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Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds

Alexey Mikhailovich Starosotnikov 1
Alexey Mikhailovich Starosotnikov
, 
Dmitry Vladimirovich Shkaev 1
Dmitry Vladimirovich Shkaev
, 
Maxim Aleksandrovich Bastrakov 1
Maxim Aleksandrovich Bastrakov
,  , 
Svyatoslav Arkad'evich Shevelev 1
Svyatoslav Arkad'evich Shevelev
, 
Igor L'vovich Dalinger 1
Igor L'vovich Dalinger
10.1016/j.mencom.2018.11.025
Published 2018-11-01
Communication , Volume 28, Issue 6, 638-640
21
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Starosotnikov A. M. et al. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 638-640.
GOST all authors (up to 50) Copy
Starosotnikov A. M., Shkaev D. V., Bastrakov M. A., Fedyanin I. V., Shevelev S. A., Dalinger I. L. Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds // Mendeleev Communications. 2018. Vol. 28. No. 6. pp. 638-640.
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TY - JOUR
DO - 10.1016/j.mencom.2018.11.025
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.025
TI - Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds
T2 - Mendeleev Communications
AU - Starosotnikov, Alexey Mikhailovich
AU - Shkaev, Dmitry Vladimirovich
AU - Bastrakov, Maxim Aleksandrovich
AU - Fedyanin, Ivan Vladimirovich
AU - Shevelev, Svyatoslav Arkad'evich
AU - Dalinger, Igor L'vovich
PY - 2018
DA - 2018/11/01
PB - Mendeleev Communications
SP - 638-640
IS - 6
VL - 28
ER -
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@article{2018_Starosotnikov,
author = {Alexey Mikhailovich Starosotnikov and Dmitry Vladimirovich Shkaev and Maxim Aleksandrovich Bastrakov and Ivan Vladimirovich Fedyanin and Svyatoslav Arkad'evich Shevelev and Igor L'vovich Dalinger},
title = {Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds},
journal = {Mendeleev Communications},
year = {2018},
volume = {28},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.025},
number = {6},
pages = {638--640},
doi = {10.1016/j.mencom.2018.11.025}
}
MLA
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Starosotnikov, Alexey Mikhailovich, et al. “Dearomatization of oxa- or selenadiazolopyridines with neutral nucleophiles as an efficient approach to pharmacologically relevant nitrogen compounds.” Mendeleev Communications, vol. 28, no. 6, Nov. 2018, pp. 638-640. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2018.11.025.

Abstract

Highly electrophilic 6-nitro-4-azabenzofuroxan and 6-nitro-4-azabenzo[1,2,5]selenadiazole add π-excessive (het)arenes and other neutral nucleophiles at 7-position to give C–C and N–C-bonded adducts, 1,4-dihydropyridines fused with furoxan or selenadiazole ring.

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