Highly Regio- and Stereoselective Acylboration, Acylsilation, and Acylstannation of Allenes Catalyzed by Phosphine-Free Palladium Complexes: An Efficient Route to a New Class of 2-Acylallylmetal Reagents
Author:
Affiliation:
1. Contribution from the Department of Chemistry, Tsing Hua University, Hsinchu, Taiwan, 300 ROC
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja036021l
Reference96 articles.
1. A new catalytic reaction involving oxidative addition of iodotrimethylsilane (Me3SiI) to palladium(0). Synthesis of stereodefined enynes by the coupling of Me3SiI, acetylenes, and acetylenic tin reagents
2. Amphiphilic Catalytic Allylating Reagent, Bis-π-allylpalladium Complex
3. Efficient Preparation of Functionalized (E,Z) Dienes Using Acetylene as the Building Block
4. Nickel-Catalyzed Asymmetric Multiple-Component Tandem Coupling. Effects of Simple Monodentate Oxazolines as Chiral Ligands
5. Highly Regio- and Chemoselective Palladium-Catalyzed Three-Component Assembly of Arylethylidene Malononitriles, Allylic Chlorides, and Allenylstannanes: A Novel Route to 1,7-Enyne Derivatives
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