Tetrahedron Letters, volume 58, issue 42, pages 3993-3997
Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade
Publication type: Journal Article
Publication date: 2017-10-01
Journal:
Tetrahedron Letters
Quartile SCImago
Q3
Quartile WOS
Q3
Impact factor: 1.8
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Abstract A simple, general, and regioselective method has been developed for the synthesis of a series of heteroarylfuroxans, including isoxazolyl-, isoxazolinyl- and (1,2,4-oxadiazolyl)furoxans. The described method is based on a cascade of one-pot processes, including the nitration of furoxancarbaldehyde oximes, thermolysis of the formed nitrolic acids to generate furoxancarbonitrile oxides, and [3+2]-cycloaddition with an appropriate dipolarophile – alkynes, olefins, or activated nitriles.
Citations by journals
1
2
3
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Mendeleev Communications
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Mendeleev Communications
3 publications, 25%
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Synthesis
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Synthesis
1 publication, 8.33%
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Advanced Synthesis and Catalysis
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Advanced Synthesis and Catalysis
1 publication, 8.33%
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Tetrahedron Letters
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Tetrahedron Letters
1 publication, 8.33%
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Asian Journal of Organic Chemistry
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Asian Journal of Organic Chemistry
1 publication, 8.33%
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Structural Chemistry
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Structural Chemistry
1 publication, 8.33%
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Russian Chemical Reviews
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Russian Chemical Reviews
1 publication, 8.33%
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Synlett
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Synlett
1 publication, 8.33%
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Comprehensive Heterocyclic Chemistry IV
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Comprehensive Heterocyclic Chemistry IV
1 publication, 8.33%
|
1
2
3
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Citations by publishers
1
2
3
4
5
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Elsevier
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Elsevier
5 publications, 41.67%
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Thieme
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Thieme
2 publications, 16.67%
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Wiley
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Wiley
2 publications, 16.67%
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Springer Nature
|
Springer Nature
1 publication, 8.33%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 8.33%
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1
2
3
4
5
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- 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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Larin A. et al. Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade // Tetrahedron Letters. 2017. Vol. 58. No. 42. pp. 3993-3997.
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Larin A., Fershtat L. L., Ananyev I. V., Makhova N. N. Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade // Tetrahedron Letters. 2017. Vol. 58. No. 42. pp. 3993-3997.
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TY - JOUR
DO - 10.1016/j.tetlet.2017.09.013
UR - https://doi.org/10.1016%2Fj.tetlet.2017.09.013
TI - Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade
T2 - Tetrahedron Letters
AU - Larin, A.V
AU - Fershtat, Leonid L.
AU - Ananyev, Ivan V
AU - Makhova, Nina N.
PY - 2017
DA - 2017/10/01 00:00:00
PB - Elsevier
SP - 3993-3997
IS - 42
VL - 58
SN - 0040-4039
SN - 1873-3581
ER -
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@article{2017_Larin
author = {A.V Larin and Leonid L. Fershtat and Ivan V Ananyev and Nina N. Makhova},
title = {Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade},
journal = {Tetrahedron Letters},
year = {2017},
volume = {58},
publisher = {Elsevier},
month = {oct},
url = {https://doi.org/10.1016%2Fj.tetlet.2017.09.013},
number = {42},
pages = {3993--3997},
doi = {10.1016/j.tetlet.2017.09.013}
}
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MLA
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Larin, A.V, et al. “Versatile approach to heteroarylfuroxan derivatives from oximinofuroxans via a one-pot, nitration/thermolysis/[3+2]-cycloaddition cascade.” Tetrahedron Letters, vol. 58, no. 42, Oct. 2017, pp. 3993-3997. https://doi.org/10.1016%2Fj.tetlet.2017.09.013.