Abstract
Abstract Addition of amines, especially benzylamine, to the reaction mixture of (E)-α-phenylcinnamic acid with a cinchonidine-modified palladium catalyst resulted in much enhanced activities and fairly increased enantioselectivities. The preferential acceleration of the selective reaction is attributable to the effective desorption, assisted by the added base, of the hydrogenated molecules from the modified sites.
References
10
Referenced
51
10.1016/S0920-5861(97)00026-6
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10.1016/S0167-2991(97)80904-4
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Dates
Type | When |
---|---|
Created | 22 years ago (Aug. 11, 2003, 10:40 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 18, 2024, 11:07 a.m.) |
Indexed | 1 year, 1 month ago (July 18, 2024, 6:33 a.m.) |
Issued | 26 years, 2 months ago (July 1, 1999) |
Published | 26 years, 2 months ago (July 1, 1999) |
Published Online | 22 years, 1 month ago (Aug. 1, 2003) |
Published Print | 26 years, 2 months ago (July 1, 1999) |
@article{Nitta_1999, title={Importance of Product Desorption in Enantioselective Hydrogenation of (E)-α-Phenylcinnamic Acid with a Cinchonidine-Modified Pd/TiO2 Catalyst: Effect of Additives}, volume={28}, ISSN={1348-0715}, url={http://dx.doi.org/10.1246/cl.1999.635}, DOI={10.1246/cl.1999.635}, number={7}, journal={Chemistry Letters}, publisher={Oxford University Press (OUP)}, author={Nitta, Yuriko}, year={1999}, month=jul, pages={635–636} }