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- W2094974762 abstract "Abstract trans‐β‐Phenylglycidic esters undergo ring opening when treated in tert‐butyl alcohol with primary amines (R–NH2, with R = secondary group or tertiary group), which attacks epoxide exclusively at C‐3 and avoids aminolysis of the ester group affording the erythro‐β‐amino‐α‐hydroxy esters as the sole product." @default.
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- W2094974762 date "2004-12-31" @default.
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- W2094974762 title "A Simple and Direct Synthesis of Erythro‐β‐amino‐α‐hydroxy Esters fromtrans‐β‐Phenylglycidic Ester" @default.
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- W2094974762 doi "https://doi.org/10.1081/scc-120038499" @default.
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