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Cited by 4 publications
(4 citation statements)
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“…In the second condition, a decreasing enzyme/substrate ratio to 1.25% led to a slower reaction rate, but after nine days, the ( S )-alcohol (68% ee) and ( R )-acetate (>99% ee) were obtained with c 41% and E > 200. 134…”
Section: Classification Of Enzymesmentioning
confidence: 99%
“…In the second condition, a decreasing enzyme/substrate ratio to 1.25% led to a slower reaction rate, but after nine days, the ( S )-alcohol (68% ee) and ( R )-acetate (>99% ee) were obtained with c 41% and E > 200. 134…”
Section: Classification Of Enzymesmentioning
confidence: 99%
“…A study of the reuse of lipase from C. antarctica type B (CAL-B, Novozym 435) was conducted for the acylation of (−)-Thiamphenicol with vinyl decanoate. The corresponding 3’-monoester was obtained in 96% yield and the enzyme was reused five times without any loss of the activity [ 37 ].…”
Section: Esterification Approachmentioning
confidence: 99%
“…Organic solvents, for example, ethyl acetate, diethyl ether, or carbon trichloride permit its comprehensive solubility at high substrate concentrations. 14 The thiamphenicol solubility in solvents affects the conversion rate and the yield of target compound. To develop the further application of thiampheni- col and improve the yield of thiamphenicol derivatives, it is necessary to know the solubility of thiamphenicol in different solvents.…”
Section: ■ Introductionmentioning
confidence: 99%
“…Conversely, the total asymmetric synthesis of derivatives of thiamphenicol remains an attractive field at present, since they show the probable enhanced biological activities in comparison with the parent substrate. Organic solvents, for example, ethyl acetate, diethyl ether, or carbon trichloride permit its comprehensive solubility at high substrate concentrations . The thiamphenicol solubility in solvents affects the conversion rate and the yield of target compound.…”
Section: Introductionmentioning
confidence: 99%