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New polyhydroxylated pyrrolidines derived from enantiopure 3,6-dihydro-2H-1,2-oxazines
Authors:Pulz Robert  Al-Harrasi Ahmed  Reissig Hans-Ulrich
Affiliation:Institut für Chemie - Organische Chemie, Freie Universit?t Berlin, Takustrasse 3, D-14195 Berlin, Germany.
Abstract:[reaction: see text] Diastereoselective hydroborations of enantiopure 3,6-dihydro-2H-1,2-oxazines led to dihydroxy-substituted 1,2-oxazines. Samarium diiodide-induced N-O bond cleavage generated 1,4-amino alcohols which were recyclized to polyhydroxylated pyrrolidines which are potential glycosidase inhibitors.
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