2-STEP STEREOSELECTIVE CONVERSION OF 5-MONOSUBSTITUTED 1,3-DIOXOLAN-4-ONES INTO SELECTIVELY PROTECTED 2,3-ERYTHRO-1,2,3-TRIOLS - A ROUTE TO POLYHYDROXYLATED MOLECULES
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UNTERSTELLER, E
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ECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCEECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCE
UNTERSTELLER, E
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XIN, YC
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ECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCEECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCE
XIN, YC
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SINAY, P
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ECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCEECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCE
SINAY, P
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[1] ECOLE NORMALE SUPER,CNRS,DEPT CHIM,F-75231 PARIS 05,FRANCE
5-Monosubstituted 1,3-dioxolan-4-one 1 are stereoselectively converted into selectively protected 2,3-erythro-1,2,9-triols 3 via Tebbe methylenation, followed by hydroboration-oxidation.