Chiral environments at alkaloid-modified
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P.B. Wells; K.E. Simons; J.A. Slipszenko; S.P. Griffiths; D.F. Ewing
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Article
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1999
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Elsevier Science
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English
⚖ 394 KB
Molecular environments at enantioselective sites are considered with reference to the adsorption of cinchonidine, Ž . epiquinidine, brucine, and oxycodone onto 6.3% Ptrsilica EUROPT-1 , using the hydrogenation of methyl pyruvate and of butane-2,3-dione as molecular probes. The mode of action of cinc