The kinetics of base hydrolysis of the cis-(chloro)-(benzimidazole)bis(ethylenediamine) cobalt(II1) ion was investigated in Methanol-water and Ethyleneglycol-water media of varying compositions and at isodielectric conditions (Ds = 61 at 25Β°C) in isopropanol-and Acetonitrilewater media at 35Β°C in th
Enzymes in asymmetric synthesis: Effect of reaction media on the PLE catalysed hydrolysis of diesters
β Scribed by Giuseppe Guanti; Luca Banfi; Enrica Narisano; Renata Riva; Sergio Thea
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 233 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Organic cosolvents and other addenda can influence
the rate and the enantioselectivity of pig Ziver esterase catalysed hydroZysis of meso diacetates and diesters, the magnitude of the effect being strongZy dependent on the nature of substrate.
Dissymmetrization of meso diesters and diacetates through enzyme catalysed hydrolysis is a powerful tool for preparation of chiral "building blocks" to be used in the synthesis of natural products.
3 In particular, pig liver esterase (PLE) has been extensively employed due to its wide specificity. Unfortunately, however, enantiomeric excesses are not always high, thus
limiting the enzyme's potential utility.
π SIMILAR VOLUMES
Homopolymers of 3-alkyl-l-vinylimidazolium bromides series have been prepared by free radical polymerization in aqueous solution or in benzene. The tendency of aggregation of these water soluble polymers was studied by viscosity measurements and fluorescence probes which have revealed the formation
The kinetics of base hydrolysis of (CUPS) (salicylato) (tetraethylenepentamine) cobalt(II1) have been investigated in aquo-organic solvent media at 15.0 f t, "C < 40.0, and I = 0.10 mol dm (C104-) using propane-2-01 (570% v/v), t-butanol(560% v/v), acetone (570% v/v, acetonitrile (550% v/v), and eth
The base hydrolysis of (apS) (salicylato) (tetraethylenepentamine)cobalt(III) has been investigated in MeOH + water and DMSO + water media (0-70% (viv) cosolvents) at 20.0 I t"C I 35.0 and I = 0.10 mol dm-3 (clod-). The phenoxide species [(tetren)Co02CC,H40]' undergoes both OH--independent and OH--c