Abstract
Starting from amino alkynes derived from glycine esters, silver(Ⅰ) catalyst was employed for a tandem intramolecular hydroamination/Michael addition process under mild conditions. This reaction provides an efficient approach to substituted 3,4-dihydro-2H-pyrroles
Abstract
Starting from amino alkynes derived from glycine esters, silver(Ⅰ) catalyst was employed for a tandem intramolecular hydroamination/Michael addition process under mild conditions. This reaction provides an efficient approach to substituted 3,4-dihydro-2H-pyrroles