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Controlling the Selectivity Patterns of Au-Catalyzed Cyclization-Migration Reactions. | LitMetric

Controlling the Selectivity Patterns of Au-Catalyzed Cyclization-Migration Reactions.

Org Lett

Department of Chemistry , University at Illinois at Chicago, 845 West Taylor Street , Chicago , Illinois 60607 , United States.

Published: March 2019

As little as 2 mol % of (XPhos)AuNTf catalyzes the transformation of a broad range of o-acetylene-substituted styrenes into 1,2-dihydronaphthalenes. Our data suggests that this transformation occurs via a gold-stabilized cyclopropyl carbinyl cation, which triggers either a [1,2] carboxylate shift or a less favorable [1,2] aryl shift. The relative rates of these migrations can be controlled by the identity of the ligand or by stabilizing the mesomeric cation.

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http://dx.doi.org/10.1021/acs.orglett.8b03888DOI Listing

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