Asymmetric synthesis of polyacetate derived building blocks with α-oxyanion functionality.: Lewis acid catalyzed opening of 2,9-dioxabicyclo[3.3.1]nonan-3-ones
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作者:
Dunkel, R
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Leibniz Univ Hannover, Dept Organ Chem, D-30167 Hannover, GermanyLeibniz Univ Hannover, Dept Organ Chem, D-30167 Hannover, Germany
Dunkel, R
[1
]
Hoffmann, HMR
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Leibniz Univ Hannover, Dept Organ Chem, D-30167 Hannover, GermanyLeibniz Univ Hannover, Dept Organ Chem, D-30167 Hannover, Germany
Hoffmann, HMR
[1
]
机构:
[1] Leibniz Univ Hannover, Dept Organ Chem, D-30167 Hannover, Germany
All four stereoisomeric cyclic 3,5,7-trihydroxyheptanoic acid equivalents of the polyacetate aldol type (Scheme 1) are obtainable from 8-oxabicyclo[3.2.1]octd-en-3-one which functions as a meso-configurated 4-way optical switch. Lewis acid assisted nucleophilic ring opening of anomeric [3.3.1] oxabicyclic lactones is a key step. The utility of the methodology is exemplified by a 6 step synthesis of the C17-C23 fragment of spongistatin (altohyrtin) and C-glycoside analogues. (C) 1999 Elsevier Science Ltd. All rights reserved.