Related Experiment Video
Updated: May 21, 2026

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
Tantallaaziridines: from synthesis to catalytic applications
Jean Michel P Lauzon1, Laurel L Schafer
1Department of Chemistry, University of British Columbia, 2036 Main Mall, Vancouver, B.C., Canada V6T 1Z1.
Abstract:
Tantallaaziridines are a class of organometallic compounds containing three-membered rings that include a tantalum, carbon and nitrogen atom. Closely related complexes containing the related iminoacyl ligand can be used as starting materials for tantallaaziridine synthesis. Tantallaaziridines can also be synthesized by reduction of imines or β-hydrogen abstraction of amides to give stable, isolable complexes. Tantallaaziridines possess a reactive Ta-C bond that can undergo stoichiometric transformations with unsaturated organic molecules to give new organometallic products. Upon quenching of such reactions with aqueous workup, selectively substituted small molecule amines can be prepared. Tantallaaziridines have also been proposed as catalytic intermediates in the direct α-alkylation of amines, hydroaminoalkylation, by exploiting the β-hydrogen abstraction route to regenerate the catalytically active species. Recent progress and remaining challenges in the field will be discussed.
Related Concept Videos
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...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Preparation of Alkynes: Dehydrohalogenation
Alkynes can be prepared by dehydrohalogenation of vicinal or geminal dihalides in the presence of a strong base like sodium amide in liquid ammonia. The reaction proceeds with the loss of two equivalents of hydrogen halide (HX) via two successive E2 elimination reactions.
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
Preparation of Amides
The DCC-promoted synthesis of amides begins with the protonation of DCC by carboxylic acid. The protonation makes it a better acceptor. Next, the addition of carboxylate to the protonated carbodiimide gives a reactive acylating agent.
Subsequently, the amine acts as a nucleophile that attacks the acylating agent to form a tetrahedral intermediate. In the...
Aryldiazonium Salts to Azo Dyes: Diazo Coupling

