Double Arylation of Diynes and Alkynylation of Functionalized Heteroaryl Halides by a Practical Heck Reaction in an Ionic Liquid
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0031-1289861.pdf
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Ionic Liquids in Metal, Photo-, Electro-, and (Bio) Catalysis;Chemical Reviews;2024-04-25
2. Mechanistic Insights and Implications of Dearomative Rearrangement in Copper-Free Sonogashira Cross-Coupling Catalyzed by Pd-Cy*Phine;Organometallics;2016-03-28
3. A Versatile and Efficient Palladium-meta-Terarylphosphine Catalyst for the Copper-Free Sonogashira Coupling of (Hetero-)Aryl Chlorides and Alkynes;European Journal of Organic Chemistry;2014-09-24
4. Effects of solvent and base on the palladium-catalyzed amination: PdCl2(Ph3P)2/Ph3P-catalyzed selective arylation of primary anilines with aryl bromides;Tetrahedron;2014-08
5. Uncommon perspectives in palladium- and copper-catalysed arylation and heteroarylation of terminal alkynes following Heck or Sonogashira protocols: Interactions copper/ligand, formation of diynes, reaction and processes in ionic liquids;Comptes Rendus Chimie;2013-06
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