Related Experiment Video
Updated: Jun 19, 2026

Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
Published on: February 7, 2019
Synthesis and catalytic application of aluminium anilido-pyrazolate complexes
1Department of Chemistry, National Chung Hsing University, Taichung, 402, Taiwan.
Abstract:
A series of aluminium complexes containing anilido-pyrazolate ligands is described. Reactions of four anilido-pyrazolate ligand precursors, HNPhPz, HNPhTriMePz, HNPhOMePz, or HNPhSMePz [HNPhPz = ortho-C6H4(NH-phenyl)(1-pyrazole); HNPhTriMePz = ortho-C6H4(NH-2,4,6-trimethylphenyl)(1-pyrazole); HNPhOMePz = ortho-C6H4(NH-2-methoxyphenyl)(1-pyrazole); HNPhSMePz = ortho-C6H4(NH-2-methylthiophenyl)(1-pyrazole)], with one molar equivalent of AlMe3 in toluene give the aluminium dimethyl complexes, (NArPz)AlMe2 [Ar = phenyl, (NPhPz)AlMe2 (1); Ar = 2,4,6-trimethylphenyl, (NPhTriMePz)AlMe2 (2); Ar = 2-methoxyphenyl, (NPhOMePz)AlMe2 (3); Ar = 2-methylthiophenyl, (NPhSMePz)AlMe2 (4)], respectively. The molecular structures are reported for compounds 1 and 3. Their catalytic activities toward the ring opening polymerisation reaction of -caprolactone in the presence of BnOH are also under investigation.
More Related Videos
04:51Synthesis of Triazole and Tetrazole-Functionalized Zr-Based Metal-Organic Frameworks Through Post-Synthetic Ligand Exchange
Published on: June 23, 2023
10:42Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
α-Alkylation of Ketones via Enolate Ions
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
In the first step of the mechanism, the acid protonates the carbonyl oxygen resulting in a resonance-stabilized cation, which subsequently loses an α-hydrogen to form an enol tautomer. The C=C bond in an enol is highly nucleophilic because of the electron-donating nature of the –OH group. Consequently, the double bond attacks an electrophilic halogen to form a...
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids