The ring-opening reactions of methyl 3,4-anhydro-2,6-dideoxy-a-and -/3-L-IJIXOand -ribo-hexopyranosides with sodium azide, ammonia, methyl-and dimethylamine, and sodium methoxide were studied. Regioselectivity is explained in terms of steric and conformational factors. SOMMAIRE L'ouverture du cycle
Synthèses et réactivité avec des nucléophiles de sels de perfluoroalkylméthylèneoxy(trisdiméthylamino) phosphonium
✍ Scribed by Mohamed Allouch; Claude Selve
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 862 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0022-1139
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