Azide-mediated detosylation of N-tosylpyrroloiminoquinones and N-tosylindole-4, 7-quinones
SP Patel, DH Nadkarni, S Murugesan, JR King…
Index: Patel, Swayamprabha P.; Nadkarni, Dwayaja H.; Murugesan, Srinivasan; King, Jason R.; Velu, Sadanandan E. Synlett, 2008 , # 18 p. 2864 - 2868
Full Text: HTML
Citation Number: 3
Abstract
Abstract The utility of NaN 3 as a reagent for the detosylation of N-tosylpyrroloiminoquinones and N-tosylindole-4, 7-quinones is described. The NaN 3-mediated detosylation is carried out in polar aprotic solvents such as DMF and DMSO. The reaction occurs under neutral, mild conditions and results in good to excellent yields of the detosylated quinones.
Related Articles:
[De Nanteuil, Florian; Waser, Jerome Angewandte Chemie - International Edition, 2011 , vol. 50, # 50 p. 12075 - 12079]
Direct synthesis of sulfonyl azides from sulfonic acids
[Kiani, Adeleh; Akhlaghinia, Batool; Rouhi-Saadabad, Hamed; Bakavoli, Mehdi Journal of Sulfur Chemistry, 2014 , vol. 35, # 2 p. 119 - 127]
Nitrosation with sodium hexanitrocobaltate (III)
[Stefane, Bogdan; Kocevar, Marijan; Polanc, Slovenko Journal of Organic Chemistry, 1997 , vol. 62, # 21 p. 7165 - 7169]
[Suarez, Jose Ramon; Kwiczak, Joanna; Grenda, Katarzyna; Jimeno, M. Luisa; Chiara, Jose Luis Advanced Synthesis and Catalysis, 2013 , vol. 355, # 5 p. 913 - 918]
[Katritzky, Alan; Widyan, Khalid; Gyanda, Kapil Synthesis, 2008 , # 8 p. 1201 - 1204]