1291103-72-4

Upstream product

• 15352-99-5 (+/-)-hex-1-yn-3-yl acetate 
• 100-61-8 N-methylaniline 
• 105-31-7 1-hexyn-3-ol 
• 1291103-58-6 1-hexyn-3-yl pentafluorobenzoate 

Relevant academic research and scientific papers

Chiral tridentate P,N,N ligands for highly enantioselective copper-catalyzed propargylic amination with both primary and secondary amines as nucleophiles

Chiral tridentate P,N,N ligands have been demonstrated to be highly efficient for the coppercatalyzed enantioselective propargylic amination of propargylic acetates with both primary and secondary amines as nucleophiles, affording the corresponding propar

Copper-catalyzed enantioselective propargylic amination of nonaromatic propargylic esters with amines

Chemical equations presented. The enantioselective propargylic amination of propargylic pentafluorobenzoates bearing an alkyl group at the propargylic position with amines in the presence of catalytic amounts of a copper complex and an optically active diphosphine such as BINAP has been found to give the corresponding propargylic amines in good yields with high enantioselectivity.