Synlett

A synthesis of oximes from olefins by cobalt (II) porphyrin-catalyzed reduction-nitrosation

K Sugamoto, Y Hamasuna, Y Matsushita, T Matsui

Index: Sugamoto, Kazuhiro; Hamasuna, Yutaka; Matsushita, Yoh-Ichi; Matsui, Takanao Synlett, 1998 , # 11 p. 1270 - 1272

Full Text: HTML

Citation Number: 12

Abstract

Abstract: Various olefins such as styrenes, α, β-unsaturated carbonyl compounds, and α, β, γ, δ-unsaturated carbonyl compounds were directly converted to the corresponding acetophenoximes, α-hydroxyimino carbonyl compounds and γ-hydroxyimino-α, β- unsaturated carbonyl compounds in good or moderate yields by reduction-nitrosation with t- butyl nitrite and triethylsilane in the presence of cobalt (II) porphyrin as a catalyst.

Related Articles:

An efficient catalytic method for the Beckmann rearrangement of ketoximes to amides and aldoximes to nitriles mediated by propylphosphonic anhydride (T3P®)

[Augustine, John Kallikat; Kumar, Rajesha; Bombrun, Agnes; Mandal, Ashis Baran Tetrahedron Letters, 2011 , vol. 52, # 10 p. 1074 - 1077]

More Articles...