Enantiocontrolled Total Syntheses of Breviones A, B, and C
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https://figshare.com/articles/dataset/Enantiocontrolled_Total_Syntheses_of_Breviones_A_B_and_C/2642314
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Enantiocontrolled total syntheses of the breviones A, B, and C have been accomplished using a highly diastereoselective oxidative coupling of an α-pyrone with a tricyclic diene prepared from an optically pure Wieland–Miescher ketone derivative through the 7-endo-trig mode of acyl radical cyclization.
创建时间：
2016-02-23
