42491-77-0Relevant articles and documents
Enantioselective Syntheses of (S)- and (R)-3-Hydroxypyrrolidin-2-ones via Lactate Dehydrogenase Catalysed Reductions of 4-Benzyloxycarbonylamino-2-oxobutanoic Acid
Bentley, Jonathan M.,Wadsworth, Harry J.,Willis, Christine L.
, p. 231 - 232 (2007/10/02)
The first examples of the BS- and SE-lactate dehydrogenase catalysed reductions of an α-keto acid incorporating a nitrogen containing function in the side chain are described: (S)- and (R)-benzyloxycarbonylamino-2-hydroxybutanoic acids were prepared in good yield and excellent enantioselectivities and were converted to the (S)- and (R)-3-hydroxypyrrolidin-2-ones respectively.
The preparation and biological activity of novel amino acid analogs of butirosin.
Haskell,Rodebaugh,Plessas,Watson,Westland
, p. 263 - 280 (2007/10/05)
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