Enantioselective synthesis of S-substituted ω-amino-α-thiohydroxycarboxylic acids via sulfenylation of 2-(ω-aminoalkyl)-oxazolines

DOI: 10.1016/S0957-4166(97)00259-0

Source and publish data:

Tetrahedron Asymmetry p. 2433 - 2446 (1997)

Update date:2022-08-04

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Authors:

Rottmann, Antje

Liebscher, Juergen

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Article abstract of DOI:10.1016/S0957-4166(97)00259-0

Optically active ω-benzenesulfonylamino-α-methylthio- and ω-benzenesulfonylamino-α-phenylthiocarboxylic acids 7 were synthesized by stereoselective α-sulfenylation of 2-(ω-benzenesulfonylaminoalkyl)-1,3-oxazolines 3 with disulfides in the presence of LDA,

Full text of DOI:10.1016/S0957-4166(97)00259-0

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Product name:Butanoic acid, 2-bromo-4-[(phenylsulfonyl)amino]-, (S)-

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