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Beyond Nature's Chiral Pool: Enantioselective Catalysis in Industry
William A. Nugent, T. V. RajanBabu and Mark J. Burk
Vol. 259, No. 5094 (Jan. 22, 1993), pp. 479-483
Published by: American Association for the Advancement of Science
Stable URL: http://www.jstor.org/stable/2880705
Page Count: 5
You can always find the topics here!Topics: Ligands, Catalysts, Catalysis, Hydrogenation, Biochemistry, Business structures, Chirality, Chemical bonding, Nitriles, Materials
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Enantioselective catalysts produce organic compounds in enantiomerically enriched form. They are highly efficient tools for the synthesis of biologically active materials, such as pharmaceuticals and crop-protection chemicals, in which enantiomeric purity can be critical. The design of chiral ligands is the key to developing new enantioselective catalysts. Three unusual families of ligands have been used to develop practical technology for enantioselective hydrocyanation of olefins, ring-opening of epoxides, and hydrogenation of various compounds.
Science © 1993 American Association for the Advancement of Science