Related Experiment Video
Updated: Feb 25, 2026

CD Spectroscopy to Study DNA-Protein Interactions
Published on: February 10, 2022
Chirality sensing of bioactive compounds with amino alcohol unit via circular dichroism
Marcin Górecki1, Grażyna Groszek2, Jadwiga Frelek1
1Institute of Organic Chemistry, Polish Academy of Sciences, Warsaw, Poland.
Abstract:
The aim of the present work was to test various chiroptical techniques, including in particular the in situ dirhodium methodology, to assign the absolute configuration of 1,2- and 1,3-amino alcohols. As models, we selected mainly compounds that have both an additional strongly absorbing and interfering chromophoric system and application in medicinal chemistry. Determination of the absolute configuration (AC) of the tested molecules such as cinchona alkaloids, Tamiflu, and others was carried out using a combination of electronic and vibrational circular dichroism (ECD, VCD) spectroscopy. It has been demonstrated that both 1,2- and 1,3-aminol moieties are subject to the same sector rule correlating stereostructure of formed Rh2 -complex with chiroptical properties, and that the changes in the position of the stereogenic center do not affect its proper use.
Related Concept Videos
Chirality in Nature
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Prochirality
Molecules with Multiple Chiral Centers
¹H NMR Chemical Shift Equivalence: Enantiotopic and Diastereotopic Protons
In chiral compounds such as 2-butanol, replacing the methylene hydrogens at C3 produces a pair of...
Properties of Enantiomers and Optical Activity

