929606-19-9Relevant academic research and scientific papers
Stereocontrol in palladium-catalyzed propargylic substitutions: Kinetic resolution to give enantioenriched 1,5-enynes and propargyl acetates
Ardolino, Michael J.,Eno, Meredith S.,Morken, James P.
supporting information, p. 3413 - 3419 (2013/12/04)
Kinetic resolution during the catalytic allyl-propargyl cross-coupling with chiral starting materials can be accomplished with a chiral palladium catalyst. These reactions offer ready access to enantiomerically enriched enyne products from simple, readily
Tandem enyne metathesis and Claisen rearrangement: A versatile approach to conjugated dienes of variable substitution patterns
Clark, Daniel A.,Kulkarni, Amol A.,Kalbarczyk, Kyle,Schertzer, Bryan,Diver, Steven T.
, p. 15632 - 15636 (2007/10/03)
To extend the versatility of the ruthenium carbene-promoted enyne metathesis, it was combined with an Ireland ester enolate Claisen rearrangement. This reaction sequence provided conjugated dienes of higher substitution pattern than that obtained through
