Enantioselective Synthesis of (+)-Estrone Exploiting a Hydrogen Bond-Promoted Diels−Alder Reaction
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https://figshare.com/articles/dataset/Enantioselective_Synthesis_of_Estrone_Exploiting_a_Hydrogen_Bond_Promoted_Diels_Alder_Reaction/2012910
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资源简介：
Starting from Dane’s diene and methylcyclopentenedione, (+)-estrone is synthesized along the Quinkert−Dane route in 24% total yield. The key step is an enantioselective Diels−Alder reaction promoted by an amidinium catalyst as efficiently as by a traditional Ti-TADDOLate Lewis acid.
创建时间：
2015-12-16
