Abstract

The reductive coupling of alkynes with aldehydes is a common method for preparing allylic alcohols. When unsymmetrical alkynes are used two regioisomeric products can be formed. Regiocontrol is possible with a strong steric or electronic bias in the alkyne. The authors have developed catalyst systems which are exceptionally sensitive to steric differences in unsymmetrical alkynes, allowing either regioisomeric trisubstituted alkene to be synthesized.

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