[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones
Publication type: Journal Article
Publication date: 2021-01-01
scimago Q4
wos Q4
SJR: 0.190
CiteScore: 1.3
Impact factor: 0.9
ISSN: 10704280, 16083393
Organic Chemistry
Abstract
Abstract [3+2]-Dipolar cycloaddition of diarylnitrones to substituted pyrroloquinoxalinetriones afforded (2a S *,3 R *,5a S *)-2a-acyl-3,4-diaryl-3,4-dihydro-1 H -[1,2]oxazolo[5′,4′:2,3]pyrrolo[1,2- a ]quinoxaline-1,2,6(2a H ,7 H )-triones that attract interest for medicinal chemistry.
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Stepanova E. E. et al. [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones // Russian Journal of Organic Chemistry. 2021. Vol. 57. No. 1. pp. 32-37.
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Stepanova E. E., Dmitriev M. V., Maslivets A. N. [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones // Russian Journal of Organic Chemistry. 2021. Vol. 57. No. 1. pp. 32-37.
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TY - JOUR
DO - 10.1134/S107042802101005X
UR - http://link.springer.com/10.1134/S107042802101005X
TI - [3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones
T2 - Russian Journal of Organic Chemistry
AU - Stepanova, E E
AU - Dmitriev, M V
AU - Maslivets, A N
PY - 2021
DA - 2021/01/01
PB - Pleiades Publishing
SP - 32-37
IS - 1
VL - 57
SN - 1070-4280
SN - 1608-3393
ER -
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BibTex (up to 50 authors)
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@article{2021_Stepanova,
author = {E E Stepanova and M V Dmitriev and A N Maslivets},
title = {[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones},
journal = {Russian Journal of Organic Chemistry},
year = {2021},
volume = {57},
publisher = {Pleiades Publishing},
month = {jan},
url = {http://link.springer.com/10.1134/S107042802101005X},
number = {1},
pages = {32--37},
doi = {10.1134/S107042802101005X}
}
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MLA
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Stepanova, E. E., et al. “[3+2]-Dipolar Cycloaddition of Nitrones to Pyrroloquinoxalinetriones.” Russian Journal of Organic Chemistry, vol. 57, no. 1, Jan. 2021, pp. 32-37. http://link.springer.com/10.1134/S107042802101005X.