Recent Progress in Oxidative Organic Transformations Employing Nitroxyl Radicals

• Iwabuchi Yoshiharu

  Graduate School of Pharmaceutical Sciences, Tohoku University

Bibliographic Information

Other Title

• 有機ニトロキシルラジカルを用いた酸化的分子変換の最近の進歩
• ユウキ ニトロキシルラジカル オ モチイタ サンカテキ ブンシ ヘンカン ノ サイキン ノ シンポ

Abstract

Nitroxyl radicals (N-oxyls or nitroxides), as exemplified by TEMPO (2,2,6,6-tetramethylpiperidinyl-1-oxy), AZADO (2-azaadamantane N-oxyl), and PINO (phthalimidiy N-oxyl), represent a stable class of organic radicals that exhibit unique properties and reactivity. The diverse and exotic chemistry of these compounds has been found versatile use in electron spin resonance (ESR) studies as spin labels, in biological studies as antioxidants, as charge carriers for energy storage, as mediators in polymerization reactions, and as catalysts in chemical and electrochemical oxidation reactions. This article describes recent synthetic applications of the two most prominent classes of N-oxyl compounds, namely, aminoxyl and imidoxyl species, to effect useful oxidative transformations.

Journal

• Journal of Synthetic Organic Chemistry, Japan

  Journal of Synthetic Organic Chemistry, Japan 77 (5), 424-432, 2019-05-01

  The Society of Synthetic Organic Chemistry, Japan

Keywords

• nitroxyl radicals
• stable radicals
• redox catalyst
• organocatalyst
• hybrid catalysis
• aerobic oxidation
• alcohol oxidation

Details

• CRID: 1390845713066870528
• NII Article ID: 130007644997
• NII Book ID: AN0024521X
• DOI: 10.5059/yukigoseikyokaishi.77.424
• ISSN: 18836526
• ISSN: 00379980
• NDL BIB ID: 029672540
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I029672540
• Web Site: https://www.jstage.jst.go.jp/article/yukigoseikyokaishi/77/5/77_424/_pdf
• Text Lang: ja
• Data Source:
  • JaLC
  • NDL
  • Crossref
  • CiNii Articles
  • KAKEN
• Abstract License Flag: Disallowed