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Transformation of “Masked” 1,3-Diols of 1,2-O-Isopropylidene-α-D-Erythro-Hexofuranose into Acyclic Forms. Chirons for Amphotericin B |
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| Authors: | David Woei-Ming Liang Bert Fraser-Reid |
| Abstract: | 3,5-Dideoxy-1,2-O-isopropylidene-α-D-erythro-hexofuranose 1 was readily converted to dithianyl amide 8, which is a convenient acyclic form of 1,3-diol, in high yield. |
| Keywords: | Carbohydrate 1 3-Diol Hexofuranose Chirons Amphotericin B |