## Abstract Reaction of 1,4โanhydroโ2,3,5โtriโ__O__โbenzylโ1โdeoxyโ1โiminoโDโarabinitol __N__โoxide (**8**) with allyl alcohol produced a 3.6โ:โ1 mixture of the two pyrrolo[1,2โ__b__]isoxazole derivatives **13** and **14**. The major adduct **13** was converted to 7โdeoxycasuarine (**7**), a potent
โฆ LIBER โฆ
Synthesis and inhibitory activity of glycosidase inhibitors, glycosylamino-oxazolines
โ Scribed by Chikara Uchida; Seiichiro Ogawa
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 542 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0968-0896
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โฆ Synopsis
In connection with structural modification of the trehalase inhibitor trehazolin (1), as a new-type of glycohydrolase inhibitor, some glycosylamino-oxazolines were designed and synthesized. Among three oxazolines beta-galacto (3), beta-gluco (5) and alpha-manno-types (6) obtained in stable form, the latter 6 has been shown to possess a moderate inhibitory activity against alpha-mannosidase.
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