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Volumn 12, Issue 11, 2011, Pages 7438-7444

Novel ionic liquid with both Lewis and Brønsted acid sites for Michael addition

Author keywords

Lewis and br nsted acid sites; Michael addition; Novel ionic liquid

Indexed keywords

BRONSTED ACID; IONIC LIQUID; LEWIS ACID; ION; IRON; WATER;

EID: 82255164621     PISSN: None     EISSN: 14220067     Source Type: Journal    
DOI: 10.3390/ijms12117438     Document Type: Article
Times cited : (10)

References (8)
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  • 2
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    • Gupta, N.S.; Kad, G.L.; Singh, J. Acidic ionic liquid [bmim]HSO4: An efficient catalyst for acetalization and thioacetalization of carbonyl compounds and their subsequent deprotection. Catal. Commun. 2007, 8, 1323-1328.
    • (2007) Catal. Commun , vol.8 , pp. 1323-1328
    • Gupta, N.S.1    Kad, G.L.2    Singh, J.3
  • 4
    • 2542450803 scopus 로고    scopus 로고
    • Investigations towards the chemoselective thioacetaliztion of carbonyl compounds by using ionic liquid [bmim]Br as a recyclable catalytic medium
    • Kamal, A.; Chouhan, G. Investigations towards the chemoselective thioacetaliztion of carbonyl compounds by using ionic liquid [bmim]Br as a recyclable catalytic medium. Adv. Synth. Catal. 2004, 346, 579-582.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 579-582
    • Kamal, A.1    Chouhan, G.2
  • 5
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    • Tungstophosphoric acid supported on silica gel (H3PW12O40/SiO2) as an eco-friendly, reusable and heterogeneous catalyst for chemoselective oxathioacetalization of carbonyl compounds in solution or under solvent-free conditions
    • Firouzabadi, H.; Iranpoor, N.; Jafari, A.A.; Jafari, M.R. Tungstophosphoric acid supported on silica gel (H3PW12O40/SiO2) as an eco-friendly, reusable and heterogeneous catalyst for chemoselective oxathioacetalization of carbonyl compounds in solution or under solvent-free conditions. J. Mol. Catal. A 2006, 247, 14-18.
    • (2006) J. Mol. Catal. A , vol.247 , pp. 14-18
    • Firouzabadi, H.1    Iranpoor, N.2    Jafari, A.A.3    Jafari, M.R.4
  • 6
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    • Insight into the mechanism of the Michael addition of malononitrile to α, βunsaturated imides catalyzed by bifunctional thiourea catalysts
    • Zhang, D.; Wang, G.; Zhu, R. Insight into the mechanism of the Michael addition of malononitrile to α, βunsaturated imides catalyzed by bifunctional thiourea catalysts. Tetrahedron Asymmetry 2008, 19, 568-576.
    • (2008) Tetrahedron Asymmetry , vol.19 , pp. 568-576
    • Zhang, D.1    Wang, G.2    Zhu, R.3
  • 7
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    • Acid catalyzed 1, 2-Michael addition reaction: A viable synthetic route in designing fullerene core starlike macromolecule
    • Singh, R.; Goswami, T. Acid catalyzed 1, 2-Michael addition reaction: A viable synthetic route in designing fullerene core starlike macromolecule. J. Phys. Org. Chem. 2008, 21, 225-236.
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    • Chiral amine-thioureas bearing multiple hydrogen bonding donors: Highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins
    • Wang, C.-J.; Zhang, Z.-H.; Dong, X.-Q.; Wu, X.-J. Chiral amine-thioureas bearing multiple hydrogen bonding donors: Highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins. Chem. Commun. 2008, 1431-1433.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.