Publication: Facile synthesis of N-aroylurea analogs as potential antioxidants
Issued Date
2009-01-01
Resource Type
ISSN
1450202X
1450216X
1450216X
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2-s2.0-67649111441
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Mahidol University
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SCOPUS
Bibliographic Citation
European Journal of Scientific Research. Vol.31, No.4 (2009), 510-518
Suggested Citation
Kitti Amornraksa, Apilak Worachartcheewan, Virapong Prachayasittikul Facile synthesis of N-aroylurea analogs as potential antioxidants. European Journal of Scientific Research. Vol.31, No.4 (2009), 510-518. Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/27075
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Title
Facile synthesis of N-aroylurea analogs as potential antioxidants
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Abstract
N,N'-Dicyclohexylcarbodiimide (DCC) is a widely used dehydrating and oxidizing agents for the synthesis such as proteins, amides and esters. The study reports synthetic application of the DCC to form N-aroylurea analogs and their antioxidant activity. Results showed that N-benzoyl-N,N'-dicyclohexylurea (Ia), N,N'-dicyclohexyl-N-3,5-dinitrobenzoylurea (Ib) and N,N'-dicyclohexyl-N-[(E)-3-phenylacryloyl]urea (Ic) were readily accomplished by facile one pot reaction of DCC with benzoic or cinnamic acid in the presence of triethylamine. The reaction took place via rearrangement of O-aroylurea intermediate to furnish relatively good yields of the analogs Ia-c. In addition, at 200 μg/mL, the urea analog Ic starts to mimic superoxide scavenging activity. © EuroJournals Publishing, Inc. 2009.