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2000
Volume 7, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

Pyrrolizidines were synthesized from 1,3-dipolar cycloaddition of N-substituted isatins, proline, and olefins. The highly diastereoselective and regioselective one-pot three-component cyclocondensation products were obtained in the presence of ionic liquids such as 1-buthyl-3-methlylimidazolium bromide.

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/content/journals/loc/10.2174/157017810791824946
2010-09-01
2025-10-03
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/content/journals/loc/10.2174/157017810791824946
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  • Article Type:
    Research Article
Keyword(s): 1,3-dipolar cycloaddition; diastereoselective; ionic liquid; isatine; Pyrrolizidines
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