Abstract
A regioselective synthesis of trisubstituted 1,2,4-triazoles through reaction of nitrile imines with guanidine derivatives is described. These 1,3-dipolar cycloaddition reactions proceeded smoothly in moderate to good yields and excellent regioselectivity under ambient conditions. This method provides fast access to a range of functionalized 3-amino-1,2,4-triazoles.
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We thank the Research Council of Tarbiat Modares University for supporting this work.
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Yavari, I., Taheri, Z. & Sheikhi, S. A synthesis of functionalized 3-amino-1,2,4-triazoles from nitrile imines and guanidine derivatives. Mol Divers 28, 11–18 (2024). https://doi.org/10.1007/s11030-022-10471-z
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DOI: https://doi.org/10.1007/s11030-022-10471-z