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Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones

Rahul R Nagawade 1
Rahul R Nagawade
, 
Sandeep A Kotharkar 2
Sandeep A Kotharkar
, 
Devanand B Shinde 2
Devanand B Shinde
10.1070/MC2005v015n04ABEH002123
Published 2005-06-28
Communication , Volume 15, Issue 4, 150-151
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Nagawade R. R., Kotharkar S. A., Shinde D. B. Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones // Mendeleev Communications. 2005. Vol. 15. No. 4. pp. 150-151.
GOST all authors (up to 50) Copy
Nagawade R. R., Kotharkar S. A., Shinde D. B. Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones // Mendeleev Communications. 2005. Vol. 15. No. 4. pp. 150-151.
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TY - JOUR
DO - 10.1070/MC2005v015n04ABEH002123
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002123
TI - Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones
T2 - Mendeleev Communications
AU - Nagawade, Rahul R
AU - Kotharkar, Sandeep A
AU - Shinde, Devanand B
PY - 2005
DA - 2005/06/28
PB - Mendeleev Communications
SP - 150-151
IS - 4
VL - 15
ER -
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@article{2005_Nagawade,
author = {Rahul R Nagawade and Sandeep A Kotharkar and Devanand B Shinde},
title = {Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002123},
number = {4},
pages = {150--151},
doi = {10.1070/MC2005v015n04ABEH002123}
}
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Nagawade, Rahul R., et al. “Titanium(IV) chloride catalyzed one-pot synthesis of 3,4-dihydropyrimidin- 2(1H)-ones and thiones.” Mendeleev Communications, vol. 15, no. 4, Jun. 2005, pp. 150-151. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n04ABEH002123.

Abstract

Titanium(IV) chloride catalyses efficiently the three-component condensation reaction of an aldehyde, 1,3-dicarbonyl compound and urea or thiourea to afford the corresponding 3,4-dihydropyrimidin-2(1H)-ones and thiones in high yields.

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