Expedient synthesis of (-)-(1S, 2R)-allonorcoronamic acid

DOI: 10.1016/0957-4166(95)00446-7

Source and publish data:

Tetrahedron Asymmetry p. 283 - 284 (1996)

Update date:2022-08-11

Topics:

Authors:

Hercouet, Alain

Bessieres, Bernard

Le Corre, Maurice

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Article abstract of DOI:10.1016/0957-4166(95)00446-7

The title amino acid was synthesized in enantiomerically pure form, starting from (S)-(+)-1,2-propanediol 2 in three steps, by condensation of cyclic sulfate 3 with methyl benzylideneglycinate.

Full text of DOI:10.1016/0957-4166(95)00446-7

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Product name:1,3,2-Dioxathiolane, 4-methyl-, 2,2- dioxide, (4S)-

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