Silver-mediated fluorination of functionalized aryl stannanes

T Furuya, AE Strom, T Ritter

Index: Furuya, Takeru; Strom, Alexandra E.; Ritter, Tobias Journal of the American Chemical Society, 2009 , vol. 131, p. 1662 - 1663

Full Text: HTML

Citation Number: 188

Abstract

We report a regiospecific silver-mediated fluorination of aryl stannanes. The presented reaction can afford complex fluoroarenes from readily available phenols in three steps. The operational simplicity and the broad substrate scope of the fluorination should render this reaction a useful tool for the synthesis of milligram to gram quantities of functionalized aryl fluorides. Silver-mediated oxidative transformations of aryl nucleophiles that proceed via ...

Simple and efficient CuI/PEG-400 system for hydroxylation of...

[Chen, Junmin; Yuan, Tangjun; Hao, Wenyan; Cai, Mingzhong Catalysis Communications, 2011 , vol. 12, # 15 p. 1463 - 1465]

Tricyclic potential neuroleptics: 2-chloro-11-[4-(4-fluoroar...

[Bartl; Dlabac; Protiva Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 11 p. 3182 - 3189]

Preparation of phenolic compounds through catalyst-free ipso...

[Gohain, Mukut; Du Plessis, Maretha; Van Tonder, Johannes H.; Bezuidenhoudt, Barend C.B. Tetrahedron Letters, 2014 , vol. 55, # 13 p. 2082 - 2084]

An efficient synthesis of phenol via CuI/8-hydroxyquinoline-...

[Maurer, Stefan; Liu, Wei; Zhang, Xiaojing; Jiang, Yongwen; Ma, Dawei Synlett, 2010 , # 6 p. 976 - 978]

2-(Trimethylsilyl) ethanol as a new alcohol equivalent for c...

[Dibakar, Mullick; Prakash, Anjanappa; Selvakumar, Kumaravel; Ruckmani, Kandasamy; Sivakumar, Manickam Tetrahedron Letters, 2011 , vol. 52, # 41 p. 5338 - 5341]