Tuesday, 27 June 2006 - 8:35 AM
Bonanza Room A (John Ascuaga’s Nugget Casino Resort)
142

Enantioselective Hydrolysis of Hydroxynitriles via Biotransformations

Stephen K. Taylor and Julie Pollock. Hope College, Holland, MI

We are currently hydrolyzing hydroxynitriles using mild biotransformation methods. For example, in the reaction below, the resulting g-hydroxycarboxylic acid spontaneously forms a lactone. We will report how this chemistry has been used to make four pheromones. We are also testing how branching of the R- group and how moving the chiral center closer to the reacting nitrile influence the enantioselectivity.


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