Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227276 | Tetrahedron | 2009 | 5 Pages |
Abstract
The addition of nucleophilic methoxyarenes to allenes proceeds at room temperature in dichloromethane with a catalytic amount of phosphite-gold(I) precatalyst and silver additive. The addition is regioselective for the allene terminus, and generates E-allylation products without the need for prefunctionalization of the synthons as organometallics or allyl bromides. Coordinating heteroaromatics and sterically hindered allenes do not participate in the reaction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Michael A. Tarselli, Ann Liu, Michel R. Gagné,