The Oxidation of Organo-Boron Compounds Using Electrochemically Generated Peroxodicarbonate

被引:8
|
作者
Kohlpaintner, Philipp J. [1 ]
Marquart, Lucas [1 ]
Goossen, Lukas J. [2 ]
Waldvogel, Siegfried R. [1 ,3 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
[2] Ruhr Univ Bochum, Evonik Chair Organ Chem, Univ Str 150, D-44901 Bochum, Germany
[3] Inst Biol & Chem Syst Funct Mol Syst IBCS FMS, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
alcohols; boron compounds; electrosynthesis; oxidation; peroxodicarbonate; IPSO-HYDROXYLATION; ARYLBORONIC ACIDS; BOND; BENZOXAZOLES; ARYL; PEROXYCARBONATE; CONVERSION; RESOLUTION; CATALYST; SOLVENT;
D O I
10.1002/ejoc.202300220
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Peroxodicarbonate represents a green and largely underexplored oxidizer generated electrochemically from aqueous carbonate solutions. Through state-of-the-art electrolyzer technology, highly concentrated solutions have now become accessible. These were successfully employed as green oxidizer in deborolative hydroxylations. A plethora of phenols and alcohols have thus been synthesized in up to 99 % from organoboron compounds using only green and non-toxic solvents. This transformation was successfully scaled-up to multi-gram batch sizes.
引用
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页数:6
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