1210927-97-1Relevant articles and documents
Palladacycle-Catalyzed Regioselective Heck Reaction Using Diaryliodonium Triflates and Aryl Iodides
Hou, Cheng,Lei, Lu,Liang, Cui,Mo, Dong-Liang,Wang, Zhi-Xin,Zou, Pei-Sen
supporting information, p. 663 - 667 (2022/01/28)
We describe a P-containing palladacycle-catalyzed regioselective Heck reaction of 2,3-dihydrofuran with diaryliodonium salts and aryl iodides to afford 2-aryl-2,5-dihydrofurans and 2-aryl-2,3-dihydrofurans, respectively, in good yields. Mechanistic studie
Use of commercially available ruthenium fischer-type carbenes for ring-closing metathesis reactions: Scope and limitations of an in situ activation procedure
Wallace, Debra J.
scheme or table, p. 2277 - 2282 (2010/02/28)
An evaluation of two commercially available Fischer-type ruthenium carbenes in a range of ring-closing diene and enyne metathesis reactions has been carried out. A method to activate such catalysts for ring-closing reactions is presented.