Facial selectivity in the cycloaddition of heterodienes to carbohydrate cyclic ketene acetals. A novel synthesis of disaccharide derivatives
Chemical Communications Pub Date: 1900-01-01 DOI: 10.1039/A800103K
Abstract
Carbohydrate ketene acetals derived from mannopyranose and glucopyranose are shown to serve as electron-rich dienophiles in facially selective, Lewis acid-catalyzed inverse electron demand hetero-Diels–Alder reactions.
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Journal Name：Chemical Communications
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CAS no.: 89640-58-4
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