FeCl3-PTSA Co-Catalysed Highly Regio- and Stereo-Selective Synthesis of β-Functionalised Enamine Derivatives
Author:
Affiliation:
1. School of Chemistry and Life Science, Guangdong University of Petrochemical Technology, 2 Guangdu Road, Maoming 525000, P. R. China
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/174751912X13306054094882
Reference39 articles.
1. Room-Temperature Synthesis of Pyrazoles, Diazepines, β-Enaminones, and β-Enamino Esters Using Silica-Supported Sulfuric Acid as a Reusable Catalyst Under Solvent-Free Conditions
2. P2O5/SiO2as a New, Efficient, and Reusable Catalyst for Preparation ofβ-Enaminones Under Solvent-Free Conditions
3. Approach to Synthesis of β-Enamino Ketones and Pyrroles Catalyzed by Gallium(III) Triflate Under Solvent-Free Conditions
4. Molecular Iodine–Catalyzed Mild and Effective Synthesis of β-Enaminones at Room Temperature
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1. Recent Trends in the Synthesis of Enaminones;HETEROCYCLES;2023
2. Approach for the Direct Synthesis ofβ-Dichlorosubstituted Acetanilides Using Iodine Trichloride (ICl3) as the Oxidant and Catalyst;Chinese Journal of Chemistry;2013-04
3. ChemInform Abstract: FeCl3-PTSA Co-Catalyzed Highly Regio- and Stereoselective Synthesis of β-Functionalized Enamine Derivatives.;ChemInform;2012-07-19
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