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Aza-Henry reaction with perfluoroalkylated cyclic ketimines

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Kutovaya I. V., Shmatova O. I., Nenajdenko V. G. Aza-Henry reaction with perfluoroalkylated cyclic ketimines // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 81-82.
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Kutovaya I. V., Shmatova O. I., Nenajdenko V. G. Aza-Henry reaction with perfluoroalkylated cyclic ketimines // Mendeleev Communications. 2017. Vol. 28. No. 1. pp. 81-82.
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TY - JOUR
DO - 10.1016/j.mencom.2018.01.027
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.027
TI - Aza-Henry reaction with perfluoroalkylated cyclic ketimines
T2 - Mendeleev Communications
AU - Kutovaya, Irina Valerievna
AU - Shmatova, Olga I
AU - Nenajdenko, Valentin Georgievich
PY - 2017
DA - 2017/12/22
PB - Mendeleev Communications
SP - 81-82
IS - 1
VL - 28
ER -
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@article{2017_Kutovaya,
author = {Irina Valerievna Kutovaya and Olga I Shmatova and Valentin Georgievich Nenajdenko},
title = {Aza-Henry reaction with perfluoroalkylated cyclic ketimines},
journal = {Mendeleev Communications},
year = {2017},
volume = {28},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.027},
number = {1},
pages = {81--82},
doi = {10.1016/j.mencom.2018.01.027}
}
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Kutovaya, Irina Valerievna, et al. “Aza-Henry reaction with perfluoroalkylated cyclic ketimines.” Mendeleev Communications, vol. 28, no. 1, Dec. 2017, pp. 81-82. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.01.027.

Abstract

Aza-Henry reaction of 5-, 6- and 7-membered cyclic imines bearing perfluorinated group with nitroalkanes affords the corresponding nitro amines in up to 95% yield. Subsequent reduction of nitro group gives perfluoroalkyl-equipped vicinal diamines.

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