Arnaud Chevalier, Abdelaaziz Ouahrouch, Alexandre Arnaud, Thibault Gallavardin, Xavier Franck
文献索引:10.1039/C8RA01546E
全文:HTML全文
Indazole derivatives are currently drawing more and more attention in medicinal chemistry as kinase inhibitors. 1H-indazole-3-carboxaldehydes are key intermediates to access to a variety of polyfunctionalized 3-substituted indazoles. We report here a general access to this motif, based on the nitrosation of indoles in a slightly acidic environment. These very mild conditions allow the conversion of both electron-rich and electron-deficient indoles into 1H-indazole-3-carboxaldehydes.
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