메뉴 건너뛰기




Volumn 15, Issue 9, 2011, Pages 1392-1422

Salt-type organic acids: A class of green acidic catalysts in organic transformations

Author keywords

Acidic ionic liquids; Br nsted acid; Lewis acid; Polyaniline salts; Protic; Salt type organic acids; Sulfamic acid

Indexed keywords

CATALYSIS; CATALYST SELECTIVITY; IONIC LIQUIDS; ORGANIC ACIDS; POLYANILINE; REUSABILITY;

EID: 79958242176     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795378245     Document Type: Review
Times cited : (10)

References (211)
  • 1
    • 0032298861 scopus 로고    scopus 로고
    • On developing cleaner organic unit processes
    • Sikdar, S. K.; Howell, S. G. On developing cleaner organic unit processes. J. Clean. Prod., 1998, 6(3-4), 253-259.
    • (1998) J. Clean. Prod , vol.6 , Issue.3-4 , pp. 253-259
    • Sikdar, S.K.1    Howell, S.G.2
  • 2
    • 44949257331 scopus 로고    scopus 로고
    • Efficient utilization of nanospace of layered transition metal oxide hnbmoo6 as a strong, water- tolerant solid acid catalyst
    • Tagusagawa, C.; Takagaki, A.; Hayashi, S.; Domen, K. Efficient utilization of nanospace of layered transition metal oxide hnbmoo6 as a strong, water- tolerant solid acid catalyst. J. Am. Chem. Soc., 2008, 130(23), 7230-7231.
    • (2008) J. Am. Chem. Soc , vol.130 , Issue.23 , pp. 7230-7231
    • Tagusagawa, C.1    Takagaki, A.2    Hayashi, S.3    Domen, K.4
  • 3
    • 47249084731 scopus 로고    scopus 로고
    • Deactivation and coke formation on nickel-tungsten supported on silica-alumina catalysts
    • Rezgui, Y.; Guemini, M. Deactivation and coke formation on nickel-tungsten supported on silica-alumina catalysts. Ind. Eng. Chem. Res., 2008, 47(12), 4056-4062.
    • (2008) Ind. Eng. Chem. Res , vol.47 , Issue.12 , pp. 4056-4062
    • Rezgui, Y.1    Guemini, M.2
  • 4
    • 34447324909 scopus 로고    scopus 로고
    • An asymmetric, bifunctional catalytic approach to non-natural α-amino acid derivatives
    • Paull, D. H.; Alden-Danforth, E.; Wolfer, J.; Dogo-isonagie, C.; abraham, C. J.; Lectka, T. An asymmetric, bifunctional catalytic approach to non-natural α-amino acid derivatives. J. Org. Chem., 2007, 72(14), 5380-5382.
    • (2007) J. Org. Chem , vol.72 , Issue.14 , pp. 5380-5382
    • Paull, D.H.1    Alden-Danforth, E.2    Wolfer, J.3    Dogo-Isonagie, C.4    Abraham, C.J.5    Lectka, T.6
  • 5
    • 58149204346 scopus 로고    scopus 로고
    • Bismuth-catalyzed intramolecular carbo-oxycarbonylation of 3-alkynyl esters
    • Komeyama, K.; Takahashi, K.; Takaki, K. Bismuth-catalyzed intramolecular carbo-oxycarbonylation of 3-alkynyl esters. Org. Lett., 2008, 10(22), 5119-5122.
    • (2008) Org. Lett , vol.10 , Issue.22 , pp. 5119-5122
    • Komeyama, K.1    Takahashi, K.2    Takaki, K.3
  • 6
    • 0002446999 scopus 로고    scopus 로고
    • The Cu(otf)2- and yb(otf)3-catalyzed claisen rearrangement of 2-alkoxycarbonyl-substituted allyl vinyl ethers
    • Hiersemann, M.; Abraham, L. The Cu(otf)2- and yb(otf)3-catalyzed claisen rearrangement of 2-alkoxycarbonyl-substituted allyl vinyl ethers. Org. Lett., 2001, 3(1), 49-52.
    • (2001) Org. Lett , vol.3 , Issue.1 , pp. 49-52
    • Hiersemann, M.1    Abraham, L.2
  • 7
    • 44949130811 scopus 로고    scopus 로고
    • Stereoselective one-pot synthesis of oxazolines
    • Hajra, S.; Bar, S.; Sinha, D.; Maji, B. Stereoselective one-pot synthesis of oxazolines. J. Org. Chem., 2008, 73(11), 4320-4322.
    • (2008) J. Org. Chem , vol.73 , Issue.11 , pp. 4320-4322
    • Hajra, S.1    Bar, S.2    Sinha, D.3    Maji, B.4
  • 8
    • 66549094328 scopus 로고    scopus 로고
    • Mild and efficient silylation of alcohols and phenols with HMDS using Bi(OTf)3 under solvent-free condition
    • Kadam, S. T.; Kim, S. S. Mild and efficient silylation of alcohols and phenols with HMDS using Bi(OTf)3 under solvent-free condition. J. Organomet. Chem., 2009, 694(16), 2562-2566.
    • (2009) J. Organomet. Chem , vol.694 , Issue.16 , pp. 2562-2566
    • Kadam, S.T.1    Kim, S.S.2
  • 9
    • 60449096215 scopus 로고    scopus 로고
    • Zr(HSO4)4 and Mg(HSO4)2 as mild and efficient catalysts for the one-pot multicomponent synthesis of α-acetamido carbonyl compounds
    • Momeni, A. R.; Sadeghi, M. Zr(HSO4)4 and Mg(HSO4)2 as mild and efficient catalysts for the one-pot multicomponent synthesis of α-acetamido carbonyl compounds. Appl. Catal. A: Gen., 2009, 357(1), 100-105.
    • (2009) Appl. Catal. A: Gen , vol.357 , Issue.1 , pp. 100-105
    • Momeni, A.R.1    Sadeghi, M.2
  • 10
    • 0037037843 scopus 로고    scopus 로고
    • B(C6F5)3 catalyzed hydrosilation of enones and silyl enol ethers
    • Blackwell, J. M.; Morrison, D. J.; Piers, W. E. B(C6F5)3 catalyzed hydrosilation of enones and silyl enol ethers. Tetrahedron, 2002, 58(41), 8247-8254.
    • (2002) Tetrahedron , vol.58 , Issue.41 , pp. 8247-8254
    • Blackwell, J.M.1    Morrison, D.J.2    Piers, W.E.3
  • 11
    • 0037037850 scopus 로고    scopus 로고
    • Lewis acid catalyzed stereoselective hydrosilylation of ketones under the control of σ-Π chelation
    • Asao, N.; Ohishi, T.; Sato, K.; Yamamoto, Y. Lewis acid catalyzed stereoselective hydrosilylation of ketones under the control of σ-Π chelation. Tetrahedron, 2002, 58, 8195-8204.
    • (2002) Tetrahedron , vol.58 , pp. 8195-8204
    • Asao, N.1    Ohishi, T.2    Sato, K.3    Yamamoto, Y.4
  • 12
    • 22844454644 scopus 로고    scopus 로고
    • Environmental benefits of methanesulfonic acid: Comparative properties and advantages
    • Gernon, M. D.; Wu, M.; Buszta, T.; Janney, P. Environmental benefits of methanesulfonic acid: comparative properties and advantages. Green Chem., 1999, 1(3), 127-140.
    • (1999) Green Chem , vol.1 , Issue.3 , pp. 127-140
    • Gernon, M.D.1    Wu, M.2    Buszta, T.3    Janney, P.4
  • 13
    • 0042709497 scopus 로고    scopus 로고
    • Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me2NSO2Cl and N, N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide
    • Wakasugi, K.; Nakamura, A.; Iida, A.; Nishii, Y.; Nakatani, N.; Fukushima, S.; Tanabe, Y. Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me2NSO2Cl and N, N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide. Tetrahedron, 2003, 59(28), 5337-5345.
    • (2003) Tetrahedron , vol.59 , Issue.28 , pp. 5337-5345
    • Wakasugi, K.1    Nakamura, A.2    Iida, A.3    Nishii, Y.4    Nakatani, N.5    Fukushima, S.6    Tanabe, Y.7
  • 14
    • 0037162857 scopus 로고    scopus 로고
    • Beckmann Rearrangement of Oximes under Very Mild Conditions
    • Luca, L. D.; Giacomelli, G.; Porcheddu, A. Beckmann Rearrangement of Oximes under Very Mild Conditions. J. Org. Chem., 2002, 67(17), 6272-6274.
    • (2002) J. Org. Chem , vol.67 , Issue.17 , pp. 6272-6274
    • Luca, L.D.1    Giacomelli, G.2    Porcheddu, A.3
  • 15
    • 5444234183 scopus 로고    scopus 로고
    • Conversion of α-Amino Acids into Nitriles by Oxidative Decarboxylation with Trichloroisocyanuric Acid
    • Hiegel, G. A.; Lewis, J. C.; Bae, J. W. Conversion of α-Amino Acids into Nitriles by Oxidative Decarboxylation with Trichloroisocyanuric Acid. Synthetic. Commun., 2004, 34(19), 3449-3454.
    • (2004) Synthetic. Commun , vol.34 , Issue.19 , pp. 3449-3454
    • Hiegel, G.A.1    Lewis, J.C.2    Bae, J.W.3
  • 16
    • 4143114533 scopus 로고    scopus 로고
    • Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels-Alder Reactions
    • Notz, W.; Tanaka, F.; Barbas, C. F. Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels-Alder Reactions. Acc. Chem. Res., 2004, 37(8), 580-591.
    • (2004) Acc. Chem. Res , vol.37 , Issue.8 , pp. 580-591
    • Notz, W.1    Tanaka, F.2    Barbas, C.F.3
  • 17
    • 55949099026 scopus 로고    scopus 로고
    • Based on Tunable Ordered Porous Silica for the von Pechmann Reaction
    • Karimi, B.; Zareyee, D. Based on Tunable Ordered Porous Silica for the von Pechmann Reaction. Org. Lett., 2008, 10(18), 3989-3992.
    • (2008) Org. Lett , vol.10 , Issue.18 , pp. 3989-3992
    • Karimi, B.1    Zareyee, D.2
  • 18
    • 12944325325 scopus 로고    scopus 로고
    • Peroxotungstate Immobilized on Ionic Liquid-Modified Silica as a Heterogeneous Epoxidation Catalyst with Hydrogen Peroxide
    • Yamaguchi, K.; Yoshida, C.; Uchida, S.; Mizuno, N. Peroxotungstate Immobilized on Ionic Liquid-Modified Silica as a Heterogeneous Epoxidation Catalyst with Hydrogen Peroxide, J. Am. Chem. Soc., 2005, 127(2), 530-531.
    • (2005) J. Am. Chem. Soc , vol.127 , Issue.2 , pp. 530-531
    • Yamaguchi, K.1    Yoshida, C.2    Uchida, S.3    Mizuno, N.4
  • 19
    • 33847299889 scopus 로고    scopus 로고
    • Recovery of chitosan from aqueous acidic solutions by salting-out. Part 2: Use of salts of organic acids
    • Dupuis, G.; LeHoux, J.-G. Recovery of chitosan from aqueous acidic solutions by salting-out. Part 2: Use of salts of organic acids. Carbohyd. Polym., 2007, 68(2), 287-294.
    • (2007) Carbohyd. Polym , vol.68 , Issue.2 , pp. 287-294
    • Dupuis, G.1    Lehoux, J.-G.2
  • 20
    • 34447098295 scopus 로고    scopus 로고
    • Catalysis in ionic liquids
    • Pârvulescu, V. I.; Hardacre, C. Catalysis in ionic liquids. Chem. Rev., 2007, 107(6), 2615-2665.
    • (2007) Chem. Rev , vol.107 , Issue.6 , pp. 2615-2665
    • Pârvulescu, V.I.1    Hardacre, C.2
  • 21
    • 61449244753 scopus 로고    scopus 로고
    • Strategy for synthesis of ionic metal-organic frameworks
    • Han, L.; Zhang, S.; Wang, Y.; Yan, X.; Lu, X. A strategy for synthesis of ionic metal-organic frameworks. Inorg. Chem., 2009, 48(3), 786-788.
    • (2009) Inorg. Chem , vol.48 , Issue.3 , pp. 786-788
    • Han, L.1    Zhang, S.2    Wang, Y.3    Yan, X.4    Lu, X.A.5
  • 23
    • 35348828491 scopus 로고    scopus 로고
    • Super acidic ionic liquids for arene carbonylation derived from dialkylimidazolium chlorides and MCl3 (M = Al, Ga, or In)
    • Angueira, E.J.; White, M.G. Super acidic ionic liquids for arene carbonylation derived from dialkylimidazolium chlorides and MCl3 (M = Al, Ga, or In). J. Mol. Catal. A: Chem., 2007, 277(1-2), 164-170.
    • (2007) J. Mol. Catal. A: Chem , vol.277 , Issue.1-2 , pp. 164-170
    • Angueira, E.J.1    White, M.G.2
  • 24
    • 33747806671 scopus 로고    scopus 로고
    • Catalysis in ionic liquids, Adv
    • Zhang, Z. C. Catalysis in ionic liquids, Adv. Catal., 2006, 49, 153-237.
    • (2006) Catal , vol.49 , pp. 153-237
    • Zhang, Z.C.1
  • 25
    • 67649803074 scopus 로고    scopus 로고
    • Isomerization of exo-tetrahydrodicyclopentadiene to adamantane using an acidity-adjustable chloroaluminate ionic liquid
    • Huang, M.-Y.; Wu, J.-C.; Shieu, F. S.; Lin, J.-J. Isomerization of exo-tetrahydrodicyclopentadiene to adamantane using an acidity-adjustable chloroaluminate ionic liquid. Catal. Commun., 2009, 10(13), 1747-1751.
    • (2009) Catal. Commun , vol.10 , Issue.13 , pp. 1747-1751
    • Huang, M.-Y.1    Wu, J.-C.2    Shieu, F.S.3    Lin, J.-J.4
  • 26
    • 34250218170 scopus 로고    scopus 로고
    • Highly selective synthesis of 2,6-dimethylnaphthanlene by green catalysts---N-alkyl-pyridinium halides- aluminum chloride ionic liquids
    • Wu, W.; Wu, G.; Zhang, M. Highly selective synthesis of 2,6-dimethylnaphthanlene by green catalysts---N-alkyl-pyridinium halides- aluminum chloride ionic liquids. Appl. Catal. A: Gen., 2007, 326(2), 189-193.
    • (2007) Appl. Catal. A: Gen , vol.326 , Issue.2 , pp. 189-193
    • Wu, W.1    Wu, G.2    Zhang, M.3
  • 27
    • 34347330150 scopus 로고    scopus 로고
    • Isobutane/2-butene alkylation catalyzed by chloroaluminate ionic liquids in the presence of aromatic additives
    • Zhang, J.; Huang, C.; Chen, B.; Ren, P.; Pu, M. Isobutane/2-butene alkylation catalyzed by chloroaluminate ionic liquids in the presence of aromatic additives. J. Catal., 2007, 249(2), 261-268.
    • (2007) J. Catal , vol.249 , Issue.2 , pp. 261-268
    • Zhang, J.1    Huang, C.2    Chen, B.3    Ren, P.4    Pu, M.5
  • 28
    • 14644445148 scopus 로고    scopus 로고
    • Friedel-Crafts alkylation reactions in pyridinium- based ionic liquids
    • Xiao, Y.; Malhotra, S. V. Friedel-Crafts alkylation reactions in pyridinium- based ionic liquids. J. Mol. Catal. A: Chem., 2005, 230(1-2), 129-133.
    • (2005) J. Mol. Catal. A: Chem , vol.230 , Issue.1-2 , pp. 129-133
    • Xiao, Y.1    Malhotra, S.V.2
  • 29
    • 1542358076 scopus 로고    scopus 로고
    • Ionic liquid- catalyzed alkylation of isobutane with 2-butene
    • Yoo, K.; Namboodiri, V. V.; Varma, R. S.; Smirniotis, P. G. Ionic liquid- catalyzed alkylation of isobutane with 2-butene. J. Catal., 2004, 222(2), 511-519.
    • (2004) J. Catal , vol.222 , Issue.2 , pp. 511-519
    • Yoo, K.1    Namboodiri, V.V.2    Varma, R.S.3    Smirniotis, P.G.4
  • 30
    • 59349099725 scopus 로고    scopus 로고
    • Friedel-Crafts acylation of anthracene with oxalyl chloride catalyzed by ionic liquid of [bmim]Cl/AlCl3
    • Yuan, X.; Chen, M.; Dai, Q.; Cheng, X.-N. Friedel-Crafts acylation of anthracene with oxalyl chloride catalyzed by ionic liquid of [bmim]Cl/AlCl3. Chem. Eng. J., 2009, 146(2), 266-269.
    • (2009) Chem. Eng. J , vol.146 , Issue.2 , pp. 266-269
    • Yuan, X.1    Chen, M.2    Dai, Q.3    Cheng, X.-N.4
  • 31
    • 0000934713 scopus 로고    scopus 로고
    • Nickel(II) heterocyclic carbene complexes as catalysts for olefin dimerization in an imidazolium chloroaluminate ionic liquid
    • McGuinness, D. S.; Mueller, W.; Wasserscheid, P.; Cavell, K. J.; Skelton, B. W.; White, A. H.; Englert, U. Nickel(II) heterocyclic carbene complexes as catalysts for olefin dimerization in an imidazolium chloroaluminate ionic liquid. Organometallics, 2002, 21(1), 175-181.
    • (2002) Organometallics , vol.21 , Issue.1 , pp. 175-181
    • McGuinness, D.S.1    Mueller, W.2    Wasserscheid, P.3    Cavell, K.J.4    Skelton, B.W.5    White, A.H.6    Englert, U.7
  • 32
    • 34249292989 scopus 로고    scopus 로고
    • Nickel-catalyzed propylene dimerization in organochloroaluminate ionic liquids: Control of the isomerization reaction
    • Fernando de Souza, R.; Leal, B. C.; Oberson de Souza, M.; Thiele, D. Nickel-catalyzed propylene dimerization in organochloroaluminate ionic liquids: control of the isomerization reaction, J. Mol. Catal. A: Chem., 2007, 272(1-2), 6-10.
    • (2007) J. Mol. Catal. A: Chem , vol.272 , Issue.1-2 , pp. 6-10
    • Fernando de Souza, R.1    Leal, B.C.2    Oberson de Souza, M.3    Thiele, D.4
  • 33
    • 0942300627 scopus 로고    scopus 로고
    • The DABCO-catalysed baylis-hillman reactions in the chloroaluminate room temperature ionic liquids: Rate promoting and recyclable media
    • Kumar, A.; Pawar, S. S. The DABCO-catalysed baylis-hillman reactions in the chloroaluminate room temperature ionic liquids: rate promoting and recyclable media. J. Mol. Catal. A: Chem., 2004, 211(1-2), 43-47.
    • (2004) J. Mol. Catal. A: Chem , vol.211 , Issue.1-2 , pp. 43-47
    • Kumar, A.1    Pawar, S.S.2
  • 34
    • 35348837781 scopus 로고    scopus 로고
    • Ionic Liquids as powerful solvent media for Improving catalytic performance of silyl borate catalyst to promote diels-alder reactions
    • Kumar, A.; Pawar, S. S. Ionic Liquids as powerful solvent media for Improving catalytic performance of silyl borate catalyst to promote diels-alder reactions. J. Org. Chem., 2007, 72(21), 8111-8114.
    • (2007) J. Org. Chem , vol.72 , Issue.21 , pp. 8111-8114
    • Kumar, A.1    Pawar, S.S.2
  • 35
    • 50949088926 scopus 로고    scopus 로고
    • An efficient one-pot synthesis of 3-glyoxylic acids of electron-deficient substituted azaindoles by ionic liquid imidazolium chloroaluminate-promoted Friedel-Crafts acylation
    • Yeung, K.-S.; Qiu, Z.; Farkas, M. E.; Xue, Q.; Regueiro-Ren, A.; Yang, Z.; Bender, J. A.; Good, A. C.; Kadow, J. F. An efficient one-pot synthesis of 3-glyoxylic acids of electron-deficient substituted azaindoles by ionic liquid imidazolium chloroaluminate-promoted Friedel-Crafts acylation. Tetrahedron Lett., 2008, 49(43), 6250-6253.
    • (2008) Tetrahedron Lett , vol.49 , Issue.43 , pp. 6250-6253
    • Yeung, K.-S.1    Qiu, Z.2    Farkas, M.E.3    Xue, Q.4    Regueiro-Ren, A.5    Yang, Z.6    Bender, J.A.7    Good, A.C.8    Kadow, J.F.9
  • 36
    • 1242329828 scopus 로고    scopus 로고
    • Converting exo-selective diels-alder reaction to endo-selective in chloroloaluminate ionic liquids
    • Kumar, A.; Pawar, S. S. Converting exo-selective diels-alder reaction to endo-selective in chloroloaluminate ionic liquids, J. Org. Chem., 2004, 69(4), 1419-1420.
    • (2004) J. Org. Chem , vol.69 , Issue.4 , pp. 1419-1420
    • Kumar, A.1    Pawar, S.S.2
  • 37
    • 33644770072 scopus 로고    scopus 로고
    • An iron-containing ionic liquid as recyclable catalyst for aryl grignard cross-coupling of alkyl halides
    • Bica, K.; Gaertner, P. An iron-containing ionic liquid as recyclable catalyst for aryl grignard cross-coupling of alkyl halides. Org. Lett., 2006, 8(4), 733-735.
    • (2006) Org. Lett , vol.8 , Issue.4 , pp. 733-735
    • Bica, K.1    Gaertner, P.2
  • 38
    • 64249130993 scopus 로고    scopus 로고
    • Oligomerization of isobutene catalyzed by iron(iii) chloride ionic liquids
    • Yang, S.; Liu, Z.; Meng, X.; Xu, C. Oligomerization of isobutene catalyzed by iron(iii) chloride ionic liquids. Energ. Fuel., 2009, 23(1), 70-73.
    • (2009) Energ. Fuel , vol.23 , Issue.1 , pp. 70-73
    • Yang, S.1    Liu, Z.2    Meng, X.3    Xu, C.4
  • 39
    • 43049164174 scopus 로고    scopus 로고
    • Highly selective catalytic friedel-crafts sulfonylation of aromatic compounds using a FeCl3-based ionic liquid
    • Bahrami, K.; Khodei, M. M.; Shahbazi, F. Highly selective catalytic friedel-crafts sulfonylation of aromatic compounds using a FeCl3-based ionic liquid. Tetrahedron Lett., 2008, 49(24), 3931-3934.
    • (2008) Tetrahedron Lett , vol.49 , Issue.24 , pp. 3931-3934
    • Bahrami, K.1    Khodei, M.M.2    Shahbazi, F.3
  • 40
    • 7444265215 scopus 로고    scopus 로고
    • Synthesis of 2,3-unsaturated glycopyranosides by ferrier rearrangement in FeCl3 based ionic liquid
    • Tilve, R. D.; Alexander, M. V.; Khandekar, A. C.; Samant, S. D.; Kanetkar, Vinod R. Synthesis of 2,3-unsaturated glycopyranosides by ferrier rearrangement in FeCl3 based ionic liquid. J. Mol. Catal. A: Chem., 2004, 223(1-2), 237-240.
    • (2004) J. Mol. Catal. A: Chem , vol.223 , Issue.1-2 , pp. 237-240
    • Tilve, R.D.1    Alexander, M.V.2    Khandekar, A.C.3    Samant, S.D.4    Kanetkar, V.R.5
  • 41
    • 47749087801 scopus 로고    scopus 로고
    • Fe-containing ionic liquids as catalysts for the dimerization of bicyclo[2.2.1]hepta-2,5-diene
    • Nguyen, M.i D.; Nguyen, L. V.; Jeon, E. H.; Kim, J. H.; Cheong, M.; Kim, H. S.; Lee, J. S. Fe-containing ionic liquids as catalysts for the dimerization of bicyclo[2.2.1]hepta-2,5-diene. J. Catal., 2008, 258(1), 5-13.
    • (2008) J. Catal , vol.258 , Issue.1 , pp. 5-13
    • Nguyen M.i, D.1    Nguyen, L.V.2    Jeon, E.H.3    Kim, J.H.4    Cheong, M.5    Kim, H.S.6    Lee, J.S.7
  • 42
    • 22944465724 scopus 로고    scopus 로고
    • Friedel-Crafts acylation reactions in pyridinium based ionic liquids
    • Xiao, Y.; Malhotra, S. V. Friedel-Crafts acylation reactions in pyridinium based ionic liquids. J. Organomet. Chem., 2005, 690(15), 3609-3613.
    • (2005) J. Organomet. Chem , vol.690 , Issue.15 , pp. 3609-3613
    • Xiao, Y.1    Malhotra, S.V.2
  • 44
    • 1542346918 scopus 로고    scopus 로고
    • Studies on an ionic liquid prepared from InCl3 and 1-methyl-3-butylimidazolium chloride
    • Yang, J.-Z.; Tian, P.; Xu, W.-G.; Xu, B.; Liu, S.-Z. Studies on an ionic liquid prepared from InCl3 and 1-methyl-3-butylimidazolium chloride. Thermochim. Acta, 2004, 412(1-2), 1-5.
    • (2004) Thermochim. Acta , vol.412 , Issue.1-2 , pp. 1-5
    • Yang, J.-Z.1    Tian, P.2    Xu, W.-G.3    Xu, B.4    Liu, S.-Z.5
  • 45
    • 0037430431 scopus 로고    scopus 로고
    • Asymmetric Mannich-type reactions catalyzed by indium(III) complexes in ionic liquids
    • Chen, S.-L.; Ji, S.-J.; Loh,T.-P. Asymmetric Mannich-type reactions catalyzed by indium(III) complexes in ionic liquids. Tetrahedron Lett., 2003, 11(10), 2405-2408.
    • (2003) Tetrahedron Lett , vol.11 , Issue.10 , pp. 2405-2408
    • Chen, S.-L.1    Ji, S.-J.2    Loh, T.-P.3
  • 46
    • 34548701110 scopus 로고    scopus 로고
    • Efficient synthesis of benzophenone derivatives in Lewis acid ionic liquids
    • Li, C.; Liu, W.; Zhao, Z. Efficient synthesis of benzophenone derivatives in Lewis acid ionic liquids. Catal. Commun., 2007, 8(11), 1834-1837.
    • (2007) Catal. Commun , vol.8 , Issue.11 , pp. 1834-1837
    • Li, C.1    Liu, W.2    Zhao, Z.3
  • 47
    • 58149352346 scopus 로고    scopus 로고
    • Novel acidic ionic liquids mediated zinc chloride: Highly effective catalysts for the Beckmann rearrangement
    • Liu, X. F.; Xiao, L.; Wu, H. Li, Z.; Chen, J.; Xia C. Novel acidic ionic liquids mediated zinc chloride: Highly effective catalysts for the Beckmann rearrangement. Catal. Commun., 2009, 10(5), 424-427.
    • (2009) Catal. Commun , vol.10 , Issue.5 , pp. 424-427
    • Liu, X.F.1    Xiao, L.2    Wu, H.3    Li, Z.4    Chen, J.5    Xia, C.6
  • 48
    • 56749128219 scopus 로고    scopus 로고
    • Desulfurization of fuel by extraction with pyridinium-based ionic liquids
    • Gao, H.; Luo, M.; Xing, J.; Wu, Y.; Li, Y.; Li, W.; Liu, Q.; Liu, H. Desulfurization of fuel by extraction with pyridinium-based ionic liquids. Ind. Eng. Chem. Res., 2008, 47(21), 8384-8388.
    • (2008) Ind. Eng. Chem. Res , vol.47 , Issue.21 , pp. 8384-8388
    • Gao, H.1    Luo, M.2    Xing, J.3    Wu, Y.4    Li, Y.5    Li, W.6    Liu, Q.7    Liu, H.8
  • 49
    • 45449113440 scopus 로고    scopus 로고
    • Extractive desulfurization using fe-containing ionic liquids
    • Ko, N. H.; Lee, J. S.; Huh, E. S.; Lee, H.; Jung, K. D.; Kim, H. S.; Cheong, M. Extractive desulfurization using fe-containing ionic liquids. Energy Fuel., 2008, 22(3), 1687-1690.
    • (2008) Energy Fuel , vol.22 , Issue.3 , pp. 1687-1690
    • Ko, N.H.1    Lee, J.S.2    Huh, E.S.3    Lee, H.4    Jung, K.D.5    Kim, H.S.6    Cheong, M.7
  • 50
    • 53349175670 scopus 로고    scopus 로고
    • Deep oxidativedesulfurization of fuels using peroxophosphomolybdate catalysts in ionic liquids
    • He, L.; Li, H.; Zhu, W.; Guo, J.; Jiang, X.; Lu, J. Yan, Y. Deep oxidativedesulfurization of fuels using peroxophosphomolybdate catalysts in ionic liquids. Ind. Eng. Chem. Res., 2008, 47(18), 6890-6895.
    • (2008) Ind. Eng. Chem. Res , vol.47 , Issue.18 , pp. 6890-6895
    • He, L.1    Li, H.2    Zhu, W.3    Guo, J.4    Jiang, X.5    Lu, J.6    Yan, Y.7
  • 51
    • 67649099549 scopus 로고    scopus 로고
    • Desulfurization of dibenzothiophene by chemical oxidation and solvent extraction with Me3NCH2C6H5Cl·2ZnCl2 ionic liquid
    • Li, F.-T.; Liu, R.-H.; Wen, J.-H.; Zhao, D.-S.; Sun, Z.-M.; Liu, Y. Desulfurization of dibenzothiophene by chemical oxidation and solvent extraction with Me3NCH2C6H5Cl·2ZnCl2 ionic liquid., Green Chem., 2009, 11(6), 883-888.
    • (2009) Green Chem , vol.11 , Issue.6 , pp. 883-888
    • Li, F.-T.1    Liu, R.-H.2    Wen, J.-H.3    Zhao, D.-S.4    Sun, Z.-M.5    Liu, Y.6
  • 52
    • 23644462120 scopus 로고    scopus 로고
    • Mannich reaction catalyzed by carboxyl- functionalized ionic liquid in aqueous media
    • Li, J.; Peng, Y.; Song, G. Mannich reaction catalyzed by carboxyl- functionalized ionic liquid in aqueous media. Catal. Lett., 2005, 102(3-4), 159-162.
    • (2005) Catal. Lett , vol.102 , Issue.3-4 , pp. 159-162
    • Li, J.1    Peng, Y.2    Song, G.3
  • 53
    • 0346366649 scopus 로고    scopus 로고
    • One-pot synthesis of silica gel confined functional ionic liquids: Effective catalysts for deoximation under mild conditions
    • Li, D.; Shi, F.; Guo, S.; Deng, Y. One-pot synthesis of silica gel confined functional ionic liquids: effective catalysts for deoximation under mild conditions. Tetrahedron Lett., 2004, 45(2), 265-268.
    • (2004) Tetrahedron Lett , vol.45 , Issue.2 , pp. 265-268
    • Li, D.1    Shi, F.2    Guo, S.3    Deng, Y.4
  • 54
    • 0037696954 scopus 로고    scopus 로고
    • The carbonylation reaction of nitrobenzene to methyl phenylcarbamate: Highly efficient promoters for the palladium-phenanthroline catalytic system based on phosphorus acids
    • Ragaini, F.; Cognolato, C.; Gasperini, M.; Cenini, S. The carbonylation reaction of nitrobenzene to methyl phenylcarbamate: Highly efficient promoters for the palladium-phenanthroline catalytic system based on phosphorus acids. Angew. Chem. Int. Ed., 2003, 42, 2886-2889.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 2886-2889
    • Ragaini, F.1    Cognolato, C.2    Gasperini, M.3    Cenini, S.4
  • 55
    • 31044437389 scopus 로고    scopus 로고
    • Developing effective catalyst system for reductive carbonylation of nitrobenzene based on the diversity of ionic liquids
    • Shi, F.; He, Y.; Li, D.; Ma, Y.; Zhang, Q.; Deng, Y. Developing effective catalyst system for reductive carbonylation of nitrobenzene based on the diversity of ionic liquids. J. Mol. Catal. A: Chem., 2006, 244(1-2), 64-67.
    • (2006) J. Mol. Catal. A: Chem , vol.244 , Issue.1-2 , pp. 64-67
    • Shi, F.1    He, Y.2    Li, D.3    Ma, Y.4    Zhang, Q.5    Deng, Y.6
  • 57
    • 3943110897 scopus 로고    scopus 로고
    • Novel Brønsted acidic ionic liquid as effcient and reusable catalyst system for esterification
    • Gui, J. Z.; Cong, X. H.; Liu, D.; Zhang, X. T.; Hu, Z. D.; Sun, Z. L. Novel Brønsted acidic ionic liquid as e cient and reusable catalyst system for esterification. Catal. Commun., 2004, 5, 473-477.
    • (2004) Catal. Commun , vol.5 , pp. 473-477
    • Gui, J.Z.1    Cong, X.H.2    Liu, D.3    Zhang, X.T.4    Hu, Z.D.5    Sun, Z.L.6
  • 58
    • 36749042024 scopus 로고    scopus 로고
    • Transesterification of cottonseeoil catalyzed by brønsted acidic ionic liquids
    • Wu, Q.; Chen, H.; Han, M.; Wang, D.; Wang, J. Transesterification of cottonseeoil catalyzed by brønsted acidic ionic liquids. Ind. Eng. Chem. Res., 2007, 46(24), 7955-7960.
    • (2007) Ind. Eng. Chem. Res , vol.46 , Issue.24 , pp. 7955-7960
    • Wu, Q.1    Chen, H.2    Han, M.3    Wang, D.4    Wang, J.5
  • 59
    • 55549091363 scopus 로고    scopus 로고
    • Novel multi-SO3H functional ionic liquid for the conjugate addition of amines to electron deficient alkenes
    • Liang, X.; Wang, Y.; Gong, G.; Yang, J. Novel multi-SO3H functional ionic liquid for the conjugate addition of amines to electron deficient alkenes. Catal. Commun., 2008, 10(3), 281-284.
    • (2008) Catal. Commun , vol.10 , Issue.3 , pp. 281-284
    • Liang, X.1    Wang, Y.2    Gong, G.3    Yang, J.4
  • 60
    • 34248231984 scopus 로고    scopus 로고
    • Synthesis of carbamates from aliphatic amines and dimethyl carbonate catalyzed by acid functional ionic liquids
    • Zhou, H.; Shi, F.; Tian, X.; Zhang, Q.; Deng. Y. Synthesis of carbamates from aliphatic amines and dimethyl carbonate catalyzed by acid functional ionic liquids. J. Mol. Catal. A: Chem., 2007, 277(1-2), 89-92.
    • (2007) J. Mol. Catal. A: Chem , vol.277 , Issue.1-2 , pp. 89-92
    • Zhou, H.1    Shi, F.2    Tian, X.3    Zhang, Q.4    Deng, Y.5
  • 61
    • 42749090618 scopus 로고    scopus 로고
    • Synthesis of chalcones via Claisen-Schmidt condensation reaction catalyzed by acyclic acidic ionic liquids
    • Fang, D.; Cheng, J.; Fei, Z.; Gong, K.; Liu, Z. Synthesis of chalcones via Claisen-Schmidt condensation reaction catalyzed by acyclic acidic ionic liquids. Catal. Commun., 2008, 9(9), 1924-1927.
    • (2008) Catal. Commun , vol.9 , Issue.9 , pp. 1924-1927
    • Fang, D.1    Cheng, J.2    Fei, Z.3    Gong, K.4    Liu, Z.5
  • 62
    • 4644271808 scopus 로고    scopus 로고
    • Nitration of aromatic compounds with nitric acid catalyzed by ionic liquids
    • Qiao, K.; Yokoyama, C. Nitration of aromatic compounds with nitric acid catalyzed by ionic liquids. Chem. Lett., 2004, 33(7), 808-809.
    • (2004) Chem. Lett , vol.33 , Issue.7 , pp. 808-809
    • Qiao, K.1    Yokoyama, C.2
  • 63
    • 10044283224 scopus 로고    scopus 로고
    • Selective alkylation of phenol with tert-butyl alcohol catalyzed by Brønsted acidic imidazolium salts
    • Gui, J. Z.; Ban, H. Y.; Cong, X. H.; Zhang, X. T.; Hu, Z. D.; Sun, Z. L. Selective alkylation of phenol with tert-butyl alcohol catalyzed by Brønsted acidic imidazolium salts. J. Mol. Catal. A: Chem., 2004, 225(1-2), 27-31.
    • (2004) J. Mol. Catal. A: Chem , vol.225 , Issue.1-2 , pp. 27-31
    • Gui, J.Z.1    Ban, H.Y.2    Cong, X.H.3    Zhang, X.T.4    Hu, Z.D.5    Sun, Z.L.6
  • 64
    • 49549106233 scopus 로고    scopus 로고
    • SO3H-Functionalized ionic liquids for selective alkylation of p-cresol with tert-butanol
    • Liu, X.; Zhou, J.; Guo, X.; Liu, M.; Ma, X.; Song, C.; Wang, C. SO3H-Functionalized ionic liquids for selective alkylation of p-cresol with tert-butanol. Ind. Eng. Chem. Res., 2008, 47(15), 5298-5303.
    • (2008) Ind. Eng. Chem. Res , vol.47 , Issue.15 , pp. 5298-5303
    • Liu, X.1    Zhou, J.2    Guo, X.3    Liu, M.4    Ma, X.5    Song, C.6    Wang, C.7
  • 65
    • 2442475205 scopus 로고    scopus 로고
    • Application of Functional ionic liquids possessing two adjacent acid sites for acetalization of aldehydes
    • Li, D.; Shi, F.; Peng, J.; Guo, S.; Deng, Y. Application of Functional ionic liquids possessing two adjacent acid sites for acetalization of aldehydes. J. Org. Chem., 2004, 69(10), 3582-3585.
    • (2004) J. Org. Chem , vol.69 , Issue.10 , pp. 3582-3585
    • Li, D.1    Shi, F.2    Peng, J.3    Guo, S.4    Deng, Y.5
  • 66
    • 5044234663 scopus 로고    scopus 로고
    • The first utilization of acidic ionic liquid for preparation of tetraarylporphyrins
    • Kitaoka, S.; Nobuoka, K.; Ishikawa, Y. The first utilization of acidic ionic liquid for preparation of tetraarylporphyrins. Chem. Commun., 2004, 41(17), 1902-1903.
    • (2004) Chem. Commun , vol.41 , Issue.17 , pp. 1902-1903
    • Kitaoka, S.1    Nobuoka, K.2    Ishikawa, Y.3
  • 67
    • 17144422866 scopus 로고    scopus 로고
    • Pechmann reaction in non-chloroaluminate acidic ionic liquids under solvent-free conditions
    • Gu, Y.; Zhang, J.; Duan, Z.; Deng, Y. Pechmann reaction in non-chloroaluminate acidic ionic liquids under solvent-free conditions. Adv. Synth. Catal., 2005, 347(4), 512-516.
    • (2005) Adv. Synth. Catal , vol.347 , Issue.4 , pp. 512-516
    • Gu, Y.1    Zhang, J.2    Duan, Z.3    Deng, Y.4
  • 68
    • 66149182887 scopus 로고    scopus 로고
    • A sulfonic acid functionalized ionic liquid as a homogeneous and recyclable catalyst for the one-pot synthesis of α-aminophosphonates
    • Akbari, J.; Heydari, A. A sulfonic acid functionalized ionic liquid as a homogeneous and recyclable catalyst for the one-pot synthesis of α-aminophosphonates. Tetrahedron Lett., 2009, 50(29), 4236-4238.
    • (2009) Tetrahedron Lett , vol.50 , Issue.29 , pp. 4236-4238
    • Akbari, J.1    Heydari, A.2
  • 69
    • 37349119737 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids derived from alkylamines as catalysts and mediums for Fischer esterification: Study of structure-activity relationship
    • Ganeshpure, P. A.; George, G.; Das, J. Brønsted acidic ionic liquids derived from alkylamines as catalysts and mediums for Fischer esterification: study of structure-activity relationship. J. Mol. Catal. A: Chem., 2008, 279(2), 182-186.
    • (2008) J. Mol. Catal. A: Chem , vol.279 , Issue.2 , pp. 182-186
    • Ganeshpure, P.A.1    George, G.2    Das, J.3
  • 70
    • 34547413385 scopus 로고    scopus 로고
    • One-pot green procedure for Biginelli reaction catalyzed by novel task-specific room-temperature ionic liquids
    • Fang, D.; L, J.; Zhou, X.; Ye, Z.; Liu, Z. One-pot green procedure for Biginelli reaction catalyzed by novel task-specific room-temperature ionic liquids. J. Mol. Catal. A: Chem., 2007, 274(1-2), 208-211.
    • (2007) J. Mol. Catal. A: Chem , vol.274 , Issue.1-2 , pp. 208-211
    • Fang, D.L.J.1    Zhou, X.2    Ye, Z.3    Liu, Z.4
  • 71
    • 38749104231 scopus 로고    scopus 로고
    • Synthesis of plasticizer ester using acid-functionalized ionic liquid as catalyst
    • Xie, C.; Li, H.; Li, L.; Yu, S.; Liu, F. Synthesis of plasticizer ester using acid-functionalized ionic liquid as catalyst. J. Hazard. Mater., 2008, 151(2-3), 847-850.
    • (2008) J. Hazard. Mater , vol.151 , Issue.2-3 , pp. 847-850
    • Xie, C.1    Li, H.2    Li, L.3    Yu, S.4    Liu, F.5
  • 72
    • 31044436897 scopus 로고    scopus 로고
    • Mannich reaction in Brønsted acidic ionic liquid: A facile synthesis of α-amino carbonyl compounds
    • Sahoo, S.; Joseph, T.; Halligudi, S. B. Mannich reaction in Brønsted acidic ionic liquid: A facile synthesis of α-amino carbonyl compounds. J. Mol. Catal. A: Chem., 2006, 244(1-2), 179-182.
    • (2006) J. Mol. Catal. A: Chem , vol.244 , Issue.1-2 , pp. 179-182
    • Sahoo, S.1    Joseph, T.2    Halligudi, S.B.3
  • 73
    • 67349208494 scopus 로고    scopus 로고
    • Brønsted acidic imidazolium salts containing perfluoroalkyl tails catalyzed one-pot synthesis of 1,8-dioxo-decahydroacridines in water
    • Shen, W.; Wang, L.-M.; Tian, H.; Tang, J.; Yu, J. Brønsted acidic imidazolium salts containing perfluoroalkyl tails catalyzed one-pot synthesis of 1,8-dioxo-decahydroacridines in water. J. Fluorine Chem., 2009, 130(6), 522-527.
    • (2009) J. Fluorine Chem , vol.130 , Issue.6 , pp. 522-527
    • Shen, W.1    Wang, L.-M.2    Tian, H.3    Tang, J.4    Yu, J.5
  • 74
    • 1642369564 scopus 로고    scopus 로고
    • SO3H-functionalized ionic liquid as effcient, green and reusable acidic catalyst system for oligomerization of olefins
    • Gu, Y.; Shi, F.; Deng, Y. SO3H-functionalized ionic liquid as effcient, green and reusable acidic catalyst system for oligomerization of olefins. Catal. Commun., 2003, 4(11), 597-601.
    • (2003) Catal. Commun , vol.4 , Issue.11 , pp. 597-601
    • Gu, Y.1    Shi, F.2    Deng, Y.3
  • 75
    • 21644435816 scopus 로고    scopus 로고
    • FTIR study on deactivation of sulfonyl chloride functionalized ionic materials as dual catalysts and media for Beckmann rearrangement of cyclohexanone oxime
    • Du, Z.; Li, Z.; Gu, Y. Zhang, J. Deng Y. FTIR study on deactivation of sulfonyl chloride functionalized ionic materials as dual catalysts and media for Beckmann rearrangement of cyclohexanone oxime, J. Mol. Catal. A: Chem., 2005, 237(1-2), 80-85.
    • (2005) J. Mol. Catal. A: Chem , vol.237 , Issue.1-2 , pp. 80-85
    • Du, Z.1    Li, Z.2    Gu, Y.3    Zhang, J.4    Deng, Y.5
  • 76
    • 3142658251 scopus 로고    scopus 로고
    • Novel Acidic Ionic Liquids Catalytic Systems fo Friedel-Crafts Alkylation of Aromatic Compounds with Alkenes
    • Qiao, K.; Yokoyama, C. Novel Acidic Ionic Liquids Catalytic Systems fo Friedel-Crafts Alkylation of Aromatic Compounds with Alkenes. Chem. Lett., 2004, 33(4), 472-473.
    • (2004) Chem. Lett , vol.33 , Issue.4 , pp. 472-473
    • Qiao, K.1    Yokoyama, C.2
  • 77
    • 11844264846 scopus 로고    scopus 로고
    • Preparation of α-caprolactam via beckmann rearrangement of cyclohexanone oxime: A mild and recyclable process
    • Qiao, K.; Deng, Y. Q.; Yokoyama, C.; Sato, H.; Yamashina, M. Preparation of α-caprolactam via beckmann rearrangement of cyclohexanone oxime: a mild and recyclable process. Chem. Lett., 2004, 33(7), 1350-1351.
    • (2004) Chem. Lett , vol.33 , Issue.7 , pp. 1350-1351
    • Qiao, K.1    Deng, Y.Q.2    Yokoyama, C.3    Sato, H.4    Yamashina, M.5
  • 78
    • 33646404392 scopus 로고    scopus 로고
    • Koch carbonylation of tertiary alcohols in the presence of acidic ionic liquids
    • Qiao, K., Yokoyama, C. Koch carbonylation of tertiary alcohols in the presence of acidic ionic liquids. Catal. Commun., 2006, 7(7) 450-453.
    • (2006) Catal Commun , vol.7 , Issue.7 , pp. 450-453
    • Qiao, K.1    Yokoyama, C.2
  • 79
    • 39249083156 scopus 로고    scopus 로고
    • Preparation of 5-hydroymethylfurfural by dehydration of fructose in the presence of acidic ionic liquid
    • Bao, Q.; Qiao, K.; Tomida, D.; Yokoyama, C. Preparation of 5-hydroymethylfurfural by dehydration of fructose in the presence of acidic ionic liquid. Catal. Commun., 2008, 9(6), 1383-1388.
    • (2008) Catal. Commun , vol.9 , Issue.6 , pp. 1383-1388
    • Bao, Q.1    Qiao, K.2    Tomida, D.3    Yokoyama, C.4
  • 80
    • 32844467648 scopus 로고    scopus 로고
    • Acidic ionic liquid modified silica gel as novel solid catalysts for esterification and nitration reactions
    • Qiao, K.; Hagiwara, H.; Yokoyama, C. Acidic ionic liquid modified silica gel as novel solid catalysts for esterification and nitration reactions. J. Mol. Catal. A: Chem., 2006, 246(1-2), 65-69.
    • (2006) J. Mol. Catal. A: Chem , vol.246 , Issue.1-2 , pp. 65-69
    • Qiao, K.1    Hagiwara, H.2    Yokoyama, C.3
  • 81
    • 62649090096 scopus 로고    scopus 로고
    • Enhancing nucleophilicity in ionic liquid [bmim]HSO4: A recyclable media and catalyst for the halogenation of alcohols
    • Gupta, N.; Kad, G. L.; Singh, Jasvinder. Enhancing nucleophilicity in ionic liquid [bmim]HSO4: A recyclable media and catalyst for the halogenation of alcohols, J. Mol. Catal. A: Chem., 2009, 302(1-2), 11-14.
    • (2009) J. Mol. Catal. A: Chem , vol.302 , Issue.1-2 , pp. 11-14
    • Gupta, N.1    Kad, G.L.2    Singh, J.3
  • 82
    • 9344259701 scopus 로고    scopus 로고
    • A Mild, Efficient, and inexpensive protocol for the selective deprotection of TBDMS ethers using KHSO4
    • Arumugam, P.; Karthikeyan, G.; Perumal, P. T. A Mild, efficient, and inexpensive protocol for the selective deprotection of TBDMS ethers using KHSO4. Chem. Lett., 2004, 33(9), 1146-1147.
    • (2004) Chem. Lett , vol.33 , Issue.9 , pp. 1146-1147
    • Arumugam, P.1    Karthikeyan, G.2    Perumal, P.T.3
  • 83
    • 64349096412 scopus 로고    scopus 로고
    • Glycolysis of poly(ethylene terephthalate) catalyzed by ionic liquids
    • Wang, H.; Liu, Y.; Li, Z.; Zhang, X.; Zhang, S.; Zhang, Y. Glycolysis of poly(ethylene terephthalate) catalyzed by ionic liquids. Eur. Polym. J., 2009, 45(5), 1535-1544.
    • (2009) Eur. Polym. J , vol.45 , Issue.5 , pp. 1535-1544
    • Wang, H.1    Liu, Y.2    Li, Z.3    Zhang, X.4    Zhang, S.5    Zhang, Y.6
  • 84
    • 2342527334 scopus 로고    scopus 로고
    • New biginelli reaction procedure using potassium hydrogen sulfate as the promoter for an efficient synthesis of 3, 4-dihydropyrimidin-2(1H)-one
    • Tu, S.; Fang, F.; Zhu, S.; Li, T.; Zhang, X.; Zhuang, Q. A New biginelli reaction procedure using potassium hydrogen sulfate as the promoter for an efficient synthesis of 3, 4-dihydropyrimidin-2(1H)-one. J. Heterocyclic Chem., 2004, 41(2), 253-257.
    • (2004) J. Heterocyclic Chem , vol.41 , Issue.2 , pp. 253-257
    • Tu, S.1    Fang, F.2    Zhu, S.3    Li, T.4    Zhang, X.5    Zhuang, Q.A.6
  • 85
    • 10944258867 scopus 로고    scopus 로고
    • Microwave accelerated preparation of [bmim]HSO4 ionic liquid: An acid catalyst for improved synthesis of coumarins
    • Singh, V.; Kaur, S.; Sapehiyia, V.; Singh, J.; Kad, G. L. Microwave accelerated preparation of [bmim]HSO4 ionic liquid: an acid catalyst for improved synthesis of coumarins. Catal. Commun., 2005, 6(1), 57-60.
    • (2005) Catal. Commun , vol.6 , Issue.1 , pp. 57-60
    • Singh, V.1    Kaur, S.2    Sapehiyia, V.3    Singh, J.4    Kad, G.L.5
  • 86
    • 67649210315 scopus 로고    scopus 로고
    • Conversion of mono/di/polysaccharides into furan compounds using 1-alkyl-3-methylimidazolium ionic liquids
    • Lima, S.; Neves, P.; Antunes, M. M.; Pillinger, M.; Ignatyev, N.; Valente, A. A. Conversion of mono/di/polysaccharides into furan compounds using 1-alkyl-3-methylimidazolium ionic liquids. Appl. Catal. A: Gen., 2009, 363(1-2), 93-99.
    • (2009) Appl. Catal. A: Gen , vol.363 , Issue.1-2 , pp. 93-99
    • Lima, S.1    Neves, P.2    Antunes, M.M.3    Pillinger, M.4    Ignatyev, N.5    Valente, A.A.6
  • 87
    • 36548999346 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids as novel catalysts for Prins reaction
    • Wang, W.; Shao, L.; Cheng, W.; Yang, J.; He, M. Brønsted acidic ionic liquids as novel catalysts for Prins reaction. Catal. Commun., 2008, 9(3), 337-341.
    • (2008) Catal. Commun , vol.9 , Issue.3 , pp. 337-341
    • Wang, W.1    Shao, L.2    Cheng, W.3    Yang, J.4    He, M.5
  • 88
    • 54049105604 scopus 로고    scopus 로고
    • Nitration of aromatic compounds with NO2/air catalyzed by sulfonic acid-functionalized ionic liquids
    • Cheng, G.; Duan, X.; Qi, X.; Lu, C. Nitration of aromatic compounds with NO2/air catalyzed by sulfonic acid-functionalized ionic liquids. Catal. Commun., 2008, 10(2), 201-204.
    • (2008) Catal. Commun , vol.10 , Issue.2 , pp. 201-204
    • Cheng, G.1    Duan, X.2    Qi, X.3    Lu, C.4
  • 89
    • 61849089322 scopus 로고    scopus 로고
    • Functionalized ionic liquid as the recyclable catalyst for mannich-type reaction in aqueous media
    • Fang, D.; Fei, Z.; Liu, Z. Functionalized ionic liquid as the recyclable catalyst for mannich-type reaction in aqueous media. Catal. Commun., 2009, 10(8), 1267-1270.
    • (2009) Catal. Commun , vol.10 , Issue.8 , pp. 1267-1270
    • Fang, D.1    Fei, Z.2    Liu, Z.3
  • 90
    • 36248989701 scopus 로고    scopus 로고
    • A practical and efficient synthesis of quinoxaline derivatives catalyzed by task-specific ionic liquid
    • Fang, D.; Gong, K.; Fei, Z.; Zhou, X.; Liu, Z. A practical and efficient synthesis of quinoxaline derivatives catalyzed by task-specific ionic liquid. Catal. Commun., 2008, 9(2), 317-320.
    • (2008) Catal. Commun , vol.9 , Issue.2 , pp. 317-320
    • Fang, D.1    Gong, K.2    Fei, Z.3    Zhou, X.4    Liu, Z.5
  • 91
    • 66949171844 scopus 로고    scopus 로고
    • A Brønsted acidic ionic liquid as an efficient and environmentally benign catalyst for biodiesel synthesis from free fatty acids and alcohols
    • Zhang, L.; Xian, M.; He, Y.; Li, L.; Yang, J.; Yu, S.; Xu, X. A Brønsted acidic ionic liquid as an efficient and environmentally benign catalyst for biodiesel synthesis from free fatty acids and alcohols. Bioresource Technol., 2009, 100(19), 4368-4373.
    • (2009) Bioresource Technol , vol.100 , Issue.19 , pp. 4368-4373
    • Zhang, L.1    Xian, M.2    He, Y.3    Li, L.4    Yang, J.5    Yu, S.6    Xu, X.7
  • 92
    • 59249093330 scopus 로고    scopus 로고
    • Bronsted acidic ionic liquid as an efficient and reusable catalyst for transesterification of α-ketoesters
    • Qureshi, Z. S.; Deshmukh, K. M.; Bhor, M. D.; Bhanage, B. M. Bronsted acidic ionic liquid as an efficient and reusable catalyst for transesterification of α-ketoesters. Catal.Commun., 2009, 10(6), 833-837.
    • (2009) Catal.Commun , vol.10 , Issue.6 , pp. 833-837
    • Qureshi, Z.S.1    Deshmukh, K.M.2    Bhor, M.D.3    Bhanage, B.M.4
  • 93
    • 57249093618 scopus 로고    scopus 로고
    • Hydrogensulfate and tetrakis (hydrogensulfato) borate ionic liquids: Synthesis and catalytic application in highly brønsted-acidic systems for friedel-crafts alkylation
    • Wasserscheid, P.; Sesing, M.; Korth, W. Hydrogensulfate and tetrakis (hydrogensulfato) borate ionic liquids: synthesis and catalytic application in highly brønsted-acidic systems for friedel-crafts alkylation. Green Chem., 2002, 4(2), 134-138.
    • (2002) Green Chem , vol.4 , Issue.2 , pp. 134-138
    • Wasserscheid, P.1    Sesing, M.2    Korth, W.3
  • 94
    • 22144492579 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids: Fast, mild, and efficient catalysts for solvent-free tetrahydropyranylation of alcohol
    • Duan, Z.; Gu, Y.; Deng, Y. Brønsted acidic ionic liquids: fast, mild, and efficient catalysts for solvent-free tetrahydropyranylation of alcohol. Synthetic Commun., 2005, 35(14), 1939-1945.
    • (2005) Synthetic Commun , vol.35 , Issue.14 , pp. 1939-1945
    • Duan, Z.1    Gu, Y.2    Deng, Y.3
  • 95
    • 37349086512 scopus 로고    scopus 로고
    • Green approach for the synthesis of long chain aliphatic acid esters at room temperature
    • Li, X.; Eli, W. A green approach for the synthesis of long chain aliphatic acid esters at room temperature. J. Mol. Catal. A: Chem., 2008, 279(2), 159-164.
    • (2008) J. Mol. Catal. A: Chem , vol.279 , Issue.2 , pp. 159-164
    • Li, X.1    Eli, W.A.2
  • 96
    • 38149139219 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids as dual catalyst and solvent for environmentally friendly synthesis of chalcone
    • Shen, J.; Wang, H.; Liu, H.; Sun, Y.; Liu, Z. Brønsted acidic ionic liquids as dual catalyst and solvent for environmentally friendly synthesis of chalcone. J. Mol. Catal. A: Chem., 2008, 280(1-2), 24-28.
    • (2008) J. Mol. Catal. A: Chem , vol.280 , Issue.1-2 , pp. 24-28
    • Shen, J.1    Wang, H.2    Liu, H.3    Sun, Y.4    Liu, Z.5
  • 97
    • 20344385743 scopus 로고    scopus 로고
    • Novel brønsted-acidic ionic liquids for esterifications
    • Xing, H.; Wang, T.; Zhou, Z.; Dai, Y. Novel brønsted-acidic ionic liquids for esterifications. Ind. Eng. Chem. Res., 2005, 44(11), 4147-4150.
    • (2005) Ind. Eng. Chem. Res , vol.44 , Issue.11 , pp. 4147-4150
    • Xing, H.1    Wang, T.2    Zhou, Z.3    Dai, Y.4
  • 99
    • 33847290523 scopus 로고    scopus 로고
    • The sulfonic acid-functionalized ionic liquids with pyridinium cations: Acidities and their acidity-catalytic activity relationships
    • Xing, H.; Wang, T.; Zhou, Z.; Dai, Y. The sulfonic acid-functionalized ionic liquids with pyridinium cations: Acidities and their acidity-catalytic activity relationships. J. Mol. Catal. A: Chem., 2007, 264(1-2), 53-59.
    • (2007) J. Mol. Catal. A: Chem , vol.264 , Issue.1-2 , pp. 53-59
    • Xing, H.1    Wang, T.2    Zhou, Z.3    Dai, Y.4
  • 100
    • 0344394380 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquid 1-methylimidazolium tetrafluoroborate: A green catalyst and recyclable medium for esterification
    • Zhu, H. P.; Yang, F.; Tang, J.; He, M. Y. Brønsted acidic ionic liquid 1-methylimidazolium tetrafluoroborate: a green catalyst and recyclable medium for esterification. Green Chem., 2003, 5(1), 38-39.
    • (2003) Green Chem , vol.5 , Issue.1 , pp. 38-39
    • Zhu, H.P.1    Yang, F.2    Tang, J.3    He, M.Y.4
  • 101
    • 27544456965 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids as efficient and recyclable catalysts for protection of carbonyls to acetals and ketals under mild conditions
    • Du, Y.; Tian, F. Brønsted acidic ionic liquids as efficient and recyclable catalysts for protection of carbonyls to acetals and ketals under mild conditions. Synthetic Commun., 2005, http://www.informaworld.com/smpp/title~db=all~content=t713597304~tab=issueslist~branches=35-v3535(20), 2703-2708.
    • (2005) Synthetic Commun , pp. 2703-2708
    • Du, Y.1    Tian, F.2
  • 102
    • 2942606279 scopus 로고    scopus 로고
    • An efficient procedure for protection of carbonyls in Brønsted acidic ionic liquid [Hmim]BF4
    • Wu, H. H.; Yang, F.; Cui, P.; Tang, J.; He, M. Y. An efficient procedure for protection of carbonyls in Brønsted acidic ionic liquid [Hmim]BF4. Tetrahedron Lett., 2004, 45(15), 4963-4965.
    • (2004) Tetrahedron Lett , vol.45 , Issue.15 , pp. 4963-4965
    • Wu, H.H.1    Yang, F.2    Cui, P.3    Tang, J.4    He, M.Y.5
  • 103
    • 33751366817 scopus 로고    scopus 로고
    • Preparation of dialkoxypropanes in simple ammonium ionic liquids
    • Jiang, H.; Wang, C.; Li, H.; Wang, Y. Preparation of dialkoxypropanes in simple ammonium ionic liquids. Green Chem., 2006, 8(12), 1076-1079.
    • (2006) Green Chem , vol.8 , Issue.12 , pp. 1076-1079
    • Jiang, H.1    Wang, C.2    Li, H.3    Wang, Y.4
  • 104
    • 33745629393 scopus 로고    scopus 로고
    • Preparation of simple ammonium ionic liquids and their application in the cracking of dialkoxypropanes
    • Wang, C.; Guo, L.; Li, H.; Wang, Y. Weng J.; and Wu, L. Preparation of simple ammonium ionic liquids and their application in the cracking of dialkoxypropanes. Green Chem., 2006, 8(7), 603-607.
    • (2006) Green Chem , vol.8 , Issue.7 , pp. 603-607
    • Wang, C.1    Guo, L.2    Li, H.3    Wang, Y.4    Weng, J.5    Wu, L.6
  • 105
    • 0344391969 scopus 로고    scopus 로고
    • Ionic liquid-promoted regiospecific friedlander annulation: Novel synthesis of quinolines and fused polycyclic quinolines
    • Palimkar, S. S.; Siddiqui, S. A.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. Ionic liquid-promoted regiospecific friedlander annulation: novel synthesis of quinolines and fused polycyclic quinolines. J. Org. Chem., 2003, 68(24), 9371-9378./
    • (2003) J. Org. Chem , vol.68 , Issue.24 , pp. 9371-9378
    • Palimkar, S.S.1    Siddiqui, S.A.2    Daniel, T.3    Lahoti, R.J.4    Srinivasan, K.V.5
  • 106
    • 67650475329 scopus 로고    scopus 로고
    • Efficient and rapid stereoselective synthesis of trans-4,5-diaminocyclopent-2-enones by acidic ionic liquid under solvent- free conditions
    • Ramesh, D.; T Reddy, S.; Narasimhulu, M.; Rajaram, S.; Suryakiran, N.; Mahesh, K. C.; Venkateswarlu, Y. Efficient and rapid stereoselective synthesis of trans-4,5-diaminocyclopent-2-enones by acidic ionic liquid under solvent- free conditions. Chem. Lett., 2009, 38(6), 586-587.
    • (2009) Chem. Lett , vol.38 , Issue.6 , pp. 586-587
    • Ramesh, D.T.1    Reddy, S.2    Narasimhulu, M.3    Rajaram, S.4    Suryakiran, N.5    Mahesh, K.C.6    Venkateswarlu, Y.7
  • 107
    • 1342268959 scopus 로고    scopus 로고
    • Mannich reaction using acidic ionic liquids as catalysts and solvents
    • Zhao, G.; Jiang, T.; Gao, H.; Han, B.; Huang, J.; Sun, D. Mannich reaction using acidic ionic liquids as catalysts and solvents. Green Chem., 2004, 6(2), 75-77.
    • (2004) Green Chem , vol.6 , Issue.2 , pp. 75-77
    • Zhao, G.1    Jiang, T.2    Gao, H.3    Han, B.4    Huang, J.5    Sun, D.6
  • 108
    • 53049086984 scopus 로고    scopus 로고
    • Novel and efficient one-pottandem synthesis of 2-styryl-substituted 4(3h)-quinazolinones
    • Dabiri, M.; Baghbanzadeh, M.; Delbari, A. S. Novel and efficient one-pottandem synthesis of 2-styryl-substituted 4(3h)-quinazolinones. J. Comb. Chem., 2008, 10(5), 700-703.
    • (2008) J. Comb. Chem , vol.10 , Issue.5 , pp. 700-703
    • Dabiri, M.1    Baghbanzadeh, M.2    Delbari, A.S.3
  • 109
    • 1642526412 scopus 로고    scopus 로고
    • Ionic liquid promoted novel and efficient one pot synthesis of 3, 4-dihydropyrimidin-2-(1H)-ones at ambient temperature under ultrasound irradiation
    • Gholap, A. R.; Venkatesan, K.; Daniel, T.; Lahoti, R. J.; Srinivasan, K. V. Ionic liquid promoted novel and efficient one pot synthesis of 3, 4-dihydropyrimidin-2-(1H)-ones at ambient temperature under ultrasound irradiation. Green Chem., 2004, 6(3), 147-150.
    • (2004) Green Chem , vol.6 , Issue.3 , pp. 147-150
    • Gholap, A.R.1    Venkatesan, K.2    Daniel, T.3    Lahoti, R.J.4    Srinivasan, K.V.5
  • 110
    • 51549103247 scopus 로고    scopus 로고
    • Ionic liquid-promoted one-pot oxidative Michael addition of TMSCN to Baylis-Hillman adducts
    • Yadav, L. D. S.; Awasthi, C.; Rai, A. Ionic liquid-promoted one-pot oxidative Michael addition of TMSCN to Baylis-Hillman adducts. Tetrahedron Lett., 2008, 49(44), 6360-6363.
    • (2008) Tetrahedron Lett , vol.49 , Issue.44 , pp. 6360-6363
    • Yadav, L.D.S.1    Awasthi, C.2    Rai, A.3
  • 111
    • 17144407949 scopus 로고    scopus 로고
    • An efficient synthesisof Bis(indolyl)methanes catalyzed by recycled acidic ionic liquid
    • Gu, D. G.; Ji, S. J.; Jiang, Z. Q.; Zhou, M. F.; Loh, T. P. An efficient synthesisof Bis(indolyl)methanes catalyzed by recycled acidic ionic liquid. Synlett, 2005, 16(6), 959-962.
    • (2005) Synlett , vol.16 , Issue.6 , pp. 959-962
    • Gu, D.G.1    Ji, S.J.2    Jiang, Z.Q.3    Zhou, M.F.4    Loh, T.P.5
  • 112
    • 67649114373 scopus 로고    scopus 로고
    • Solvent-free synthesis of unsaturated ketones by the Saucy-Marbet reaction using simple ammonium ionic liquid as a catalyst
    • Wang, C.; Zhao, W.; Li H.; Guo, L. Solvent-free synthesis of unsaturated ketones by the Saucy-Marbet reaction using simple ammonium ionic liquid as a catalyst. Green Chem., 2009, 11(6), 843-847.
    • (2009) Green Chem , vol.11 , Issue.6 , pp. 843-847
    • Wang, C.1    Zhao, W.2    Li, H.3    Guo, L.4
  • 113
    • 57749091290 scopus 로고    scopus 로고
    • Mild and efficient method forpreparation of azides from alcohols using acidic ionic liquid [H-NMP]HSO4
    • Hajipour, A. R.; Rajaei, A.; Ruoho, A. E. Mild and efficient method forpreparation of azides from alcohols using acidic ionic liquid [H-NMP]HSO4. Tetrahedron Lett., 2009, 50(6), 708-711.
    • (2009) Tetrahedron Lett , vol.50 , Issue.6 , pp. 708-711
    • Hajipour, A.R.1    Rajaei, A.2    Ruoho, A.E.3
  • 114
    • 35848952952 scopus 로고    scopus 로고
    • Brönsted acidic ionic liquid as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions
    • Hajipour, A. R.; Khazdooz, L.; Ruoho, A. E. Brönsted acidic ionic liquid as an efficient catalyst for chemoselective synthesis of 1,1-diacetates under solvent-free conditions. Catal. Commun., 2008, 9(1), 89-96.
    • (2008) Catal. Commun , vol.9 , Issue.1 , pp. 89-96
    • Hajipour, A.R.1    Khazdooz, L.2    Ruoho, A.E.3
  • 115
    • 38849145148 scopus 로고    scopus 로고
    • 1-Methylimidazolium triflouroacetate ([Hmim]TFA): An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines
    • Dabiri, M.; Baghbanzadeh, M.; Arzroomchilar, E. 1-Methylimidazolium triflouroacetate ([Hmim]TFA): An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo-octahydroxanthenes and 1,8-dioxo-decahydroacridines. Catal. Commun., 2008, 9(5), 939-942.
    • (2008) Catal. Commun , vol.9 , Issue.5 , pp. 939-942
    • Dabiri, M.1    Baghbanzadeh, M.2    Arzroomchilar, E.3
  • 116
    • 27544454975 scopus 로고    scopus 로고
    • Investigation of physicochemical properties of lactam-based brønsted acidic ionic liquids
    • Du, Z.; Li, Z.; Guo, S.; Zhang, J.; Zhu, L.; Deng, Y. Investigation of physicochemical properties of lactam-based brønsted acidic ionic liquids. J. Phys. Chem. B, 2005, 109(41), 19542-19546.
    • (2005) J. Phys. Chem. B , vol.109 , Issue.41 , pp. 19542-19546
    • Du, Z.1    Li, Z.2    Guo, S.3    Zhang, J.4    Zhu, L.5    Deng, Y.6
  • 117
    • 33644751841 scopus 로고    scopus 로고
    • Clean beckmann rearrangement of cyclohexanone oxime in caprolactambased brønsted acidic ionic liquids
    • Guo, S.; Du, Z.; Zhang, S.; Li, D.; Li, Z.; Deng, Y. Clean beckmann rearrangement of cyclohexanone oxime in caprolactambased brønsted acidic ionic liquids. Green Chem., 2006, 8(3), 296-300.
    • (2006) Green Chem , vol.8 , Issue.3 , pp. 296-300
    • Guo, S.1    Du, Z.2    Zhang, S.3    Li, D.4    Li, Z.5    Deng, Y.6
  • 118
    • 33646021312 scopus 로고    scopus 로고
    • Protic pyridinium ionic liquids: Synthesis, acidity determination and their performances for acid catalysis
    • Duan, Z.; Gu, Y.; Zhang, J.; Zhu, L.; Deng, Y. Protic pyridinium ionic liquids: synthesis, acidity determination and their performances for acid catalysis. J. Mol. Catal. A: Chem., 2006, 250(1-2), 163-168.
    • (2006) J. Mol. Catal. A: Chem , vol.250 , Issue.1-2 , pp. 163-168
    • Duan, Z.1    Gu, Y.2    Zhang, J.3    Zhu, L.4    Deng, Y.5
  • 120
    • 11944251255 scopus 로고    scopus 로고
    • Tunable dimerization of a-methylstyrene catalyzed by acidic ionic liquids
    • Cai, Q.; Li, J.; Bao, F.; Shan, Y. Tunable dimerization of a-methylstyrene catalyzed by acidic ionic liquids. Appl, Catal, A: Gen., 2005, 279(1-2), 139-143.
    • (2005) Appl, Catal, A: Gen , vol.279 , Issue.1-2 , pp. 139-143
    • Cai, Q.1    Li, J.2    Bao, F.3    Shan, Y.4
  • 121
    • 33645968949 scopus 로고    scopus 로고
    • Temperature-controlled highly selective dimerization of a-methylstyrene catalyzed by brønsted acidic ionic liquid under solvent-free conditions
    • Wang, H.; Cui, P.; Zou, G.; Yang, F.; Tang, J. Temperature-controlled highly selective dimerization of a-methylstyrene catalyzed by brønsted acidic ionic liquid under solvent-free conditions. Tetrahedron, 2006, 62(17), 3985-3988.
    • (2006) Tetrahedron , vol.62 , Issue.17 , pp. 3985-3988
    • Wang, H.1    Cui, P.2    Zou, G.3    Yang, F.4    Tang, J.5
  • 122
    • 4444354020 scopus 로고    scopus 로고
    • Anti-microbial activities of protic ionic liquids with lactate anion
    • Pernak, J.; Goc, I.; Mirska, I. Anti-microbial activities of protic ionic liquids with lactate anion. Green Chem., 2004, 6(7), 323-329.
    • (2004) Green Chem , vol.6 , Issue.7 , pp. 323-329
    • Pernak, J.1    Goc, I.2    Mirska, I.3
  • 123
    • 33745627525 scopus 로고    scopus 로고
    • Preparation, characterization and application of amino acid-based green ionic liquids
    • Tao, G.-H.; He, L.; Liu, W.-S.; Xu, L.; Xiong, W.; Wang, T.; Kou, Y. Preparation, characterization and application of amino acid-based green ionic liquids. Green Chem., 2006, 8(7), 639-646.
    • (2006) Green Chem , vol.8 , Issue.7 , pp. 639-646
    • Tao, G.-H.1    He, L.2    Liu, W.-S.3    Xu, L.4    Xiong, W.5    Wang, T.6    Kou, Y.7
  • 124
    • 15044358033 scopus 로고    scopus 로고
    • Rationalisation of solvent effects in the diels-alder reaction between cyclopentadiene and methyl acrylate in room temperature ionic liquids
    • Vidi, A.; Ohlin, C. A.; Laurenczy, G.; Küsters, E.; Sedelmeier, G.; Dyson, P. J.; Rationalisation of solvent effects in the diels-alder reaction between cyclopentadiene and methyl acrylate in room temperature ionic liquids. Adv. Synth. Catal., 2005, 347(2-3), 266-274.
    • (2005) Adv. Synth. Catal , vol.347 , Issue.2-3 , pp. 266-274
    • Vidi, A.1    Ohlin, C.A.2    Laurenczy, G.3    Küsters, E.4    Sedelmeier, G.5    Dyson, P.J.6
  • 125
    • 37349005208 scopus 로고    scopus 로고
    • Amino acid ionic liquids
    • Ohno, H.; Fukumoto, K. Amino acid ionic liquids. Acc. Chem. Res., 2007, 40(11), 1122-1129.
    • (2007) Acc. Chem. Res , vol.40 , Issue.11 , pp. 1122-1129
    • Ohno, H.1    Fukumoto, K.2
  • 127
    • 0035858618 scopus 로고    scopus 로고
    • Ionic liquids as recyclable reaction media for the tetrahydropyranylation of alcohols
    • Branco, L. C.; Afonso, C. A. M. Ionic liquids as recyclable reaction media for the tetrahydropyranylation of alcohols. Tetrahedron, 2001, 57(20), 4405-4410.
    • (2001) Tetrahedron , vol.57 , Issue.20 , pp. 4405-4410
    • Branco, L.C.1    Afonso, C.A.M.2
  • 128
    • 18144381931 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids: A green, efficient and reusable catalyst system and reaction medium for fischer esterification
    • Joseph, T.; Sahoo, S.; Halligudi, S. B. Brønsted acidic ionic liquids: A green, efficient and reusable catalyst system and reaction medium for fischer esterification. J. Mol. Catal. A: Chem., 2005, 234(1-2), 107-110.
    • (2005) J. Mol. Catal. A: Chem , vol.234 , Issue.1-2 , pp. 107-110
    • Joseph, T.1    Sahoo, S.2    Halligudi, S.B.3
  • 129
    • 0001744693 scopus 로고
    • Triphenylphosphine hydrobromide: A mild and efficient catalyst for tetrahydropyranylation of tertiary alcohols
    • Bolitt, V.; Mioskowski, C.; Shin, D. S.; J Falck,. R. Triphenylphosphine hydrobromide: A mild and efficient catalyst for tetrahydropyranylation of tertiary alcohols. Tetrahedron Lett., 1988, 29(36), 4583-4586.
    • (1988) Tetrahedron Lett , vol.29 , Issue.36 , pp. 4583-4586
    • Bolitt, V.1    Mioskowski, C.2    Shin, D.S.3    Falck, J.R.4
  • 130
    • 0032482514 scopus 로고    scopus 로고
    • Comparative studies of the deprotection of various acid sensitive protecting groups with pyridinium p-toluenesulphonate
    • Zaidi, J. H.; Fauq, A. H.; Ahmed, N. Comparative studies of the deprotection of various acid sensitive protecting groups with pyridinium p-toluenesulphonate. Tetrahedron Lett., 1998, 39(23), 4137-4138.
    • (1998) Tetrahedron Lett , vol.39 , Issue.23 , pp. 4137-4138
    • Zaidi, J.H.1    Fauq, A.H.2    Ahmed, N.3
  • 131
    • 44249125453 scopus 로고    scopus 로고
    • Polymer-supported protic functionalized ionic liquids for nucleophilic substitution reactions: Superior catalytic activity compared to other ionic resins
    • Shinde, S. S.; Lee, B. S.; Chi, D. Y. Polymer-supported protic functionalized ionic liquids for nucleophilic substitution reactions: superior catalytic activity compared to other ionic resins. Tetrahedron Lett., 2008, 4(27), 4245-4248.
    • (2008) Tetrahedron Lett , vol.4 , Issue.27 , pp. 4245-4248
    • Shinde, S.S.1    Lee, B.S.2    Chi, D.Y.3
  • 132
    • 0038506180 scopus 로고    scopus 로고
    • A novel greener glycosidation using an acid-ionic liquid containing a protic acid
    • Sasaki, K.; Nagai, H.; Matsumura, S.; Toshima, K. A novel greener glycosidation using an acid-ionic liquid containing a protic acid, Tetrahedron Lett., 2003, 44(30), 5605-5608.
    • (2003) Tetrahedron Lett , vol.44 , Issue.30 , pp. 5605-5608
    • Sasaki, K.1    Nagai, H.2    Matsumura, S.3    Toshima, K.4
  • 133
    • 34248531272 scopus 로고    scopus 로고
    • Aryl C-glycosylation using an ionic liquid containing a protic acid
    • Yamada, C.; Sasaki, K.; Matsumura, S.; Toshima, K. Aryl C-glycosylation using an ionic liquid containing a protic acid. Tetrahedron Letters, 2007, 48(24), 4223-4227.
    • (2007) Tetrahedron Letters , vol.48 , Issue.24 , pp. 4223-4227
    • Yamada, C.1    Sasaki, K.2    Matsumura, S.3    Toshima, K.4
  • 134
    • 70349769318 scopus 로고    scopus 로고
    • Baylis-Hillman reaction promoted by a recyclable protic-ionic-liquid solvent-catalyst system: DABCO-AcOH-H2O
    • Song, Y.; Ke, H.; Wang, N.; Wang, L.; Zou, G. Baylis-Hillman reaction promoted by a recyclable protic-ionic-liquid solvent-catalyst system: DABCO-AcOH-H2O. Tetrahedron, 2009, 65(45), 9086-9090.
    • (2009) Tetrahedron , vol.65 , Issue.45 , pp. 9086-9090
    • Song, Y.1    Ke, H.2    Wang, N.3    Wang, L.4    Zou, G.5
  • 135
  • 136
    • 1242317728 scopus 로고    scopus 로고
    • Esterification of aliphatic acids with olefin promoted by brønsted acidic ionic liquids
    • Gu, Y.; Shi, F; Deng, Y. Esterification of aliphatic acids with olefin promoted by brønsted acidic ionic liquids. J. Mol. Catal. A: Chem., 2004, 212(1-2), 71-75.
    • (2004) J. Mol. Catal. A: Chem , vol.212 , Issue.1-2 , pp. 71-75
    • Gu, Y.1    Shi, F.2    Deng, Y.3
  • 137
    • 1642561840 scopus 로고    scopus 로고
    • Determination of the lewis acidity of ionic liquids by means of an IR spectroscopic probe
    • Yang, Y.; Kou, Y. Determination of the lewis acidity of ionic liquids by means of an IR spectroscopic probe. Chem. Commun., 2004, 2, 226-227.
    • (2004) Chem. Commun , vol.2 , pp. 226-227
    • Yang, Y.1    Kou, Y.2
  • 138
    • 5444234125 scopus 로고    scopus 로고
    • Brønsted acidic ionic liquids and their zwitterions: Synthesis, characterization and pka determination
    • Fei, Z.; Zhao, D.; Geldbach, T. J.; Scopelliti, R.; Dyson, P. J. Brønsted acidic ionic liquids and their zwitterions: synthesis, characterization and pka determination. Chem. Eur. J., 2004, 10, 4886-4893.
    • (2004) Chem. Eur. J , vol.10 , pp. 4886-4893
    • Fei, Z.1    Zhao, D.2    Geldbach, T.J.3    Scopelliti, R.4    Dyson, P.J.5
  • 140
    • 1642567251 scopus 로고    scopus 로고
    • Biodegradable ionic liquids: Part I. concept, preliminary targets and evaluation
    • Gathergood, N.; Garcia, M. T.; Scammells, P. J. Biodegradable ionic liquids: Part I. concept, preliminary targets and evaluation. Green Chem., 2004, 6(3), 166-175.
    • (2004) Green Chem , vol.6 , Issue.3 , pp. 166-175
    • Gathergood, N.1    Garcia, M.T.2    Scammells, P.J.3
  • 141
    • 1542786165 scopus 로고    scopus 로고
    • Designing Safer Chemicals
    • Boethling, R. S. Designing Safer Chemicals, ACS Symp. Ser. 640, 1996, 156.
    • (1996) ACS Symp. Ser , vol.640 , pp. 156
    • Boethling, R.S.1
  • 143
    • 34447107806 scopus 로고    scopus 로고
    • Biodegradability of imidazolium and pyridinium ionic liquids by an activated sludge microbial community
    • Docherty, K. M.; Dixon, J. K.; Kulpa Jr, C. F. Biodegradability of imidazolium and pyridinium ionic liquids by an activated sludge microbial community. Biodegradation, 2007, 18(4), 481-493.
    • (2007) Biodegradation , vol.18 , Issue.4 , pp. 481-493
    • Docherty, K.M.1    Dixon, J.K.2    Kulpa, C.F.3
  • 144
    • 64149089656 scopus 로고    scopus 로고
    • Toxicity of imidazolium and pyridinium based ionic liquids towards algae. Chlorella vulgaris, Oocystis submarina (green algae) and Cyclotella meneghiniana, Skeletonema marinoi (diatoms)
    • Lataĺa, A.; Nédzi, M.; Stepnowski, P. Toxicity of imidazolium and pyridinium based ionic liquids towards algae. Chlorella vulgaris, Oocystis submarina (green algae) and Cyclotella meneghiniana, Skeletonema marinoi (diatoms). Green Chem., 2009, 11(4), 580-588.
    • (2009) Green Chem , vol.11 , Issue.4 , pp. 580-588
    • Lataĺa, A.1    Nédzi, M.2    Stepnowski, P.3
  • 145
    • 69949166905 scopus 로고    scopus 로고
    • Toxicity of imidazolium and pyridinium based ionic liquids towards algae. Bacillaria paxillifer (a microphytobenthic diatom) and Geitlerinema amphibium (a microphytobenthic blue green alga
    • Lataĺa, A.; Nédzi, M.; Stepnowski, P. Toxicity of imidazolium and pyridinium based ionic liquids towards algae. Bacillaria paxillifer (a microphytobenthic diatom) and Geitlerinema amphibium (a microphytobenthic blue green alga. Green Chem., 2009, 11(9), 1371-1376.
    • (2009) Green Chem , vol.11 , Issue.9 , pp. 1371-1376
    • Lataĺa, A.1    Nédzi, M.2    Stepnowski, P.3
  • 146
    • 0000134287 scopus 로고
    • The Crystal structure of sulfamic acid
    • Kanda, F. A.; King, A. J. The Crystal structure of sulfamic acid. J. Am. Chem. Soc., 1951, 73(5), 2315-2319.
    • (1951) J. Am. Chem. Soc , vol.73 , Issue.5 , pp. 2315-2319
    • Kanda, F.A.1    King, A.J.2
  • 147
    • 0037058068 scopus 로고    scopus 로고
    • Quadrupolar, 14N 14N and 15N Chemical Shift, and 14N-1H Dipolar Tensors of Sulfamic Acid
    • Harbison, G. S.; Kye, Y. -S.; Penner, G. H.; Grandin, M.; Monette, M. 14N Quadrupolar, 14N and 15N Chemical Shift, and 14N-1H Dipolar Tensors of Sulfamic Acid. J. Phys. Chem. B, 2002, 106(40), 10285-10291.
    • (2002) J. Phys. Chem. B , vol.106 , Issue.40 , pp. 10285-10291
    • Harbison, G.S.1    Kye, Y.-S.2    Penner, G.H.3    Grandin, M.4    Monette, M.5
  • 148
    • 0002724051 scopus 로고
    • Sulfamic Acid, sulfamide, and related aquo-ammonosulfuric acids
    • Audrieth, L. F.; Sveda, M.; Sisler, H. H.; Butler, M. J. Sulfamic Acid, sulfamide, and related aquo-ammonosulfuric acids. Chem. Rev., 1940, 26(1), 49-94.
    • (1940) Chem. Rev , vol.26 , Issue.1 , pp. 49-94
    • Audrieth, L.F.1    Sveda, M.2    Sisler, H.H.3    Butler, M.J.4
  • 149
    • 33847086479 scopus 로고
    • Sulfamic Acid and its N-substituted derivatives
    • Benson, G. A.; Spillane, W. J. Sulfamic Acid and its N-substituted derivatives. Chem. Rev., 1980, 80(2), 151-186.
    • (1980) Chem. Rev , vol.80 , Issue.2 , pp. 151-186
    • Benson, G.A.1    Spillane, W.J.2
  • 150
    • 19944374090 scopus 로고    scopus 로고
    • Sulfamic Acid: A Very Useful Catalyst
    • Wang, B. Sulfamic Acid: A Very Useful Catalyst. Synlett, 2005, 16(8), 1342-1343.
    • (2005) Synlett , vol.16 , Issue.8 , pp. 1342-1343
    • Wang, B.1
  • 151
    • 85024684657 scopus 로고
    • Sulfamic Acid, A new industrial chemical
    • Cupery, M. E. Sulfamic Acid, A new industrial chemical. Ind. Eng. Chem., 1938, 30(6), 627-631.
    • (1938) Ind. Eng. Chem , vol.30 , Issue.6 , pp. 627-631
    • Cupery, M.E.1
  • 153
    • 33947092999 scopus 로고
    • Reaction between nitric and sulfamic acids in aqueous solution
    • Dzelzkalns, L. S.; Ronner, F. T. Reaction between nitric and sulfamic acids in aqueous solution. Inorg. Chem., 1978, 17(12), 3710-3711.
    • (1978) Inorg. Chem , vol.17 , Issue.12 , pp. 3710-3711
    • Dzelzkalns, L.S.1    Ronner, F.T.2
  • 154
    • 33947455672 scopus 로고
    • Reaction of sodium nitrite and sulfamic acid
    • Brasted, R. C. Reaction of sodium nitrite and sulfamic acid. Anal. Chem., 1952, 24(7), 1111-1114.
    • (1952) Anal. Chem , vol.24 , Issue.7 , pp. 1111-1114
    • Brasted, R.C.1
  • 155
    • 33947440097 scopus 로고
    • Reaction of diazo compounds with sulfamic acid
    • Grimmel, H. W.; Morgan, J. F. Reaction of diazo compounds with sulfamic acid. J. Am. Chem. Soc., 1948, 70(5), 1750-1751.
    • (1948) J. Am. Chem. Soc , vol.70 , Issue.5 , pp. 1750-1751
    • Grimmel, H.W.1    Morgan, J.F.2
  • 156
    • 0034309252 scopus 로고    scopus 로고
    • 15N CIDNP during reaction of the oxoperoxonitrate- CO2 adduct with bovine albumin and L-tyrosine derivatives
    • Lehnig, M.; Jakobi, K. 15N CIDNP during reaction of the oxoperoxonitrate- CO2 adduct with bovine albumin and L-tyrosine derivatives. J. Chem. Soc., Perkin Trans., 2000, 10(2), 2016-2021.
    • (2000) J. Chem. Soc., Perkin Trans , vol.10 , Issue.2 , pp. 2016-2021
    • Lehnig, M.1    Jakobi, K.2
  • 157
    • 0042365090 scopus 로고    scopus 로고
    • Simplified and convenient laboratory-scale preparation of 14N or 15N high molecular weight poly(dichlorophosphazene) directly from PCl5
    • Carriedo, G. A.; Alonso, F. J. G.; Elipe, P. G.; Fidalgo, J. I.; Álvarez, J. L. G.; Presa-Soto, A. A Simplified and convenient laboratory-scale preparation of 14N or 15N high molecular weight poly(dichlorophosphazene) directly from PCl5.Chem. Eur. J., 2003, 9(16), 3833-3836.
    • (2003) Chem Eur. J , vol.9 , Issue.16 , pp. 3833-3836
    • Carriedo, G.A.1    Alonso, F.J.G.2    Elipe, P.G.3    Fidalgo, J.I.4    Álvarez, J.L.G.5    Presa-Soto, A.A.6
  • 158
    • 3543029364 scopus 로고
    • The Synthesis of polymeric ethers
    • Rhoad, M. J.; Hory, P. J. The Synthesis of polymeric ethers. J. Am. Chem. Soc., 1950, 72(5), 2216-2219.
    • (1950) J. Am. Chem. Soc , vol.72 , Issue.5 , pp. 2216-2219
    • Rhoad, M.J.1    Hory, P.J.2
  • 159
    • 26444589070 scopus 로고    scopus 로고
    • An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound
    • Li, J.-T.; Dai, H.-G.; Xu, W.-Z.; Li, T.-S. An efficient and practical synthesis of bis(indolyl)methanes catalyzed by aminosulfonic acid under ultrasound. Ultrasonic Sonochem., 2006, 13(1), 24-27.
    • (2006) Ultrasonic Sonochem , vol.13 , Issue.1 , pp. 24-27
    • Li, J.-T.1    Dai, H.-G.2    Xu, W.-Z.3    Li, T.-S.4
  • 160
    • 33947711966 scopus 로고    scopus 로고
    • Sulfamic acid catalyzed direct condensation of aldehydes, amines, and TMSCN to [1]-aminonitriles at ambient temperature
    • Li, Z.; Sun, Y.; Ren, X.; Wei, P.; Shi, Y.; Ouyang, P. Sulfamic acid catalyzed direct condensation of aldehydes, amines, and TMSCN to [1]-aminonitriles at ambient temperature. Synlett, 2007, 18(5), 803-805.
    • (2007) Synlett , vol.18 , Issue.5 , pp. 803-805
    • Li, Z.1    Sun, Y.2    Ren, X.3    Wei, P.4    Shi, Y.5    Ouyang, P.6
  • 161
    • 0031928770 scopus 로고    scopus 로고
    • Sulfamic acid catalysed acetylation of alcohols and phenols with acetic anhydride
    • Jin, T. S.; Ma, Y. R.; Zhang, Z. H.; Li, T. S. Sulfamic acid catalysed acetylation of alcohols and phenols with acetic anhydride. Synthetic. Commun., 1998, 28(17), 3173-3177.
    • (1998) Synthetic. Commun , vol.28 , Issue.17 , pp. 3173-3177
    • Jin, T.S.1    Ma, Y.R.2    Zhang, Z.H.3    Li, T.S.4
  • 162
    • 57249088466 scopus 로고    scopus 로고
    • An efficient and convenient procedure for the preparation of 1, 1-diacetates from aldehydes catalyzed by H2NSO3H
    • Jin, T. S.; Sun, G.; Li, Y. W.; Li, T. S. An efficient and convenient procedure for the preparation of 1, 1-diacetates from aldehydes catalyzed by H2NSO3H. Green Chem., 2002, 4(3), 255-256.
    • (2002) Green Chem , vol.4 , Issue.3 , pp. 255-256
    • Jin, T.S.1    Sun, G.2    Li, Y.W.3    Li, T.S.4
  • 163
    • 0037231329 scopus 로고    scopus 로고
    • A facile and efficient procedure for deprotection of 1, 1-diacetates catalyzed by H2NSO3H
    • Jin, T. S.; Sun, G.; Li, Y. W.; Li, T. S. A facile and efficient procedure for deprotection of 1, 1-diacetates catalyzed by H2NSO3H. J. Chem. Res., Synop., 2003, 1, 30-32.
    • (2003) J. Chem. Res., Synop , vol.1 , pp. 30-32
    • Jin, T.S.1    Sun, G.2    Li, Y.W.3    Li, T.S.4
  • 164
    • 10644249884 scopus 로고    scopus 로고
    • Sulfamic acid as a cost-effective and recyclable catalyst for protection of carbonyls to acetals and ketals under mild conditions
    • Gong, W. Z.; Wang, B.; Gu, Y. L.; Yan, L.; Yang, L. M. Suo, J. S. Sulfamic acid as a cost-effective and recyclable catalyst for protection of carbonyls to acetals and ketals under mild conditions. Synthetic Commun., 2004, 34(23), 4243-4247.
    • (2004) Synthetic Commun , vol.34 , Issue.23 , pp. 4243-4247
    • Gong, W.Z.1    Wang, B.2    Gu, Y.L.3    Yan, L.4    Yang, L.M.5    Suo, J.S.6
  • 165
    • 24944461938 scopus 로고    scopus 로고
    • Sulfamic acid: An efficient, cost-effective and recyclable solid acid catalyst for the Friedlander quinoline synthesis
    • Yadav, J. S.; Rao, P. P.; Sreenu, D.; Rao, R. S.; Kumar, V. N.; Nagaiah, K.; Prasad, A. R. Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the Friedlander quinoline synthesis. Tetrahedron Lett., 2005, 46(42), 7249-7253.
    • (2005) Tetrahedron Lett , vol.46 , Issue.42 , pp. 7249-7253
    • Yadav, J.S.1    Rao, P.P.2    Sreenu, D.3    Rao, R.S.4    Kumar, V.N.5    Nagaiah, K.6    Prasad, A.R.7
  • 166
    • 27744468959 scopus 로고    scopus 로고
    • Sulfamic acid: A novel and efficient catalyst for the synthesis of aryl-14H-dibenzo[a.j]xanthenes under conventional heating and microwave irradiation
    • Rajitha, B.; Kumar, B. S.; Reddy, Y. T.; Reddy, P. N.; Sreenivasulu, N. Sulfamic acid: a novel and efficient catalyst for the synthesis of aryl-14H-dibenzo[a.j]xanthenes under conventional heating and microwave irradiation. Tetrahedron Lett., 2005, 46(50), 8691-8693.
    • (2005) Tetrahedron Lett , vol.46 , Issue.50 , pp. 8691-8693
    • Rajitha, B.1    Kumar, B.S.2    Reddy, Y.T.3    Reddy, P.N.4    Sreenivasulu, N.5
  • 167
    • 34248566954 scopus 로고    scopus 로고
    • Sulfamic acid-catalyzed Michael addition of indoles and pyrrole to electron-deficient nitroolefins under solvent-free condition
    • An, L.-T.; Zou, J.-P.; Zhang, L.-L.; Zhang Y. Sulfamic acid-catalyzed Michael addition of indoles and pyrrole to electron-deficient nitroolefins under solvent-free condition. Tetrahedron Lett., 2007, 48(24), 4297-4300.
    • (2007) Tetrahedron Lett , vol.48 , Issue.24 , pp. 4297-4300
    • An, L.-T.1    Zou, J.-P.2    Zhang, L.-L.3    Zhang, Y.4
  • 168
    • 27644549976 scopus 로고    scopus 로고
    • I2-catalyzed Michael addition of indole and pyrrole to nitroolefins
    • Lin, C.; Hsu, J.; Sastry, M. N. V.; Fang, H.; Tu, Z.; Liu, J.-T.; Yao, C.-F. I2-catalyzed Michael addition of indole and pyrrole to nitroolefins. Tetrahedron, 2005, 61(49), 11751-11757.
    • (2005) Tetrahedron , vol.61 , Issue.49 , pp. 11751-11757
    • Lin, C.1    Hsu, J.2    Sastry, M.N.V.3    Fang, H.4    Tu, Z.5    Liu, J.-T.6    Yao, C.-F.7
  • 169
    • 0346057826 scopus 로고    scopus 로고
    • Inter- and intramolecular imino diels-alder reactions catalyzed by sulfamic acid: A mild and efficient catalyst for a one-pot synthesis of tetrahydroquinolines
    • Nagarajan, R.; Magesh, C. J.; Perumal, T. Inter- and intramolecular imino diels-alder reactions catalyzed by sulfamic acid: a mild and efficient catalyst for a one-pot synthesis of tetrahydroquinolines. Synthesis, 2004, 36(1), 69-74.
    • (2004) Synthesis , vol.36 , Issue.1 , pp. 69-74
    • Nagarajan, R.1    Magesh, C.J.2    Perumal, T.3
  • 170
    • 4544253640 scopus 로고    scopus 로고
    • Sulphamic acid-an efficient and cost-effective solid acid catalyst for the pechmann reaction
    • Singh, P. R.; Singh, D. U.; Samant, S. D. Sulphamic acid-an efficient and cost-effective solid acid catalyst for the pechmann reaction. Synlett, 2004, 15(11), 1909-1912.
    • (2004) Synlett , vol.15 , Issue.11 , pp. 1909-1912
    • Singh, P.R.1    Singh, D.U.2    Samant, S.D.3
  • 171
    • 60549106717 scopus 로고    scopus 로고
    • Alimadadi, B. Three-component one-pot synthesis of 4,6-diarylpyrimidin-2(1H)-ones under solvent-free conditions in the presence of sulfamic acid as a green and reusable catalyst
    • Heravi, M. M.; Ranjbar, L.; Derikvand, F.; Alimadadi, B. Three-component one-pot synthesis of 4,6-diarylpyrimidin-2(1H)-ones under solvent-free conditions in the presence of sulfamic acid as a green and reusable catalyst. Mol. Divers., 2008, 12(3-4), 191-196.
    • (2008) Mol. Divers , vol.12 , Issue.3-4 , pp. 191-196
    • Heravi, M.M.1    Ranjbar, L.2    Derikvand, F.3
  • 172
    • 33845537940 scopus 로고    scopus 로고
    • Recyclableand highly effective sulfamic acid/MeOH catalytic system for the synthesis of quinoxalines at room temperature
    • Darabi, H. R.; Mohandessi, S.; Aghapoor, K.; Mohsenzadeh, F. A recyclableand highly effective sulfamic acid/MeOH catalytic system for the synthesis of quinoxalines at room temperature. Catal. Commun., 2007, 8(3), 389-392.
    • (2007) Catal. Commun , vol.8 , Issue.3 , pp. 389-392
    • Darabi, H.R.1    Mohandessi, S.2    Aghapoor, K.3    Mohsenzadeh, F.A.4
  • 173
    • 42749094387 scopus 로고    scopus 로고
    • Sulfamic acid: An efficient and cost-effective solid acid catalyst for the synthesis of α -aminophosphonates at ambient temperature
    • Mitragotri, S. D.; Pore, D. M.; Desai, U. V.; Wadgaonkar, P. P. Sulfamic acid: An efficient and cost-effective solid acid catalyst for the synthesis of [1]-aminophosphonates at ambient temperature. Catal. Commun., 2008, 9(9), 1822-1826.
    • (2008) Catal. Commun , vol.9 , Issue.9 , pp. 1822-1826
    • Mitragotri, S.D.1    Pore, D.M.2    Desai, U.V.3    Wadgaonkar, P.P.4
  • 174
    • 34247396213 scopus 로고    scopus 로고
    • Ultrasound-promoted synthesis of 1-amidoalkyl-2-naphthols via a three-component condensation of 2-naphthol, ureas/amides, and aldehydes, catalyzed by sulfamic acid under ambient conditions
    • Patil, S. B.; Singh, P. R.; Surpur, M. P.; Samant, S. D. Ultrasound-promoted synthesis of 1-amidoalkyl-2-naphthols via a three-component condensation of 2-naphthol, ureas/amides, and aldehydes, catalyzed by sulfamic acid under ambient conditions. Ultrasonic. Sonochem., 2007, 14(5), 515-518.
    • (2007) Ultrasonic. Sonochem , vol.14 , Issue.5 , pp. 515-518
    • Patil, S.B.1    Singh, P.R.2    Surpur, M.P.3    Samant, S.D.4
  • 175
    • 34548594002 scopus 로고    scopus 로고
    • Sulfamic acid as a cost-effective catalyst instead of metal-containing acids for the one-pot synthesis of α-acetamido ketones
    • Heravi, M. M.; Ranjbar, L.; Derikvand, F.; Bamoharram, F. F. Sulfamic acid as a cost-effective catalyst instead of metal-containing acids for the one-pot synthesis of α-acetamido ketones. J. Mol. Catal. A: Chem., 2007, 276(1-2), 226-229.
    • (2007) J. Mol. Catal. A: Chem , vol.276 , Issue.1-2 , pp. 226-229
    • Heravi, M.M.1    Ranjbar, L.2    Derikvand, F.3    Bamoharram, F.F.4
  • 176
    • 33746340605 scopus 로고    scopus 로고
    • A novel direct and one-pot Mannich synthesis of fluorinated α-aminobutanones with sulfamic acid as a green catalyst
    • Xia, M.; Lu, Y.-D. A novel direct and one-pot Mannich synthesis of fluorinated α-aminobutanones with sulfamic acid as a green catalyst. J. Fluorine Chem., 2006, 127(8), 1119-1124.
    • (2006) J. Fluorine Chem , vol.127 , Issue.8 , pp. 1119-1124
    • Xia, M.1    Lu, Y.-D.2
  • 177
    • 67349278502 scopus 로고    scopus 로고
    • One-pot three-component mannich-type reactions using sulfamic acid catalyst under ultrasound irradiation
    • Zeng, H.; Li, H.; Shao, H. One-pot three-component mannich-type reactions using sulfamic acid catalyst under ultrasound irradiation. Ultrasonic. Sonochem., 2009, 16(6), 758-762.
    • (2009) Ultrasonic. Sonochem , vol.16 , Issue.6 , pp. 758-762
    • Zeng, H.1    Li, H.2    Shao, H.3
  • 178
    • 34247860574 scopus 로고    scopus 로고
    • Sulfamic acid: An efficient, cost-effective and recyclable solid acid catalyst for the three-component synthesis of α-amino nitriles
    • Heydari, A.; Khaksar, S.; Pourayoubi, M.; Mahjoub, A. R. Sulfamic acid: an efficient, cost-effective and recyclable solid acid catalyst for the three-component synthesis of α-amino nitriles. Tetrahedron Lett., 2007, 48(23), 4059-4060.
    • (2007) Tetrahedron Lett , vol.48 , Issue.23 , pp. 4059-4060
    • Heydari, A.1    Khaksar, S.2    Pourayoubi, M.3    Mahjoub, A.R.4
  • 179
    • 0037404613 scopus 로고    scopus 로고
    • An effcient synthesis of 3,4-dihydropyrimidin-2-ones catalyzed by NH2SO3H under ultrasound irradiation
    • Li, J. T.; Han, J. F.; Yang, J. H.; Li, T. S. An effcient synthesis of 3,4-dihydropyrimidin-2-ones catalyzed by NH2SO3H under ultrasound irradiation. Ultrasonic. Sonochem., 2003, 10(3), 119-122.
    • (2003) Ultrasonic. Sonochem , vol.10 , Issue.3 , pp. 119-122
    • Li, J.T.1    Han, J.F.2    Yang, J.H.3    Li, T.S.4
  • 180
    • 14844350074 scopus 로고    scopus 로고
    • Oxaziridine- mediated amination of primary amines: Scope and application to a one-pot pyrazole synthesis
    • Armstrong, A.; Jones, L. H.; Knight, J. D.; Kelsey, R. D. Oxaziridine- mediated amination of primary amines: scope and application to a one-pot pyrazole synthesis. Org. Lett., 2005, 7(4), 713-716.
    • (2005) Org. Lett , vol.7 , Issue.4 , pp. 713-716
    • Armstrong, A.1    Jones, L.H.2    Knight, J.D.3    Kelsey, R.D.4
  • 181
    • 33646555402 scopus 로고    scopus 로고
    • A convenient preparation of aliphatic and aromatic N-sulfonylimines mediated by sulfamic acid in aqueous media
    • Li, Z.; Ren, X.; Wei, P.; Wan, H.; Shi, Y.; Ouyang, P. A convenient preparation of aliphatic and aromatic N-sulfonylimines mediated by sulfamic acid in aqueous media. Green Chem., 2006, 8(5), 433-436.
    • (2006) Green Chem , vol.8 , Issue.5 , pp. 433-436
    • Li, Z.1    Ren, X.2    Wei, P.3    Wan, H.4    Shi, Y.5    Ouyang, P.6
  • 182
    • 0028346095 scopus 로고
    • Highly Stereocontrolled and Efficient Preparation of the Protected, Esterification-Ready Docetaxel (Taxotere) Side Chain
    • Kanazawa, A. M.; Denis, J.-N.; Greene, A. E. Highly Stereocontrolled and Efficient Preparation of the Protected, Esterification-Ready Docetaxel (Taxotere) Side Chain. J. Org. Chem., 1994, 59(6), 1238-1240.
    • (1994) J. Org. Chem , vol.59 , Issue.6 , pp. 1238-1240
    • Kanazawa, A.M.1    Denis, J.-N.2    Greene, A.E.3
  • 183
    • 4143147493 scopus 로고    scopus 로고
    • Sulfamic acid as a cost-effective catalyst instead of metal-containing acids for acetolysis of cyclic ethers
    • Wang, B.; Gu, Y. L.; Gong, W. Z.; Kang, Y. R.; Yang, L. M.; Suo, J. S. Sulfamic acid as a cost-e[1]ective catalyst instead of metal-containing acids for acetolysis of cyclic ethers. Tetrahedron Lett., 2004, 45(35), 6599-6602.
    • (2004) Tetrahedron Lett , vol.45 , Issue.35 , pp. 6599-6602
    • Wang, B.1    Gu, Y.L.2    Gong, W.Z.3    Kang, Y.R.4    Yang, L.M.5    Suo, J.S.6
  • 184
    • 58149280405 scopus 로고    scopus 로고
    • Stereoselective Synthesis of Bishomo-inositols as Glycosidase Inhibitors
    • Baran, A.; Balci, M. Stereoselective Synthesis of Bishomo-inositols as Glycosidase Inhibitors. J. Org. Chem., 2009, 74(1), 88-95.
    • (2009) J. Org. Chem , vol.74 , Issue.1 , pp. 88-95
    • Baran, A.1    Balci, M.2
  • 185
    • 34548241470 scopus 로고    scopus 로고
    • Sulfamic acid as an efficient and recyclable catalyst for the ring opening of epoxides with amines and anilines: An easy synthesis of α-amino alcohols under solvent-free conditions
    • Kamal, A.; Prasad, B. R.; Reddy, A. M.; Khan, M. N. A. Sulfamic acid as an efficient and recyclable catalyst for the ring opening of epoxides with amines and anilines: An easy synthesis of α-amino alcohols under solvent-free conditions. Catal. Commun., 2007, 8(12), 1876-1880.
    • (2007) Catal. Commun , vol.8 , Issue.12 , pp. 1876-1880
    • Kamal, A.1    Prasad, B.R.2    Reddy, A.M.3    Khan, M.N.A.4
  • 186
    • 0344413580 scopus 로고    scopus 로고
    • Solvent-free tetrahydropyranylation of alcohols with sulfamic acid as reusable catalyst
    • Wang, B.; Yang, L. M.; Suo, J. S. Solvent-free tetrahydropyranylation of alcohols with sulfamic acid as reusable catalyst. Synthetic. Commun., 2003, 33(22), 3929-3934.
    • (2003) Synthetic. Commun , vol.33 , Issue.22 , pp. 3929-3934
    • Wang, B.1    Yang, L.M.2    Suo, J.S.3
  • 187
    • 1842788776 scopus 로고    scopus 로고
    • Sulfamic acid as a cost-effective and recyclable catalyst for liquid beckmann rearrangement, a green process to produce amides from ketoximes without waste
    • Wang, B.; Gu, Y. L.; Luo, C.; Yang, T.; Yang, L. M.; Suo, J. S. Sulfamic acid as a cost-effective and recyclable catalyst for liquid beckmann rearrangement, a green process to produce amides from ketoximes without waste. Tetrahedron Lett., 2004, 45(17), 3369-3372.
    • (2004) Tetrahedron Lett , vol.45 , Issue.17 , pp. 3369-3372
    • Wang, B.1    Gu, Y.L.2    Luo, C.3    Yang, T.4    Yang, L.M.5    Suo, J.S.6
  • 188
    • 33646423822 scopus 로고    scopus 로고
    • Sulphamic acid: An efficient, cost-effective and recyclable solid acid catalyst for highly chemoselective allylation of aldehydes
    • Prasad, A. R. Sulphamic acid: an efficient, cost-effective and recyclable solid acid catalyst for highly chemoselective allylation of aldehydes. Appl. Catal., A: Gen., 2006, 306(1), 192-196.
    • (2006) Appl. Catal., A: Gen , vol.306 , Issue.1 , pp. 192-196
    • Prasad, A.R.1
  • 189
    • 35348962570 scopus 로고    scopus 로고
    • Efficient, solventless N-Boc protection of amines carried out at room temperature using sulfamic acid as recyclable catalyst
    • Upadhyaya, D. J.; Barge, A.; Stefania, R.; Cravotto, G. Efficient, solventless N-Boc protection of amines carried out at room temperature using sulfamic acid as recyclable catalyst. Tetrahedron Lett., 2007, 48(47), 8318-8322
    • (2007) Tetrahedron Lett , vol.48 , Issue.47 , pp. 8318-8322
    • Upadhyaya, D.J.1    Barge, A.2    Stefania, R.3    Cravotto, G.4
  • 190
    • 0141483247 scopus 로고    scopus 로고
    • Epoxidation of α,β-unsaturated carbonyl compounds in ionic liquid/water biphasic system under mild conditions
    • Wang, B.; Kang, Y. R.; Yang, L. M.; Suo, J. S. Epoxidation of α,β-unsaturated carbonyl compounds in ionic liquid/water biphasic system under mild conditions. J. Mol. Catal. A: Chem., 2003, 203(1-2), 29-36.
    • (2003) J. Mol. Catal. A: Chem , vol.203 , Issue.1-2 , pp. 29-36
    • Wang, B.1    Kang, Y.R.2    Yang, L.M.3    Suo, J.S.4
  • 191
    • 1842788687 scopus 로고    scopus 로고
    • Pyrrole synthesis in ionic liquids by Paal-Knorr condensation under mild conditions
    • Wang, B.; Gu, Y. L.; Luo, C.; Yang, T.; Yang, L. M.; Suo, J. S. Pyrrole synthesis in ionic liquids by Paal-Knorr condensation under mild conditions. Tetrahedron Lett., 2004, 45(17), 3417-3419.
    • (2004) Tetrahedron Lett , vol.45 , Issue.17 , pp. 3417-3419
    • Wang, B.1    Gu, Y.L.2    Luo, C.3    Yang, T.4    Yang, L.M.5    Suo, J.S.6
  • 192
    • 1242276715 scopus 로고    scopus 로고
    • Leaching separation of taurine and sodium sulfate solid mixture using ionic liquids
    • Gu, Y. L.; Shi, F.; Yang, H. Z.; Deng, Y. Q. Leaching separation of taurine and sodium sulfate solid mixture using ionic liquids. Sep. Purif. Technol., 2004, 35(2), 153-159.
    • (2004) Sep. Purif. Technol , vol.35 , Issue.2 , pp. 153-159
    • Gu, Y.L.1    Shi, F.2    Yang, H.Z.3    Deng, Y.Q.4
  • 193
    • 0037505228 scopus 로고    scopus 로고
    • Ionic liquid-regulated sulfamic acid: Chemoselective catalyst for the transesterification of α-ketoesters
    • Wang, B.; Yang, L. M.; Suo, J. S. Ionic liquid-regulated sulfamic acid: chemoselective catalyst for the transesterification of α-ketoesters. Tetrahedron Lett., 2003, 44(27), 5037-5039.
    • (2003) Tetrahedron Lett , vol.44 , Issue.27 , pp. 5037-5039
    • Wang, B.1    Yang, L.M.2    Suo, J.S.3
  • 194
    • 0035969741 scopus 로고    scopus 로고
    • Antiferromagnetic pairing in polyaniline salt-zeolite nanocomposites
    • Frisch, H. L.; Song, H.; and Ma, J.; Rafailovich, M. Zhu, S. Yang, N.L. Yan, X. Antiferromagnetic pairing in polyaniline salt-zeolite nanocomposites. J. Phys. Chem. B, 2001, 105(47), 11901-11905.
    • (2001) J. Phys. Chem. B , vol.105 , Issue.47 , pp. 11901-11905
    • Frisch, H.L.1    Song, H.2    Ma, J.3    Rafailovich, M.4    Zhu, S.5    Yang, N.L.6    Yan, X.7
  • 195
    • 40149086085 scopus 로고    scopus 로고
    • On the stabilization of conducting pernigraniline salt by the synthesis and oxidation of polyaniline in hydrophobic ionic liquids
    • Bazito, F. F. C.; Silveira, L. T.; Torresi, R. M.; Córdoba de Torresi, S. I. On the stabilization of conducting pernigraniline salt by the synthesis and oxidation of polyaniline in hydrophobic ionic liquids. Phys. Chem. Chem. Phys., 2008, 10(10), 1457-1462.
    • (2008) Phys. Chem. Chem. Phys , vol.10 , Issue.10 , pp. 1457-1462
    • Bazito, F.F.C.1    Silveira, L.T.2    Torresi, R.M.3    de Torresi, C.S.I.4
  • 196
    • 0028416309 scopus 로고
    • Composition and spectral studies of polyaniline salts
    • Palaniappan, S.; Narayana, B. H. Composition and spectral studies of polyaniline salts. Polym. Adv. Technol., 1994, 5(4), 225-230.
    • (1994) Polym. Adv. Technol , vol.5 , Issue.4 , pp. 225-230
    • Palaniappan, S.1    Narayana, B.H.2
  • 197
    • 57249096919 scopus 로고    scopus 로고
    • Tetrahydropyranylation of alcohols catalyzed by polyaniline salts
    • Palaniappan, S.; Sai, M. R.; Amarnath, C. A. Tetrahydropyranylation of alcohols catalyzed by polyaniline salts. Green Chem., 2002, 4(4), 369-371.
    • (2002) Green Chem , vol.4 , Issue.4 , pp. 369-371
    • Palaniappan, S.1    Sai, M.R.2    Amarnath, C.A.3
  • 198
    • 0036428827 scopus 로고    scopus 로고
    • Benzoyl peroxide oxidation route to polyaniline salt and its use as catalyst in tetrahydropyranylation of decanol
    • Palaniappan, S.; Amarnath, C. A. Benzoyl peroxide oxidation route to polyaniline salt and its use as catalyst in tetrahydropyranylation of decanol. New J. Chem., 2002, 26(11), 1671-1674
    • (2002) New J. Chem , vol.26 , Issue.11 , pp. 1671-1674
    • Palaniappan, S.1    Amarnath, C.A.2
  • 199
    • 57249104573 scopus 로고    scopus 로고
    • Esterification of carboxylic acids with alcohols catalyzed by polyaniline salts
    • Palaniappan, S.; Ram, M. S. Esterification of carboxylic acids with alcohols catalyzed by polyaniline salts. Green Chem., 2002, 4(1), 53-55.
    • (2002) Green Chem , vol.4 , Issue.1 , pp. 53-55
    • Palaniappan, S.1    Ram, M.S.2
  • 200
    • 49649096434 scopus 로고    scopus 로고
    • Use of pyridinium chlorochromate and reusable polyaniline salt catalyst combination for the oxidation of indoles
    • Kumar, C.N.S.S.P.; Devi, C. L.; Rao, V. J.; Palaniappan, S. Use of pyridinium chlorochromate and reusable polyaniline salt catalyst combination for the oxidation of indoles. Synlett, 2008, 19(13), 2023-2027.
    • (2008) Synlett , vol.19 , Issue.13 , pp. 2023-2027
    • Kumar, C.N.S.S.P.1    Devi, C.L.2    Rao, V.J.3    Palaniappan, S.4
  • 201
    • 3142710156 scopus 로고    scopus 로고
    • Polyaniline salts and complexes as catalyst in bisindole synthesis
    • Palaniappan, S.; Saravanan, C.; Amarnath, C. A.; Rao, V. J. Polyaniline salts and complexes as catalyst in bisindole synthesis. Catal. Lett., 2004, 97(1-2), 77-81.
    • (2004) Catal. Lett , vol.97 , Issue.1-2 , pp. 77-81
    • Palaniappan, S.1    Saravanan, C.2    Amarnath, C.A.3    Rao, V.J.4
  • 202
    • 2942597944 scopus 로고    scopus 로고
    • Mannich-type reaction in solvent free condition using reusable polyaniline catalyst
    • Palaniappan, S.; John, A.; Amarnath, C. A.; Rao, V. J. Mannich-type reaction in solvent free condition using reusable polyaniline catalyst. J. Mol. Catal. A: Chem., 2004, 218(1), 47-53.
    • (2004) J. Mol. Catal. A: Chem , vol.218 , Issue.1 , pp. 47-53
    • Palaniappan, S.1    John, A.2    Amarnath, C.A.3    Rao, V.J.4
  • 203
    • 1042266450 scopus 로고    scopus 로고
    • Synthesis of 7-hydroxy-4-methyl coumarin using polyaniline supported acid catalyst
    • Palaniappan, S.; Shekhar, R. C. Synthesis of 7-hydroxy-4-methyl coumarin using polyaniline supported acid catalyst. J. Mol. Catal. A: Chem., 2004, 209(1-2), 117-124.
    • (2004) J. Mol. Catal. A: Chem , vol.209 , Issue.1-2 , pp. 117-124
    • Palaniappan, S.1    Shekhar, R.C.2
  • 204
    • 0037496996 scopus 로고    scopus 로고
    • Benzoyl peroxide oxidation route to polyaniline salt and its use as catalyst in the esterification reaction
    • Ram, M. S.; Palaniappan, S. Benzoyl peroxide oxidation route to polyaniline salt and its use as catalyst in the esterification reaction. J. Mol. Catal. A:Chem., 2003, 201(1-2), 289-296.
    • (2003) J. Mol. Catal. A:Chem , vol.201 , Issue.1-2 , pp. 289-296
    • Ram, M.S.1    Palaniappan, S.2
  • 205
    • 33645391803 scopus 로고    scopus 로고
    • Clean synthesis of 1,8-dioxo-dodecahydroxanthene derivatives catalyzed by polyaniline- p-toluenesulfonate salt in aqueous media
    • John, A.; Yadav, P. J. P.; Palaniappan, S. Clean synthesis of 1,8-dioxo-dodecahydroxanthene derivatives catalyzed by polyaniline- p-toluenesulfonate salt in aqueous media. J.Mol. Catal. A: Chem., 2006, 248(1-2), 121-125.
    • (2006) J.Mol. Catal A: Chem , vol.248 , Issue.1-2 , pp. 121-125
    • John, A.1    Yadav, P.J.P.2    Palaniappan, S.3
  • 206
    • 33847687134 scopus 로고    scopus 로고
    • Efficient,convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives
    • Srinivas, C.; Kumar, C. N. S. S. P.; Rao, V. J.; Palaniappan, S. Efficient, convenient and reusable polyaniline-sulfate salt catalyst for the synthesis of quinoxaline derivatives. J. Mol. Catal. A: Chem., 2007, 265(1-2), 227-230.
    • (2007) J. Mol. Catal. A: Chem , vol.265 , Issue.1-2 , pp. 227-230
    • Srinivas, C.1    Kumar, C.N.S.S.P.2    Rao, V.J.3    Palaniappan, S.4
  • 207
    • 39149131713 scopus 로고    scopus 로고
    • Green approach for the synthesis of quinoxaline derivatives in water medium using reusable polyaniline-sulfate salt catalyst and sodium laurylsulfate
    • Srinivas, C.; Kumar, C. N. S. S. P.; Rao, V. J.; Palaniappan, S. Green approach for the synthesis of quinoxaline derivatives in water medium using reusable polyaniline-sulfate salt catalyst and sodium laurylsulfate. Catal. Lett., 2008, 121(3-4), 291-296.
    • (2008) Catal. Lett , vol.121 , Issue.3-4 , pp. 291-296
    • Srinivas, C.1    Kumar, C.N.S.S.P.2    Rao, V.J.3    Palaniappan, S.4
  • 208
    • 33750982142 scopus 로고    scopus 로고
    • Polyaniline- sulfate salt as an efficient and reusable catalyst for the synthesis of 1,5-benzodiazepines and 2-phenyl benzimidazoles
    • Srinivas, U.; Srinivas, C.; Narender, P.; Rao, V. J; Palaniappan, S. Polyaniline- sulfate salt as an efficient and reusable catalyst for the synthesis of 1,5-benzodiazepines and 2-phenyl benzimidazoles. Catal. Commun., 2006, 8(1), 107-110.
    • (2006) Catal. Commun , vol.8 , Issue.1 , pp. 107-110
    • Srinivas, U.1    Srinivas, C.2    Narender, P.3    Rao, V.J.4    Palaniappan, S.5
  • 209
    • 33749459372 scopus 로고    scopus 로고
    • Polyaniline salts and complexes: Efficient and reusable catalyst for the one-pot synthesis of 5-(methoxycarbonyl)-6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one
    • Gangadasu, B.; Palaniappan, S.; Amarnath, C. A.; Rao, V. J. Polyaniline salts and complexes: efficient and reusable catalyst for the one-pot synthesis of 5-(methoxycarbonyl)-6-methyl-4-phenyl-3,4-dihydropyrimidin-2(1H)-one. J. Appl. Polym. Sci., 2006, 102(2), 1741-1745.
    • (2006) J. Appl. Polym. Sci , vol.102 , Issue.2 , pp. 1741-1745
    • Gangadasu, B.1    Palaniappan, S.2    Amarnath, C.A.3    Rao, V.J.4
  • 210
    • 34548271994 scopus 로고    scopus 로고
    • Cycloaddition of CO2 to epoxides catalyzed by polyaniline salts
    • He, J.; Wu, T.; Zhang, Z.; Ding, K.; Han, B.; Xie, Y.; Jiang, T.; Liu, Z. Cycloaddition of CO2 to epoxides catalyzed by polyaniline salts. Chem. Eur. J., 2007, 13(24), 6992-6997.
    • (2007) Chem. Eur. J , vol.13 , Issue.24 , pp. 6992-6997
    • He, J.1    Wu, T.2    Zhang, Z.3    Ding, K.4    Han, B.5    Xie, Y.6    Jiang, T.7    Liu, Z.8
  • 211
    • 68349139369 scopus 로고    scopus 로고
    • Polyaniline-supported Acid as an efficient and reusable catalyst for a one-pot synthesis of α-acetamido ketones via a four-component condensation reaction
    • Nabid, M. R.; Rezaei, S. J. T. Polyaniline-supported Acid as an efficient and reusable catalyst for a one-pot synthesis of α-acetamido ketones via a four-component condensation reaction. Appl. Catal. A: Gen., 2009, 366(1), 108-113.
    • (2009) Appl. Catal. A: Gen , vol.366 , Issue.1 , pp. 108-113
    • Nabid, M.R.1    Rezaei, S.J.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.