A pendant phosphorus Lewis acid: route to a palladium-benzoyl derived phosphorane
Kelly F Firth1, Juri Möbus1, Douglas W Stephan1
1Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario, CanadaM5S 3H6. dstephan@chem.utoronto.ca.
Abstract:
The traditional use of phosphorus compounds is as ligands for transition metals, however herein we synthesize Lewis acidic fluorophosphonium cation appended to a palladium complex and effect CO insertion into a Pd-C bond to obtain an unprecedented metal-benzoyl derived phosphorane.
Related Concept Videos
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism
The reaction begins with the nucleophilic addition between a phosphorus ylide and the carbonyl compound. Due to its carbanionic character, phosphorus ylide acts as a strong nucleophile and attacks the electrophilic carbonyl group. This generates a charge-separated dipolar intermediate called betaine. The negatively charged oxygen atom and...
Aldehydes and Ketones to Alkenes: Wittig Reaction Overview
Carboxylic Acids to Acid Chlorides
Electrophilic Aromatic Substitution: Chlorination and Bromination of Benzene
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)

