Rampulla, David M.; Gellman, Andrew J. published an article about the compound: (S)-Methyl 3-hydroxybutanoate( cas:53562-86-0,SMILESS:C[C@H](O)CC(OC)=O ).Electric Literature of C5H10O3. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:53562-86-0) through the article.
Of the three types of chiral surfaces described in this entry, the most well-developed ones are those that are produced by templating with chiral organic modifiers. Although the mechanisms and adsorbate/substrate interactions that impart enantioselectivity on these surfaces are not understood in great detail, some such surfaces have been highly optimized to give highly enantioselective separations and catalytic reactions. Naturally chiral surfaces can be generated from materials that are chiral in bulk, or achiral materials cleaved to expose surface structures that are chiral at the nanoscale. The crystalline nature of these structures makes them good candidates for a detailed study of the origins of enantiospecificity on their surfaces.
In addition to the literature in the link below, there is a lot of literature about this compound((S)-Methyl 3-hydroxybutanoate)Electric Literature of C5H10O3, illustrating the importance and wide applicability of this compound(53562-86-0).
Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics