A cascade process for directly converting nitriles (RCN) to cyanamides (RNHCN) <i>via</i> SO<sub>2</sub>F<sub>2</sub>-activated Tiemann rearrangement
作者:Guofu Zhang、Yiyong Zhao、Chengrong Ding
DOI:10.1039/c9ob01547g
日期:——
practical process for the direct conversion of nitriles to cyanamides was newly discovered and exhibited a wide substrate scope as well as great functional group-tolerability (36 examples). In this efficient strategy, the in situ generated amidoximes obtained from the reaction of nitriles with hydroxylamine subsequently underwent Tiemann rearrangement, producing the corresponding cyanamides with great
Novel N2-substituted -2,6-diaminonebularines of the formula (I):
wherein R is 2-pyridyl or 3-pyridyl, which may be susbstifuted, or acid addition salts thereof, have an excellent coronary vasodilator action.