Metal??Free Synthesis of Imido Derivatives by Direct Oxidation of α??Amido Sulfones
F Martinelli, A Palmieri, M Petrini
Index: Martinelli, Fabio; Palmieri, Alessandro; Petrini, Marino European Journal of Organic Chemistry, 2010 , # 26 p. 5085 - 5089
Full Text: HTML
Citation Number: 3
Abstract
Abstract Oxidation of α-amidoaryl sulfones with m-chloroperoxybenzoic acid under mild conditions readily provides the corresponding imides in satisfactory yields. The overall process probably involves formation of an N-acyliminium ion intermediate, which by attack of the peroxyacid anion generates the final imido derivatives.
Related Articles:
Practical syntheses of a CXCR3 antagonist
[Chan, Johann; Baucom, Kyle D.; Murry, Jerry A. Journal of the American Chemical Society, 2007 , vol. 129, # 46 p. 14106 - 14107]
Development of an Acyl Sulfonamide Anti-Proliferative Agent, LY573636· Na†
[Yates, Matthew H.; Kallman, Neil J.; Ley, Christopher P.; Wei, Jeffrey N. Organic Process Research and Development, 2009 , vol. 13, # 2 p. 255 - 262]
[Ton, Thi My Uyen; Tejo, Ciputra; Tania, Stefani; Chang, Joyce Wei Wei; Chan, Philip Wai Hong Journal of Organic Chemistry, 2011 , vol. 76, # 12 p. 4894 - 4904]
[Adibi, Hadi; Massah, Ahmad Reza; Majnooni, Mohammad Bagher; Shahidi, Sherita; Afshar, Maryam; Abiri, Ramin; Naghash, Hamid Javaherian Synthetic Communications, 2010 , vol. 40, # 18 p. 2753 - 2766]
Practical copper (I)-catalysed amidation of aldehydes
[Chang, Joyce Wei Wei; Ton, Thi My Uyen; Tania, Stefani; Taylor, Paul C.; Chan, Philip Wai Hong Chemical Communications, 2010 , vol. 46, # 6 p. 922 - 924]