1600518-03-3Relevant academic research and scientific papers
Copper(I)-catalyzed nucleophilic addition of ynamides to acyl chlorides and activated N-heterocycles
Zhang, Peng,Cook, Andrea M.,Liu, Yang,Wolf, Christian
, p. 4167 - 4173 (2014/05/20)
The addition of ynamides to acyl chlorides and N-heterocycles activated in situ with ethyl chloroformate has been accomplished at room temperature using copper iodide as catalyst. This economical and practical carbon-carbon bond formation provides convenient access to a variety of 3-aminoynones from aliphatic and aromatic acyl chlorides in up to 99% yield. The addition to pyridines and quinolines occurs under almost identical conditions and proceeds with good to high regioselectivity, producing the corresponding 1,2-dihydro-N-heterocycles in up to 95% yield.
