467426-60-4Relevant articles and documents
BuMgNiPr2: A new base for stoichiometric, position-selective deprotonation of cyclopropane carboxamides and other weak CH acids
Zhang, Mao-Xi,Eaton, Philip E.
, p. 2169 - 2171 (2002)
Using the irreversible formation of an alkane, the proton-removing ability of a magnesiated amine, and the activating effect of a carboxamido group, weakly acidic CH groups E in a variety of systems can be selectively converted into useful amido-Grignard