FACIAL SELECTIVITY IN THE CYCLOADDITION OF HETERODIENES TO CARBOHYDRATE CYCLIC KETENE ACETALS - A NOVEL SYNTHESIS OF DISACCHARIDE DERIVATIVES

Authors
JOHNSON SC CRASTO C HECHT SM
Citation
Sc. Johnson et al., FACIAL SELECTIVITY IN THE CYCLOADDITION OF HETERODIENES TO CARBOHYDRATE CYCLIC KETENE ACETALS - A NOVEL SYNTHESIS OF DISACCHARIDE DERIVATIVES, Chemical communications, (9), 1998, pp. 1019-1020
Citations number
17
Categorie Soggetti
Chemistry
Journal title
Chemical communications → ACNP
ISSN journal
13597345
Issue
9
Year of publication
1998
Pages
1019 - 1020
Database
ISI
SICI code
1359-7345(1998):9<1019:FSITCO>2.0.ZU;2-S
Abstract
Carbohydrate ketene acetals derived from mannopyranose and glucopyrano se are shown to serve as electron-rich dienophiles in facially selecti ve, Lewis acid-catalyzed inverse electron demand hetero-Diels-Alder re actions.