Abstract
The enantioselective synthesis of 2-amino-4H-chromenesviathe cascade rhodium-catalysed conjugate addition/hetero Thorpe-Ziegler reaction is reported. Moderate to good yields (up to 98%) and high enantioselectivities (up to 92% ee) were obtained with a chiral diene-coordinated rhodium complex as the catalyst. This protocol remedies the methodological deficiency in the asymmetric synthesis of 4-aryl 2-amino-4H-chromenes.
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CITATION STYLE
Chang, Z., Zhu, H., Wu, C., Xing, J., & Dou, X. (2021). A rhodium-catalysed conjugate addition/cyclization cascade for the asymmetric synthesis of 2-amino-4H-chromenes. Organic and Biomolecular Chemistry, 19(4), 785–788. https://doi.org/10.1039/d0ob02404j
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