Molecular modelling and chemical synthesis of molecular 'mappemondes' designed from a calix[4]-bis-crown

Tetrahedron Letters

Volumn 37, Issue 19, 1996, Pages 3325-3328

  Asfar, Zouhair ^a   Naumann, Christoph ^a   Kaufmann, Gérard ^b   Vicens, Jacques ^a  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CALIXARENE; MACROCYCLIC COMPOUND;

ARTICLE; COMPUTER SIMULATION; DRUG DESIGN; DRUG SYNTHESIS;

EID: 0029878939     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00568-0     Document Type: Article

References (12)

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3. Sauvage, J. P. Acc. Chem. Res. 1990, 23, 319.
4. Sijbesma, R. P.; Nolte, R. J. M. Topics in Current Chemistry 1995, 175, 25.
5. Kelly, T. R.; Bowyer, M. C.; Bhaskar, K. V.; Bebbington, D.; Garcia, A.; Lang, F.; Kim, M. H.; Jette, M. P. J. Amer. Chem. Soc. 1994, 116, 3657.
6. Yamato, T.; Doamekpor, L. K.; Tsuzuki, H.; Tashiro, M. Chem. Lett. 1995, 89.
7. Asfari, Z.; Wenger, S.; Vicens, J. Pure App. Chem. 1995, 67, 1037; Asfari, Z.; Wenger, S.; Vicens, J. Supramol.Sci. 1994, 1, 103.
8. Asfari, Z.; Wenger, S.; Vicens, J. Pure App. Chem. 1995, 67, 1037; Asfari, Z.; Wenger, S.; Vicens, J. Supramol.Sci. 1994, 1, 103.
9. All molecular modelling calculations were carried out with the SYBYL 6.1 program from Tripos Inc. The geometrical parameters of the different models were calculated on a Silicon Graphics Indigo/2 worstation, with help of the Tripos force field and the MAXIMIN2 energy minimizer.
10. Abidi, R.; Asfari, Z.; Harrowfield, J. M. Nauman, C.; Sobolev, A. N.; Vicens, J. Aust. J. Chem. to be published.
11. 27: C, 68.82; H, 6.91. Yield 33%.
12. Asfari, Z.; Abidi, R.; Arnaud, F.; Vicens, J. J. Incl. Phenom. Mol. Recognit. Chem. 1992, 13, 163.