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Some Diels-Alder Reactions in water solution 1. Faster in water than in other solvents. 2. Even in a case in which reaction is faster in isooctane than in methanol. 3. Reaction speeds with additives that increase the hydrophobic effect (LiCl) but slows with an antihydrophobic additive (guanidinium chloride). 4. More selective for endo addition in water, and ON WATER. Selective Diels-Alder Reactions in Aqueous Solutions and Suspensions R. Breslow, U. Maitra, and D. Rideout Tetrahedron Lett. 1983, 24, 1901-1904 Abstract: Diels-Alder reactions show high endo/exo selectivities in aqueous suspensions “Even with a considerable layer of “neat” diene- dienophile solution the selectivities suggest that much of the reaction occurs in or at the water phase. This is consistent with our rough rate measurements.” “Thus water as a medium for Diels-Alder reactions, and other processes, is of practical interest even with poorly soluble substrates.” Hydrophobic Effects on Simple Organic Reactions in Water R. Breslow, Acts. Chem. Res. 1991, 24, 159-164 Interestingly, a high preference for endo addition was found even with suspensions in which the cyclopentadiene was over 90% undissolved. Selectivity Produced by Hydrophobic Packing of Reagents and Substrate in Water O H OH O + - Li RBH 3 + H O 2 O SO O SO O SO 3 3 3 H OH O O A B A:B ratio R D O 4M LiCl/D O 1:1 CD OD/D O 2 2 3 2 H 13:87 14:86 10:90 Ph 60:40 69:31 32:68 C F 78:22 85:15 46:54 6 5 Mark R. Biiscoe, Christopher Uyeda, and RB Org. Lett. 2004, 6, 4331-4334 Considerations in Choosing a Hydrophobic Oxidant: T.S. Geometry O O O O O O H Or Peracid Dioxirane Hydrophobic packing is not permitted Hydrophobic packing is permitted in peracid transition state. in dioxirane transition state. Houk, K. N.; Liu, J.; DeMello, N. C.; Condroski, K. R. J. Am. Chem. Soc. 1997, 119, 10147-10152
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