ACCESS TO POLYHYDROXYLATED CYCLOHEPTANE DERIVATIVES THROUGH STEREOSELECTIVE NITRILE OXIDE INTRAMOLECULAR CYCLOADDITION - SYNTHESIS OF AN ANALOG OF CALYSTEGINE B-2
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DUCLOS, O
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UNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCEUNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCE
DUCLOS, O
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DUREAULT, A
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UNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCEUNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCE
DUREAULT, A
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DEPEZAY, JC
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UNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCEUNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCE
DEPEZAY, JC
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[1] UNIV PARIS 05,CNRS,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,45 RUE ST PERES,F-75270 PARIS 06,FRANCE
A hydroxymethyl substituted calystegine B2 has been synthesized stereoselectively by intramolecular cycloaddition of an olefinic nitrile oxide derived from D-glucose.