Enzymes as selective reagents in organic synthesis: Enantioselective preparation of “asymmetrized tris (hydroxymethyl)methane”
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Baker's yeast-mediated synthesis of protected α-hydroxy-aldehydes
2. Microbiological synthesis of variously protected L-glyceraldehydes in high optical purity
3. Enzymes in asymmetric synthesis: Effect of reaction media on the PLE catalysed hydrolysis of diesters
4. Bifunctional chiral synthons via biochemical methods, 4. Chiral precursors to (+)-biotin and (−)-a-factor.
5. Synthesis of both enantiomeric forms of 2-substituted 1,3-propanediol monoacetates starting from a common prochiral precursor, using enzymatic transformations in aqueous and in organic media
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1. Development of a Practical and Scalable Synthesis of (R)- and (S)-3-Amino-2-[(benzyloxy)methyl]propan-1-ol Monohydrochloride: A Useful C-4 Chiral Building Block;Organic Process Research & Development;2012-08-29
2. Hydrolysis and Formation of Carboxylic Acid Esters;Enzyme Catalysis in Organic Synthesis;2012-04-20
3. Enzymatic optical resolution of norbornanecarboxylic esters using pig liver esterase;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Asymmetric Syntheses of Highly Functionalized Bicyclo[2.2.2]octene Derivatives;HETEROCYCLES;2010
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