Sunjic, Vitomir et al. published their research in Gazzetta Chimica Italiana in 1989 | CAS: 59960-32-6

Asymmetric hydrogenation of α-arylpropenoic acids catalyzed by rhodium(I) complexes of chiral ligands derived from some monosaccharides was written by Sunjic, Vitomir;Habus, Ivan;Comisso, Giovanni;Moimas, Flavio. And the article was included in Gazzetta Chimica Italiana in 1989.Electric Literature of C16H16O3 This article mentions the following:

Prochiral precursors, I and II, of (+)-Ketoprofen and (+)-Naproxen are hydrogenated in the presence of various Rh(I) complexes of chiral dephenylphosphines and diphenylphosphinites. Four ligands are derived from the monosaccharides, D-glucose, D-xylose, D-galactose, and L-arabinose. The optical yields (e.e.s. in %) varied from 10-50%, indicating that none of the substrates I and II behave as bidentate ligand within any of the examined catalytic species. The highest e.e. (45%) was obtained with II using the Rh(I) complex of chiral phosphine III as catalyst. No double asym. induction, e.g., with amide IV, has been reached when hydrogenation with the diastereomer of III was tried. In the experiment, the researchers used many compounds, for example, 2-(3-(Hydroxy(phenyl)methyl)phenyl)propanoic acid (cas: 59960-32-6Electric Literature of C16H16O3).

2-(3-(Hydroxy(phenyl)methyl)phenyl)propanoic acid (cas: 59960-32-6) belongs to alcohols. The oxygen atom of the strongly polarized O―H bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Electric Literature of C16H16O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts