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Application of the asymmetric hetero Diels-Alder reaction for synthesising carbohydrate derivatives and glycosidase inhibitors

Osborn, H.M.I. and Coisson, D. (2004) Application of the asymmetric hetero Diels-Alder reaction for synthesising carbohydrate derivatives and glycosidase inhibitors. Mini-Reviews in Organic Chemistry, 1 (1). pp. 41-54. ISSN 1570-193X

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To link to this item DOI: 10.2174/1570193043488953

Abstract/Summary

This review provides a discussion of recent developments in the asymmetric hetero Diels-Alder reaction (AHDAR), with particular emphasis on the synthesis of carbohydrates, their derivatives, and inhibitors of carbohydrate processing enzymes.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
ID Code:11539
Uncontrolled Keywords:heterodiene, heterodienophile, stereocontrol, enantiocontrol, diastereocontrol, INVERSE ELECTRON DEMAND, NITROSO-COMPOUNDS, METHYL, (E)-4-METHOXY-2-OXO-3-BUTENOATE, ENANTIOSELECTIVE SYNTHESIS, STRAIGHTFORWARD SYNTHESIS, CYCLOADDITION REACTIONS, ALUMINUM COMPLEXES, CHIRAL AUXILIARIES, CARBONYL-COMPOUNDS, ACTIVATED DIENES

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