Silylboronate-Mediated Defluorosilylation of Aryl Fluorides with or without Ni-Catalyst
The defluorosilylation of aryl fluorides to access aryl silanes was achieved under transition-metal-free conditions via an inert C–F bond activation. The defluorosilylation, mediated by silylboronates and KOtBu, proceeded smoothly at room temperature to afford various aryl silanes in good yields. Al...
Main Authors: | Jun Zhou, Zhengyu Zhao, Norio Shibata |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2021-10-01
|
Series: | Frontiers in Chemistry |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fchem.2021.771473/full |
Similar Items
-
Transition-metal-free silylboronate-mediated cross-couplings of organic fluorides with amines
by: Jun Zhou, et al.
Published: (2023-04-01) -
From Academia to the Market – Air-stable Ni(ii)/Josiphos Catalysts
by: Florian Bächle, et al.
Published: (2021-11-01) -
Synthesis of Carbonyl-Containing Oxindoles via Ni-Catalyzed Reductive Aryl-Acylation and Aryl-Esterification of Alkenes
by: Zhengtian Ding, et al.
Published: (2022-09-01) -
Advances in Catalytic C–F Bond Activation and Transformation of Aromatic Fluorides
by: Rongqing Ma, et al.
Published: (2022-12-01) -
“Doing More with Less”: Ni(II)@ORMOSIL, a Novel Sol-Gel Pre-Catalyst for the Reduction of Nitrobenzene
by: Michael Meistelman, et al.
Published: (2021-11-01)