Enzyme-mediated enantioselective acylation of secondary amines in organic solvents
β Scribed by Gregorio Asensio; Cecilia Andreu; J.Alberto Marco
- Book ID
- 104216270
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 154 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Llpases and esterases catalyze armde synthesis from pnmary ammes in the presence of various esters Llpase SP 382 exhlblted a very high activity and speclficlty Enzymatic synthesis m orgamc solvents 1s now well recognized (1,2) Transesterlficatlon catalyzed by hydrolases has been widely used (2,3) wh
Porcine pancreatic lipase mediated acylation of l,n-diols and triols affords primary acytated products in high yields. The regio-and stereospecificity of enzyme catalyzed reactions are the envy of synthetic chemists.1 The use of enzymes in organic synthesis has become increasingly popular since it