Add time:08/18/2019         Source:sciencedirect.com

The Lewis acid-catalyzed regioselective azidolysis of 2,3-three membered heterocyclic amines has been investigated. The results obtained demonstrated that using TMSN3 as a source of azide, the appropriate choice of Lewis acid allowed to obtain different regio- and stereocontrolled precursors of aminoalcoholic and triaminic sequences. Considering the occurrence of these moieties in the structure of many biologically active compounds, the present methodologies could represent a powerful tool in organic synthesis for the preparation of interesting molecules.

We also recommend Trading Suppliers and Manufacturers of N,N-diethyl-N-(piperidin-4-ylmethyl)amine (cas 116905-90-9). Pls Click Website Link as below: cas 116905-90-9 suppliers