Tetrahedron Letters

Efficient oxidation of alcohols electrochemically mediated by azabicyclo-N-oxyls

Y Demizu, H Shiigi, T Oda, Y Matsumura, O Onomura

Index: Demizu, Yosuke; Shiigi, Hirofumi; Oda, Takahisa; Matsumura, Yoshihiro; Onomura, Osamu Tetrahedron Letters, 2008 , vol. 49, # 1 p. 48 - 52

Full Text: HTML

Citation Number: 47

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Preparation of azabicyclo-N-oxyls and the electrochemical oxidation of alcohols using them as mediators have been exploited. This oxidation was applicable to a transformation of sterically hindered secondary alcohols into the corresponding ketones in high yields.

Related Articles:

Asymmetric synthesis catalyzed by chiral ferrocenylphosphine transition metal complexes. 10 gold (i)-catalyzed asymmetric aldol reaction of isocyanoacetate

[Hayashi, Tamio; Sawamura, Masaya; Ito, Yoshihiko Tetrahedron, 1992 , vol. 48, # 11 p. 1999 - 2012]

Asymmetric synthesis catalyzed by chiral ferrocenylphosphine transition metal complexes. 10 gold (i)-catalyzed asymmetric aldol reaction of isocyanoacetate

[Hayashi, Tamio; Sawamura, Masaya; Ito, Yoshihiko Tetrahedron, 1992 , vol. 48, # 11 p. 1999 - 2012]

Nonenzymatic biomimetic oxidation systems: theory and application to transformation studies of environmental chemicals

[Perrone; Carbonara; Tortorella Archiv der Pharmazie, 1984 , vol. 317, # 7 p. 635 - 639]

More Articles...