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- W2013828399 abstract "O-(p-Biphenoyl)-N-tosyl-(l)-allo-threonine methyl ester is synthesized in three steps (65% overall yield) starting from commercially available (l)-allo-threonine methyl ester hydrochloride by N-acylation followed by N,O-acyl migration with inversion of the β carbinol carbon and N-tosylation. Treatment of the methyl ester with dibromophenylborane gives oxazaborolidinone 1, which can be used as a Lewis acid catalyst for the asymmetric Michael and Diels−Alder reactions." @default.
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- W2013828399 date "2006-01-07" @default.
- W2013828399 modified "2023-09-24" @default.
- W2013828399 title "Short and Practical Synthesis of <i>O</i>-(<i>p</i>-Biphenoyl)-<i>N-</i>tosyl-<i>a</i><i>llo</i>-threonine-Derived Oxazaborolidinone Catalyst" @default.
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- W2013828399 doi "https://doi.org/10.1021/jo0522299" @default.
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