Journal2005
Mild and Efficient Deprotection of 1,3-Dithianes withN,N′- Diiodo-N,N′-1,2-Ethanediyl-Bis(p-Toluenesulphonamide)
Journal of the Chinese Chemical Society Vol. 52, No. 2, 327–330
چکیده
Aliphatic and aromatic 1,3-dithiane are oxidized to the corresponding carbonyl compounds in good yields under mild conditions by N,N′-diiodo-N,N′-1,2-ethanediyl-bis(p-toluenesulphonamide) [NIBTS] and silver nitrate.
موضوعات و کلیدواژهها
Chemical Synthesis and ReactionsOxidative Organic Chemistry ReactionsVanadium and Halogenation ChemistryChemistryMedicinal chemistryStereochemistryCombinatorial chemistry
ارجاع علمی
Ramin Ghorbani‐Vaghei, Mohammad Ali Zolfigol. “Mild and Efficient Deprotection of 1,3-Dithianes withN,N′- Diiodo-N,N′-1,2-Ethanediyl-Bis(p-Toluenesulphonamide).” Journal of the Chinese Chemical Society, 2005. https://doi.org/10.1002/jccs.200500049