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Hydroxynitrile lyases reaction systems

Griengl reported the first example of hydroxynitrile lyase-catalyzed cyanohydrin formation in a mixed solvent system of [bmim][BF4] and buffer (pH 3.7) (1 1) (Fig. 19). In the reaction, a mixed solvent system was essential, but excellent results were obtained. [Pg.16]

In particular, the use of hydroxynitrile lyase has proved to be a general and reliable method for obtaining a-hydroxy nitriles of both configurations [22]. An interesting approach is the Upase- and baseacyl-cyanohydrin for a synthetic DKR [23]. This is a combination of two reaction systems the dynamic, base-catalyzed equiUbrium between acetone cyanohydrin, acetone, HCN, aldehyde and a racemic cyanohydrin and the lipase-catalyzed enantioselective and irreversible acylation of the hydroxyl group. The combination yields the... [Pg.201]


See other pages where Hydroxynitrile lyases reaction systems is mentioned: [Pg.104]    [Pg.213]    [Pg.216]    [Pg.201]    [Pg.260]    [Pg.144]    [Pg.393]    [Pg.85]   
See also in sourсe #XX -- [ Pg.620 , Pg.621 ]




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