Intermolecular Alkyne Hydroacylation. Mechanistic Insight from the Isolation of the Vinyl Intermediate That Precedes Reductive Elimination
The isolation of the branched alkenyl intermediate that directly precedes reductive elimination of the final α,β-unsaturated ketone product is reported for the hydroacylation reaction between two alkyne.
Unit Operation: Reaction
Objective: Kinetics
Company: University of Bristol, University of Oxford
Source: Copyright © 2012 American Chemical Society
Authors: Miguel A. Huertos (University of Oxford), Guy C. Lloyd-Jones (University of Bristol), Rebekah J. Pawley (University of Oxford), Andrew S. Weller (University of Oxford), Michael C. Willis (University of Oxford)
Publish Date: 26-Jul-2012
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