Abstract
The present investigation reports an easy access to a library of novel spiro-oxindole-pyrrolizine or pyrrolo[1,2-c]thiazole fused coumarin hybrid heterocycles through a one-pot sequential four-component reactions of 2,2-dimethyl-1,3-dioxane-4,6-dione, salicylaldehydes, isatins, and cyclic α-amino acids under ultrasound irradiation.
Keywords:
1,3-dipolar cycloaddition; coumarin; pyrrolizine; pyrrolothiazole; sequential; spiro-oxindole.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acids / chemistry
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Combinatorial Chemistry Techniques / methods*
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Coumarins / chemical synthesis*
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Coumarins / chemistry
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Heterocyclic Compounds / chemical synthesis
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Indicators and Reagents
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Models, Molecular
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Molecular Conformation
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Spiro Compounds / chemistry
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Ultrasonics / methods*
Substances
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Amino Acids
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Coumarins
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Heterocyclic Compounds
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Indicators and Reagents
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Spiro Compounds