13274-75-4Relevant articles and documents
Investigating Bicyclobutane-Triazolinedione Cycloadditions as a Tool for Peptide Modification
Schwartz, Brett D.,Smyth, Aidan P.,Nashar, Philippe E.,Gardiner, Michael G.,Malins, Lara R.
, p. 1268 - 1273 (2022/02/07)
Acyl bicyclobutanes are shown to engage in strain-promoted cycloaddition reactions with a diverse array of triazolinedione reagents. The synthesis of an orthogonally protected urazole building block enabled the facile preparation of amino acid- and peptid
N2O4 chemisorbed onto n-propylsilica kryptofix 21 and kriptofix 22 as two new functional polymers for the fast oxidation of urazoles and 1,4-dihydropyridines
Chehardoli, Gholamabbas,Zolfigol, Mohammad Ali,Ghaemi, Ezat,Madrakian, Elaheh,Niknam, Khodabakhsh,Mallakpour, Shadpour
experimental part, p. 596 - 599 (2012/09/07)
3-Chloropropylsilica was reacted with Kriptofix 21 or 22 in the presence of triethylamine to form N-propylsilica Kryptofix 21 and Kriptofix 22. Then N 2O4 was added to each of these polymers to chemisorb onto cavity of aza-crown ethers. These functionalized polymers were applied for the fast and simple oxidation of urazoles and 1,4-dihydropyridines, respectively.
Green and metal-free catalytic oxidation of urazoles into triazolinediones by guanidinium nitrate and catalytic amounts of silica sulfuric acid
Nikoorazm, Mohsen,Choghamarani, Arash Ghorbani,Goudarziafshar, Hamid,Mallakpour, Shadpour
experimental part, p. 2389 - 2391 (2010/11/18)
-