Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans
Publication type: Journal Article
Publication date: 2022-08-01
scimago Q3
SJR: 0.305
CiteScore: 2.8
Impact factor: —
ISSN: 10665285, 15739171
General Chemistry
Abstract
An efficient synthesis of N- and S-substituted arylglyoximes via one-pot transformations of available monoarylfuroxans was developed. The proposed approach includes furoxan ring cleavage followed by the generation of α-oximinoacetonitrile oxides which further add N- and S-nucleophiles.
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Chaplygin D. A. et al. Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans // Russian Chemical Bulletin. 2022. Vol. 71. No. 8. pp. 1745-1749.
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Chaplygin D. A., Larin A. A., Fershtat L. L. Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans // Russian Chemical Bulletin. 2022. Vol. 71. No. 8. pp. 1745-1749.
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TY - JOUR
DO - 10.1007/s11172-022-3585-0
UR - https://link.springer.com/10.1007/s11172-022-3585-0
TI - Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans
T2 - Russian Chemical Bulletin
AU - Chaplygin, D A
AU - Larin, A A
AU - Fershtat, L L
PY - 2022
DA - 2022/08/01
PB - Springer Nature
SP - 1745-1749
IS - 8
VL - 71
SN - 1066-5285
SN - 1573-9171
ER -
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@article{2022_Chaplygin,
author = {D A Chaplygin and A A Larin and L L Fershtat},
title = {Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans},
journal = {Russian Chemical Bulletin},
year = {2022},
volume = {71},
publisher = {Springer Nature},
month = {aug},
url = {https://link.springer.com/10.1007/s11172-022-3585-0},
number = {8},
pages = {1745--1749},
doi = {10.1007/s11172-022-3585-0}
}
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MLA
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Chaplygin, D. A., et al. “Synthesis of N- and S-substituted arylglyoximes via transformations of 4-arylfuroxans.” Russian Chemical Bulletin, vol. 71, no. 8, Aug. 2022, pp. 1745-1749. https://link.springer.com/10.1007/s11172-022-3585-0.