Sjoberg, Berndt published the artcileStereochemical studies. IV. The enantiomers of ¦Á-(2-thianaphthenyl)propionic acid, Quality Control of 1949-41-3, the publication is Arkiv foer Kemi (1958), 565-71, database is CAplus.
cf. C.A. 52, 20124h. To study the synthetic plant growth regulants, ¦Á-hydroxy-¦Á-(2-thianaphthenyl)propionic acid was prepared and reduced to the title compound After resolving it into the optical antipodes employing morphine and (+)-¦Á-2-naphthyl)ethylamine, the rotary power measured was [¦Á]25D 31.2¡ã and [¦Á]25D -31.4¡ã (absolute EtOH), resp. The configuration was determined by desulfurization of the (+)-form to (+)-¦Á-methyl-¦Ã-phenylbutyric acid which was ozonized to (+)-¦Á-methylglutaric acid.
Arkiv foer Kemi published new progress about 1949-41-3. 1949-41-3 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene, name is 2-Methyl-4-phenylbutanoic acid, and the molecular formula is C16H24BF4Ir, Quality Control of 1949-41-3.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia