Enantioselective Ester Hydrolysis by Hydroxamic Acids of N-Benzyloxycarbonyl-L-amino Acids or Optically Active Amines in Cetyltrimethylammonium Bromide Micelles

DOI: 10.1021/jo01297a016

Source and publish data:

Journal of Organic Chemistry p. 1623 - 1625 (1980)

Update date:2022-08-05

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Authors:

Ihara, Hirotaka

Ono, Shuji

Shosenji, Hideto

Yamada, Kimiho

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Article abstract of DOI:10.1021/jo01297a016

Hydrolysis of p-nitrophenyl esters of amino acids by hydroxamic acids of N-benzyloxycarbonyl-L-amino acids or optically active amines of L-amino acids in the presence of CTABr micelles showed effective enantioselectivities (D/L = 2.51 and 2.65, respective

Full text of DOI:10.1021/jo01297a016

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