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By D. Stevenson, I.D. Wilson

This quantity represents the complaints of a two-day foreign assembly on chiral chromatography held on the college of Surrey among 3-4 September 1987. The assembly was once together geared up through the Chromatographic SOCiety and the Robens Institute of the college of Surrey in accordance with the burgeoning curiosity during this speedy maturing box of chromatography. Nowhere is that this curiosity extra obtrusive than within the agrochemical and pharmaceutical industries the place the results of alternative pharmacological and toxicological task for the person enantiomers found in a racemic drug ol" insecticide is an expanding zone of outrage. advancements within the sector of chiral separations are ultimately commencing to supply SCientists with the mandatory instruments to check how animals and guy deal with racemates and relate their obseIVations to the obseIVed organic results of those ingredients. the improvement of strong and straightforward equipment for the separation of enantiomers will hence have a profound effect on security assessment and drug layout. The assembly proved to be very winning. with over one hundred sixty delegates from 13 nations in Europe and the United States current to benefit from the reports of specialists within the box of chiral chromatography and to listen to in regards to the most recent advancements. expectantly. in destiny symposia on chiral separations on the college of Surrey.

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W. Wainer, M. C. Alembik and C. R. Chromotogr361:374 (1986). S. Allenmark and B. Chromatogr. 252:297 (1982). 21 SYSTEMATIC STUDIES OF CHIRAL RECOGNmON MECHANISMS William H. Pirkle. Thomas C. Pochapsky. John A. Burke III and Kris C. Deming School of Chemical Sciences. University of Illinois at Urbana-Champaign. Urbana. IL 61801. USA SUMMARY A general discussion of chiral stationary phase structure/activity relationships is presented. Against this background. a discussion of the systematic approach used in our development of broad-spectrum chiral stationary phases suitable for liquid chromatographic separation of enantiomers is given.

Kuwata, M. Uebori and Y. , 211:375 (1981). K. G. Feitsma, B. F. H. Drenth and R A. , 387:447 (1987). R. T. GhiJsen, B. F. H. Drenth, F. Overzet and R. A. HighResolut. , 5:192 (1982). C. Pettersson and G. , 204:179 (1981). R. Dappen, H. Ann and V. R. , 373:1 (1986). I. W. Wainer, T. D. Doyle and C. D. , 7:731 (1984). J. , 298:67 (1984). G. Schill, I. W. Wainer and S. A. , 9:641 (1986). J. Hermansson and M. Ltq. , 9:621 (1986). D. W. , 7:353 (1984). B. Testa, Xenobiotica, 16:265 (1986). J. Hermansson and M.

EnantioPac®. LKB-AB. Bromma. Sweden). 50 C. 1 M sodium chlOride. 3 ml/min. Detection was by UV at 205 run and/or diode array (200-350 run). Apparatus The HPLC solvent delivery systems used were a Waters M45 pump. a Perkin Elmer Series 10 pump or a Spectra Physics 3500B pump. The experiments were performed using a Spectra Physics 770 UV detector and/or a HP 8450A (Hewlett-Packard) multi-channel UVvisible diode array spectrophotometer. a Rheodyne 7125 sample injector equipped with a 20 38 III loop and a Kipp BD40 recorder.

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