An Improved Procedure for the Conversion of Alkenes and Glycals to 1,2-Diazides Using Mn(OAc)<sub>3</sub>·2H<sub>2</sub>O in Acetonitrile Containing Trifluoroacetic Acid
作者:Barry B. Snider*、Hong Lin
DOI:10.1080/00397919808007024
日期:1998.5
Abstract Alkenes and Glycals react with Mn(OAc3)·2H2O and NaN3 in 9:1 acetonitrile-trifluoroacetic acid to give 1,2-diazides in >80% yield. Allylic azides are formed by slow addition of NaN3 to a mixture of alkene, Mn(OAc)3·2H2O and Cu(OAc)2.