𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Stereoselective pig liver esterase-catalyzed hydrolysis of fluorinated bicyclic esters

✍ Scribed by Sames Sicsic; Jacques Leroy; Clause Wakselman

Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
29 KB
Volume
35
Category
Article
ISSN
0022-1139

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Enantioselective hydrolysis of racemic e
Enantioselective hydrolysis of racemic esters using pig liver esterase
✍ Jean-Michel Herdan; Margareta Balulescu; Ovidiu Cira πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 English βš– 356 KB

The utilization of enzymes is a recent achievement in organic synthesis. There are many good reasons for the organic chemist to consider this approach. Enzymatic reactions are very fast and specific. The same transformations carried out by classical means in several days or weeks, can be achieved in

A Study of Stereoselective Hydrolysis of
A Study of Stereoselective Hydrolysis of Symmetrical Diesters with Pig Liver Esterase
✍ Peter Mohr; Nada Waespe-Ε arčeviΔ‡; Christoph Tamm; Krystyna Gawronska; Jacek K. G πŸ“‚ Article πŸ“… 1983 πŸ› John Wiley and Sons 🌐 German βš– 757 KB

## Abstract Pig liver esterase‐(PLE) catalyzed hydrolysis of dimethyl esters of symmetrical dicarboxylic acids, including __meso__‐diacids, __cis__‐1,2‐cycloalkanedicarboxylic acids, and diacids with a prochiral center, was studied with 14 substrates. The products of these stereoselective hydrolyse