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• W2100136287 startingPage "2718" @default.
• W2100136287 abstract "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." @default.
• W2100136287 created "2016-06-24" @default.
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• W2100136287 date "2010-03-19" @default.
• W2100136287 modified "2023-10-12" @default.
• W2100136287 title "Enantioselective Synthesis of (+)-Estrone Exploiting a Hydrogen Bond-Promoted Diels−Alder Reaction" @default.
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• W2100136287 doi "https://doi.org/10.1021/jo100053j" @default.
• W2100136287 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2852147" @default.
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