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Fullerene-Sensitized [2 + 3] Cycloaddition between Maleimides and Iminodiacetic Ester: Formation of Pyrrolidine Derivatives

Name: Fullerene-Sensitized [2 + 3] Cycloaddition between Maleimides and Iminodiacetic Ester: Formation of Pyrrolidine Derivatives
Published: 2000-02-11T00:00:00+00:00
License: https://creativecommons.org/licenses/by-nc/4.0/
Keywords: derivative, photolysi, maleimide, Ester, cycloaddition, dimethoxycarbonylpyrrolidine, Formation, dimethyliminodiacetate, Pyrrolidine Derivatives Fullerene catalyzes, Iminodiacetic, Maleimide, Cycloaddition

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posted on 2000-02-11, 00:00 authored by Yaru Shi, Liangbing Gan, Xiaolan Wei, Shi Jin, Sheng Zhang, Fanyu Meng, Zheming Wang, Chunhua Yan

Fullerene catalyzes the cycloaddition of dimethyliminodiacetate to maleimides under photolysis to form 2,5-dimethoxycarbonylpyrrolidine derivatives.

Fullerene-Sensitized [2 + 3] Cycloaddition between Maleimides and Iminodiacetic Ester: Formation of Pyrrolidine Derivatives

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