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LIST of PUBLICATIONS


1. Partially OH-Depleted Calixarenes.
By F. Grynszpan, Z. Goren and S. E. Biali, J. Org. Chem., 56, 532-536 (1990).
2. Reductive and Oxidative Reactions of Calix[4]arene Derivatives
By F. Grynszpan, N. Dinoor and S. E. Biali, Tetrahedron Lett., 32, 1909-1912 (1991).
3. Solution Conformation and Inversion Barrier in Dihydroxycalixarene.
By F. Grynszpan and S. E. Biali, Tetrahedron Lett., 32, 5155-5158 (1991).
4. The source of the Intraannular Hydrogens in the Dehydroxylation of Calix[4]arene Diethyl Phosphate Ester Derivatives.
By F. Grynszpan and S. E. Biali, J. Phys. Org. Chem., 5, 155-159 (1992).
5. Proximal Intraannular Modifications of Calix[4]arene via its Spirodienone Derivative.
By O. Aleksiuk, F. Grynszpan and S. E. Biali, J. Chem. Soc., Chem. Commun., 11-13 (1993).
6. Phosphorus Polybridged Calixarenes
By F. Grynszpan, O. Aleksiuk and S. E. Biali, J. Chem. Soc., Chem. Commun., 13-16 (1993).
7. Preparation, Stereochemistry and Reactions of the Bis(spirodienone) Derivatives of p-tert-Butylcalix[4]arene.
By A. M. Litwak, F. Grynszpan, O. Aleksiuk, Sh. Cohen and S. E. Biali, J. Org. Chem., 58, 393-402 (1993).
8. The Spirodienone Route for Aminodehydroxylation: Monoaminotrihydroxy-p-tert-butylcalix[4]arene.
By O. Aleksiuk, F. Grynszpan and S. E. Biali, J. Org. Chem., 58, 1994-1996 (1993).
9. Transmission of Internal Rotations: Correlated, Uncorrelated and Localized Disrotatory Rotation in Propeller Chains.
By A. B. Lindner, F. Grynszpan and S. E. Biali, J. Org. Chem., 58, 6662-6670 (1993).
10. Cyclization and Reductive Cleavage of Monospirodienone Calix[4]arene Derivatives. Trihydroxy-p-tert- butylcalixarene Revisited.
By F. Grynszpan, O. Aleksiuk and S. E. Biali, J. Org. Chem., 59, 2070-2074 (1994).
11. Preparation, Structure and Stereodynamics of Phosphorus Bridged Calixarenes.
By O. Aleksiuk, F. Grynszpan and S. E. Biali, J. Inclus. Phenom., 19, 237-256 (1994).
12. Calix[4]arenes with Alkylidene Bridges, Synthesis and Conformational Properties.
By C. Grüttner, V. Böhmer, W. Vogt, I. Thondorf, S. E. Biali and F. Grynszpan, Tetrahedron Lett., 35, 6267-6270 (1994).
13. Large Macrocyclic Rings with Complex Architectures:Polyspirodienone Calix[6]arene Derivatives.
By F. Grynszpan and S. E. Biali, J. Chem. Soc., Chem. Commun., 2545-2546 (1994).
14. NMR Diffusion Coefficients of p-tert-butylcalix[n]arene Systems.
By O. Mayzel, O. Aleksiuk, F. Grynszpan and S. E. Biali, Y. Cohen, J. Chem. Soc., Chem. Commun, 1183-1184 (1995).
15. Preparation, Structure and Stereodynamics of Phosphorus Bridged Calixarenes.
By O. Aleksiuk, F. Grynszpan, and S. E. Biali., “Calixarenes 50th Annivrsary”, pp. 199-221. J. Vicens, Z. Asfari, J. M. Harrowfied, Ed., Kluwer Academic Publishers; Dordrecht/Boston/London, 1995.
16. Spirodienone Calixarene Derivatives.
By O. Aleksiuk, F. Grynszpan, A. M. Litwak, and S. E. Biali, New J. Chem., 20, 473-482 (1996).
17. Synthesis and Reactions of Large - Ring Spirodienone Calixarene Derivatives.
By F. Grynszpan, O. Aleksiuk, and S. E. Biali, Pure and Appl. Chem., 68 (6), 1249-1254 (1996).
18. From Calixarenes to Macrocyclic Polyethers.
By F. Grynszpan and S. E. Biali, J. Chem. Soc., Chem. Commun., 195-196 (1996).
19. Alkanediyl Bridged Calix[4]arenes: Synthesis, Conformational Analysis and Rotational Barriers.
By S. E. Biali, V. Böhmer, Sh. Cohen, G. Ferguson, C. Grüttner, F. Grynszpan, E. Paulus, I. Thondorf and W. Vogt, J. Am. Chem. Soc., 118, 12938-12949 (1996).
20. Using Antibodies to Perturb the Coordination Sphere of a Transition Metal Complex.
By P. Ghosh, D. Shabat, S. Kumar, S. C. Sinha, F. Grynszpan, J. Li, L. Noodelman and E. Keinan, Nature, 382, 339-341 (1996). (Summarized in Chem. & Eng. News, July 29, 1996; p. 40, Science/Tech. Concentrates).
21. Structure and Equilibration Studies of Bis - and Tris(spirodienone) Derivatives of Medium - Sized Calixarenes.
By F. Grynszpan and S. E. Biali, J. Org. Chem., 61, 9512-9521 (1996).
22. An Efficient Sol-Gel Reactor for Antibody Catalyzed Transformations.
By D. Shabat, F. Grynszpan, S. Saphier, A. Turniansky, D. Avnir and E. Keinan, Chem. Mat., 9, 2258-2260 (1997).
23. Spirodienone Calixarene Derivatives as Blocking Groups for Selective Functionalizations: Conformation and Stereodynamics of Monodioxamethylene Calix[4]arene Derivatives.
By J. Wöhnert, J. Brenn, M. Stoldt, O. Aleksiuk, F. Grynszpan, I. Thondorf and S. E. Biali, J. Org. Chem., 63, 3866-3874 (1998).
24. Use of Antibodies to Dissect the Components of a Catalytic Event. The Cyclopropenone Hapten.
By F. Grynszpan and E. Keinan, Chem. Commun., 865-866 (1998).
25. Conformational Studies of Calix[5]arenes Containing a Single Alkanediyl Bridge.
By S. E. Biali, V. Böhmer, I. Columbus, G. Fergurson, C. Grüttner, F. Grynszpan, E. F. Paulus and I. Thondorf. J. Chem. Soc. Perkin Trans 2, 2261-1170 (1998).
26. Opsin Shift in an Aldolase Antibody.
By F. Grynszpan and E. Keinan. Bioorg. Med. Chem. Lett. 9, 2419-2425 (1999).
27. Stereochemistry of a Spherand-Type Calixarene.
By K. Agbaria, S.E. Biali, V. Böhmer, J. Brenn, Sh. Cohen, M. Frings, F. Grynszpan, J.McB. Harrowfield, A.N. Sobolev and I. Thondorf, J. Org. Chem. 66, 2900-2906, (2001).
28. Multiple Reactive Immunization Towards the Hydrolysis of Organophosphorous Nerve Agents: Hapten Design and Synthesis.
By H. Huang, W.-G. Han, L. Noodleman and F. Grynszpan. Bioorg. Med. Chem. 9, 3185-3195, (2001).
29. Prediction of the Protein-Protein interaction in the LFA-1 I-Domain / ICAM-1 D1-D2 complex.
By G.B. Legge, G. Morris, M.F. Sanner, Y. Takada, A.J. Olson and F. Grynszpan. Proteins, Struct. Func. Gen. 48, 151-160 (2002).
30. Click Chemistry in situ: Acetylcholinesterase as a Molecular-Scale Reaction Vessel for the Selective Assembly of a Femtomolar Inhibitor from an Array of Building Blocks.
By W. Lewis, L.G. Green, F. Grynszpan, Z. Radic, P.R. Carlier, P. Taylor, M.G. Finn, and K.B. Sharpless. Angew. Chem. 114, 1095-1099, (2002). Angew. Chem. Int. Ed., 41, 1053-1057, (2002). (Highlighted in Chem. & Eng. News, Feb. 11, 2002; 80(6), p. 29-34, Cover Story. Highlighted in The Union Tribune, San Diego, City Edition, B1. Highlighted in Nature, Drug Discovery Reviews, 1, 254, (2002)).
31. Mutants of 4-oxalocrotonate tautomerase catalyze the decarboxylation of oxaloacetate through an imine mechanism.
By A. Brik, L.J. D’Souza, E. Keinan, F. Grynszpan and P.E. Dawson. ChemBioChem, In press (2002).

 

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