Optical resolution of some racemates by HPLC using chiral polymers having (+)-5-oxobornyl moieties

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Natl Cheng Kung Univ, Tainan, Taiwan ^{[1
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J Appl Polym Sci | / 5卷 / 677-682期

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[1] Optical resolution of some racemates by HPLC using chiral polymers having (+)-5-oxobornyl moieties
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[2] SYNTHESIS OF CHIRAL POLYMERS HAVING CAMPHANEDIOL MOIETIES AND THEIR APPLICATIONS ON THE OPTICAL RESOLUTION OF SOME RACEMATES
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[3] Synthesis of chiral polymers having camphanediol moieties and their applications on the optical resolution of some racemates
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[4] Optical resolution ability of chiral polymers having camphanediol moieties
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[5] Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin. II. Enzyme chiral separations
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[6] Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin.: II.: Enzyme chiral separations
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[7] Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin.: I.: Structural chiral separations
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[8] Stereochemical resolution of racemates, in HPLC, using a chiral stationary phase based upon immobilized α-chymotrypsin. I. Structural chiral separations
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[9] OPTICAL RESOLUTION OF CARBOXYLIC DRUGS BY REVERSED PHASE HPLC USING CHIRAL STATIONARY PHASES
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[10] ENANTIOFACE DIFFERENTIATION BY CHIRAL POLYMERS HAVING (+)-5,6-EXO-BORNANEDIOL MOIETIES .2. ASYMMETRIC REDUCTION OF PROCHIRAL KETONES BY CHIRAL POLYMERS CONTAINING (+)-5,6-EXO-BORNANEDIOL DERIVATIVES
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