Thiazole Masked Chiral Butanals from D-Glyceraldehyde Acetonide and 2-Trimethylsilylthiazole

DOI: 10.1055/s-1988-27671

Source and publish data:

Synthesis p. 685 - 689 (1988)

Update date:2022-07-30

Topics: Synthesis Yield NMR spectroscopy Reactants Chiral Resolution Thiazole D-Glyceraldehyde Acetonide

Authors:

Dondoni, Alessandro

Fantin, Giancarlo

Fogagnolo, Marco

Medici, Alessandro

Pedrini, Paola

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Article abstract of DOI:10.1055/s-1988-27671

1,2-O-Isopropylidene-3-(2-thiazolyl) glycerol 3 (thiazole D-erythrose) obtained from (R)-2,3-O-isopropylideneglyceraldehyde (1) and 2-trimethylsilylthiazole (2) is elaborated into thiazole-masked chiral hydroxy-, epoxy-, and azidobutanals.

Full text of DOI:10.1055/s-1988-27671

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