Investigation of the configurational stabilities of chiral isocyanoacetates in multicomponent reactions
Isocyanoacetates are uniquely reactive compounds characterized by an ambivalent isocyano functional group and an enolizable α-carbon. It is widely believed that chiral α-substituted isocyanoacetates are configurationally unstable in some synthetically use
Carney, Daniel W.,Truong, Jonathan V.,Sello, Jason K.
p. 10279 - 10285
(2012/02/14)
More Articles about upstream products of 1346414-03-6