1,3-Dipolar Cycloaddition Reaction of Dibenzalaceton with Non-stabilized Azomethinylides: Synthesis of New Spirooxindolo(pyrrolizidines/ pyrrolidines)

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Abstract:

1,3-dipolar cycloaddition reaction of 1 mol or 2 mol of dibenzalaceton with 1 mol of non-stabilized azomethinylides generated in situ by decarboxylative condensation of isatin and proline or sarcosine give the novel new spiro-oxindolo(pyrrolizidines/ pyrrolidines) instead of bis-spirooxindolo( pyrrolizidines/ pyrrolidines).

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Journal title

International Journal of Bio-Inorganic Hybrid Nanomaterials

volume 2 issue 3

pages 457- 464

publication date 2013-10-01

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Keywords

1,3-Dipolar cycloaddition Azomethinylides Spiro-oxindolo(pyrrolizidines/ pyrrolidines) isatin Proline Sarcosine

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