Related Experiment Video
Updated: May 26, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Diterpenoids from Euphorbia neriifolia
Jun-Hua Liu1, Abdul Latif, Mumtaz Ali
1School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, PR China.
Nine diterpenoids were isolated from Euphorbia neriifolia Linn. stems. Their structures and relative stereochemistries were confirmed using advanced spectroscopic and X-ray methods.
Area of Science:
- Natural Products Chemistry
- Organic Chemistry
- Phytochemistry
Background:
- Euphorbia neriifolia Linn. is a plant species with a history of traditional medicinal use.
- The chemical constituents of Euphorbia species are known to possess diverse biological activities.
- Detailed structural elucidation of compounds from this plant can contribute to understanding its medicinal properties.
Purpose of the Study:
- To isolate and characterize diterpenoids from the stems of Euphorbia neriifolia Linn.
- To elucidate the complete structures of the isolated compounds.
- To determine the relative stereochemistry of the identified diterpenoids.
Main Methods:
- Extraction and isolation of chemical constituents from plant material.
- Spectroscopic techniques including 1D and 2D Nuclear Magnetic Resonance (NMR) for structural determination.
- ROESY (Rotating-frame Overhauser Effect Spectroscopy) for relative stereochemistry assignment.
- Single-crystal X-ray diffraction for definitive structural confirmation.
Main Results:
- Isolation of nine diterpenoids from the stems of Euphorbia neriifolia Linn.
- Complete structural elucidation of all nine compounds using comprehensive NMR data.
- Determination of the relative stereochemistries for the isolated diterpenoids through ROESY and X-ray crystallography.
Conclusions:
- The study successfully identified nine diterpenoids from Euphorbia neriifolia Linn. stems.
- The structural and stereochemical information provides a basis for further pharmacological investigations.
- This research expands the knowledge of the phytochemical profile of Euphorbia neriifolia Linn.
Related Concept Videos
Structure of Conjugated Dienes
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the double...
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent groups, ethers can be classified into two...
Aromatic Compounds: Overview
In 1825, Faraday isolated benzene...
UV–Vis Spectroscopy: Woodward–Fieser Rules
Structure and Nomenclature of Epoxides
Diels–Alder Reaction: Characteristics of Dienes
Characteristics of the diene
Conformation
The simplest example of a diene is 1,3-butadiene, an acyclic conjugated π system. At room temperature, the molecule exists as a mixture of s-cis and s-trans conformers by virtue of rotation around the carbon–carbon single bond. Although the s-trans isomer is more stable, the...
