• Bulletin of the Korean Chemical Society
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• 제10권1호
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• pp.33-34
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• 1989

Pig Liver Esterase (PLE) which has been known to cleave a broad range of diesters to prepare stereoselective enantiomers is applied to hydrolysis of ${\beta}-lactam$ esters imparting the corresponding acids in various yields.

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.439-443
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• 1995

Both enantiomers of (S)-(-)-2-(diphenylphosphino)-2'-mercapto-1,1'-binaphthyl and their derivatives were obtained by synthesis from racemic 2,2'-dihydroxy-1,1'-binaphthyl and subsequent resolution. The utilities of these ligands were investigated briefly. And among these, S-methyl derivative 15 has proved to be an effective ligand for Pd-catalyzed allylic alkylation.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.559-563
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• 1989

Optically active (R)- and (S)-2-benzyloxy-1-butanol have been prepared by a previously described asymmetric synthesis based on a chiral oxathiane and have been converted into (R)-(+)-4-hexanolide, a component of the pheromone secreted by the female of the dermestid beetle, and its enantiomer.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.578-581
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• 1989

Two enantiomers of various 2-hydroxy acid esters have been resolved as the 3,5-dinitrophenyl carbamates on chiral stationary phases (CSPs) derived from ${\alpha}-arylalkylamines.$ Two CSPs, each of which contains the same type of chiral moiety, but shows different mode of connection to a silica support, have been found to show the contrasting resolution behaviors. From the contrasting resolution behaviours of two CSPs used in this study, two competing chiral recognition mechanisms are proposed.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.398.1-398.1
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• 2002

A new chiral derivatization agent with sugar moiety. 2, 3.4, 6-tetra-O-acetyl-D-galactopyranosyl isothiocyanate (GATC) was synthesized. Several $\beta$-blockers were investigated for the possible separation of the enantiomers by reversed-phase HPLC after derivatization with this new chiral derivatization agent (GATC). GATC was reacted readily with $\beta$-blockers at room temperature and the reaction mixture could directly be injected into the HPLC system. (omitted)

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.400.1-400.1
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• 2002

Because of the differences in pharmacological properties between enantiomers of chiral acidic non-steroidal antiinflammatory drugs (NSAIDs) in human body. accurate determinations of their optical purities have been in great need. An efficient capillary electrophoretic (CE) profiling method was developed for the enantioseparation of NSAIDs. Capillary electrophoretic conditions were optimized using TM$\beta$-cyclodextrin as the chiral selectors under MES buffer. (omitted)

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.275.2-276
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• 2003

Several ${\beta}$-agonists were investigated for the possible separation of the enantiomers by reversed-phase high-performance liquid chromatography after derivatization with a new chiral derivatization agent, GATC. The derivatization proceeded quantitatively within 1 h at room temperature. The corresponding diastereomers were well resolved an ODS column with acetonitrile-acetate buffers a mobile phase and monitored at UV 254nm. (omitted)

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.224.2-224.2
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• 2003

Pyrethroic acids are essential chiral intermediates of the pyrethroids, which account for about 25% of the world insecticide market and are found to be some of the most effective commercially available pesticides. It was demonstrated that polysaccharide-derived chiral stationary phases (CSPs) are very efficient for the separation of the enantiomers of pyrethroid acids. It was observed that the enantioseparation of pyrethroic methyl ester and ethyl derivatives was well accomplished on brush-type WhelkO-1. (omitted)

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2418-2422
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• 2011

The enantiomeric separation of lactic acid for its absolute configuration has become important task for understanding its biological origin and metabolic process involved in the formation of lactic acid. It involves the conversion of enantiomers as diastereomeric O-pentafluoropropionylated (S)-(+)-3-methyl-2-butyl ester and the direct separation by gas chromatography-mass spectrometry on a achiral capillary column. The (R)- and (S)-lactic acids were completely separated with a high resolution of 1.9. The newly developed method showed good linearity (r ${\geq}$ 0.999), precision (% relative standard deviation = 3.4-6.2), and accuracy (% relative error = -7.7-1.4) with the detection limit of 0.011 ${\mu}g/mL$. When the method was applied to determine the absolute configuration of lactic acid in Lactobacillus delbrueckii subsp. lactis 304 (LAB 304), the composition (%) of (R)-lactic acid in the cell pellet and in the culture medium were $89.0{\pm}0.1$ and $78.2{\pm}0.4$, respectively. Thus, it was verified that the present method is useful for the identification and composition test of lactic enantiomers in microorganisms.

• KSBB Journal
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• 제22권3호
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• pp.123-128
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• 2007

에폭사이드 가수분해 효소를 이용하여 라세믹 에폭사이드 기질로부터 광학활성 에폭사이드 또는 vic-diol을 제조하는 동력학적 분할법은 이론 수율이 50%로 제한된다는 단점이 있다. 이러한 문제점을 해결하기 위하여 이론 수율 100%를 얻을 수 있는 다양한 생물전환 방법들이 최근에 개발되고 있다. 서로 상보적인 입체 및 위치특이성을 가진 에폭사이드 가수분해효소에 의한 광학수렴반응을 이용한 광학활성 vic-diol 제조법, 에폭사이드 가수분해효소가 촉발하는 cascade 반응을 통해 라세믹 haloalkyl 에폭사이드로부터 광학활성 epoxy alcohol 또는 THF를 제조하는 방법, ADH를 이용하여 haloketone을 환원시킨 다음 자발적인 cyclization 반응을 통해 광학활성 에폭사이드를 제조하는 방법들이 개발되었다. 이러한 방법들은 높은 광학순도를 가진 광학활성 물질들을 이론수율 100%로 제조할 수 있으므로 향후에 상업화 사례가 많아질 것으로 기대된다.