Abstract
Cp∗Co(III)-catalyzed annulations of 2-alkenylphenols with CO for the synthesis of coumarin derivatives have been developed. The reaction features mild reaction conditions, broad substrate scope, and good functional group tolerance. Preliminary mechanistic studies were conducted, suggesting that C-H activation is the turnover limiting step. Furthermore, the efficiency of this reaction was demonstrated by the rapid total synthesis of three natural products herniarin, xanthyletin, and seselin.
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CITATION STYLE
Liu, X. G., Zhang, S. S., Jiang, C. Y., Wu, J. Q., Li, Q., & Wang, H. (2015). Cp∗Co(III)-Catalyzed Annulations of 2-Alkenylphenols with CO: Mild Access to Coumarin Derivatives. Organic Letters, 17(21), 5404–5407. https://doi.org/10.1021/acs.orglett.5b02728
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