Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction
Publication type: Journal Article
Publication date: 2013-12-10
scimago Q2
wos Q2
SJR: 0.528
CiteScore: 5.7
Impact factor: 3.5
ISSN: 09226168, 15685675
General Chemistry
Abstract
A mild, green, and facile method for the synthesis of naphthyridine derivatives is described in high yields using ionic liquids as a green media. The method involves a three-component reaction of aldehyde, enamine, and tert-butyl 2,4-dioxopiperidine-1-carboxylate.Graphical Abstract
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Total citations:
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Xu J. et al. Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction // Research on Chemical Intermediates. 2013. Vol. 41. No. 6. pp. 3873-3884.
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Xu J., Cao Y. S., Li Yu. L., Liu Y., Wang X. Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction // Research on Chemical Intermediates. 2013. Vol. 41. No. 6. pp. 3873-3884.
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TY - JOUR
DO - 10.1007/s11164-013-1496-2
UR - https://doi.org/10.1007/s11164-013-1496-2
TI - Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction
T2 - Research on Chemical Intermediates
AU - Xu, Jing
AU - Cao, Yi Sen
AU - Li, Yu Ling
AU - Liu, Yun
AU - Wang, Xiang-Shan
PY - 2013
DA - 2013/12/10
PB - Springer Nature
SP - 3873-3884
IS - 6
VL - 41
SN - 0922-6168
SN - 1568-5675
ER -
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BibTex (up to 50 authors)
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@article{2013_Xu,
author = {Jing Xu and Yi Sen Cao and Yu Ling Li and Yun Liu and Xiang-Shan Wang},
title = {Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction},
journal = {Research on Chemical Intermediates},
year = {2013},
volume = {41},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s11164-013-1496-2},
number = {6},
pages = {3873--3884},
doi = {10.1007/s11164-013-1496-2}
}
Cite this
MLA
Copy
Xu, Jing, et al. “Green synthesis of naphthyridine derivatives in ionic liquid via three-component reaction.” Research on Chemical Intermediates, vol. 41, no. 6, Dec. 2013, pp. 3873-3884. https://doi.org/10.1007/s11164-013-1496-2.