Home / Publications / Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium

Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium

16
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Zheng J., Li Y. Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium // Mendeleev Communications. 2012. Vol. 22. No. 3. pp. 148-149.
GOST all authors (up to 50) Copy
Zheng J., Li Y. Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium // Mendeleev Communications. 2012. Vol. 22. No. 3. pp. 148-149.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2012.05.012
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.012
TI - Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium
T2 - Mendeleev Communications
AU - Zheng, Jia
AU - Li, Yiqun
PY - 2012
DA - 2012/04/27
PB - Mendeleev Communications
SP - 148-149
IS - 3
VL - 22
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2012_Zheng,
author = {Jia Zheng and Yiqun Li},
title = {Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.012},
number = {3},
pages = {148--149},
doi = {10.1016/j.mencom.2012.05.012}
}
MLA
Cite this
MLA Copy
Zheng, Jia, and Yiqun Li. “Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium.” Mendeleev Communications, vol. 22, no. 3, Apr. 2012, pp. 148-149. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.05.012.

Abstract

The basic ionic liquid (benzyl)(dimethyl)(N,N-dimethylaminoethyl)ammonium chloride was found to be an efficient and reusable catalyst for the synthesis of spiroacenaphthylenes via the multicomponent reaction between acenaphthenequinone, malononitrile and α-methylenecarbonyl compounds (β-diketones, pyrazolones) in water.

References

1.
Hydrophobic acceleration of Diels-Alder reactions
Rideout D.C., Breslow R.
Journal of the American Chemical Society, 1980
2.
Organic Reactions on Silica in Water
Minakata S., Komatsu M.
Chemical Reviews, 2008
3.
Water-Promoted Organic Reactions
Lubineau A., Augé J., Queneau Y.
Synthesis, 1994
4.
Multi-Component Reactions in Water
Kumaravel K., Vasuki G.
Current Organic Chemistry, 2009
7.
A synthon approach to spiro compounds
Pradhan R., Patra M., Behera A.K., Mishra B.K., Behera R.K.
Tetrahedron, 2006
8.
(a) L. L. Andreani and E. Lapi, Bull. Chim. Farm., 1960, 99, 583;
9.
Synthesis and pharmacological activity of 2-oxo-(2H) 1-benzopyran-3-carboxamide derivatives
Bonsignore L., Loy G., Secci D., Calignano A.
European Journal of Medicinal Chemistry, 1993
10.
(c) G. R. Green, J.M. Evans and A. K. Vong, in Comprehensive Heterocyclic Chemistry II, eds. A. R. Katritzky, C.W. Rees and E. F. V. Scriven, Pergamon Press, Oxford, 1995, vol. 5, p. 469.
16.
Efficient One-Pot Synthesis of Spirooxindole Derivatives Catalyzed by l-Proline in Aqueous Medium
Li Y., Chen H., Shi C., Shi D., Ji S.
Journal of Combinatorial Chemistry, 2010
17.
Multi-component supramolecular synthesis of spirooxindoles catalyzed by β-cyclodextrin in water
Sridhar R., Srinivas B., Madhav B., Reddy V.P., Nageswar Y.V., Rao K.R.
Canadian Journal of Chemistry, 2009
19.
One-pot three-component synthesis of the spiroacenaphthylene derivatives
Saeedi M., Heravi M.M., Beheshtiha Y.S., Oskooie H.A.
Tetrahedron, 2010
20.
One-pot multicomponent synthesis and anti-microbial evaluation of 2′-(indol-3-yl)-2-oxospiro(indoline-3,4′-pyran) derivatives
Nandakumar A., Thirumurugan P., Perumal P.T., Vembu P., Ponnuswamy M.N., Ramesh P.
Bioorganic and Medicinal Chemistry Letters, 2010