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Chapter 6 References

(200) Breslow, R.; Halfon, S.: Quantitative effects of antihydrophobic agents on binding constants and solubilities in water. In Proceedings of the National Academy of Sciences, USA, 1992; Vol. 89; pp 6916-6918.

(201) Keay, B. A.: Intramolecular Diels–Alder reaction of the diene unit of furan in 2.0 M CaCl2. Chemical Communications 1987, 6, 419-421.

(202) Blokzijl, W.; Blandamer, M. J.; Engberts, J. B. F. N.: Diels-Alder reactions in aqueous solutions. Enforced hydrophobic interactions between diene and dienophile. Journal of the American Chemical Society 1991, 113, 4241-6.

(203) Otto, S.: Catalysis of Diels-Alder reactions in water. University of Groningen, 1998.

(204)Breslow, R.; Zhu, Z.: Quantitative Antihydrophobic Effects as Probes for Transition State Structures. 2. Diels-Alder Reactions. Journal of the American Chemical Society 1995, 117, 9923-4.

(205) Schneider, H. J.; Sangwan, N. K.: Changes of Stereoselectivity in Diels–Alder Reactions by Hydrophobic Solvent Effects and by β‐Cyclodextrin. Angewandte Chemie International Edition 1987, 26, 896-897.

(206)Hirst, S. C.; Hamilton, A. D.: Complexation control of pericyclic reactions: supramolecular effects on the intramolecular Diels-Alder reaction. Journal of the American Chemical Society 1991, 113, 382-383.

(207) Kang, J.; Rebek, J.: Acceleration of a Diels–Alder reaction by a self-assembled molecular capsule. Nature 1997, 385, 50-52.

(208) Gouverneur, V.; Houk, K.; de Pascual-Teresa, B.; Beno, B.; Janda, K.; Lerner, R.: Control of the exo and endo pathways of the Diels-Alder reaction by antibody catalysis. Science 1993, 262, 204-208.

(209) Siegel, J. B.; Zanghellini, A.; Lovick, H. M.; Kiss, G.; Lambert, A. R.; St.Clair, J. L.; Gallaher, J. L.; Hilvert, D.; Gelb, M. H.; Stoddard, B. L.; Houk, K. N.; Michael, F. E.; Baker, D.: Computational Design of an Enzyme Catalyst for a Stereoselective Bimolecular Diels-Alder Reaction. Science 2010, 329, 309-313.

(210)Yoshizawa, M.; Tamura, M.; Fujita, M.: Diels-Alder in Aqueous Molecular Hosts: Unusual Regioselectivity and Efficient Catalysis. Science 2006, 312, 251- 254.

(211) Rose, K. N.; Hardie, M. J.; Atwood, J. L.; Raston, C. L.: Oxygen-center laden C2h symmetry resorcin[4]arenes. Journal of Supramolecular Chemistry 2001, 1, 35- 38.

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chapter references breslowhalfon quantitative effects antihydrophobic agents constants solubilities proceed
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