Open Access
RSC Advances, volume 10, issue 24, pages 14122-14133
Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes
Filatov Vadim
1
,
Kukushkin Maksim
1
,
Kuznetsova Juliana
1
,
Skvortsov Dmitry
1, 2
,
Tafeenko Viktor
1
,
Zyk Nikolay
1
,
Majouga Alexander
1, 3, 4
,
2
Publication type: Journal Article
Publication date: 2020-04-06
General Chemistry
General Chemical Engineering
Abstract
Two experimental techniques of the ketene–imine Staudinger reaction allowed different diastereomers of spiro-indolinone-β-lactams to be obtained.
Citations by journals
1
|
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ACS Omega
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ACS Omega
1 publication, 10%
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International Journal of Molecular Sciences
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International Journal of Molecular Sciences
1 publication, 10%
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Mendeleev Communications
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Mendeleev Communications
1 publication, 10%
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Molecules
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Molecules
1 publication, 10%
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Chinese Chemical Letters
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Chinese Chemical Letters
1 publication, 10%
|
European Journal of Medicinal Chemistry
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European Journal of Medicinal Chemistry
1 publication, 10%
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Advanced Synthesis and Catalysis
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Advanced Synthesis and Catalysis
1 publication, 10%
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ChemistrySelect
|
ChemistrySelect
1 publication, 10%
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Journal of Biomolecular Structure and Dynamics
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Journal of Biomolecular Structure and Dynamics
1 publication, 10%
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AIP Conference Proceedings
|
AIP Conference Proceedings
1 publication, 10%
|
1
|
Citations by publishers
1
2
3
|
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Elsevier
|
Elsevier
3 publications, 30%
|
Multidisciplinary Digital Publishing Institute (MDPI)
|
Multidisciplinary Digital Publishing Institute (MDPI)
2 publications, 20%
|
Wiley
|
Wiley
2 publications, 20%
|
American Chemical Society (ACS)
|
American Chemical Society (ACS)
1 publication, 10%
|
Taylor & Francis
|
Taylor & Francis
1 publication, 10%
|
American Institute of Physics (AIP)
|
American Institute of Physics (AIP)
1 publication, 10%
|
1
2
3
|
- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Filatov V. et al. Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes // RSC Advances. 2020. Vol. 10. No. 24. pp. 14122-14133.
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Filatov V., Kukushkin M., Kuznetsova J., Skvortsov D., Tafeenko V., Zyk N., Majouga A., Beloglazkina E. K. Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes // RSC Advances. 2020. Vol. 10. No. 24. pp. 14122-14133.
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TY - JOUR
DO - 10.1039/D0RA02374D
UR - https://doi.org/10.1039%2FD0RA02374D
TI - Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes
T2 - RSC Advances
AU - Filatov, Vadim
AU - Kukushkin, Maksim
AU - Kuznetsova, Juliana
AU - Skvortsov, Dmitry
AU - Tafeenko, Viktor
AU - Zyk, Nikolay
AU - Majouga, Alexander
AU - Beloglazkina, Elena K.
PY - 2020
DA - 2020/04/06 00:00:00
PB - Royal Society of Chemistry (RSC)
SP - 14122-14133
IS - 24
VL - 10
SN - 2046-2069
ER -
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@article{2020_Filatov
author = {Vadim Filatov and Maksim Kukushkin and Juliana Kuznetsova and Dmitry Skvortsov and Viktor Tafeenko and Nikolay Zyk and Alexander Majouga and Elena K. Beloglazkina},
title = {Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes},
journal = {RSC Advances},
year = {2020},
volume = {10},
publisher = {Royal Society of Chemistry (RSC)},
month = {apr},
url = {https://doi.org/10.1039%2FD0RA02374D},
number = {24},
pages = {14122--14133},
doi = {10.1039/D0RA02374D}
}
Cite this
MLA
Copy
Filatov, Vadim, et al. “Synthesis of 1,3-diaryl-spiro[azetidine-2,3′-indoline]-2′,4-diones: Via the Staudinger reaction: Cis - Or trans -diastereoselectivity with different addition modes.” RSC Advances, vol. 10, no. 24, Apr. 2020, pp. 14122-14133. https://doi.org/10.1039%2FD0RA02374D.