Study on iodocyclization of S-allyl derivatives of 3-mercapto- 1,2,4-triazoles

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It was found that the interaction between S-allyl derivatives of 3-mercapto-l,2,4-triazoles and iodine resulted in a mixture of several products of iodocyclization being formed (linear and angular closure of five-and six-membered rings). The structures of original and synthesized compounds were examined by gas chromatography-mass spectrometry and 1H NMR spectroscopy.

4-triazole, gas chromatography-mass spectrometry, 1h nmr spectroscopy, 3-(allylthio)-l, 5-methyl-3-(allylthio)-l, 5-tert-butyl-3-(allylthio)-1, l-acetyl-5-methyl-3-(allylthio)-l, iodocyclization

Короткий адрес: https://sciup.org/147160168

IDR: 147160168

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