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• W2953080911 endingPage "1495" @default.
• W2953080911 startingPage "1485" @default.
• W2953080911 abstract "Essentially, enantiopure syn- and anti-propionate aldol adducts were divergently synthesized using a novel strategy which utilizes both the highly enantioselective 1,3,2-oxazaborolidin-5-one-promoted aldol reaction with a ketene silyl acetal derived from ethyl 2-bromo propionate and a highly diastereoselective radical debromination reaction. These procedures provide yields that increase to a level available for practical synthesis." @default.
• W2953080911 created "2019-06-27" @default.
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• W2953080911 date "2001-08-01" @default.
• W2953080911 modified "2023-09-24" @default.
• W2953080911 title "A Divergent Synthesis of Essentially Enantiopuresyn- andanti-Propionate Aldol Adducts Based on the Chiral 1,3,2-Oxazaborolidin-5-one-Promoted Asymmetric Aldol Reaction Followed by Diastereoselective Radical Reduction" @default.
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• W2953080911 doi "https://doi.org/10.1246/bcsj.74.1485" @default.
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