T3P/DMSO is shown to be an effective and mild reagent for the one-pot synthesis of furo[2,3-d]pyrimidine-2,4(1H,3H)-diones from a variety of alcohols. Alcohols are oxidized in situ to aldehydes under mild conditions, which undergo a three-component reaction with N,N'-dimethylbarbituric acid and various isocyanides to afford furo[2,3-d]pyrimidine-2,4(1H,3H)-diones in good yields.
Soleimani, E., Khodaei, M. M., Yazdani, H., & Mohammad Nejhad, J. (2017). Synthesis of Furo[2,3-d]pyrimidine-2,4(1H,3H)-diones From Alcohols Using T3P/DMSO. Organic Chemistry Research, 3(1), 32-36. doi: 10.22036/org.chem..2017.50939.1053
MLA
Ebrahim Soleimani; Mohammad Mehdi Khodaei; Hossein Yazdani; Jafar Mohammad Nejhad. "Synthesis of Furo[2,3-d]pyrimidine-2,4(1H,3H)-diones From Alcohols Using T3P/DMSO". Organic Chemistry Research, 3, 1, 2017, 32-36. doi: 10.22036/org.chem..2017.50939.1053
HARVARD
Soleimani, E., Khodaei, M. M., Yazdani, H., Mohammad Nejhad, J. (2017). 'Synthesis of Furo[2,3-d]pyrimidine-2,4(1H,3H)-diones From Alcohols Using T3P/DMSO', Organic Chemistry Research, 3(1), pp. 32-36. doi: 10.22036/org.chem..2017.50939.1053
VANCOUVER
Soleimani, E., Khodaei, M. M., Yazdani, H., Mohammad Nejhad, J. Synthesis of Furo[2,3-d]pyrimidine-2,4(1H,3H)-diones From Alcohols Using T3P/DMSO. Organic Chemistry Research, 2017; 3(1): 32-36. doi: 10.22036/org.chem..2017.50939.1053
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