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
✦ LIBER ✦
The crystal structure of ethyl 2,3-dideoxy-α-d-erythro-hex-2-enopyranoside
✍ Scribed by Lavinia M. Wingert; John R. Ruble; George A. Jeffrey
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 576 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0008-6215
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