Reactions of methyl 4,6-O-benzylidene-2,3-dideoxy-3-nitro-α- and-β-d-erythro-hex-2-enopyranosides with phenylacetonitrile: Preparation and structural determination of adducts and an isoxazole derivative
✍ Scribed by Tohru Sakakibara; Rokuro Sudoh
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 522 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0008-6215
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## Nucleophilic addition-reactions of the title compound, prepared from the corresponding 3-nitrohex-2-enitol, were investigated under kinetically controlled conditions; such sterically bulky nucleophiles as tert-butyl peroxide and 2,4-pentanedionate ions (except in 1,Cdioxane) were found to enga
IZUMI TAKAI, YOSHIFUSA TACHIMORI, AZUMA YAMAMOTO, YOSHIHARU ISHIDO\*, AND (the late) ROKURO SUWH
4,6-Di-O-acetyl-2,3-dideoxy-D-erythro-hex-2-enopyranose (4,6-di-o-acetyl-D-pseudoglucal), prepared from 3,4,6-tri-O-acetyl-1,5-anhydro-2-deoxy-D-arubinohex-1-enitol (tri-0-acetyl-D-glucal), was condensed, by catalysis with boron trifluoride, with an equivalent of the original glycal, to give crystal