Deracemization of aryl substituted α-hydroxy esters using Candida parapsilosis ATCC 7330: effect of substrate structure and mechanism was written by Baskar, B.;Pandian, N. G.;Priya, K.;Chadha, Anju. And the article was included in Tetrahedron in 2005.Synthetic Route of C11H14O3 This article mentions the following:
Candida parapsilosis ATCC 7330 was found to be an efficient biocatalyst for the deracemization of aryl α-hydroxy esters (65-85% yield and 90-99% ee). A variety of α-hydroxy esters were synthesized to reflect steric and electronic effects on biocatalytic deracemization. The mechanism of this biocatalytic deracemization was found to be stereoinversion. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0Synthetic Route of C11H14O3).
Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Synthetic Route of C11H14O3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics