Nathalie Belair scite author profile

331ChemInform Abstract The enzymatic hydrolysis of the malonic acid diesters (I) produces the monoesters (II) when pig liver esterase is used as the bio-agent. The monoalkylmalonic acid ester (IIa) shows no significant enantioselectivity, whereas the dialkylmalonates (IIb) and (IIc) are formed with a high enantiomeric excess. Similar results are obtained with the bio-agent horse liver acetonic powder. Pig pancreatic lipase and α-chymotrypsine show no enzymatic activity with the substrates (I).

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Nathalie Belair

Enzymes in organic synthesis : VI scope and enantioselectivity of enzymatic hydrolyses of organosilyl-substituted esters

ChemInform Abstract: Enzymes in Organic Synthesis. Part 6. Scope and Enantioselectivity of Enzymatic Hydrolyses of Organosilyl‐Substituted Esters.

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