Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 69, Issue 17, Pages 5752-5755Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo049325e
Keywords
-
Categories
Ask authors/readers for more resources
Conditions for an efficient ligand-, copper-, and amine-free palladium-catalyzed Sonogashira reaction of aryl iodides and bromides with terminal alkynes have been developed. Critical to the success of this new protocol is the use of tetrabutylammonium acetate as the base. Noteworthy features of this method are room-temperature conditions and the tolerance of a broad range of functional groups in both reaction partners.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available