A literature-unprecedented three-component aryne coupling reaction has been developed, utilizing pyrroline, imine, dihydroisoquinoline, imidazoline or oxazoline as nucleophiles and acrylonitrile as a third component, which acts as both a proton donor and a nucleophile.
A literature-unprecedented three-component aryne coupling reaction with pyrroline, imine, dihydroisoquinoline, imidazoline or oxazoline as a nucleophile, and acrylonitrile as a third component, acting as both a proton donor and a nucleophile, has been developed. With imidazoline or oxazoline as the substrate, the initially formed three-component reaction product could react further to provide tetrahydro-1,4-diazepine or tetrahydro-1,4-oxazepine, respectively.
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