Direct Nucleophilic Substitution of Alcohols Using an Immobilized Oxovanadium Catalyst
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences Osaka University 1-6, Yamadaoka, Suita Osaka 565-0871 Japan
2. Current address: Max-Planck-Institut für Kohlenforschung 45470 Mülheim/Ruhr Germany
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100569
Reference40 articles.
1. Key green chemistry research areas—a perspective from pharmaceutical manufacturers
2. Direct Nucleophilic S N 1‐Type Reactions of Alcohols
3. Recent Advances in the Direct Nucleophilic Substitution of Allylic Alcohols through SN1-Type Reactions
4. Recent Advances in Direct Catalytic Dehydrative Substitution of Alcohols
5. Palladium-Catalyzed SN1 Reactions of Secondary Benzylic Alcohols: Etherification, Amination, and Thioetherification
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1. Nucleophilic Deprotection of <i>p</i>-Methoxybenzyl Ethers Using Heterogeneous Oxovanadium Catalyst;Chemical and Pharmaceutical Bulletin;2024-02-21
2. Access to thioethers from thiols and alcohols via homogeneous and heterogeneous catalysis;Scientific Reports;2023-11-23
3. Oxovanadium-Catalyzed Direct Nucleophilic Substitution of Alcohols;Synfacts;2021-10-19
4. Chemo- and regioselective cross-dehydrogenative coupling reaction of 3-hydroxycarbazoles with arenols catalyzed by a mesoporous silica-supported oxovanadium;RSC Advances;2021
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