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Stereoselectivity in the cycloaddition reactions of 2-ethoxy-3-methylisoquinolinium salts

✍ Scribed by Chen, Teh-Kuei; Bradsher, Charles K.


Book ID
127136457
Publisher
American Chemical Society
Year
1979
Tongue
English
Weight
516 KB
Volume
44
Category
Article
ISSN
0022-3263

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Cycloaddition Reactions of 1,3-Diaza-2-a
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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