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note
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Triazoles are known to undergo tautomerism. From the X-ray crystal studies of the compounds reported in this manuscript, it is clear that the position of the NH is dependent on the substituents on the triazole ring. Hence, for consistency in the drawings of our figures and schemes, we have placed all the NH on position 2.
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23
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note
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Attempts to carry out the cycloaddition with organic azides did not give the desired triazole, and the starting materials were recovered.
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