NDLI: An Efficient Procedure for Palladium-Catalyzed Reduction of Aryl/Enol Triflates

Content Provider	Scilit
Author	Kotsuki, Hiyoshizo Datta, Probal Kanti Hayakawa, Hiroyuki Suenaga, Hitoshi
Copyright Year	1995
Description	An efficient procedure to deoxygenate phenols and enols via trifluoromethanesulfonates is presented. Their reduction with triethylsilane in the presence of a catalytic amount of palladium acetate and bidentate phosphine ligands such as 1,3-bis(diphenylphosphino)propane or 1,1’-bis(diphenylphosphino)ferrocene proceeds efficiently to afford a variety of aromatic, heteroaromatic, and olefinic compounds.
Related Links	http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-1995-4120.pdf
Ending Page	1350
Page Count	3
Starting Page	1348
ISSN	00397881
e-ISSN	1437210X
DOI	10.1055/s-1995-4120
Journal	Synthesis
Issue Number	11
Volume Number	1995
Language	English
Publisher	Georg Thieme Verlag KG
Publisher Date	1995-11-01
Access Restriction	Open
Subject Keyword	Journal: Synthesis Organic Chemistry Aryl/enol Triflates Palladium-catalyzed Reaction
Content Type	Text
Resource Type	Article
Subject	Organic Chemistry Catalysis

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An Efficient Procedure for Palladium-Catalyzed Reduction of Aryl/Enol Triflates