Enantioselectivity in Ruthenium‐Catalyzed Propargylic Substitution Reactions of Propargylic Alcohols with Acetone: A DFT Study
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences Toho University, Miyama Funabashi Chiba 274-8510 Japan
2. Department of Applied Chemistry School of Engineering The University of Tokyo, Hongo Bunkyo-ku Tokyo 113-8656 Japan
Publisher
Wiley
Subject
General Chemistry,Biochemistry,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.202100984
Reference51 articles.
1. Novel Propargylic Substitution Reactions Catalyzed by Thiolate-Bridged Diruthenium Complexes via Allenylidene Intermediates
2. For reviews:
3. Transition‐Metal‐Catalyzed Propargylic Substitution of Propargylic Alcohol Derivatives Bearing an Internal Alkyne Group
4. Scope and advances in the catalytic propargylic substitution reaction
5. Catalyzed Propargylic Substitution
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1. Enantioselective propargylic amination and related tandem sequences to α-tertiary ethynylamines and azacycles;Nature Chemistry;2024-03-19
2. Asymmetric Propargylic C−C Bond Formation Using Metal–Allenylidene Species;European Journal of Organic Chemistry;2023-11-22
3. Biomimetic asymmetric catalysis;Science China Chemistry;2023-04-25
4. Interplay of diruthenium catalyst in controlling enantioselective propargylic substitution reactions with visible light-generated alkyl radicals;Nature Communications;2023-02-23
5. Effect of Propargylic Substituents on Enantioselectivity and Reactivity in Ruthenium-Catalyzed Propargylic Substitution Reactions: A DFT Study;ACS Omega;2022-10-04
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