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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
The conversion also occurs with serine methylester but it decomposes very quickly.
📌 3 Key Takeaways
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Objective & Hypothesis:The conversion of the amino group of amino dicarboxylicacid esters and an aryl amine into N-substituted pyrrolinone derivatives with dimethoxydihydrofurane is described.
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Key Findings & Data:The conversion of the amino group of amino dicarboxylicacid esters and an aryl amine into N-substituted pyrrolinone derivatives with dimethoxydihydrofurane is described.
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Conclusion & Impact:The conversion also occurs with serine methylester but it decomposes very quickly.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Pyrrolinone · synthesis · amino acids
Abstract
The conversion of the amino group of amino dicarboxylicacid esters and an aryl amine into N-substituted pyrrolinone derivatives with dimethoxydihydrofurane is described. The conversion also occurs with serine methylester but it decomposes very quickly.
Özet
The conversion of the amino group of amino dicarboxylicacid esters and an aryl amine into N-substituted pyrrolinone derivatives with dimethoxydihydrofurane is described. The conversion also occurs with serine methylester but it decomposes very quickly.
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Cite This Article
SAYGILI, N., AYDOĞAN, C. (2012). Synthesis of 3-pyrroline-2-ones from amino acids and an aryl amine. Turkish Journal of Chemistry, Cilt: 36 - Sayı: 6, 860–866. https://ajindex.com/articles/184815