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Regioselective hydrolysis of diesters of (Z)- and (E)-2-methyl-butenedioic acids by PLE

โœ Scribed by Rudolf Schmid; Vassilia Partali; Thorleif Anthonsen; Henrik W Anthonsen; Lise Kvittingen


Book ID
104231881
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
78 KB
Volume
42
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


Dimethyl, diethyl and dipropyl esters of (Z)-and (E)-2-methyl-butenedioic acids (citraconic and mesaconic acid) were hydrolysed by pig live esterase, PLE. For the diethyl esters the enzyme showed low regioselectivity for both the (Z)-and the (E)-isomers. However, the hydrolysis of dimethyl and dipropyl (Z)-2-methyl-butenedioic acid gave a ratio of the monoesters of 95:5 and 85:15.


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EI fragmentation of E,Z-3-iodo-2-alkenoi
โœ J. C. Herrera; N. A. Urdaneta ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 148 KB ๐Ÿ‘ 1 views

The electron ionization mass spectra of some E,Z-3-iodo-2-alkenoic acids and methyl E,Z-3-iodo-2alkenoates were investigated. A semi-empirical method was used to examine the thermochemical and molecular properties of the species. Two fragmentation paths of the molecular ions are determined by the ge