A Highly Regio- and Stereoselective Nickel-Catalyzed Ring-Opening Reaction of Alkyl- and Allylzirconium Reagents to 7-Oxabenzonorbornadienes
Author:
Affiliation:
1. Department of Chemistry, Tsing Hua University, Hsinchu, Taiwan 30013
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo051660v
Reference49 articles.
1. Palladium-Catalyzed Coupling Reactions of 1-Bromoadamantane with Styrenes and Arenes
2. Advances in Functional-Group-Tolerant Metal-Catalyzed Alkyl–Alkyl Cross-Coupling Reactions
3. Transition Metal-Catalyzed Activation of Aliphatic C−X Bonds in Carbon−Carbon Bond Formation
4. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides
5. Boronic Acids: New Coupling Partners in Room-Temperature Suzuki Reactions of Alkyl Bromides. Crystallographic Characterization of an Oxidative-Addition Adduct Generated under Remarkably Mild Conditions
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1. Palladium-catalyzed stereocontrolled ring-opening of 7-oxabenzonorbornadienes with organic carboxylic acids;Chemical Communications;2023
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3. Chemistry of Unsymmetrical C1-Substituted Oxabenzonorbornadienes;Current Organic Synthesis;2021-08
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