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Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides

Issa Yavari 1
Issa Yavari
Tayebeh Sanaeishoar 1
Tayebeh Sanaeishoar
Leila Azad 1
Leila Azad
Maryam Ghazvini 1
Maryam Ghazvini
1 Department of Chemistry, Science and Research Branch, Islamic Azad Univeristy, Ponak, Tehran, Iran
Published 2011-03-10
CommunicationVolume 21, Issue 2, 108-109
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Yavari I. et al. Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides // Mendeleev Communications. 2011. Vol. 21. No. 2. pp. 108-109.
GOST all authors (up to 50) Copy
Yavari I., Sanaeishoar T., Azad L., Ghazvini M. Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides // Mendeleev Communications. 2011. Vol. 21. No. 2. pp. 108-109.
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TY - JOUR
DO - 10.1016/j.mencom.2011.03.018
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.03.018
TI - Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides
T2 - Mendeleev Communications
AU - Yavari, Issa
AU - Sanaeishoar, Tayebeh
AU - Azad, Leila
AU - Ghazvini, Maryam
PY - 2011
DA - 2011/03/10
PB - Mendeleev Communications
SP - 108-109
IS - 2
VL - 21
ER -
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@article{2011_Yavari,
author = {Issa Yavari and Tayebeh Sanaeishoar and Leila Azad and Maryam Ghazvini},
title = {Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.03.018},
number = {2},
pages = {108--109},
doi = {10.1016/j.mencom.2011.03.018}
}
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Yavari, Issa, et al. “Ketenimine N-functionalization of thiazolidine-2,4-diones with acetylenes and isocyanides.” Mendeleev Communications, vol. 21, no. 2, Mar. 2011, pp. 108-109. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.03.018.

Abstract

The zwitterionic 1:1 intermediates formed in the reaction between alkyl isocyanides and dialkyl acetylenedicarboxylates are trapped by 2,4-thiazolidine-2,4-diones to afford N-functionalized 2,4-dioxothiazolidines containing a ketenimine moiety.

References

1.
Small ring systems from isocyanides. I. Reaction of isocyanides with hexafluorobutyne-2
Oakes T.R., David H.G., Nagel F.J.
Journal of the American Chemical Society, 1969
2.
Reactions of isocyanides with activated acetylenes in protic solvents
Oakes T.R., Donovan D.J.
Journal of Organic Chemistry, 1973
3.
A facile route to highly functionalized ketenimines
Yavari I., Davar-Panah M., Heydari M., Najafian K., Zonouzi A.
Monatshefte fur Chemie, 1996
8.
Synthesis of Highly Functionalized 1-Azadienes and Ketenimines
Yavari I., Djahaniani H., Nasiri F.
Monatshefte fur Chemie, 2004
12.
Simple Synthesis of Highly Functionalized Ketenimines
Bayat M., Imanieh H., Hossieninejad E.
Synthetic Communications, 2008
14.
One-pot synthesis of highly functionalized stable ketenimines of 2,2,2-trifluoro-N-aryl-acetamides
Anary-Abbasinejad M., Moslemine M.H., Anaraki-Ardakani H.
Journal of Fluorine Chemistry, 2009
15.
Synthesis and aldose reductase inhibitory activity of 5-arylidene-2,4-thiazolidinediones
Bruno G., Costantino L., Curinga C., Maccari R., Monforte F., Nicolò F., Ottanà R., Vigorita M.G.
Bioorganic and Medicinal Chemistry, 2002