Ficarra, Paola published the artcileDirect enantiomeric separation of flavanones by high performance liquid chromatography using various chiral stationary phases, Synthetic Route of 69097-99-0, the publication is Planta Medica (1995), 61(2), 171-6, database is CAplus and MEDLINE.
The performance of four chiral liquid chromatog. columns (Chiralcel OA, OJ, OC, OD) was studied with respect to the enantioseparation of flavanones and some derivatives The effect of mobile phase composition on the retention time and stereoselectivity was studied. A good enantioseparation (α up to 1.45) was achieved for most of the racemates. Further, the elution order of the enantiomers from the chiral stationary phases has been determined by using a CD based detection system.
Planta Medica published new progress about 69097-99-0. 69097-99-0 belongs to tetrahydropyran, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Ether,Inhibitor, name is 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one, and the molecular formula is C16H14O6, Synthetic Route of 69097-99-0.
Referemce:
https://en.wikipedia.org/wiki/Tetrahydropyran,
Tetrahydropyran – an overview | ScienceDirect Topics