Related Experiment Video
Updated: Oct 26, 2026

Applications of Liquid-Chromatography Tandem Mass Spectrometry in Natural Products Research: Tropane Alkaloids as a Case Study
Published on: March 8, 2024
The Use of TMS for Determining the Absolute Configuration of Natural Products Bearing Hydroxyl Groups
Gregor Talajić1, Edi Topić1, Emanuel Pištan1
1Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, Zagreb10000, Croatia.
Abstract:
Compounds isolated from natural sources continue to make invaluable contributions across many fields of chemistry. Structures elucidated and reported in the literature often serve as starting points for the total synthesis of bioactive compounds. In this painstaking process of separation and structural elucidation, one of the most complex steps is the determination of absolute configuration. In this work we present a combination of a simple molecular modification, which is fast, robust and selective, with traditional single-crystal X-ray diffraction to achieve high precision in determining absolute configuration. The method can be employed on a wide variety of compounds bearing at least one hydroxylic group, which includes a significant proportion of natural products.
Related Concept Videos
2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)
Proton (¹H) NMR: Chemical Shift
Absorption signals of all the protium nuclei in a...
NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR
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...
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.

