Abstract
It has been established that the iodocyclization of 2-allythio-4-(3H)-pyrimidinones occurs at the N(1) nitrogen atom with the formation of 3-iodomethyl-7-oxo-2,3-dihydro-8H-thiazolo[3,2-d]pyrimidinium iodides and triiodides.
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Additional information
Chelyabinsk State University, Chelyabinsk, 454136. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 211–213, February, 1995. Original articel submitted January 26, 1995.
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Khim, D.G., Shmygarev, V.I. Iodocyclization of 2-allythio-4(3H)-pyrimidinones. Chem Heterocycl Compd 31, 183–185 (1995). https://doi.org/10.1007/BF01169677
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DOI: https://doi.org/10.1007/BF01169677