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Volumn 25, Issue 2, 2014, Pages 341-347

One-pot synthesis of various xanthene derivatives using ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable catalyst under solvent-free conditions

Author keywords

1,3 Disulfonic acid imidazolium hydrogen sulfate; Ionic liquid; One pot reaction; Solvent free conditions; Xanthene derivatives

Indexed keywords


EID: 84895910804     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2013.11.016     Document Type: Article
Times cited : (65)

References (77)
  • 3
    • 34447132417 scopus 로고    scopus 로고
    • Innovations and green chemistry
    • I.T. Horváth, and P.T. Anastas Innovations and green chemistry Chem. Rev. 107 2007 2169 2173
    • (2007) Chem. Rev. , vol.107 , pp. 2169-2173
    • Horváth, I.T.1    Anastas, P.T.2
  • 4
    • 0347417134 scopus 로고    scopus 로고
    • Room-temperature ionic liquids. Solvents for synthesis and catalysis
    • T. Welton Room-temperature ionic liquids. Solvents for synthesis and catalysis Chem. Rev. 99 1999 2071 2084
    • (1999) Chem. Rev. , vol.99 , pp. 2071-2084
    • Welton, T.1
  • 5
    • 9644264300 scopus 로고    scopus 로고
    • Ionic liquids in catalysis
    • T. Welton Ionic liquids in catalysis Coord. Chem. Rev. 248 2004 2459 2477
    • (2004) Coord. Chem. Rev. , vol.248 , pp. 2459-2477
    • Welton, T.1
  • 6
    • 0000034575 scopus 로고    scopus 로고
    • Ionic liquids-new "solutions" for transition metal catalysis
    • P. Wasserscheid, and W. Keim Ionic liquids-new "solutions" for transition metal catalysis Angew. Chem. Int. Ed. 39 2000 3772 3789
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3772-3789
    • Wasserscheid, P.1    Keim, W.2
  • 7
    • 77955931938 scopus 로고    scopus 로고
    • 3-Methyl-1-sulfonic acid imidazolium chloride as a new, efficient and recyclable catalyst and solvent for the preparation of N-sulfonyl imines at room temperature
    • M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, and A. Zare 3-Methyl-1-sulfonic acid imidazolium chloride as a new, efficient and recyclable catalyst and solvent for the preparation of N-sulfonyl imines at room temperature J. Iran. Chem. Soc. 7 2010 646 651
    • (2010) J. Iran. Chem. Soc. , vol.7 , pp. 646-651
    • Zolfigol, M.A.1    Khazaei, A.2    Moosavi-Zare, A.R.3    Zare, A.4
  • 8
    • 77950229847 scopus 로고    scopus 로고
    • Ionic liquid 3-methyl-1-sulfonic acid imidazolium chloride as a novel and highly efficient catalyst for the very rapid synthesis of bis(indolyl)methanes under solvent-free conditions
    • M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, and A. Zare Ionic liquid 3-methyl-1-sulfonic acid imidazolium chloride as a novel and highly efficient catalyst for the very rapid synthesis of bis(indolyl)methanes under solvent-free conditions Org. Prep. Proced. Int. 42 2010 95 102
    • (2010) Org. Prep. Proced. Int. , vol.42 , pp. 95-102
    • Zolfigol, M.A.1    Khazaei, A.2    Moosavi-Zare, A.R.3    Zare, A.4
  • 9
    • 79951660356 scopus 로고    scopus 로고
    • An efficient method for the nitration of phenols with nano2 in the presence of 3-methyl-1-sulfonic acid imidazolium
    • A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, and A. Zare An efficient method for the nitration of phenols with nano2 in the presence of 3-methyl-1-sulfonic acid imidazolium Sci. Iran. Trans. C: Chem. Chem. Eng. 17 2010 31 36
    • (2010) Sci. Iran. Trans. C: Chem. Chem. Eng. , vol.17 , pp. 31-36
    • Khazaei, A.1    Zolfigol, M.A.2    Moosavi-Zare, A.R.3    Zare, A.4
  • 10
    • 79958176359 scopus 로고    scopus 로고
    • Rapid synthesis of 1-amidoalkyl-2-naphthols over sulfonic acid functionalized imidazolium salts
    • M.A. Zolfigol, A. Khazaei, A.R. Moosavi-Zare, A. Zare, and V. Khakyzadeh Rapid synthesis of 1-amidoalkyl-2-naphthols over sulfonic acid functionalized imidazolium salts Appl. Catal. A: Gen. 400 2011 70 81
    • (2011) Appl. Catal. A: Gen. , vol.400 , pp. 70-81
    • Zolfigol, M.A.1    Khazaei, A.2    Moosavi-Zare, A.R.3    Zare, A.4    Khakyzadeh, V.5
  • 11
    • 0034678033 scopus 로고    scopus 로고
    • Target-oriented and diversity-oriented organic synthesis in drug discovery
    • S.L. Schreiber Target-oriented and diversity-oriented organic synthesis in drug discovery Science 287 2000 1964 1969
    • (2000) Science , vol.287 , pp. 1964-1969
    • Schreiber, S.L.1
  • 12
    • 0036603766 scopus 로고    scopus 로고
    • Recent advances in isocyanide-based multicomponent chemistry
    • A. Domling Recent advances in isocyanide-based multicomponent chemistry Curr. Opin. Chem. Biol. 6 2002 306 313
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , pp. 306-313
    • Domling, A.1
  • 14
    • 41549157869 scopus 로고    scopus 로고
    • Greener and expeditious synthesis of bioactive heterocycles using microwave irradiation
    • V. Polshettiwar, and R.S. Varma Greener and expeditious synthesis of bioactive heterocycles using microwave irradiation Pure. Appl. Chem. 80 2008 777 790
    • (2008) Pure. Appl. Chem. , vol.80 , pp. 777-790
    • Polshettiwar, V.1    Varma, R.S.2
  • 15
    • 78650176189 scopus 로고    scopus 로고
    • Highly efficient synthesis of triazolo[1, 2-A]indazole-triones and novel spiro triazolo[1,2-a]indazole-tetraones under solvent-free conditions
    • A. Hasaninejad, A. Zare, and M. Shekouhy Highly efficient synthesis of triazolo[1, 2-a]indazole-triones and novel spiro triazolo[1,2-a]indazole- tetraones under solvent-free conditions Tetrahedron 67 2011 390 400
    • (2011) Tetrahedron , vol.67 , pp. 390-400
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3
  • 16
    • 80052251126 scopus 로고    scopus 로고
    • 4 as a versatile mediator or catalyst in organic synthesis
    • 4 as a versatile mediator or catalyst in organic synthesis Molecules 16 2011 6432 6464
    • (2011) Molecules , vol.16 , pp. 6432-6464
    • Stavber, S.1
  • 17
    • 0017796644 scopus 로고
    • 40 catalyzed one-pot synthesis of 12-aryl-8, 9,10,12-tetrahydrobenzo[a] xanthen-11-ones under solvent-free conditions
    • 40 catalyzed one-pot synthesis of 12-aryl-8, 9,10,12-tetrahydrobenzo[a] xanthen-11-ones under solvent-free conditions Eur. J. Med. Chem. 13 1978 67 71
    • (1978) Eur. J. Med. Chem. , vol.13 , pp. 67-71
    • Poupelin, J.P.1    Saint-Ruf, G.2    Foussard-Blanpin, O.3
  • 19
    • 0026100365 scopus 로고
    • Potential antitumor agents. 61. Structure-activity relationships for in vivo colon 38 activity among disubstituted 9-oxo-9H-xanthene-4-acetic acids
    • G.W. Rewcastle, G.J. Atwell, L. Zhuang, B.C. Baguley, and W.A. Denny Potential antitumor agents. 61. Structure-activity relationships for in vivo colon 38 activity among disubstituted 9-oxo-9H-xanthene-4-acetic acids J. Med. Chem. 34 1991 217 222
    • (1991) J. Med. Chem. , vol.34 , pp. 217-222
    • Rewcastle, G.W.1    Atwell, G.J.2    Zhuang, L.3    Baguley, B.C.4    Denny, W.A.5
  • 20
    • 0021898150 scopus 로고
    • Amino derivatives of 1,8-naphthalic anhydride and derived dyes for synthetic-polymer fibres
    • A.T. Peters, and M.J. Bide Amino derivatives of 1,8-naphthalic anhydride and derived dyes for synthetic-polymer fibres Dyes Pigm. 6 1985 349 375
    • (1985) Dyes Pigm. , vol.6 , pp. 349-375
    • Peters, A.T.1    Bide, M.J.2
  • 21
    • 0024559378 scopus 로고
    • Xanthene-dye-labelled phosphatidylethanolamines as probes of interfacial pH. Studies in phospholipid vesicles
    • C.G. Knight, and T. Stephens Xanthene-dye-labelled phosphatidylethanolamines as probes of interfacial pH. Studies in phospholipid vesicles Biochem. J. 258 1989 683 687
    • (1989) Biochem. J. , vol.258 , pp. 683-687
    • Knight, C.G.1    Stephens, T.2
  • 22
    • 0037036547 scopus 로고    scopus 로고
    • Performance and photostability of xanthene and pyrromethene laser dyes in sol-gel phases
    • M. Ahmad, T.A. King, D.K. Ko, B.H. Cha, and J. Lee Performance and photostability of xanthene and pyrromethene laser dyes in sol-gel phases J. Phys. D: Appl. Phys. 35 2002 1473 1476
    • (2002) J. Phys. D: Appl. Phys. , vol.35 , pp. 1473-1476
    • Ahmad, M.1    King, T.A.2    Ko, D.K.3    Cha, B.H.4    Lee, J.5
  • 24
    • 0034741381 scopus 로고    scopus 로고
    • The first efficient method for the intramolecular trapping of benzynes by phenols: A new approach to xanthenes
    • D.W. Knight, and P.B. Little The first efficient method for the intramolecular trapping of benzynes by phenols: a new approach to xanthenes J. Chem. Soc. Perkin Trans. 1 15 2001 1771 1777
    • (2001) J. Chem. Soc. Perkin Trans. 1 , vol.15 , pp. 1771-1777
    • Knight, D.W.1    Little, P.B.2
  • 25
    • 0035013269 scopus 로고    scopus 로고
    • Synthesis of xanthenes, indanes, and tetrahydronaphthalenes via intramolecular phenyl-carbonyl coupling reactions
    • C.W. Kuo, and J.M. Fang Synthesis of xanthenes, indanes, and tetrahydronaphthalenes via intramolecular phenyl-carbonyl coupling reactions Synth. Commun. 31 2001 877 892
    • (2001) Synth. Commun. , vol.31 , pp. 877-892
    • Kuo, C.W.1    Fang, J.M.2
  • 26
    • 0037100385 scopus 로고    scopus 로고
    • Synthesis of polycyclic xanthenes and furans via palladium-catalyzed cyclization of polycyclic aryltriflate esters
    • J.Q. Wang, and R.G. Harvey Synthesis of polycyclic xanthenes and furans via palladium-catalyzed cyclization of polycyclic aryltriflate esters Tetrahedron 58 2002 5927 5931
    • (2002) Tetrahedron , vol.58 , pp. 5927-5931
    • Wang, J.Q.1    Harvey, R.G.2
  • 27
    • 70349125333 scopus 로고    scopus 로고
    • Ferric hydrogen sulfate as an efficient heterogeneous catalyst for environmentally friendly greener synthesis of 1,8-dioxo-octahydroxanthenes
    • H.R. Shaterian, A. Hosseinian, and M. Ghashang Ferric hydrogen sulfate as an efficient heterogeneous catalyst for environmentally friendly greener synthesis of 1,8-dioxo-octahydroxanthenes Turk. J. Chem. 33 2009 233 240
    • (2009) Turk. J. Chem. , vol.33 , pp. 233-240
    • Shaterian, H.R.1    Hosseinian, A.2    Ghashang, M.3
  • 28
    • 77950021958 scopus 로고    scopus 로고
    • A new strategy for the synthesis of benzoxanthenes catalyzed by proline triflate in water
    • J. Li, L. Lu, and W. Su A new strategy for the synthesis of benzoxanthenes catalyzed by proline triflate in water Tetrahedron Lett. 51 2010 2434 2437
    • (2010) Tetrahedron Lett. , vol.51 , pp. 2434-2437
    • Li, J.1    Lu, L.2    Su, W.3
  • 29
    • 37749004900 scopus 로고    scopus 로고
    • An efficient and convenient protocol for the synthesis of novel 12-aryl- or 12-alkyl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-one derivatives
    • B. Das, K. Laxminarayana, M. Krishnaiah, and Y. Srinivas An efficient and convenient protocol for the synthesis of novel 12-aryl- or 12-alkyl-8,9,10,12- tetrahydrobenzo[a]xanthen-11-one derivatives Synlett 2007 3107 3112
    • (2007) Synlett , pp. 3107-3112
    • Das, B.1    Laxminarayana, K.2    Krishnaiah, M.3    Srinivas, Y.4
  • 30
    • 54449089713 scopus 로고    scopus 로고
    • Strontium triflate catalyzed one-pot condensation of β-naphthol, aldehydes and cyclic 1,3-dicarbonyl compounds
    • J. Li, W. Tang, L. Lu, and W. Su Strontium triflate catalyzed one-pot condensation of β-naphthol, aldehydes and cyclic 1,3-dicarbonyl compounds Tetrahedron Lett. 49 2008 7117 7120
    • (2008) Tetrahedron Lett. , vol.49 , pp. 7117-7120
    • Li, J.1    Tang, W.2    Lu, L.3    Su, W.4
  • 31
    • 77951224178 scopus 로고    scopus 로고
    • A catalytic and green procedure for synthesis of 12-aryl- or 12-alkyl-8,9,10,12-tetrahydrobenzo[α]xanthen-11-one derivatives under solvent-free conditions
    • N. Foroughifar, A. Mobinikhaledi, and H. Moghanian A catalytic and green procedure for synthesis of 12-aryl- or 12-alkyl-8,9,10,12- tetrahydrobenzo[α]xanthen-11-one derivatives under solvent-free conditions Int. J. Green Nanotechnol. Phys. Chem. 1 2009 57 63
    • (2009) Int. J. Green Nanotechnol. Phys. Chem. , vol.1 , pp. 57-63
    • Foroughifar, N.1    Mobinikhaledi, A.2    Moghanian, H.3
  • 32
    • 80051517015 scopus 로고    scopus 로고
    • One-pot synthesis of tetrahydrobenzo[a]xanthen-11-one derivatives catalyzed by ruthenium chloride hydrate as a homogeneous catalyst
    • K. Tabatabaeian, A. Khorshidi, M. Mamaghani, A. Dadashi, and M.K. Jalali One-pot synthesis of tetrahydrobenzo[a]xanthen-11-one derivatives catalyzed by ruthenium chloride hydrate as a homogeneous catalyst Can. J. Chem. 89 2011 623 627
    • (2011) Can. J. Chem. , vol.89 , pp. 623-627
    • Tabatabaeian, K.1    Khorshidi, A.2    Mamaghani, M.3    Dadashi, A.4    Jalali, M.K.5
  • 34
    • 52049108246 scopus 로고    scopus 로고
    • 2: An efficient alternative for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes
    • 2: an efficient alternative for the synthesis of 14-aryl or alkyl-14H-dibenzo[a,j]xanthenes Tetrahedron Lett. 49 2008 6454 6456
    • (2008) Tetrahedron Lett. , vol.49 , pp. 6454-6456
    • Mirjalili, B.B.1    Bamoniri, A.2    Akbari, A.3
  • 35
    • 52049119030 scopus 로고    scopus 로고
    • Oxalic acid as a catalyst for efficient synthesis of bis-(indolyl) methanes, and 14-aryl-14H-dibenzo[a,j]xanthenes in water
    • N.D. Kokare, J.N. Sangshetti, and D.B. Shinde Oxalic acid as a catalyst for efficient synthesis of bis-(indolyl)methanes, and 14-aryl-14H-dibenzo[a,j] xanthenes in water Chin. Chem. Lett. 19 2008 1186 1189
    • (2008) Chin. Chem. Lett. , vol.19 , pp. 1186-1189
    • Kokare, N.D.1    Sangshetti, J.N.2    Shinde, D.B.3
  • 36
    • 84867333049 scopus 로고    scopus 로고
    • 1,3-Dibromo-5,5-dimethylhydantoin (DBH)/kaolin: An efficient reagent system for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under solvent-free conditions
    • F. Shirini, N.G. Khaligh, G.H. Imanzadeh, and P.G. Ghasem-Abadi 1,3-Dibromo-5,5-dimethylhydantoin (DBH)/kaolin: an efficient reagent system for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthenes under solvent-free conditions Chin. Chem. Lett. 23 2012 1145 1148
    • (2012) Chin. Chem. Lett. , vol.23 , pp. 1145-1148
    • Shirini, F.1    Khaligh, N.G.2    Imanzadeh, G.H.3    Ghasem-Abadi, P.G.4
  • 37
    • 84868481398 scopus 로고    scopus 로고
    • Zinc oxide nanoparticles: A highly efficient and readily recyclable catalyst for the synthesis of xanthenes
    • J. Safaei-Ghomi, and M.A. Ghasemzadeh Zinc oxide nanoparticles: a highly efficient and readily recyclable catalyst for the synthesis of xanthenes Chin. Chem. Lett. 23 2012 1225 1229
    • (2012) Chin. Chem. Lett. , vol.23 , pp. 1225-1229
    • Safaei-Ghomi, J.1    Ghasemzadeh, M.A.2
  • 38
    • 33746025668 scopus 로고    scopus 로고
    • Iodine catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j]xanthenes
    • B. Das, B. Ravikanth, R. Ramu, K. Laxminarayana, and B.V. Rao Iodine catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j] xanthenes J. Mol. Catal. A: Chem. 255 2006 74 77
    • (2006) J. Mol. Catal. A: Chem. , vol.255 , pp. 74-77
    • Das, B.1    Ravikanth, B.2    Ramu, R.3    Laxminarayana, K.4    Rao, B.V.5
  • 39
    • 33846240529 scopus 로고    scopus 로고
    • Molecular iodine catalyzed synthesis of aryl-14H-dibenzo[a,j]xanthenes under solvent-free condition
    • A.P. Mohamed, and P.J. Vaderapura Molecular iodine catalyzed synthesis of aryl-14H-dibenzo[a,j]xanthenes under solvent-free condition Bioorg. Med. Chem. Lett. 17 2007 621 623
    • (2007) Bioorg. Med. Chem. Lett. , vol.17 , pp. 621-623
    • Mohamed, A.P.1    Vaderapura, P.J.2
  • 40
    • 34047182689 scopus 로고    scopus 로고
    • Heteropolyacid: An efficient and eco-friendly catalyst for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthene
    • M. Mohammadpour Amini, M. Seyyedhamzeh, and A. Bazgir Heteropolyacid: an efficient and eco-friendly catalyst for the synthesis of 14-aryl-14H-dibenzo[a, j]xanthene Appl. Catal. A: Gen. 323 2007 242 245
    • (2007) Appl. Catal. A: Gen. , vol.323 , pp. 242-245
    • Mohammadpour Amini, M.1    Seyyedhamzeh, M.2    Bazgir, A.3
  • 41
    • 34347256754 scopus 로고    scopus 로고
    • Facile heteropolyacid-promoted synthesis of 14-substituted-14-H- dibenzo[a,j] xanthene derivatives under solvent-free conditions
    • M.M. Heravi, Kh. Bakhtiari, Z. Daroogheha, and F.F. Bamoharram Facile heteropolyacid-promoted synthesis of 14-substituted-14-H-dibenzo[a,j] xanthene derivatives under solvent-free conditions J. Mol. Catal. A: Chem. 273 2007 99 101
    • (2007) J. Mol. Catal. A: Chem. , vol.273 , pp. 99-101
    • Heravi, M.M.1    Bakhtiari, Kh.2    Daroogheha, Z.3    Bamoharram, F.F.4
  • 42
    • 34548526815 scopus 로고    scopus 로고
    • One-pot synthesis of aryl 14H-dibenzo[a,j]xanthene leuco-dye derivatives
    • H.R. Shaterian, M. Ghashang, and A. Hassankhani One-pot synthesis of aryl 14H-dibenzo[a,j]xanthene leuco-dye derivatives Dyes Pigm. 76 2008 564 568
    • (2008) Dyes Pigm. , vol.76 , pp. 564-568
    • Shaterian, H.R.1    Ghashang, M.2    Hassankhani, A.3
  • 43
    • 34548661513 scopus 로고    scopus 로고
    • Solvent-free synthesis of aryl-14H-dibenzo[a,j]xanthenes and 1,8-dioxo-octahydro-xanthenes using silica sulfuric acid as catalyst
    • M. Seyyedhamzeh, P. Mirzaei, and A. Bazgir Solvent-free synthesis of aryl-14H-dibenzo[a,j]xanthenes and 1,8-dioxo-octahydro-xanthenes using silica sulfuric acid as catalyst Dyes Pigm. 76 2008 836 839
    • (2008) Dyes Pigm. , vol.76 , pp. 836-839
    • Seyyedhamzeh, M.1    Mirzaei, P.2    Bazgir, A.3
  • 44
    • 33751080407 scopus 로고    scopus 로고
    • Heterogeneous catalyst: Amberlyst-15 catalyzes the synthesis of 14-substituted-14H-dibenzo[a,j]xanthenes under solvent-free conditions
    • S. Ko, and C.F. Yao Heterogeneous catalyst: amberlyst-15 catalyzes the synthesis of 14-substituted-14H-dibenzo[a,j]xanthenes under solvent-free conditions Tetrahedron Lett. 47 2006 8827 8829
    • (2006) Tetrahedron Lett. , vol.47 , pp. 8827-8829
    • Ko, S.1    Yao, C.F.2
  • 45
  • 46
    • 37649004405 scopus 로고    scopus 로고
    • Eco-friendly and efficient one-pot synthesis of alkyl- or aryl-14H-dibenzo[a,j]xanthenes in water
    • M. Dabiri, M. Baghbanzadeh, M.S. Nikcheh, and E. Arzroomchilar Eco-friendly and efficient one-pot synthesis of alkyl- or aryl-14H-dibenzo[a,j] xanthenes in water Bioorg. Med. Chem. Lett. 18 2008 436 438
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 436-438
    • Dabiri, M.1    Baghbanzadeh, M.2    Nikcheh, M.S.3    Arzroomchilar, E.4
  • 48
    • 50649110696 scopus 로고    scopus 로고
    • Facile montmorillonite k-10-supported synthesis of xanthene derivatives under microwave and thermal conditions
    • A. Sharifi, M.S. Abaee, A. Tavakkoli, M. Mirzaei, and A. Zolfaghari Facile montmorillonite k-10-supported synthesis of xanthene derivatives under microwave and thermal conditions Synth. Commun. 38 2008 2958 2966
    • (2008) Synth. Commun. , vol.38 , pp. 2958-2966
    • Sharifi, A.1    Abaee, M.S.2    Tavakkoli, A.3    Mirzaei, M.4    Zolfaghari, A.5
  • 49
    • 17144400729 scopus 로고    scopus 로고
    • A facile, simple and convenient method for the synthesis of 14-alkyl or aryl-14-H-dibenzo[a,j]xanthenes catalyzed by pTSA in solution and solvent-free conditions
    • A.R. Khosropour, M.M. Khodaei, and H. Moghannian A facile, simple and convenient method for the synthesis of 14-alkyl or aryl-14-H-dibenzo[a,j] xanthenes catalyzed by pTSA in solution and solvent-free conditions Synlett 2005 955 958
    • (2005) Synlett , pp. 955-958
    • Khosropour, A.R.1    Khodaei, M.M.2    Moghannian, H.3
  • 50
    • 34548314184 scopus 로고    scopus 로고
    • Wet cyanuric chloride catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j]xanthenes
    • N.A. Bigdeli, M.M. Heravi, and G.H. Mahdavinia Wet cyanuric chloride catalyzed simple and efficient synthesis of 14-aryl or alkyl-14-H-dibenzo[a,j] xanthenes Catal Commun. 8 2007 1595 1598
    • (2007) Catal Commun. , vol.8 , pp. 1595-1598
    • Bigdeli, N.A.1    Heravi, M.M.2    Mahdavinia, G.H.3
  • 52
    • 42649087436 scopus 로고    scopus 로고
    • 3 catalyzed condensation reaction of β-naphthol and aldehyde in ionic liquids: A green synthesis of aryl-14H-dibenzo[a,j] xanthenes
    • 3 catalyzed condensation reaction of β-naphthol and aldehyde in ionic liquids: a green synthesis of aryl-14H-dibenzo[a,j]xanthenes Tetrahedron Lett. 49 2008 3391 3394
    • (2008) Tetrahedron Lett. , vol.49 , pp. 3391-3394
    • Su, W.1    Yang, D.2    Jin, C.3    Zhang, B.4
  • 53
    • 84865865852 scopus 로고    scopus 로고
    • Succinimide-N-sulfonic acid: An efficient catalyst for the synthesis of xanthene derivatives under solvent-free conditions
    • F. Shirini, and N.G. Khaligh Succinimide-N-sulfonic acid: an efficient catalyst for the synthesis of xanthene derivatives under solvent-free conditions Dyes Pigm. 95 2012 789 794
    • (2012) Dyes Pigm. , vol.95 , pp. 789-794
    • Shirini, F.1    Khaligh, N.G.2
  • 54
    • 84867572447 scopus 로고    scopus 로고
    • Preparation, characterization and use of 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient, halogen-free and reusable ionic liquid catalyst for the trimethylsilyl protection of hydroxyl groups and deprotection of the obtained trimethylsilanes
    • F. Shirini, N.G. Khaligh, and S. Akbari-Dadamahaleh Preparation, characterization and use of 1,3-disulfonic acid imidazolium hydrogen sulfate as an efficient, halogen-free and reusable ionic liquid catalyst for the trimethylsilyl protection of hydroxyl groups and deprotection of the obtained trimethylsilanes J. Mol. Catal. A: Chem. 365 2012 15 23
    • (2012) J. Mol. Catal. A: Chem. , vol.365 , pp. 15-23
    • Shirini, F.1    Khaligh, N.G.2    Akbari-Dadamahaleh, S.3
  • 55
    • 84870680727 scopus 로고    scopus 로고
    • 1,3-Disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable ionic liquid catalyst for the N-Boc protection of amines
    • F. Shirini, and N.G. Khaligh 1,3-Disulfonic acid imidazolium hydrogen sulfate as an efficient and reusable ionic liquid catalyst for the N-Boc protection of amines J. Mol. Liq. 177 2013 386 393
    • (2013) J. Mol. Liq. , vol.177 , pp. 386-393
    • Shirini, F.1    Khaligh, N.G.2
  • 58
    • 79957468402 scopus 로고    scopus 로고
    • 1,3,5-Trichloro-2,4,6-triazinetrion: A versatile heterocycle for the one-pot synthesis of 14-aryl- or alkyl-14H-dibenzo[a,j]xanthene, 1,8-dioxooctahydroxanthene and 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11- one derivatives under solvent-free conditions
    • B. Maleki, M. Gholizadeh, and Z. Sepehr 1,3,5-Trichloro-2,4,6- triazinetrion: a versatile heterocycle for the one-pot synthesis of 14-aryl- or alkyl-14H-dibenzo[a,j]xanthene, 1,8-dioxooctahydroxanthene and 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-one derivatives under solvent-free conditions Bull. Korean Chem. Soc. 32 2011 1697 1702
    • (2011) Bull. Korean Chem. Soc. , vol.32 , pp. 1697-1702
    • Maleki, B.1    Gholizadeh, M.2    Sepehr, Z.3
  • 59
    • 84874545236 scopus 로고    scopus 로고
    • 4-Dodecylbenzenesulfonic acid (DBSA) as an efficient and recyclable catalyst for synthesis of 14-aryl- and 14-alkyl-14-H-dibenzo[a,j]xanthenes under solvent-free conditions
    • H. Hashemi, and A.R. Sardarian 4-Dodecylbenzenesulfonic acid (DBSA) as an efficient and recyclable catalyst for synthesis of 14-aryl- and 14-alkyl-14-H-dibenzo[a,j]xanthenes under solvent-free conditions Iran. J. Sci. Technol. A1 2013 75 82
    • (2013) Iran. J. Sci. Technol. , vol.1 A , pp. 75-82
    • Hashemi, H.1    Sardarian, A.R.2
  • 60
    • 84857522734 scopus 로고    scopus 로고
    • Organocatalyst trityl chloride efficiently promoted the solvent-free synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-ones by in situ formation of carbocationic system in neutral media
    • A. Khazaei, M.A. Zolfigol, and A.R. Moosavi-Zare et al. Organocatalyst trityl chloride efficiently promoted the solvent-free synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]-xanthen-11-ones by in situ formation of carbocationic system in neutral media Catal. Commun. 20 2012 54 57
    • (2012) Catal. Commun. , vol.20 , pp. 54-57
    • Khazaei, A.1    Zolfigol, M.A.2    Moosavi-Zare, A.R.3
  • 61
    • 67650529102 scopus 로고    scopus 로고
    • An efficient one-pot synthesis of tetrahydrobenzo[a]xanthene-11-one and diazabenzo[a]anthracene-9,11-dione derivatives under solvent free condition
    • G.C. Nandi, S. Samai, R. Kumar, and M.S. Singh An efficient one-pot synthesis of tetrahydrobenzo[a]xanthene-11-one and diazabenzo[a]anthracene-9,11- dione derivatives under solvent free condition Tetrahedron 65 2009 7129 7134
    • (2009) Tetrahedron , vol.65 , pp. 7129-7134
    • Nandi, G.C.1    Samai, S.2    Kumar, R.3    Singh, M.S.4
  • 62
    • 78650180331 scopus 로고    scopus 로고
    • Sulfamic acid catalyzed solvent-free synthesis of 10-aryl-7,7-dimethyl-6, 7,8,10-tetrahydro-9H-[1,3]-dioxolo [4,5-b]xanthen-9-ones and 12-aryl-9,9-dimethyl-8,9,10,12-tetrahydro-11H-benzo[a]xanthen-11-ones
    • M.M. Heravi, H. Alinejhad, K. Bakhtiari, and H.A. Oskooie Sulfamic acid catalyzed solvent-free synthesis of 10-aryl-7,7-dimethyl-6,7,8,10-tetrahydro-9H- [1,3]-dioxolo [4,5-b]xanthen-9-ones and 12-aryl-9,9-dimethyl-8,9,10,12- tetrahydro-11H-benzo[a]xanthen-11-ones Mol. Divers. 14 2010 621 626
    • (2010) Mol. Divers. , vol.14 , pp. 621-626
    • Heravi, M.M.1    Alinejhad, H.2    Bakhtiari, K.3    Oskooie, H.A.4
  • 63
    • 84875367294 scopus 로고    scopus 로고
    • Rice husk: A mild, efficient, green and recyclable catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydro[a]xanthene-11-ones and quinoxaline derivatives
    • F. Shirini, S. Akbari-Dadamahaleh, A. Mohammad-Khah, and A.R. Aliakbar Rice husk: a mild, efficient, green and recyclable catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydro[a]xanthene-11-ones and quinoxaline derivatives C.R. Chim. 16 2013 207 216
    • (2013) C.R. Chim. , vol.16 , pp. 207-216
    • Shirini, F.1    Akbari-Dadamahaleh, S.2    Mohammad-Khah, A.3    Aliakbar, A.R.4
  • 64
    • 44249124484 scopus 로고    scopus 로고
    • An efficient synthesis of 1,8-dioxo-octahydro-xanthene derivatives promoted by a room temperature ionic liquid at ambient conditions under ultrasound irradiation
    • K. Venkatesan, S.S. Pujari, R.J. Lahoti, and K.V. Srinivasan An efficient synthesis of 1,8-dioxo-octahydro-xanthene derivatives promoted by a room temperature ionic liquid at ambient conditions under ultrasound irradiation Ultrason. Sonochem. 15 2008 548 553
    • (2008) Ultrason. Sonochem. , vol.15 , pp. 548-553
    • Venkatesan, K.1    Pujari, S.S.2    Lahoti, R.J.3    Srinivasan, K.V.4
  • 65
    • 84880488314 scopus 로고    scopus 로고
    • β-Cyclodextrin mediated synthesis of 1,8-dioxooctahydroxanthenes in water
    • S. Kokkirala, N.M. Sabbavarapu, and V.D.N. Yadavalli β-Cyclodextrin mediated synthesis of 1,8-dioxooctahydroxanthenes in water Eur. J. Chem. 2 2011 272 275
    • (2011) Eur. J. Chem. , vol.2 , pp. 272-275
    • Kokkirala, S.1    Sabbavarapu, N.M.2    Yadavalli, V.D.N.3
  • 66
    • 84857359152 scopus 로고    scopus 로고
    • 3H]Cl} as a novel, highly efficient and homogeneous catalyst for the synthesis of β-acetamido ketones, 1,8-dioxo-octahydroxanthenes and 14-aryl-14H-dibenzo[a,j]xanthenes
    • 3H]Cl} as a novel, highly efficient and homogeneous catalyst for the synthesis of β-acetamido ketones, 1,8-dioxo-octahydroxanthenes and 14-aryl-14H- dibenzo[a,j]xanthenes J. Mol. Liq. 167 2012 69 77
    • (2012) J. Mol. Liq. , vol.167 , pp. 69-77
    • Zare, A.1    Moosavi-Zare, A.R.2    Merajoddin, M.3
  • 68
    • 84864587971 scopus 로고    scopus 로고
    • Preparation of various xanthene derivatives over sulfonic acid functionalized imidazolium salts (SAFIS) as novel, highly efficient and reusable catalysts
    • M.A. Zolfigol, V. Khakyzadeh, and A.R. Moosavi-Zare et al. Preparation of various xanthene derivatives over sulfonic acid functionalized imidazolium salts (SAFIS) as novel, highly efficient and reusable catalysts C.R. Chim. 15 2012 719 736
    • (2012) C.R. Chim. , vol.15 , pp. 719-736
    • Zolfigol, M.A.1    Khakyzadeh, V.2    Moosavi-Zare, A.R.3
  • 69
    • 51249112772 scopus 로고    scopus 로고
    • The one-pot synthesis of 14-alkyl- or aryl-14H-dibenzo[a,j]xanthenes catalyzed by task-specific ionic liquid
    • K. Gong, D. Fang, H.L. Wang, X.L. Zhou, and Z.L. Liu The one-pot synthesis of 14-alkyl- or aryl-14H-dibenzo[a,j]xanthenes catalyzed by task-specific ionic liquid Dyes Pigm. 80 2009 30 33
    • (2009) Dyes Pigm. , vol.80 , pp. 30-33
    • Gong, K.1    Fang, D.2    Wang, H.L.3    Zhou, X.L.4    Liu, Z.L.5
  • 70
    • 79960295345 scopus 로고    scopus 로고
    • Task-specific ionic liquid catalyzed efficient microwave-assisted synthesis of 12-alkyl or aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones under solvent-free conditions
    • D. Kundu, A. Majee, and A. Hajra Task-specific ionic liquid catalyzed efficient microwave-assisted synthesis of 12-alkyl or aryl-8,9,10,12- tetrahydrobenzo[a]xanthen-11-ones under solvent-free conditions Green Chem. Lett. Rev. 4 2011 205 209
    • (2011) Green Chem. Lett. Rev. , vol.4 , pp. 205-209
    • Kundu, D.1    Majee, A.2    Hajra, A.3
  • 71
    • 84895824432 scopus 로고    scopus 로고
    • An efficient synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11- ones using (4-sulfobutyl)tris(4-sulfophenyl)phosphonium hydrogen sulphate as catalyst under neat conditions
    • B. Janardhan, S. Vijaya Laxmi, and B. Rajitha An efficient synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones using (4-sulfobutyl)tris(4- sulfophenyl)phosphonium hydrogen sulphate as catalyst under neat conditions J. Chem. Pharm. Res. 4 2012 519 525
    • (2012) J. Chem. Pharm. Res. , vol.4 , pp. 519-525
    • Janardhan, B.1    Vijaya Laxmi, S.2    Rajitha, B.3
  • 72
    • 67649372523 scopus 로고    scopus 로고
    • PTSA-catalyzed one-pot synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a] xanthen-11-ones in ionic liquid and neat conditions
    • J.M. Khurana, and D. Magoo pTSA-catalyzed one-pot synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones in ionic liquid and neat conditions Tetrahedron Lett. 50 2009 4777 4780
    • (2009) Tetrahedron Lett. , vol.50 , pp. 4777-4780
    • Khurana, J.M.1    Magoo, D.2
  • 74
    • 84895904767 scopus 로고    scopus 로고
    • 3H]Cl} as an efficient and homogeneous catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a]xanthen-11-ones
    • 3H]Cl} as an efficient and homogeneous catalyst for the synthesis of 12-aryl-8,9,10,12-tetrahydrobenzo[a] xanthen-11-ones Iran. J. Catal. 2 2012 107 114
    • (2012) Iran. J. Catal. , vol.2 , pp. 107-114
    • Zare, A.1    Khanivar, R.2    Merajoddin, M.3
  • 75
    • 69549095915 scopus 로고    scopus 로고
    • 4: An efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo- octahydroxanthenes
    • 4: an efficient reusable acidic ionic liquid for the synthesis of 1,8-dioxo-octahydroxanthenes J. Chin. Chem. Soc. 56 2009 659 665
    • (2009) J. Chin. Chem. Soc. , vol.56 , pp. 659-665
    • Niknam, K.1    Damya, M.2
  • 76
    • 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
    • M. Dabiri, M. Baghbanzadeh, and E. Arzroomchilar 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. 9 2008 939
    • (2008) Catal. Commun. , vol.9 , pp. 939
    • Dabiri, M.1    Baghbanzadeh, M.2    Arzroomchilar, E.3
  • 77
    • 84861668857 scopus 로고    scopus 로고
    • 4] as a cheap and mild acidic ionic liquid
    • 4] as a cheap and mild acidic ionic liquid Arabian J. Chem. 5 2012 319 323
    • (2012) Arabian J. Chem. , vol.5 , pp. 319-323
    • Kalantari, M.1


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