Related Experiment Video
Updated: Jul 1, 2025

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Catalytic Light-Driven Strategy for Transforming Oximes to Carbonyls
Brandon White1, Travis Dudding1
1Department of Chemistry, Brock University, 1812 Sir Isaac Brock Way, St. Catharines, Ontario L2 S3A1, Canada.
Abstract:
Oxime and carbonyl functional groups serve as powerful chemical hubs for constructing complex synthetic targets and valuable molecular scaffolds. In furthering this value, we report a photopromoted catalytic deoximation protocol for converting oximes and their derivatives to carbonyl functional groups. This strategic approach benefits from the use of renewable light energy input and ambient air conditions, in addition to demonstrating good substrate scope, functional group tolerance, and product yields. In offering, insights into these reactivity mechanistic studies are communicated, and the value of this protocol is further shown through one-pot operations.
More Related Videos
06:34Synthesis of Antiviral Tetrahydrocarbazole Derivatives by Photochemical and Acid-catalyzed C-H Functionalization via Intermediate Peroxides CHIPS
Published on: June 20, 2014
07:36Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Related Concept Videos
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Oxidative Cleavage of Alkenes: Ozonolysis
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Oxymercuration-Reduction of Alkenes
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of...
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate