Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons
B Kalita, AA Lamar, KM Nicholas
Index: Kalita, Biswajit; Lamar, Angus A.; Nicholas, Kenneth M. Chemical Communications, 2008 , # 36 p. 4291 - 4293
Full Text: HTML
Citation Number: 12
Abstract
The direct N-functionalization of hydrocarbons by the activation of C–H and C C bonds is a challenging and important goal because of the value of the derived amines and the abundance of the hydrocarbon substrates. The most well-developed of these reactions are the transition metal-catalyzed hydroamination, 1 aziridination 2 and allylic amination 3 of alkenes. Reactions that effect direct benzylic C–H amination are receiving increasing attention, employing imido-iodinanes ...
Related Articles:
Building a sulfonamide library by eco-friendly flow synthesis
[Gioiello, Antimo; Rosatelli, Emiliano; Teofrasti, Michela; Filipponi, Paolo; Pellicciari, Roberto ACS Combinatorial Science, 2013 , vol. 15, # 5 p. 235 - 239]
Reactivity of β-Lactamido N-Sulfonyl Radicals
[Leca, Dominique; Fensterbank, Louis; Lacote, Emmanuel; Malacria, Max Organic Letters, 2002 , vol. 4, # 23 p. 4093 - 4095]
Direct conversion of thiols and disulfides into sulfonamides
[Bahrami, Kiumars; Khodaei, Mohammad M.; Soheilizad, Mehdi Tetrahedron Letters, 2010 , vol. 51, # 37 p. 4843 - 4846]
[Mahalingam; Wu, Xiongyu; Wan, Yiqian; Alterman, Mathias Synthetic Communications, 2005 , vol. 35, # 3 p. 417 - 425]
[McKay, William R.; Proctor, George R. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 2443 - 2450]