jr. Chem. Rev. 1997, 97, 1647-1668. (b) Linton, B.; Hamilton, A. D. Chem. Rev. 1997, 97, 1669-1680. (c) Philp, D.; Stoddart, J. F. Angew. Chem., Int. Ed. Engl. 1996, 35, 1154-1196. (d) Lawrence, D. S.; Jiang, T.; Levett, M. Chem. Rev. 1995, 95, 2229-2260.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 1154-1196
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    • 4243714728 scopus 로고
    • For reviews, see: (a) Conn, M. M.; Rebek, J., Jr. Chem. Rev. 1997, 97, 1647-1668. (b) Linton, B.; Hamilton, A. D. Chem. Rev. 1997, 97, 1669-1680. (c) Philp, D.; Stoddart, J. F. Angew. Chem., Int. Ed. Engl. 1996, 35, 1154-1196. (d) Lawrence, D. S.; Jiang, T.; Levett, M. Chem. Rev. 1995, 95, 2229-2260.
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    • For a short review, see: (a) Sanders, J. K. M. Chem. Eur. J. 1998, 4, 1378-1383. (b) Kang, J.; Santamaria, J.; Hilmersson, G.; Rebek, J., Jr. J. Am. Chem. Soc. 1998, 120, 7389-7390.
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    • Sanders, J.K.M.1
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    • note
    • The orientation of the two melamines can either be clockwise (P) or counterclockwise (M). In the absence of additional chiral centers present in the building blocks, the staggered isomer exists as a racemic mixture of the P and M assembly.
  • 34
    • 0342540540 scopus 로고    scopus 로고
    • note
    • This is only the case when the substituents on each melamine are identical.
  • 37
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    • For the synthesis of BisBAR, see: Lipkowski, P.; Bielejewska, A.; Kooijman, H.; Spek, A. L.; Timmerman, P.; Reinhoudt, D. N. Chem. Commun. 1999, 1311-1312. For the synthesis of calix[4]arene dimelamine 6, see ref 22. For the syntheses of HexCYA and TripCYA, see: Mathias, J. P.; Seto, C. T.; Simanek, E. E.; Whitesides, G. M. J. Am. Chem. Soc. 1994, 116, 1725-1736.
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  • 38
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    • see ref 22
    • For the synthesis of BisBAR, see: Lipkowski, P.; Bielejewska, A.; Kooijman, H.; Spek, A. L.; Timmerman, P.; Reinhoudt, D. N. Chem. Commun. 1999, 1311-1312. For the synthesis of calix[4]arene dimelamine 6, see ref 22. For the syntheses of HexCYA and TripCYA, see: Mathias, J. P.; Seto, C. T.; Simanek, E. E.; Whitesides, G. M. J. Am. Chem. Soc. 1994, 116, 1725-1736.
  • 39
    • 0000416572 scopus 로고
    • For the synthesis of BisBAR, see: Lipkowski, P.; Bielejewska, A.; Kooijman, H.; Spek, A. L.; Timmerman, P.; Reinhoudt, D. N. Chem. Commun. 1999, 1311-1312. For the synthesis of calix[4]arene dimelamine 6, see ref 22. For the syntheses of HexCYA and TripCYA, see: Mathias, J. P.; Seto, C. T.; Simanek, E. E.; Whitesides, G. M. J. Am. Chem. Soc. 1994, 116, 1725-1736.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1725-1736
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    • Mascal, M.; Fallon, P. S.; Batsanov, A. S.; Heywood, B. R.; Champ, S.; Colclough, M. J. Chem. Soc., Chem. Commun. 1995, 805-806. Shieh, H. S.; Voet, D. Acta Crystallogr., Sect. B 1976, 32, 3254-3260
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    • Shieh, H.S.1    Voet, D.2
  • 50
    • 0342540535 scopus 로고    scopus 로고
    • note
    • mels in the outer ring of the rosette motif temporarily rotate away.
  • 51
    • 0343846062 scopus 로고    scopus 로고
    • note
    • 3h isomer instead of two.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.