《Diastereoselective and enantioselective microbial reduction of cyclic α-alkyl β-keto esters》 was published in Tetrahedron Letters in 1986. These research results belong to Buisson, Didier; Azerad, Robert. Safety of Cis-methyl 2-hydroxycyclohexanecarboxylate The article mentions the following:
The reduction of racemic cyclopenta- and cyclohexanone 2-carboxyesters by various yeast and mold strains produced different amounts of isomeric β-hydroxyesters with predominant (1S) stereochem. With several strains, only one optically pure cis or trans stereoisomer was obtained in high yield, indicating a diastereoselective and enantioselective reduction In the part of experimental materials, we found many familiar compounds, such as Cis-methyl 2-hydroxycyclohexanecarboxylate(cas: 936-03-8Safety of Cis-methyl 2-hydroxycyclohexanecarboxylate)
Cis-methyl 2-hydroxycyclohexanecarboxylate(cas: 936-03-8) belongs to esters. Esters are more polar than ethers but less polar than alcohols. Safety of Cis-methyl 2-hydroxycyclohexanecarboxylate They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics