Transition-Metal-Free and Chemoselective NaOtBu–O2-Mediated Oxidative Cleavage Reactions of vic-1,2-Diols to Carboxylic Acids and Mechanistic Insight into the Reaction Pathways
Author:
Affiliation:
1. Department of Energy Science, Sungkyunkwan University, Suwon 440-746, Republic of Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol501012f
Reference33 articles.
1. Modern Reduction Methods
2. Transition metal-free, NaOtBu-O2-mediated one-pot cascade oxidation of allylic alcohols to α,β-unsaturated carboxylic acids
3. An efficient organocatalytic method for constructing biaryls through aromatic C–H activation
4. tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative
5. Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C−H Arylation of Unactivated Benzene
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