A Practical Synthetic Route to Enantiopure 3-Aryloxy-1,2-propanediols from Chiral Glycidol

DOI: 10.1016/0040-4039(95)00282-H

Source and publish data:

Tetrahedron Letters p. 2379 - 2380 (1995)

Update date:2022-08-22

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Authors:

Chen, Jian

Shum, Wilfred

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Article abstract of DOI:10.1016/0040-4039(95)00282-H

Chiral 3-aryloxy-1,2-propanediols of >98percent ee can be obtained in high yield by the nucleophilic addition of substituted phenols to chiral glycidol in the presence of triethylamine catalyst followed by recrystallization in absolute ethanol.Several enantiopure compounds of pharmaceutical significance are presented as examples.

Full text of DOI:10.1016/0040-4039(95)00282-H

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