Bench-stable oxidant sodium percarbonate for functional group transformation of arylboronic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference77 articles.
1. (a) D. Hall, Boronic Acids: Preparation and Applications in Organic Synthesis, Medicine and Materials, Ed. D. G. Hall, Wiley-VCH, Weinheim, 2nd Ed, 2011
2. (b) C. Zhu and J. R. Falck, Adv. Synth. Catal. 2014, 356, 2395.
3. Mild and Rapid Hydroxylation of Aryl/Heteroaryl Boronic Acids and Boronate Esters with N-Oxides
4. Oxidation of Organotrifluoroborates via Oxone
5. C−H Activation/Borylation/Oxidation: A One-Pot Unified Route To Meta-Substituted Phenols Bearing Ortho-/Para-Directing Groups
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1. Removal of tetracycline by ultraviolet/sodium percarbonate (UV/SPC)advanced oxidation process in water;Environmental Research;2024-04
2. Arylazopyrazole linked Schiff bases as organocatalysts for the ipso-hydroxylation of arylboronic acids for the synthesis of phenols;Tetrahedron Letters;2023-11
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