The Key to Oxidative Addition of Acyclic Vinyl Sulfide to M(0) Complex
Author:
Affiliation:
1. Department of Applied Chemistry, Faculty of Engineering Osaka University, Suita, Osaka 565-0871, Japan
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja993796e
Reference38 articles.
1. Ring Opening of Methylbenzothiophenes and Methyldibenzothiophenes by Tris(triethylphosphine)platinum(0)
2. Reversible oxidative addition and reductive elimination of diaryl sulphide involving C–S bond cleavage and formation: exchange of two aryl groups in aryl(arylthiolato)nickel complexes having tertiary phosphine ligands
3. The First Example of Facile Oxidative Addition of Carbon−Tellurium Bonds to Zero-Valent Pt, Pd, and Ni Complexes
4. Cleavage of aryl carbon-sulfur bonds by a trinuclear cluster. Reaction of alkyl phenyl sulfides with dodecacarbonyltriosmium
5. Interaction of palladium(0) complexes with allylic acetates, allyl ethers, allyl phenyl chalcogenides, allylic alcohols, and allylamines. Oxidative addition, condensation, disproportionation, and .pi.-complex formation
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1. Palladium-Catalyzed Highly Chemo- and Stereoselective Bisthiolation of Terminal Alkynes with Allyl Phenyl Sulfides via C–S Bond Cleavage;The Journal of Organic Chemistry;2022-06-06
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