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Information Journal Paper

Title

STUDY OF ONE POT REACTION OF DIMEDONE AND NITRO BENZALDEHYDE IN THE PRESENT OR ABSENCE OF CYANOGEN BROMIDE

Pages

  51-55

Abstract

 Reaction of 1,3-dimethyl pyrimidine-(1H,3H,5H)-2,4,6-trione (1,3-dimethyl barbituric acid) with cyanogen bromide and aromatic dialdehydes in the presence of N-methyl Morpholine leads to the selective and efficient formation of a novel class of bifunctionalized linkaged heterocyclic stable bis-spiro [furo[2,3-d] pyrimidine-6,5'-pyrimidine] 2,2',4,4',6'(3H,3'H,5H)-pentaones which are dimeric forms of barbiturate (uracil and thiouracil derivatives) at the range of 0oC to ambient temperature. Structure elucidation was carried out by 1H NMR, 13C NMR and FT-IR spectroscopy. A proposed mechanism was discussed for the formation of products.

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    APA: Copy

    SHAHINFAR, ZAHRA, & JALILZADEH HEDAYATI, MOHAMMAD. (2012). STUDY OF ONE POT REACTION OF DIMEDONE AND NITRO BENZALDEHYDE IN THE PRESENT OR ABSENCE OF CYANOGEN BROMIDE. THE APPLICATION OF CHEMISTRY IN ENVIRONMENT, 3(9), 51-55. SID. https://sid.ir/paper/236350/en

    Vancouver: Copy

    SHAHINFAR ZAHRA, JALILZADEH HEDAYATI MOHAMMAD. STUDY OF ONE POT REACTION OF DIMEDONE AND NITRO BENZALDEHYDE IN THE PRESENT OR ABSENCE OF CYANOGEN BROMIDE. THE APPLICATION OF CHEMISTRY IN ENVIRONMENT[Internet]. 2012;3(9):51-55. Available from: https://sid.ir/paper/236350/en

    IEEE: Copy

    ZAHRA SHAHINFAR, and MOHAMMAD JALILZADEH HEDAYATI, “STUDY OF ONE POT REACTION OF DIMEDONE AND NITRO BENZALDEHYDE IN THE PRESENT OR ABSENCE OF CYANOGEN BROMIDE,” THE APPLICATION OF CHEMISTRY IN ENVIRONMENT, vol. 3, no. 9, pp. 51–55, 2012, [Online]. Available: https://sid.ir/paper/236350/en

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