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Published in 2022 at "Chemical communications"
DOI: 10.1039/d1cc06975f
Abstract: We report that the use of a diaminoalkyne in the azide-alkyne cycloaddition with aryl azides leads to 3H-indoles under mild, uncatalysed conditions. Computations reveal that N2 extrusion from, in one case, isolable triazoles is facile,…
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Keywords:
cycloadditions electronically;
activated alkyne;
alkyne cycloadditions;
electronically activated ... See more keywords