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Polar cycloaddition reactions of some 2,3-disubstituted isoquinolinium salts

โœ Scribed by C. K. Bradsher; F. Howard Day

Book ID
112123105
Publisher
Journal of Heterocyclic Chemistry
Year
1974
Tongue
English
Weight
324 KB
Volume
11
Category
Article
ISSN
0022-152X

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Only a few reports deal with Diels-Alder or 1,3-dipolar cycloaddition reactions of glycals . For instance, azodicarboxylates undergo Diels-Alder cycloaddition with glycals to afford oxadiazines [2 -9]. The method allows the stereoselective introduction of a nitrogen atom on C-2 of a carbohydrate, an