Boronic Acid‐Mediated Photocatalysis Enables the Intramolecular Hydroacylation of Olefins Using Carboxylic Acids
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences Kyoto University Yoshida, Sakyo-ku Kyoto 606-8501 Japan
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202200082
Reference59 articles.
1. For selected reviews and reports of photocatalytic decarboxylative transformations of carboxylic acids see:
2. Visible-Light Photocatalysis as an Enabling Tool for the Functionalization of Unactivated C(sp3 )-Substrates
3. Decarboxylative reactions with and without light – a comparison
4. Decarboxylative Arylation of α-Amino Acids via Photoredox Catalysis: A One-Step Conversion of Biomass to Drug Pharmacophore
5. Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp 3 -carbons with aryl halides
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1. A Benzophenothiazine/Boronic Acid Hybrid Photocatalyst Enables the Single Electron Transfer (SET) to Carboxy Groups: SET-Initiated Cyclization of α,β-Unsaturated Carboxylic Acids;ACS Catalysis;2023-09-18
2. The xanthate route to tetralones, tetralins, and naphthalenes. A brief account;Organic & Biomolecular Chemistry;2023
3. Boron Catalysis in the Transformation of Carboxylic Acids and Carboxylic Acid Derivatives;European Journal of Organic Chemistry;2022-12-15
4. Boronic Acid‐Mediated Photocatalysis Enables the Intramolecular Hydroacylation of Olefins Using Carboxylic Acids;European Journal of Organic Chemistry;2022-03-23
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