Process for the enzymatic cleavage of vinyl 2-aryl-propionates

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing heterocyclic carbon compound having only o – n – s,...

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435 42, 435121, 435123, 435126, 435132, 435135, 435136, 435147, 435197, 435280, C12P 4100, C12P 740, C12N 914, C12N 954

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active

051550288

ABSTRACT:
In the enzymatic stereoselective ester cleavages of 2-arylpropionate, the reaction rate of the hydrolyzing enzymes can be drastically increased if the vinyl ester of the 2-arylpropionate is employed as the substrate.

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M. Degueil-Castaing et al., Enzymatic Reactions In Organic Synthesis: 2-Ester Interchange of Vinyl Esters, Tet. Letters, V.28,N.9, pp. 953-954, 1987.
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Klaus Mosbach, Methods in Enzymology, vol. XLIV, Academic Press, (1976) pp. 263-267; 551-556.
Iriuchijima et al. "Asymmetric Hydrolysis of (.+-.)--alpha-Substituted Carboxylic Acid Esters with Microorganisms" Agric. Biol. Chem. 45 (6), pp. 1389-1392 (1981).

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