Home / Publications / Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles

Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles

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Muzalevskiy V. M. et al. Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 17-19.
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Muzalevskiy V. M., Mamedzade M. N., Chertkov V. A., Bakulev V. A., Nenajdenko V. G. Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 17-19.
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TY - JOUR
DO - 10.1016/j.mencom.2018.01.003
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.003
TI - Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles
T2 - Mendeleev Communications
AU - Muzalevskiy, Vasilii Mikhailovich
AU - Mamedzade, Mansim Natig
AU - Chertkov, Vyacheslav Alekseevich
AU - Bakulev, Vasiliy Alekseevich
AU - Nenajdenko, Valentin Georgievich
PY - 2017
DA - 2017/12/22
PB - Mendeleev Communications
SP - 17-19
IS - 1
VL - 28
ER -
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@article{2017_Muzalevskiy,
author = {Vasilii Mikhailovich Muzalevskiy and Mansim Natig Mamedzade and Vyacheslav Alekseevich Chertkov and Vasiliy Alekseevich Bakulev and Valentin Georgievich Nenajdenko},
title = {Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles},
journal = {Mendeleev Communications},
year = {2017},
volume = {28},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.003},
number = {1},
pages = {17--19},
doi = {10.1016/j.mencom.2018.01.003}
}
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Muzalevskiy, Vasilii Mikhailovich, et al. “Reaction of CF3-ynones with azides. An efficient regioselective and metal-free route to 4-trifluoroacetyl-1,2,3-triazoles.” Mendeleev Communications, vol. 28, no. 1, Dec. 2017, pp. 17-19. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.003.

Abstract

[3+2] Cycloaddition of CF3-ynones with azides proceeds regioselectively to give 1-R-4-trifluoroacetyl-1H-1,2,3-triazoles as the major products.

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