Original paper

Nickel-Catalyzed Reaction of Benzamides with Bicylic Alkenes: Cleavage of C–H and C–N Bonds

Volume: 21, Issue: 6, Pages: 1774 - 1778
Published: Mar 5, 2019
Abstract
The nickel-catalyzed reaction of aromatic amides that contain an 8-aminoquinoline as a directing group with bicyclic alkenes, such as norbornene and 1,4-dihydro-1,4-epoxynaphthalene, results in the cleavage of both the C-H bond at the ortho-position of the benzene ring and the C(O)-N bond to give methanofluoren-9-one and 1,4-epoxyfluoren-9-one derivatives. Both Ni(OTf)2 and Ni(cod)2 show a high catalytic activity. The presence of AgOAc is...
Paper Details
Title
Nickel-Catalyzed Reaction of Benzamides with Bicylic Alkenes: Cleavage of C–H and C–N Bonds
Published Date
Mar 5, 2019
Volume
21
Issue
6
Pages
1774 - 1778
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