Now showing items 1-10 of 160
NMR as a tool for simultaneous study of diastereoisomeric inclusion complexes formed by racemic mixture of 4′-hydroxyflavanone and heptakis-(2,6-O-dimethyl)-β-cyclodextrin
The complexes formed by (±)-4′-hydroxyflavanone (OHFL) and heptakis-(2,6-O-dimethyl)-β-cyclodextrin (DM-β-CD) were obtained using the racemic mixture of OHFL. These complexes were able to be studied due to their ...
Determination of the Binary and Ternary Phase Diagrams of R(+)-/S(-)-Ketamine Using Differential Scanning Calorimetry
(Amer Chemical SocWashingtonEUA, 2009)
TERNARY PHASE DIAGRAM OF KETAMINE ((R,S)-2-(2-CHLOROPHENYL)-2-METHYLAMINOCYCLOHEXANONE) IN ETHANOL AND PRELIMINARY STUDIES AIMING AT ENANTIOSELECTIVE CRYSTALLIZATION OF S-KETAMINE
(Brazilian Soc Chemical EngSao PauloBrasil, 2009)
NMR as a tool for simultaneous study of diasteroisomeric inclusion complexes, part 2: Complexes formed by racemic mixture of 4′- hydroxyflavanone and two cyclodextrins
Complexes formed by (±)-4′-hydroxyflavanone (OHFL) and the cyclodextrins β-cyclodextrin and (2-hydroxypropyl)-β-CD were obtained using the racemic mixture of the OHFL. These complexes were able to be studied due to their ...
Stereochemical nomenclature: racemization and resolution [Freshman organic chemistry]
(Yale University, Open Yale Courses, 2016)