Catalytic hypervalent iodine oxidation of p-dialkoxybenzenes to p-quinones using 4-iodophenoxyacetic acid and oxone

T Yakura, Y Yamauchi, Y Tian, M Omoto

Index: Chemical and Pharmaceutical Bulletin, , vol. 56, # 11 p. 1632 - 1634

Full Text: HTML

Citation Number: 25

Abstract

... Development of efficient methods for quinone synthesis is quite important in synthetic organic chemistry because they are structural components of numerous pharmacologically active compounds and useful synthetic intermediates.1,2) Oxi ... Vol. ... 2008 Pharmaceutical Society of ...

Related Articles:

Effects of reaction conditions on quinone/diquinone product ratios in the oxidation of 1, 4-dimethoxybenzene derivatives with ceric ammonium nitrate

[Tetrahedron Letters, , vol. 55, # 12 p. 1994 - 1997]

Studies on Quinones. XI. Synthesis of Quinones from Hydroquinones by Using Manganese Dioxide and Acid-Impregnated Manganese Dioxide1

[Synthetic Communications, , vol. 13, # 5 p. 347 - 356]

Catalytic hypervalent iodine oxidation using 4-iodophenoxyacetic acid and Oxone: oxidation of p-alkoxyphenols to p-benzoquinones

[Chemical and Pharmaceutical Bulletin, , vol. 57, # 3 p. 252 - 256]

μ-Oxo-Bridged Hypervalent Iodine (III) Compound as an Extreme Oxidant for Aqueous Oxidations

[Synthesis, , vol. 44, # 8 p. 1183 - 1189]

IBS-Catalyzed Regioselective Oxidation of Phenols to 1, 2-Quinones with Oxone®

[Molecules, , vol. 17, # 7 p. 8604 - 8616]

More Articles...