Highly Stereoselective 1,4-Conjugate Addition of Organocopper Reagents to Methyl -D-Glucopyranoside Derivativ
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文摘
The 1,4-conjugate additions of a variety of organocopper reagents to some 4-O-crotonyl derivatives of methyl -D-glucopyranoside proceededwith a high level of diastereochemical induction to provide the adducts carrying a -substituted butanoic ester at C-4. The 1,4-conjugateaddition to a 6-O-crotonyl derivative afforded the adduct with reverse configuration at the -carbon to that obtained from the 4-O-crotonylderivatives.

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