Related Experiment Video
Updated: Jun 4, 2026

Synthesis of Metal Nanoparticles Supported on Carbon Nanotube with Doped Co and N Atoms and its Catalytic Applications in Hydrogen Production
Published on: December 6, 2021
Titanium-Mediated Deoxygenation of Sulfoxides into Sulfides with Ammonia Borane under Mild Conditions
Xincheng Liu1, Junzheng Sun1, Xuke Liu1
1National Key Laboratory of Advanced Drug Delivery and Release Systems, School of Pharmaceutical Sciences & Institute of Materia Medica, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250117, P. R. China.
Abstract:
A facile and selective room-temperature deoxygenation of both aromatic and aliphatic sulfoxides to thioethers has been achieved by using a TiCl4-AB reduction system in good to excellent yields. This first, practical titanium-mediated ammonia borane reduction process is compatible with various potentially sensitive functional groups. The successful execution of a gram-scale reaction confirms the practical utility of this reduction system. Moreover, its effective application to the synthesis and modification of diverse pharmaceutical molecules further demonstrates its versatility. This work also expands the application scope of ammonia borane in the reduction chemistry.
Related Concept Videos
Preparation and Reactions of Sulfides
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation and Reactions of Thiols
Hydroboration-Oxidation of Alkenes
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
