Chemoenzymatic syntheses of each stereoisomer of (4,5)-epoxy-(2E)-hexenoates

DOI: 10.1016/0957-4166(96)00333-3

Source and publish data:

Tetrahedron Asymmetry p. 2595 - 2602 (1996)

Update date:2022-08-03

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Authors:

Ono, Machiko

Saotome, Chikako

Akita, Hiroyuki

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Article abstract of DOI:10.1016/0957-4166(96)00333-3

The highly stereoselective syntheses of each of the four stereoisomers of (4,5)-epoxy-(2E)-hexenoate ((4S,5S)-2, (4R,5R)-3 and (4R,5S)-3) based on a chemoenzymatic method were achieved from the achiral precursor, methyl sorbate.

Full text of DOI:10.1016/0957-4166(96)00333-3

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