147188-32-7Relevant academic research and scientific papers
Enantioselective Radical Construction of 5-Membered Cyclic Sulfonamides by Metalloradical C-H Amination
Hu, Yang,Lang, Kai,Li, Chaoqun,Gill, Joseph B.,Kim, Isaac,Lu, Hongjian,Fields, Kimberly B.,Marshall, McKenzie,Cheng, Qigan,Cui, Xin,Wojtas, Lukasz,Zhang, X. Peter
supporting information, p. 18160 - 18169 (2019/11/19)
Both arylsulfonyl and alkylsulfonyl azides can be effectively activated by the cobalt(II) complexes of D2-symmetric chiral amidoporphyrins for enantioselective radical 1,5-C-H amination to stereoselectively construct 5-membered cyclic sulfonami
Sulfonyl fluoride inhibitors of fatty acid amide hydrolase
Alapafuja, Shakiru O.,Nikas, Spyros P.,Bharathan, Indu T.,Shukla, Vidyanand G.,Nasr, Mahmoud L.,Bowman, Anna L.,Zvonok, Nikolai,Li, Jing,Shi, Xiaomeng,Engen, John R.,Makriyannis, Alexandros
, p. 10074 - 10089 (2013/01/16)
Sulfonyl fluorides are known to inhibit esterases. Early work from our laboratory has identified hexadecyl sulfonylfluoride (AM374) as a potent in vitro and in vivo inhibitor of fatty acid amide hydrolase (FAAH). We now report on later generation sulfonyl
Microwave-assisted synthesis of sodium sulfonates precursors of sulfonyl chlorides and fluorides
Alapafuja, Shakiru O.,Nikas, Spyros P.,Shukla, Vidyanand G.,Papanastasiou, Ioannis,Makriyannis, Alexandros
experimental part, p. 7028 - 7031 (2010/02/28)
We describe the use of a microwave reaction for the conversion of various bromides to sodium sulfonates that have been further elaborated to sulfonyl chlorides. This new approach leads to much improved yields and shorter reaction times. Representative sul
COMPOUNDS AND METHODS FOR CONTROLLING BACTERIAL VIRULENCE
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Page 33, (2010/02/04)
Novel sulfonated homoserine lactones formula I have been found to act ac quorum sensing inhibitors. As such, they may be useful in the treatment of bacterial infections.
