Monoacetylation of Carbohydrate Diols via Transesterification with Ethyl Acetate
Monoacetylation of secondary diols in protected monosaccharides was achieved with ethyl acetate as acyl donor and sodium tert-butoxide as a base. The regioseletivity of the reaction varied depending on the substrate. This new method provides a simple, fast, and efficient method to access selectively acetylated carbohydrates that is compatible with acid-sensitive protecting groups.
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2019 ◽
Vol 34
(02)
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pp. 2055006
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2014 ◽
Vol 2014
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pp. 1-7
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1993 ◽
Vol 58
(7)
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pp. 1705-1710
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2016 ◽
Vol 11
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pp. 155892501601100
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