Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid
Тип публикации: Journal Article
Дата публикации: 2014-01-28
scimago Q2
wos Q3
БС1
SJR: 0.493
CiteScore: 5
Impact factor: 2.5
ISSN: 11440546, 13699261
Materials Chemistry
General Chemistry
Catalysis
Краткое описание
An efficient solvent-free protocol for the synthesis of tetrahydrobenzo[b]pyrans by the condensation of malononitrile, dimedone and various aldehydes in the presence of acetic acid functionalized imidazolium salts (1-carboxymethyl-3-methylimidazolium bromide {[cmmim]Br} and 1-carboxymethy1-3-methylimidazolium tetrafluoroborate {[cmmim][BF4]}) as reusable catalysts has been reported. The turn over frequency (TOF) values of the catalysts are higher than some of the previously reported catalysts. Also, thermal gravimetric analysis (TGA), differential thermal gravimetry (DTG), X-ray diffraction analysis (XRD) and calculations of the size and inter-planer distance of the catalysts have been reported in this work.
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Moosavi Zare A. R. et al. Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid // New Journal of Chemistry. 2014. Vol. 38. No. 6. p. 2342.
ГОСТ со всеми авторами (до 50)
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Moosavi Zare A. R., Zolfigol M. A., Khaledian O., Khakyzadeh V., Farahani M. D., Kruger H. G. Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid // New Journal of Chemistry. 2014. Vol. 38. No. 6. p. 2342.
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TY - JOUR
DO - 10.1039/c3nj01509b
UR - https://doi.org/10.1039/c3nj01509b
TI - Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid
T2 - New Journal of Chemistry
AU - Moosavi Zare, Ahmad Reza
AU - Zolfigol, Mohammad Ali
AU - Khaledian, Omid
AU - Khakyzadeh, Vahid
AU - Farahani, Majid D
AU - Kruger, Hendrik G
PY - 2014
DA - 2014/01/28
PB - Royal Society of Chemistry (RSC)
SP - 2342
IS - 6
VL - 38
SN - 1144-0546
SN - 1369-9261
ER -
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@article{2014_Moosavi Zare,
author = {Ahmad Reza Moosavi Zare and Mohammad Ali Zolfigol and Omid Khaledian and Vahid Khakyzadeh and Majid D Farahani and Hendrik G Kruger},
title = {Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid},
journal = {New Journal of Chemistry},
year = {2014},
volume = {38},
publisher = {Royal Society of Chemistry (RSC)},
month = {jan},
url = {https://doi.org/10.1039/c3nj01509b},
number = {6},
pages = {2342},
doi = {10.1039/c3nj01509b}
}
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MLA
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Moosavi Zare, Ahmad Reza, et al. “Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid.” New Journal of Chemistry, vol. 38, no. 6, Jan. 2014, p. 2342. https://doi.org/10.1039/c3nj01509b.