Abstract:A convenient procedure of synthesis of N-carbamoyl-protected propargylic amines substituted with a cyclopropyl group from α-amido sulfones and cyclopropylacetylene is described. The reaction is catalyzed by a chiral BINOL-type zinc complex and provides the corresponding products in good yields and enantioselectivities.
The first ZnCl2-catalyzed alkynylation of aldimines with tetra(phenylethynyl)tin was achieved under solvent-free conditions. The present methodology provides propargylamines in 38–62% yields.
The first ZnCl2-catalyzed alkynylation of aldimines with tetra(phenylethynyl)tin was achieved under solvent-free conditions. The present methodology provides propargylamines in 38–62% yields.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.