Reaction of α-Stannyl α,β-Unsaturated Esters with Acid Chlorides Catalized by Palladium
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918808060900
Reference11 articles.
1. A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium
2. Mild, selective, general method of ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium
3. Unsymmetrical monoprotected α-diketones via the palladium-catalyzed vinylation of acid chlorides with organotin compounds
4. Synthetic utility of the palladium-catalyzed coupling reaction of acid chlorides with organotins
5. Mechanisms of the palladium-catalyzed couplings of acid chlorides with organotin reagents
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1. Hydrostannylation-Cross-Coupling Strategy for the Stereoselective Synthesis of Alkylidenemalonates and Related α,β-Unsaturated Esters;European Journal of Organic Chemistry;2015-01-12
2. A torquoselective extrusion of isoxazoline N-oxides. Application to the synthesis of aryl vinyl and divinyl ketones for Nazarov cyclization;Tetrahedron;2009-04
3. Effect of Ligands and Additives on the Palladium-Promoted Carbonylative Coupling of Vinyl Stannanes and Electron-Poor Enol Triflates;The Journal of Organic Chemistry;2000-08-26
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5. COUPLING REACTIONS BETWEEN ACETYLENIC BROMIDES AND ALKENYLTIN COMPOUNDS;Main Group Metal Chemistry;1997-01
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