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. Author manuscript; available in PMC: 2018 Apr 7.
Published in final edited form as: Org Lett. 2017 Mar 30;19(7):1878–1881. doi: 10.1021/acs.orglett.7b00647

Figure 4.

Figure 4

Multicomponent condensation reaction with acetals, phenols, and olefins.a a Reaction conditions: 2.0 mmol of phenol, 2.0 mmol of acetal, and 1.0 mmol of dienophile, 0.5 M with respect to and 10 mol % FeCl3·6H2O with respect to phenol unless otherwise stated; isolated yields; diastereomeric ratio determined by 1H NMR; detailed experimental conditions are provided in the Supporting Information. b Yield and dr after trituration with hot hexanes.