A Simple, Broad-Scope Nickel(0) Precatalyst System for the Direct Amination of Allyl Alcohols
Author:
Affiliation:
1. Department of Chemistry; Lancaster University; Lancaster LA1 4YB UK
2. Department of Chemical Sciences; University of Huddersfield; Queensgate Huddersfield HD1 3DH UK
Publisher
Wiley
Subject
General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201805611/fullpdf
Reference96 articles.
1. Organic syntheses by means of noble metal compounds XVII. Reaction of π-allylpalladium chloride with nucleophiles
2. New synthetic reactions. Allylic alkylation
3. Asymmetric Transition Metal-Catalyzed Allylic Alkylations
4. Asymmetric Transition-Metal-Catalyzed Allylic Alkylations: Applications in Total Synthesis
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1. Carbonylative Cross‐Coupling Reaction of Allylic Alcohols and Organoalanes with 1 atm CO Enabled by Nickel Catalysis;Angewandte Chemie International Edition;2022-08-16
2. Carbonylative Cross‐Coupling Reaction of Allylic Alcohols and Organoalanes with 1 atm CO Enabled by Nickel Catalysis;Angewandte Chemie;2022-08-16
3. Nickel‐Catalyzed Allylic Substitution Reactions: An Evolving Alternative;European Journal of Inorganic Chemistry;2021-12-06
4. Access to 1,3‐Dinitriles by Enantioselective Auto‐tandem Catalysis: Merging Allylic Cyanation with Asymmetric Hydrocyanation;Angewandte Chemie;2020-04-20
5. Access to 1,3‐Dinitriles by Enantioselective Auto‐tandem Catalysis: Merging Allylic Cyanation with Asymmetric Hydrocyanation;Angewandte Chemie International Edition;2020-02-28
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