CHIRAL OXETANES FROM SUGAR LACTONES - SYNTHESIS OF DERIVATIVES OF 3,5-ANHYDRO-1,2-O-ISOPROPYLIDENE-ALPHA-D-GLUCURONIC ACID AND OF 3,5-ANHYDRO-1,2-O-ISOPROPYLIDENE-BETA-L-IDURONIC ACID

CHIRAL OXETANES FROM SUGAR LACTONES - SYNTHESIS OF DERIVATIVES OF 3,5-ANHYDRO-1,2-O-ISOPROPYLIDENE-ALPHA-D-GLUCURONIC ACID AND OF 3,5-ANHYDRO-1,2-O-ISOPROPYLIDENE-BETA-L-IDURONIC ACID

Ring contraction reactions of triflates of α-hydroxy-γ-lactones provide an approach to the synthesis of chiral polyfunctionalised oxetanes from sugars. Treatment of 1,2-0-isopropylidene-5-0-trifluoromethanesulphonyl-α-D-glucuronolactone with benzylamine or with potassium carbonate in methanol gave r...

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Bibliographic Details
Main Authors:	Austin, G, Fleet, G, Peach, J, Prout, K, Son, J
Format:	Journal article
Language:	English
Published:	1987

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