Thermal-Mediated Synthesis of Hydantoin Derivatives from Amino Acids via Carbodiimide Reagents

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Georg Thieme Verlag Kg

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info:eu-repo/semantics/closedAccess

Özet

We introduce an innovative methodology for synthesizinghydantoins from amino acids using readily available carbodiimides, em-phasizing the crucial role of temperature in the reaction process. Thisapproach presents significant advantages over conventional methodsinvolving isocyanates, facilitating easier handling and minimizing asso-ciated risks. Our strategy not only allows for the efficient production ofa diverse array of hydantoin derivatives but also adheres to environ-mentally sustainable practices. The optimized reaction conditions enhance efficiency, marking a significant advancement in the field of organic synthesis. This method presents significant advantages for industrial applications, as it is a heat-mediated process that does not re-quire the use of any bases or catalysts. By eliminating the need for additional reagents, this approach simplifies the reaction conditions, reduces potential side reactions, and minimizes the overall environmental impact. Additionally, the absence of catalysts streamlines the purification process, making it more cost-effective and efficient for large-scale production.

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hydantoin, carbodiimide, amino acid, urea, N-heterocyclic organic compound

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Synlett

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36

Sayı

10

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Onay

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