메뉴 건너뛰기




Volumn , Issue , 2013, Pages

An efficient one-pot three-component synthesis of novel sulfanyl tetrazoles using ionic liquids

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84867768931     PISSN: 20909063     EISSN: 20909071     Source Type: Journal    
DOI: 10.1155/2013/104690     Document Type: Article
Times cited : (7)

References (46)
  • 2
    • 31544434530 scopus 로고    scopus 로고
    • Recent developments in isocyanide based multicomponent reactions in applied chemistry
    • DOI 10.1021/cr0505728
    • Dömling A., Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chemical Reviews 2006 106 1 17 89 2-s2.0-31544434530 10.1021/cr0505728 (Pubitemid 43159621)
    • (2006) Chemical Reviews , vol.106 , Issue.1 , pp. 17-89
    • Domling, A.1
  • 4
    • 0036836947 scopus 로고    scopus 로고
    • 5-Substituted-1H-tetrazoles as carboxylic acid isosteres: Medicinal chemistry and synthetic methods
    • 2-s2.0-0036836947 10.1016/S0968-0896(02)00239-0
    • Herr R. Jason, 5-Substituted-1H-tetrazoles as carboxylic acid isosteres: medicinal chemistry and synthetic methods. Bioorganic and Medicinal Chemistry 2002 10 11 3379 3393 2-s2.0-0036836947 10.1016/S0968-0896(02)00239-0
    • (2002) Bioorganic and Medicinal Chemistry , vol.10 , Issue.11 , pp. 3379-3393
    • Herr, R.J.1
  • 6
    • 0014067035 scopus 로고
    • Heterocyclic tetrazoles, a new class of lipolysis inhibitors
    • 2-s2.0-0014067035
    • Holland G. F., Pereira J. N., Heterocyclic tetrazoles, a new class of lipolysis inhibitors. Journal of Medicinal Chemistry 1967 10 2 149 154 2-s2.0-0014067035
    • (1967) Journal of Medicinal Chemistry , vol.10 , Issue.2 , pp. 149-154
    • Holland, G.F.1    Pereira, J.N.2
  • 7
    • 0010633373 scopus 로고
    • The fate and excretion of C14-labeled pentylenetetrazol in the rat, with comments on analytical methods for pentylenetetrazol
    • Esplin D. W., Woodbury D. M., The fate and excretion of C14-labeled pentylenetetrazol in the rat, with comments on analytical methods for pentylenetetrazol. The Journal of Pharmacology and Experimental Therapeutics 1956 118 2 129 138
    • (1956) The Journal of Pharmacology and Experimental Therapeutics , vol.118 , Issue.2 , pp. 129-138
    • Esplin, D.W.1    Woodbury, D.M.2
  • 8
    • 17044379443 scopus 로고    scopus 로고
    • Preparation of 1,5-fused tetrazoles under solvent-free conditions
    • Eshghi H., Hassankhani A., Preparation of 1,5-fused tetrazoles under solvent-free conditions. Synthetic Communications 2005 35 1115 1120
    • (2005) Synthetic Communications , vol.35 , pp. 1115-1120
    • Eshghi, H.1    Hassankhani, A.2
  • 9
    • 0025931099 scopus 로고
    • Directed metalation and new synthetic transformations of 5-aryltetrazoles
    • 2-s2.0-0025931099 10.1016/0040-4039(91)80425-6
    • Flippin L. A., Directed metalation and new synthetic transformations of 5-aryltetrazoles. Tetrahedron Letters 1991 32 47 6857 6860 2-s2.0-0025931099 10.1016/0040-4039(91)80425-6
    • (1991) Tetrahedron Letters , vol.32 , Issue.47 , pp. 6857-6860
    • Flippin, L.A.1
  • 10
    • 0037156375 scopus 로고    scopus 로고
    • On the relative strength of the 1H-tetrazol-5-yl- and the 2-(triphenylmethyl)-2H-tetrazol-5-yl-group in directed ortho-lithiation
    • DOI 10.1016/S0040-4039(02)00490-2, PII S0040403902004902
    • Rhonnstad P., Wensbo D., On the relative strength of the 1H-tetrazol-5-yl- and the 2-(triphenylmethyl)-2H-tetrazol-5-yl-group in directed ortho-lithiation. Tetrahedron Letters 2002 43 17 3137 3139 2-s2.0-0037156375 10.1016/S0040-4039(02)00490-2 (Pubitemid 34310392)
    • (2002) Tetrahedron Letters , vol.43 , Issue.17 , pp. 3137-3139
    • Rhonnstad, P.1    Wensbo, D.2
  • 11
    • 0042158496 scopus 로고    scopus 로고
    • Synthesis of fused tetrazole- and imidazole derivatives via iodocyclization
    • DOI 10.1016/S0040-4020(03)00818-4
    • Ek F., Wistrand L.-G., Frejd T., Synthesis of fused tetrazole- and imidazole derivatives via iodocyclization. Tetrahedron 2003 59 35 6759 6769 2-s2.0-0042158496 10.1016/S0040-4020(03)00818-4 (Pubitemid 36976660)
    • (2003) Tetrahedron , vol.59 , Issue.35 , pp. 6759-6769
    • Ek, F.1    Wistrand, L.-G.2    Frejd, T.3
  • 13
    • 0001627205 scopus 로고    scopus 로고
    • Preparation of Tetrazoles from Organic Nitriles and Sodium Azide in Micellar Media
    • Jursic B. S., Le Blanc B. W., Preparation of tetrazoles from organic nitriles and sodium azide in micellar media. Journal of Heterocyclic Chemistry 1998 35 2 405 408 2-s2.0-0001627205 (Pubitemid 128494367)
    • (1998) Journal of Heterocyclic Chemistry , vol.35 , Issue.2 , pp. 405-408
    • Jursic, B.S.1    LeBlanc, B.W.2
  • 15
    • 0029091063 scopus 로고
    • Large scale synthesis of oligoribonucleotides on high-loaded polystyrene (HLP) support
    • 2-s2.0-0029091063
    • Tsou D., Hampel A., Andrus A., Vinayak R., Large scale synthesis of oligoribonucleotides on high-loaded polystyrene (HLP) support. Nucleosides and Nucleotides 1995 14 7 1481 1492 2-s2.0-0029091063
    • (1995) Nucleosides and Nucleotides , vol.14 , Issue.7 , pp. 1481-1492
    • Tsou, D.1    Hampel, A.2    Andrus, A.3    Vinayak, R.4
  • 16
    • 0000361401 scopus 로고
    • Synthesis and properties of 5-(substituted) mercaptotetrazoles
    • 2-s2.0-0000361401
    • Lieber E., Enkoji T., Synthesis and properties of 5-(substituted) mercaptotetrazoles. Journal of Organic Chemistry 1961 26 11 4472 4479 2-s2.0-0000361401
    • (1961) Journal of Organic Chemistry , vol.26 , Issue.11 , pp. 4472-4479
    • Lieber, E.1    Enkoji, T.2
  • 17
    • 33645470355 scopus 로고    scopus 로고
    • Chemistry and biological activity of natural and synthetic prenyloxycoumarins
    • 2-s2.0-33645470355 10.2174/092986706775197890
    • Curini M., Cravotto G., Epifano F., Giannone G., Chemistry and biological activity of natural and synthetic prenyloxycoumarins. Current Medicinal Chemistry 2006 13 2 199 222 2-s2.0-33645470355 10.2174/092986706775197890
    • (2006) Current Medicinal Chemistry , vol.13 , Issue.2 , pp. 199-222
    • Curini, M.1    Cravotto, G.2    Epifano, F.3    Giannone, G.4
  • 18
    • 15944389028 scopus 로고    scopus 로고
    • Simple coumarins and analogues in medicinal chemistry: Occurrence, synthesis and biological activity
    • DOI 10.2174/0929867053507315
    • Borges F., Roleira F., Milhazes N., Santana L., Uriarte E., Simple coumarins and analogues in medicinal chemistry: occurrence, synthesis and biological activity. Current Medicinal Chemistry 2005 12 8 887 916 2-s2.0-15944389028 10.2174/0929867053507315 (Pubitemid 40443846)
    • (2005) Current Medicinal Chemistry , vol.12 , Issue.8 , pp. 887-916
    • Borges, F.1    Roleira, F.2    Milhazes, N.3    Santana, L.4    Uriarte, E.5
  • 19
    • 6944222563 scopus 로고    scopus 로고
    • Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities
    • DOI 10.2174/1381612043382710
    • Fylaktakidou K. C., Hadjipavlou-Litina D. J., Litinas K. E., Nicolaides D. N., Natural and synthetic coumarin derivatives with anti-inflammatory/ antioxidant activities. Current Pharmaceutical Design 2004 10 30 3813 3833 2-s2.0-6944222563 10.2174/1381612043382710 (Pubitemid 39409872)
    • (2004) Current Pharmaceutical Design , vol.10 , Issue.30 , pp. 3813-3833
    • Fylaktakidou, K.C.1    Hadjipavlou-Litina, D.J.2    Litinas, K.E.3    Nicolaides, D.N.4
  • 20
    • 0035282630 scopus 로고    scopus 로고
    • Anti-AIDS agents. 42. Synthesis and anti-HIV activity of disubstituted (3′R,4′R)-3′,4′-di-O-(S)-camphanoyl-(+)-cis- khellactone analogues
    • DOI 10.1021/jm000070g
    • Xie L., Takeuchi Y., Cosentino L. M., McPhail A. T., Lee K.-H., Anti-AIDS agents. 42. Synthesis and anti-HIV activity of disubstituted (3′R,4′R)-3′4′-di-O-(S)-camphanoyl-(+)-cis- khellactone analogues. Journal of Medicinal Chemistry 2001 44 5 664 671 2-s2.0-0035801775 10.1021/jm000070g (Pubitemid 32171663)
    • (2001) Journal of Medicinal Chemistry , vol.44 , Issue.5 , pp. 664-671
    • Xie, L.1    Takeuchi, Y.2    Cosentino, L.M.3    McPhail, A.T.4    Lee, K.-H.5
  • 21
    • 0001250488 scopus 로고
    • Three synthetic routes to a sterically hindered tetrazole. A new one-step mild conversion of an amide into a tetrazole
    • 2-s2.0-0027209127
    • Duncia J. V., Pierce M. E., Santella III J. B., Three synthetic routes to a sterically hindered tetrazole. A new one-step mild conversion of an amide into a tetrazole. Journal of Organic Chemistry 1991 56 7 2395 2400 2-s2.0-0027209127
    • (1991) Journal of Organic Chemistry , vol.56 , Issue.7 , pp. 2395-2400
    • Duncia, J.V.1    Pierce, M.E.2    Santella Iii, J.B.3
  • 22
    • 1542497706 scopus 로고
    • Formation of organo tin-nitrogen bonds. III. N-trial-kyltin-5-substituted tetrazoles
    • Sisido K., Nabika K., Isida T., Kozima S., Formation of organo tin-nitrogen bonds. III. N-trial-kyltin-5-substituted tetrazoles. Journal of Organometallic Chemistry 1971 33 3 337 346
    • (1971) Journal of Organometallic Chemistry , vol.33 , Issue.3 , pp. 337-346
    • Sisido, K.1    Nabika, K.2    Isida, T.3    Kozima, S.4
  • 24
    • 33751384910 scopus 로고
    • Dialkyltin oxide mediated addition of trimethylsilyl azide to nitriles. A novel preparation of 5-substituted tetrazoles
    • 2-s2.0-33751384910
    • Wittenberger S. J., Donner B. G., Dialkyltin oxide mediated addition of trimethylsilyl azide to nitriles. A novel preparation of 5-substituted tetrazoles. Journal of Organic Chemistry 1993 58 15 4139 4141 2-s2.0-33751384910
    • (1993) Journal of Organic Chemistry , vol.58 , Issue.15 , pp. 4139-4141
    • Wittenberger, S.J.1    Donner, B.G.2
  • 25
    • 70249109718 scopus 로고    scopus 로고
    • Zinc chloride catalyzed synthesis of 5-substituted 1H-tetrazoles under solvent free condition
    • 2-s2.0-70249109718 10.1016/j.cclet.2009.06.020
    • Rostamizadeh S., Ghaieni H., Aryan R., Amani A., Zinc chloride catalyzed synthesis of 5-substituted 1H-tetrazoles under solvent free condition. Chinese Chemical Letters 2009 20 11 1311 1314 2-s2.0-70249109718 10.1016/j.cclet.2009. 06.020
    • (2009) Chinese Chemical Letters , vol.20 , Issue.11 , pp. 1311-1314
    • Rostamizadeh, S.1    Ghaieni, H.2    Aryan, R.3    Amani, A.4
  • 26
    • 0001839856 scopus 로고    scopus 로고
    • Parallel synthesis of alkyl tetrazole derivatives using solid support chemistry
    • 2-s2.0-0001839856
    • Matthews D. P., Green J. E., Shuker A. J., Parallel synthesis of alkyl tetrazole derivatives using solid support chemistry. Journal of Combinatorial Chemistry 2000 2 1 19 23 2-s2.0-0001839856
    • (2000) Journal of Combinatorial Chemistry , vol.2 , Issue.1 , pp. 19-23
    • Matthews, D.P.1    Green, J.E.2    Shuker, A.J.3
  • 27
    • 0000806709 scopus 로고    scopus 로고
    • Rearrangement reactions of (hydroxyphenyl)carbenes
    • Kumar A., Narayanan R., Shechter H., Rearrangement reactions of (hydroxyphenyl)carbenes. Journal of Organic Chemistry 1996 61 13 4462 4465 2-s2.0-0000806709 (Pubitemid 126527953)
    • (1996) Journal of Organic Chemistry , vol.61 , Issue.13 , pp. 4462-4465
    • Kumar, A.1    Narayanan, R.2    Shechter, H.3
  • 28
    • 67149099426 scopus 로고    scopus 로고
    • 2 as a reusable heterogeneous catalyst for the synthesis of 5-substituted 1H-tetrazoles via [2+3] cycloaddition of nitriles and sodium azide
    • 2-s2.0-67149099426 10.1016/j.tetlet.2009.05.048
    • 2 as a reusable heterogeneous catalyst for the synthesis of 5-substituted 1H-tetrazoles via [2+3] cycloaddition of nitriles and sodium azide. Tetrahedron Letters 2009 50 31 4435 4438 2-s2.0-67149099426 10.1016/j.tetlet.2009.05.048
    • (2009) Tetrahedron Letters , vol.50 , Issue.31 , pp. 4435-4438
    • Nasrollahzadeh, M.1    Bayat, Y.2    Habibi, D.3    Moshaee, S.4
  • 29
    • 0034729170 scopus 로고    scopus 로고
    • Regiospecific synthesis of 2-allylated-5-substituted tetrazoles via palladium-catalyzed reaction of nitriles, trimethylsilyl azide, and allyl acetates
    • PII S0040403900005633
    • Gyoung Y. S., Shim J. G., Yamamoto Y., Regiospecific synthesis of 2-allylated-5-substituted tetrazoles via palladium-catalyzed reaction of nitriles, trimethylsilyl azide, and allyl acetates. Tetrahedron Letters 2000 41 21 4193 4196 2-s2.0-0034729170 (Pubitemid 30367364)
    • (2000) Tetrahedron Letters , vol.41 , Issue.21 , pp. 4193-4196
    • Gyoung, Y.S.1    Shim, J.-G.2    Yamamoto, Y.3
  • 30
    • 1842688821 scopus 로고    scopus 로고
    • TBAF-Catalyzed Synthesis of 5-Substituted 1H-Tetrazoles under Solventless Conditions
    • Amantini D., Beleggia R., Fringuelli F., Pizzo F., Vaccaro L., TBAF-catalyzed synthesis of 5-substituted 1H-tetrazoles under solventless conditions. Journal of Organic Chemistry 2004 69 8 2896 2898 2-s2.0-1842688821 (Pubitemid 38469057)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.8 , pp. 2896-2898
    • Amantini, D.1    Beleggia, R.2    Fringuelli, F.3    Pizzo, F.4    Vaccaro, L.5
  • 31
    • 33644609512 scopus 로고    scopus 로고
    • An efficient synthesis of 5-substituted 1H-tetrazoles using Zn/Al hydrotalcite catalyst
    • 2-s2.0-33644609512 10.1016/j.molcata.2005.11.046
    • Kantam M. L., Shiva Kumar K. B., Phani Raja K., An efficient synthesis of 5-substituted 1H-tetrazoles using Zn/Al hydrotalcite catalyst. Journal of Molecular Catalysis A 2006 247 1-2 186 188 2-s2.0-33644609512 10.1016/j.molcata.2005.11.046
    • (2006) Journal of Molecular Catalysis A , vol.247 , Issue.1-2 , pp. 186-188
    • Kantam, M.L.1    Shiva Kumar, K.B.2    Phani Raja, K.3
  • 32
    • 22944484712 scopus 로고    scopus 로고
    • Nanocrystalline ZnO as an efficient heterogeneous catalyst for the synthesis of 5-substituted 1H-tetrazoles
    • DOI 10.1002/adsc.200505011
    • Lakshmi Kantam M., Shiva Kumar K. B., Sridhar Ch., Nanocrystalline ZnO as an efficient heterogeneous catalyst for the synthesis of 5-substituted 1H-tetrazoles. Advanced Synthesis and Catalysis 2005 347 9 1212 1214 2-s2.0-84862025844 10.1002/adsc.200505011 (Pubitemid 41044809)
    • (2005) Advanced Synthesis and Catalysis , vol.347 , Issue.9 , pp. 1212-1214
    • Lakshmi Kantam, M.1    Shiva Kumar, K.B.2    Sridhar, Ch.3
  • 33
    • 40949093468 scopus 로고    scopus 로고
    • Copper-catalyzed synthesis of 5-substituted 1H-tetrazoles via the [3+2] cycloaddition of nitriles and trimethylsilyl azide
    • 2-s2.0-40949093468 10.1016/j.tetlet.2008.02.115
    • Jin T., Kitahara F., Kamijo S., Yamamoto Y., Copper-catalyzed synthesis of 5-substituted 1H-tetrazoles via the [3+2] cycloaddition of nitriles and trimethylsilyl azide. Tetrahedron Letters 2008 49 17 2824 2827 2-s2.0-40949093468 10.1016/j.tetlet.2008.02.115
    • (2008) Tetrahedron Letters , vol.49 , Issue.17 , pp. 2824-2827
    • Jin, T.1    Kitahara, F.2    Kamijo, S.3    Yamamoto, Y.4
  • 34
    • 0031656451 scopus 로고    scopus 로고
    • Preparation of 5-alkylthio and 5-arylthiotetrazoles from thiocyanates using phase transfer catalysis
    • LeBlanc B. W., Jursic B. S., Preparation of 5-alkylthio and 5-arylthiotetrazoles from thiocyanates using phase transfer catalysis. Synthetic Communications 1998 28 19 3591 3599 2-s2.0-0031656451 (Pubitemid 28409086)
    • (1998) Synthetic Communications , vol.28 , Issue.19 , pp. 3591-3599
    • LeBlanc, B.W.1    Jursic, B.S.2
  • 35
    • 0035977262 scopus 로고    scopus 로고
    • Preparation of 5-substituted 1H-tetrazoles from nitriles in water
    • DOI 10.1021/jo010635w
    • Demko Z. P., Sharpless K. B., Preparation of 5-substituted 1H-tetrazoles from nitriles in water. Journal of Organic Chemistry 2001 66 24 7945 7950 2-s2.0-0035977262 10.1021/jo010635w (Pubitemid 34182824)
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.24 , pp. 7945-7950
    • Demko, Z.P.1    Sharpless, K.B.2
  • 37
    • 0035824303 scopus 로고    scopus 로고
    • Catalytic reactions in ionic liquids
    • Sheldon R., Catalytic reactions in ionic liquids. Chemical Communications 2001 23 2399 2407 2-s2.0-0035923960 (Pubitemid 33124059)
    • (2001) Chemical Communications , Issue.23 , pp. 2399-2407
    • Sheldon, R.1
  • 38
    • 0347417134 scopus 로고    scopus 로고
    • Room-Temperature Ionic Liquids. Solvents for Synthesis and Catalysis
    • Welton T., Room-temperature ionic liquids. Solvents for synthesis and catalysis. Chemical Reviews 1999 99 8 2071 2083 2-s2.0-0032737289 (Pubitemid 129585179)
    • (1999) Chemical Reviews , vol.99 , Issue.8 , pp. 2071-2083
    • Welton, T.1
  • 39
    • 57249093659 scopus 로고    scopus 로고
    • A short history of ionic liquidsfrom molten salts to neoteric solvents
    • 2-s2.0-57249093659 10.1039/b110838g
    • Wilkes J. S., A short history of ionic liquidsfrom molten salts to neoteric solvents. Green Chemistry 2002 4 2 73 80 2-s2.0-57249093659 10.1039/b110838g
    • (2002) Green Chemistry , vol.4 , Issue.2 , pp. 73-80
    • Wilkes, J.S.1
  • 40
    • 12344296667 scopus 로고    scopus 로고
    • Chemical and biochemical transformations in ionic liquids
    • DOI 10.1016/j.tet.2004.10.070, PII S0040402004017867
    • Jain N., Kumar A., Chauhan S., Chauhan S. M. S., Chemical and biochemical transformations in ionic liquids. Tetrahedron 2005 61 5 1015 1060 2-s2.0-45849140910 10.1016/j.tet.2004.10.070 (Pubitemid 40126710)
    • (2005) Tetrahedron , vol.61 , Issue.5 , pp. 1015-1060
    • Jain, N.1    Kumar, A.2    Chauhan, S.3    Chauhan, S.M.S.4
  • 41
    • 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 Chemistry 2004 6 3 147 150 2-s2.0-1642526412 (Pubitemid 38406303)
    • (2004) Green Chemistry , 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
  • 42
    • 1842638573 scopus 로고    scopus 로고
    • Room temperature ionic liquid promoted regioselective synthesis of 2-aryl benzimidazoles, benzoxazoles and benzthiazoles under ambient conditions
    • 2-s2.0-30544449129 10.1016/j.molcata.2003.10.064
    • Nadaf R. N., Siddiqui S. A., Daniel T., Lahoti R. J., Srinivasan K. V., Room temperature ionic liquid promoted regioselective synthesis of 2-aryl benzimidazoles, benzoxazoles and benzthiazoles under ambient conditions. Journal of Molecular Catalysis A 2004 214 1 155 160 2-s2.0-30544449129 10.1016/j.molcata.2003.10.064
    • (2004) Journal of Molecular Catalysis A , vol.214 , Issue.1 , pp. 155-160
    • Nadaf, R.N.1    Siddiqui, S.A.2    Daniel, T.3    Lahoti, R.J.4    Srinivasan, K.V.5
  • 43
    • 33748801514 scopus 로고    scopus 로고
    • Ionic liquid promoted facile one-pot synthesis of 1-pyridylimidazo[1,5-a] pyridines from dipyridylketone and aryl aldehydes
    • DOI 10.1055/s-2006-942522
    • Siddiqui S. A., Potewar T. M., Lahoti R. J., Srinivasan K. V., Ionic liquid promoted facile one-pot synthesis of 1-pyridylimidazo[1,5-a] pyridines from dipyridylketone and aryl aldehydes. Synthesis 2006 17 2849 2854 2-s2.0-33846781421 10.1055/s-2006-942522 (Pubitemid 44407831)
    • (2006) Synthesis , Issue.17 , pp. 2849-2854
    • Siddiqui, S.A.1    Potewar, T.M.2    Lahoti, R.J.3    Srinivasan, K.V.4
  • 44
    • 14844342306 scopus 로고    scopus 로고
    • Room temperature ionic liquid promoted improved and rapid synthesis of 2,4,5-triaryl imidazoles from aryl aldehydes and 1,2-diketones or α-hydroxyketone
    • DOI 10.1016/j.tet.2005.01.116
    • Siddiqui S. A., Narkhede U. C., Palimkar S. S., Daniel T., Lahoti R. J., Srinivasan K. V., Room temperature ionic liquid promoted improved and rapid synthesis of 2,4,5-triaryl imidazoles from aryl aldehydes and 1,2-diketones or α -hydroxyketone. Tetrahedron 2005 61 14 3539 3546 2-s2.0-14844342306 10.1016/j.tet.2005.01.116 (Pubitemid 40357943)
    • (2005) Tetrahedron , vol.61 , Issue.14 , pp. 3539-3546
    • Siddiqui, S.A.1    Narkhede, U.C.2    Palimkar, S.S.3    Daniel, T.4    Lahoti, R.J.5    Srinivasan, K.V.6
  • 45
    • 52249088667 scopus 로고    scopus 로고
    • One pot synthesis of benzoxazoles, benzthiazoles and benzimidazoles from carboxylic acids using ionic liquids
    • 2-s2.0-30544449129
    • Maradolla M. B., Allam S. K., Mandha A., Chandramouli G. V. P., One pot synthesis of benzoxazoles, benzthiazoles and benzimidazoles from carboxylic acids using ionic liquids. Arkivoc 2008 2008 15 42 46 2-s2.0-30544449129
    • (2008) Arkivoc , vol.2008 , Issue.15 , pp. 42-46
    • Maradolla, M.B.1    Allam, S.K.2    Mandha, A.3    Chandramouli, G.V.P.4
  • 46
    • 84862069065 scopus 로고    scopus 로고
    • Ionic liquid catalyzed one-pot multi-component synthesis, characterization and antibacterial activity of novel chromeno[2,3-d]pyrimidin-8- amine derivatives
    • 2-s2.0-84862069065 10.1016/j.molstruc.2012.02.044
    • Kanakaraju S., Prasanna B., Basavoju S., Chandramouli G. V. P., Ionic liquid catalyzed one-pot multi-component synthesis, characterization and antibacterial activity of novel chromeno[2,3-d]pyrimidin-8-amine derivatives. Journal of Molecular Structure 2012 1017 60 64 2-s2.0-84862069065 10.1016/j.molstruc.2012.02.044
    • (2012) Journal of Molecular Structure , vol.1017 , pp. 60-64
    • Kanakaraju, S.1    Prasanna, B.2    Basavoju, S.3    Chandramouli, G.V.P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.