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CuI-mediated modification of polyamines with fluorophore groups

Maksim Viktorovich Anokhin 1
Maksim Viktorovich Anokhin
Alexei Dmitrievich Averin 1
Alexei Dmitrievich Averin
Svetlana Petrovna Panchenko 1
Svetlana Petrovna Panchenko
Olga Aleksandrovna Maloshitskaya
Published 2015-07-08
CommunicationVolume 25, Issue 4, 245-247
3
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Anokhin M. V. et al. CuI-mediated modification of polyamines with fluorophore groups // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 245-247.
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Anokhin M. V., Averin A. D., Panchenko S. P., Maloshitskaya O. A., Beletskaya I. P. CuI-mediated modification of polyamines with fluorophore groups // Mendeleev Communications. 2015. Vol. 25. No. 4. pp. 245-247.
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TY - JOUR
DO - 10.1016/j.mencom.2015.07.002
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.002
TI - CuI-mediated modification of polyamines with fluorophore groups
T2 - Mendeleev Communications
AU - Anokhin, Maksim Viktorovich
AU - Averin, Alexei Dmitrievich
AU - Panchenko, Svetlana Petrovna
AU - Maloshitskaya, Olga Aleksandrovna
AU - Beletskaya, Irina Petrovna
PY - 2015
DA - 2015/07/08
PB - Mendeleev Communications
SP - 245-247
IS - 4
VL - 25
ER -
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@article{2015_Anokhin,
author = {Maksim Viktorovich Anokhin and Alexei Dmitrievich Averin and Svetlana Petrovna Panchenko and Olga Aleksandrovna Maloshitskaya and Irina Petrovna Beletskaya},
title = {CuI-mediated modification of polyamines with fluorophore groups},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.002},
number = {4},
pages = {245--247},
doi = {10.1016/j.mencom.2015.07.002}
}
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Anokhin, Maksim Viktorovich, et al. “CuI-mediated modification of polyamines with fluorophore groups.” Mendeleev Communications, vol. 25, no. 4, Jul. 2015, pp. 245-247. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.07.002.

Abstract

Copper(i)-catalyzed amination of halonaphthalenes and 6-bromoquinoline with α,ω-diamines A[(CH2)3NH2]2 [A = NH, NH(NH2)2NH, O(CH2CH2O)2] affords α-mono- and/or α,ω-disubstitution products.

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