Oxidatively sonochemical dealkylation of various N-alkylsulfonamides to free sulfonamides and aldehydes
M Katohgi, H Togo
Index: Katohgi, Masashi; Togo, Hideo Tetrahedron, 2001 , vol. 57, # 35 p. 7481 - 7486
Full Text: HTML
Citation Number: 21
Abstract
Various N-alkylsulfonamides were easily dealkylated to give the corresponding free sulfonamides in moderate to good yields in the presence of (diacetoxyiodo) benzene and iodine under ultrasonic irradiation. Application of this methodology to various N-protected alkylamines with sulfonyl, phosphonyl, and acyl groups was carried out, and the oxidative conversion occurred only in N-sulfonyl-protected phenylalkylamines to give the ...
Related Articles:
[Vellakkaran, Mari; Andappan, Murugaiah M.S.; Kommu, Nagaiah Green Chemistry, 2014 , vol. 16, # 5 p. 2788 - 2797]
Hydroformylation of monosubstituted alkenes catalyzed by W-Rh bimetallic complex
[Yamane, Motoki; Yukimura, Noriaki; Ishiai, Hiroshi; Narasaka, Koichi Chemistry Letters, 2006 , vol. 35, # 5 p. 540 - 541]
Hydroformylation of monosubstituted alkenes catalyzed by W-Rh bimetallic complex
[Yamane, Motoki; Yukimura, Noriaki; Ishiai, Hiroshi; Narasaka, Koichi Chemistry Letters, 2006 , vol. 35, # 5 p. 540 - 541]