Synthesis of ester derivatives of chloramphenicol by lipase-catalyzed transesterification in organic solvents
โ Scribed by Ottolina, Gianluca; Carrea, Giacomo; Riva, Sergio
- Book ID
- 126998662
- Publisher
- American Chemical Society
- Year
- 1990
- Tongue
- English
- Weight
- 552 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0022-3263
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๐ SIMILAR VOLUMES
Short chain fatty acid esters of geraniol and citronellol WCR synthesized by lipase-catalyzed transesterification with yields as high as 98% molar conversion. Triacylglycerols were the best substrates and immohili~edCf/nrlitfri tmturcticu lipase, SP435 gave the highest overall yields. The lipases te
Lipase-catalyzed transesterifications of cis-and Iran.+4-methylcyclohexanols with vinyl acetate in various organic solvents have been studied, and the cffcct of' solvent on activity and stereoselectivity of lipase has been investigated. Initial rate of the reaction increases with the increase in hyd