Related Experiment Video
Updated: Aug 22, 2026

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Microwave-Assisted Natural Catalyst-Promoted Astaxanthin Z‑Isomerization in Deep Eutectic Solvent Systems
1College of Agriculture and Bioengineering, Taizhou Vocational College of Science and Technology, 288 Jiamu Road, Huangyan District, Taizhou 318020, Zhejiang, China.
None:
To improve the solubility and bioavailability of astaxanthin while enhancing its processing properties, this study established an eco-friendly, highly efficient microwave-assisted Z-isomerization system. We first conducted a systematic screening of various menthol-based deep eutectic solvents (DESs) to identify the most effective medium for this conversion. Following the selection of the optimal DES, we investigated the catalytic effect of three representative natural sulfur-containing compoundsmethyl isothiocyanate (MITC), hexyl isothiocyanate, and dimethyltrisulfideunder microwave irradiation. Furthermore, we systematically evaluated the influence of other key process parameters, including heating method, catalyst dosage, astaxanthin mass concentration, microwave power, temperature, and duration, through single-factor experiments. The results demonstrated that the menthol-acetic acid-based DES provided the most effective reaction environment, and MITC exhibited the highest catalytic efficacy, achieving a peak total Z-isomer proportion of 36.2% at 60 mg/mL, compared to a baseline of 6.82% in the catalyst-free control group. Mechanistic analysis suggests that the electrophilicity of isothiocyanates and the steric effects of their side chains play critical roles in the isomerization process. These findings demonstrate that this green processing system can serve as an efficient and sustainable approach for the production of Z-isomer-enriched astaxanthin.
More Related Videos
Related Concept Videos
Sharpless Epoxidation
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
E1 Reaction: Stereochemistry and Regiochemistry
Carboxylic Acids to Methylesters: Alkylation using Diazomethane

