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Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles

Mukattis Barievich Gazizov 1
Mukattis Barievich Gazizov
Rafail Asrarovich Khairullin 1
Rafail Asrarovich Khairullin
Alina Albertovna Minnikhanova 1
Alina Albertovna Minnikhanova
Anastasiya Ivanovna Alekhina 1
Anastasiya Ivanovna Alekhina
Rashid Zagitovich Musin 2
Rashid Zagitovich Musin
Published 2011-07-01
CommunicationVolume 21, Issue 4, 198-200
4
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Gazizov M. B. et al. Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles // Mendeleev Communications. 2011. Vol. 21. No. 4. pp. 198-200.
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Gazizov M. B., Khairullin R. A., Minnikhanova A. A., Alekhina A. I., Musin R. Z., Sinyashin O. G. Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles // Mendeleev Communications. 2011. Vol. 21. No. 4. pp. 198-200.
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TY - JOUR
DO - 10.1016/j.mencom.2011.07.009
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.009
TI - Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles
T2 - Mendeleev Communications
AU - Gazizov, Mukattis Barievich
AU - Khairullin, Rafail Asrarovich
AU - Minnikhanova, Alina Albertovna
AU - Alekhina, Anastasiya Ivanovna
AU - Musin, Rashid Zagitovich
AU - Sinyashin, Oleg Gerol'dovich
PY - 2011
DA - 2011/07/01
PB - Mendeleev Communications
SP - 198-200
IS - 4
VL - 21
ER -
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@article{2011_Gazizov,
author = {Mukattis Barievich Gazizov and Rafail Asrarovich Khairullin and Alina Albertovna Minnikhanova and Anastasiya Ivanovna Alekhina and Rashid Zagitovich Musin and Oleg Gerol'dovich Sinyashin},
title = {Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.009},
number = {4},
pages = {198--200},
doi = {10.1016/j.mencom.2011.07.009}
}
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Gazizov, Mukattis Barievich, et al. “Phosphorylated aziridinium salts: synthesis and ring opening with nucleophiles.” Mendeleev Communications, vol. 21, no. 4, Jul. 2011, pp. 198-200. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.07.009.

Abstract

Treatment of 1-tert-butyl-2-dimethoxyphosphoryl-3,3-dimethylaziridine with picric, perchloric or fluoboric acid affords the stable corresponding aziridinium salts, which are prone to undergo ring opening on reaction with alcohols, carboxylate and thiocyanate ions.

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