Conjugate Addition of α‐Substituted Acyl Imidazoles to Nitroalkenes Catalyzed by Nickel Bisoxazoline and B(C 6 F 5 ) 3
Author:
Affiliation:
1. Center for Supramolecular Chemistry and Catalysis and Department of Chemistry College of Sciences Shanghai University 99 Shangda Lu Shanghai 200444 People's Republic of China
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
Organic Chemistry,Catalysis
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202200476
Reference86 articles.
1. For reviews see:
2. Acyl‐Imidazoles: A Privileged Ester Surrogate for Enantioselective Synthesis
3. α,β‐Unsaturated 2‐Acyl‐Imidazoles in Asymmetric Biohybrid Catalysis
4. Enantioselective Friedel−Crafts Alkylations of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine−Scandium(III) Triflate Complexes
5. Catalytic Enantioselective Pyrrole Alkylations of α,β-Unsaturated 2-Acyl Imidazoles
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1. Enantio- and diastereoselective conjugate addition of pyridyl alkyl ketones to enones by Cu(ii)-Lewis acid/Brønsted base catalysis;Organic Chemistry Frontiers;2024
2. Synergistic Ni/Pd Catalysis for Asymmetric Allylic Alkylation of 2-Acyl Imidazoles;Organic Letters;2023-07-14
3. B(C6F5)3‐Catalyzed 1,4‐Allylation of Azadienes with Allyltrimethylsilanes;European Journal of Organic Chemistry;2023-02-20
4. Recent developments in enantioselective nickel(ii)-catalyzed conjugate additions;Organic Chemistry Frontiers;2022
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