144951-88-2Relevant articles and documents
Facile and quantitative synthesis of 1,3-diazaheterocycle-fused 1,2,3-triazole derivatives using fluoroalkanesulfonyl azide as a diazo transfer reagent
Gu, Jiwei,Xiong, Wanting,Zhang, Zhenhua,Zhu, Shizheng
body text, p. 1717 - 1722 (2011/07/29)
A series of 1,3-diazaheterocycle-fused 1,2,3-triazoles were conveniently and quantitatively prepared by 1,3-dipolar cycloaddition of heterocyclic ketene aminals with fluoroalkanesulfonyl azide, followed by elimination of fluoroalkanesulfonyl amide at room
Synthesis and Reactions of Fluoroalkanesulfonyl Azides and N,N-Dichlorofluoroalkanessulfonamides
Zhu, Shi-Zheng
, p. 2077 - 2082 (2007/10/02)
Thermolysis or photolysis of fluoroalkanesulfonyl azides RFSO2N3 afforded the corresponding nitrene intermediates RFSo2N which reacted readily with alkanes, alkenes, benzene, dimethyl sulfide, dimethyl sulfoxide, pyridine and triphenylphosphine to give insertion or addition products.Similar results were obtained by the reactions of N,N-dichlorofluoroalkanesulfonamides, RFSO2NCl2, with the same reagents in the presence of zinc powder.Treatment of RFSO2NCl2 with alkene in the absence of zinc powder gave only a 1:1 adduct via a free-radical intermediate RfSO2NCl.
Synthesis of fluoroalkanesulfonyl azides and their reactions as fluoroalkanesulfonyl nitrene precursors
Zhu, Shi-Zheng
, p. 6503 - 6504 (2007/10/02)
Thermolysis or photolysis of the title compounds with cyclohexane, Me2C = CMe2, methyl sulfide and triphenyl phosphine gave the corresponding insertion or addition products via the perfluoroalkanesulfonyl nitrene intermediate.