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Volumn 14, Issue 3, 2010, Pages 473-477

An efficient, multicomponent approach for solvent-free synthesis of 2-amino-4H-chromene scaffold

Author keywords

2 Amino 4H chromenes; Domino reactions; Knoevenagel Michael addition; Multicomponent reactions; Solvent free

Indexed keywords

1H NAPHTHO[2,1 B]PYRAN 2 CARBONITRILE, 3 AMINO 1 (3 NITROPHENYL); 1H NAPHTHO[2,1 B]PYRAN 2 CARBONITRILE, 3 AMINO 1 (4 CHLOROPHENYL); 4H NAPHTHO[1,2 B]PYRAN 3 CARBONITRILE, 2 AMINO 4 (2 NITROPHENYL); CHROMENE DERIVATIVE; H NAPHTHO[1,2 B]PYRAN 3 CARBONITRILE, 2 AMINO 4 (4 CHLOROPHENYL); SODIUM CARBONATE; UNCLASSIFIED DRUG;

EID: 78650171299     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11030-010-9246-5     Document Type: Article
Times cited : (95)

References (37)
  • 2
    • 0000917692 scopus 로고
    • Nitriles in heterocyclic synthesis-novel synthesis of benzo[c]-coumarin and of benzo[c]pyrano[3,2-c] quinoline derivatives
    • 10.3987/R-1987-04-0903 1:CAS:528:DyaL1cXlvVOr 10.3987/R-1987-04-0903
    • EAA Hafez MH Elnagdi AGA Elagemey FMAA El-Taweel 1987 Nitriles in heterocyclic synthesis-novel synthesis of benzo[c]-coumarin and of benzo[c]pyrano[3,2-c] quinoline derivatives Heterocycles 26 903 907 10.3987/R-1987-04-0903 1:CAS:528:DyaL1cXlvVOr 10.3987/R-1987-04-0903
    • (1987) Heterocycles , vol.26 , pp. 903-907
    • Hafez, E.A.A.1    Elnagdi, M.H.2    Elagemey, A.G.A.3    Fmaa, E.4
  • 3
    • 15444374352 scopus 로고    scopus 로고
    • 2(3H)-benzoxazolone and bioisosters as 'privileged scaffold' in the design of pharmacological probes
    • DOI 10.2174/0929867053507388
    • J Poupaert P Carato E Colacino 2005 2(3H)-benzoxazolone and bioisosters as "privileged scaffold" in the design of pharmacological probes Curr Med Chem 12 877 885 10.2174/0929867053507388 1:CAS:528:DC%2BD2MXivVCqur4%3D 10.2174/0929867053507388 15853716 (Pubitemid 40394335)
    • (2005) Current Medicinal Chemistry , vol.12 , Issue.7 , pp. 877-885
    • Poupaert, J.1    Carato, P.2    Colacino, E.3
  • 4
    • 0038390401 scopus 로고    scopus 로고
    • 1,4-Dihydropyridines as calcium channel ligands and privileged structures
    • DOI 10.1023/A:1023632419813
    • DJ Triggle 2003 1,4-Dihydropyridines as calcium channel ligands and privileged structures Cell Mol Neurobiol 23 293 303 10.1023/A:1023632419813 1:CAS:528:DC%2BD3sXjsFWisbg%3D 10.1023/A:1023632419813 12825828 (Pubitemid 36676276)
    • (2003) Cellular and Molecular Neurobiology , vol.23 , Issue.3 , pp. 293-303
    • Triggle, D.J.1
  • 5
    • 23944522335 scopus 로고    scopus 로고
    • Aqua mediated synthesis of substituted 2-amino-4H-chromenes and in vitro study as antibacterial agents
    • DOI 10.1016/j.bmcl.2005.06.041, PII S0960894X05008139
    • M Kidwai S Saxena MKR Khan SS Thukral 2005 Aqua mediated synthesis of substituted 2-amino-4H-chromenes and in vitro study as antibacterial agents Bioorg Med Chem Lett 15 4295 4298 10.1016/j.bmcl.2005.06.041 1:CAS:528:DC%2BD2MXpt1WnsLc%3D 10.1016/j.bmcl.2005.06.041 16040241 (Pubitemid 41188006)
    • (2005) Bioorganic and Medicinal Chemistry Letters , vol.15 , Issue.19 , pp. 4295-4298
    • Kidwai, M.1    Saxena, S.2    Khan, M.K.R.3    Thukral, S.S.4
  • 6
    • 0016787227 scopus 로고
    • Pyran copolymer as an effective adjuvant to chemotherapy against a murine leukemia and solid tumor
    • 1:CAS:528:DyaE28XosVShtA%3D%3D 1192431
    • SJ Mohr MA Chirigos FS Fuhrman JW Pryor 1975 Pyran copolymer as an effective adjuvant to chemotherapy against a murine leukemia and solid tumor Cancer Res 35 12 3750 3754 1:CAS:528:DyaE28XosVShtA%3D%3D 1192431
    • (1975) Cancer Res , vol.35 , Issue.12 , pp. 3750-3754
    • Mohr, S.J.1    Chirigos, M.A.2    Fuhrman, F.S.3    Pryor, J.W.4
  • 7
    • 70449521080 scopus 로고    scopus 로고
    • Synthesis of carbon-11-labeled 4-aryl-4H-chromens as new PET agents for imaging of apoptosis in cancer
    • 10.1016/j.apradiso.2009.09.067 1:CAS:528:DC%2BD1MXhsVCqtrfO 10.1016/j.apradiso.2009.09.067 19818636
    • M Gao KD Miller GD Hutchins Q-H Zheng 2010 Synthesis of carbon-11-labeled 4-aryl-4H-chromens as new PET agents for imaging of apoptosis in cancer Appl Radiat Isot 68 110 116 10.1016/j.apradiso.2009.09.067 1:CAS:528: DC%2BD1MXhsVCqtrfO 10.1016/j.apradiso.2009.09.067 19818636
    • (2010) Appl Radiat Isot , vol.68 , pp. 110-116
    • Gao, M.1    Miller, K.D.2    Hutchins, G.D.3    Zheng, Q.-H.4
  • 8
    • 0037079610 scopus 로고    scopus 로고
    • Multi-component reactions and evolutionary chemistry
    • 10.1016/S1359-6446(02)00010-7 1:CAS:528:DC%2BD38XktVOgug%3D%3D 11790626
    • L Weber 2002 Multi-component reactions and evolutionary chemistry Drug Discov Today 7 143 147 10.1016/S1359-6446(02)00010-7 1:CAS:528: DC%2BD38XktVOgug%3D%3D 11790626
    • (2002) Drug Discov Today , vol.7 , pp. 143-147
    • Weber, L.1
  • 9
    • 0036603766 scopus 로고    scopus 로고
    • Recent advances in isocyanide-based multicomponent chemistry
    • DOI 10.1016/S1367-5931(02)00328-9
    • A Doemling 2002 Recent advances in isocyanide-based multicomponent chemistry Curr Opin Chem Biol 6 306 313 10.1016/S1367-5931(02)00328-9 10.1016/S1367-5931(02)00328-9 (Pubitemid 34522055)
    • (2002) Current Opinion in Chemical Biology , vol.6 , Issue.3 , pp. 306-313
    • Domling, A.1
  • 10
    • 0034127641 scopus 로고    scopus 로고
    • Recent applications of polymer-supported reagents and scavengers in combinatorial, parallel, or multistep synthesis
    • DOI 10.1016/S1367-5931(00)00096-X
    • LA Thompson 2000 Recent applications of polymer-supported reagents and scavengers in combinatorial, parallel, or multistep synthesis Curr Opin Chem Biol 4 324 337 10.1016/S1367-5931(00)00096-X 1:CAS:528:DC%2BD3cXktFWrsbk%3D 10.1016/S1367-5931(00)00096-X 10826975 (Pubitemid 30319057)
    • (2000) Current Opinion in Chemical Biology , vol.4 , Issue.3 , pp. 324-337
    • Thompson, L.A.1
  • 11
    • 7444256652 scopus 로고    scopus 로고
    • The current status of heterocyclic combinatorial libraries
    • 10.1021/cr960010b 1:CAS:528:DyaK2sXhslamtb4%3D 10.1021/cr960010b 11848878
    • A Nefzi JM Ostresh RA Houghten 1997 The current status of heterocyclic combinatorial libraries Chem Rev 97 449 472 10.1021/cr960010b 1:CAS:528:DyaK2sXhslamtb4%3D 10.1021/cr960010b 11848878
    • (1997) Chem Rev , vol.97 , pp. 449-472
    • Nefzi, A.1    Ostresh, J.M.2    Houghten, R.A.3
  • 12
    • 49849099886 scopus 로고    scopus 로고
    • Catalysis of salicylaldehydes and two different C-H acids with electricity: First example of an efficient multicomponent approach to the design of functionalized medicinally privileged 2-Amino-4H-Chromene scaffolds
    • 10.1002/adsc.200700493 1:CAS:528:DC%2BD1cXlt1Witb8%3D 10.1002/adsc.200700493
    • MN Elinson AS Dorofeev FM Miloserdov AI Ilovaisky SK Feducovich PA Belyakov GI Nikishin 2008 Catalysis of salicylaldehydes and two different C-H acids with electricity: first example of an efficient multicomponent approach to the design of functionalized medicinally privileged 2-Amino-4H-Chromene scaffolds Adv Synth Catal 350 591 601 10.1002/adsc.200700493 1:CAS:528:DC%2BD1cXlt1Witb8%3D 10.1002/adsc.200700493
    • (2008) Adv Synth Catal , vol.350 , pp. 591-601
    • Elinson, M.N.1    Dorofeev, A.S.2    Miloserdov, F.M.3    Ilovaisky, A.I.4    Feducovich, S.K.5    Belyakov, P.A.6    Nikishin, G.I.7
  • 13
    • 0024998196 scopus 로고
    • Nitriles in heterocyclic synthesis: Synthesis of condensed pyrans
    • AGA Elagamay FMAA El-Taweel 1990 Nitriles in heterocyclic synthesis: synthesis of condensed pyrans Indian J Chem B 29 885 886
    • (1990) Indian J Chem B , vol.29 , pp. 885-886
    • Elagamay, A.G.A.1    Fmaa, E.2
  • 17
    • 0035843369 scopus 로고    scopus 로고
    • Three-component process for the synthesis of 2-amino-2-chromenes in aqueous media
    • DOI 10.1016/S0040-4020(00)01121-2, PII S0040402000011212
    • R Ballini G Bosica ML Conforti R Maggi A Mazzacanni P Righi G Sartori 2001 Three-component process for the synthesis of 2-amino-2-chrome in aqueous media Tetrahedron 57 1395 1398 10.1016/S0040-4020(00)01121-2 1:CAS:528:DC%2BD3MXhtFyrsr4%3D 10.1016/S0040-4020(00)01121-2 (Pubitemid 32150051)
    • (2001) Tetrahedron , vol.57 , Issue.7 , pp. 1395-1398
    • Ballini, R.1    Bosica, G.2    Conforti, M.L.3    Maggi, R.4    Mazzacani, A.5    Righi, P.6    Sartori, G.7
  • 18
    • 4043063679 scopus 로고    scopus 로고
    • Ultrasound-assisted synthesis of 2-amino-2-chromenes with cetyltrimethylammonium bromide in aqueous media
    • DOI 10.1016/j.ultsonch.2003.10.002, PII S1350417703001834
    • TS Jin JC Xiao SJ Wang TS Li 2004 Ultrasound-assisted synthesis of 2-amino-2-chromenes with cetyltrimethylammonium bromide in aqueous media Ultrason Sonochem 11 393 397 10.1016/j.ultsonch.2003.10.002 1:CAS:528: DC%2BD2cXmtlyrs7o%3D 15302025 (Pubitemid 39070483)
    • (2004) Ultrasonics Sonochemistry , vol.11 , Issue.6 , pp. 393-397
    • Jin, T.-S.1    Xiao, J.-C.2    Wang, S.-J.3    Li, T.-S.4
  • 19
    • 0034226276 scopus 로고    scopus 로고
    • Multicomponent reactions under clay catalysis
    • 10.1016/S0920-5861(00)00347-3 1:CAS:528:DC%2BD3cXlsFGrsb8%3D 10.1016/S0920-5861(00)00347-3
    • R Ballini F Bigi ML Conforti 2000 Multicomponent reactions under clay catalysis Catal Today 60 305 309 10.1016/S0920-5861(00)00347-3 1:CAS:528:DC%2BD3cXlsFGrsb8%3D 10.1016/S0920-5861(00)00347-3
    • (2000) Catal Today , vol.60 , pp. 305-309
    • Ballini, R.1    Bigi, F.2    Conforti, M.L.3
  • 21
    • 33846183638 scopus 로고    scopus 로고
    • Efficient synthesis of benzo[g]-and benzo[h]chromene derivatives by one-pot three-component condensation of aromatic aldehydes with active methylene compounds and naphthols
    • 10.1134/S1070428006120098 10.1134/S1070428006120098
    • B Sunil Kumar N Srinivasulu R Udupi B Rajitha Y Thirupathi Reddy P Narsimha Reddy P Kumar 2006 Efficient synthesis of benzo[g]-and benzo[h]chromene derivatives by one-pot three-component condensation of aromatic aldehydes with active methylene compounds and naphthols Russ J Org Chem 42 1813 1815 10.1134/S1070428006120098 10.1134/S1070428006120098
    • (2006) Russ J Org Chem , vol.42 , pp. 1813-1815
    • Sunil Kumar, B.1    Srinivasulu, N.2    Udupi, R.3    Rajitha, B.4    Thirupathi Reddy, Y.5    Narsimha Reddy, P.6    Kumar, P.7
  • 22
    • 0036996892 scopus 로고    scopus 로고
    • Molecular and crystal structure of 2-amino-3-cyano-6-hydroxy-4-phenyl-4H- benzo[f]chromene
    • 10.1023/A:1022135402451 1:CAS:528:DC%2BD3sXns1CntA%3D%3D 10.1023/A:1022135402451
    • AM Shestopalov YM Emelianova VN Nesterov 2002 Molecular and crystal structure of 2-amino-3-cyano-6-hydroxy-4-phenyl-4H-benzo[f]chromene Russ Chem Bull 51 2238 2243 10.1023/A:1022135402451 1:CAS:528:DC%2BD3sXns1CntA%3D%3D 10.1023/A:1022135402451
    • (2002) Russ Chem Bull , vol.51 , pp. 2238-2243
    • Shestopalov, A.M.1    Emelianova, Y.M.2    Nesterov, V.N.3
  • 23
    • 1242270591 scopus 로고    scopus 로고
    • Basic alumina catalysed synthesis of substituted 2-amino-2-chromenes via three-component reaction
    • DOI 10.1016/j.tetlet.2004.01.115
    • R Maggi R Ballini G Sartori 2004 Basic alumina catalysed synthesis of substituted 2-amino-2-chromenes via three-component reaction Tetrahedron Lett. 45 2297 2299 10.1016/j.tetlet.2004.01.115 1:CAS:528:DC%2BD2cXhsFemsrk%3D 10.1016/j.tetlet.2004.01.115 (Pubitemid 38230321)
    • (2004) Tetrahedron Letters , vol.45 , Issue.11 , pp. 2297-2299
    • Maggi, R.1    Ballini, R.2    Sartori, G.3    Sartorio, R.4
  • 24
    • 33847641039 scopus 로고    scopus 로고
    • Nanosized magnesium oxide as catalyst for the rapid and green synthesis of substituted 2-amino-2-chromenes
    • DOI 10.1016/j.tet.2007.02.019, PII S004040200700213X
    • D Kumar VB Reddy BK Mishra GR Rana N Mallikarjuna R Nadagouda S Varma 2007 Nanosized magnesium oxide as catalyst for the rapid and green synthesis of substituted 2-amino-2-chromenes Tetrahedron 63 3093 3097 10.1016/j.tet.2007.02. 019 1:CAS:528:DC%2BD2sXis1Oit70%3D 10.1016/j.tet.2007.02.019 (Pubitemid 46365777)
    • (2007) Tetrahedron , vol.63 , Issue.15 , pp. 3093-3097
    • Kumar, D.1    Reddy, V.B.2    Mishra, B.G.3    Rana, R.K.4    Nadagouda, M.N.5    Varma, R.S.6
  • 25
    • 34447108076 scopus 로고    scopus 로고
    • Aqua mediated synthesis of substituted 2-amino-4H-chromenes catalyzed by green and reusable Preyssler heteropolyacid
    • DOI 10.1016/j.bmcl.2007.05.023, PII S0960894X07005768
    • MM Heravi Kh Bakhtiari V Zadsirjan FF Bamoharram MO Heravi 2007 Aqua mediated synthesis of substituted 2-amino-4H-chromenes catalyzed by green and reusable Preyssler heteropolyacid Bioorg Med Chem Lett 17 4262 4265 10.1016/j.bmcl.2007.05.023 1:CAS:528:DC%2BD2sXnsVKntbs%3D 10.1016/j.bmcl.2007. 05.023 17537629 (Pubitemid 47028597)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.15 , pp. 4262-4265
    • Heravi, M.M.1    Bakhtiari, K.2    Zadsirjan, V.3    Bamoharram, F.F.4    Heravi, O.M.5
  • 26
    • 38849106907 scopus 로고    scopus 로고
    • Basic ionic liquid as catalyst for the rapid and green synthesis of substituted 2-amino-2-chromenes in aqueous media
    • DOI 10.1016/j.catcom.2007.07.010, PII S156673670700324X
    • K Gong HL Wang Z-L Fang Liu 2008 Basic ionic liquid as catalyst for the rapid and green synthesis of substituted 2-amino-2-chromenes in aqueous media Catal Commun 9 650 653 10.1016/j.catcom.2007.07.010 1:CAS:528: DC%2BD1cXhvFyitbw%3D 10.1016/j.catcom.2007.07.010 (Pubitemid 351191838)
    • (2008) Catalysis Communications , vol.9 , Issue.5 , pp. 650-653
    • Gong, K.1    Wang, H.-L.2    Fang, D.3    Liu, Z.-L.4
  • 27
    • 39349117900 scopus 로고    scopus 로고
    • 3 in aqueous medium
    • DOI 10.1016/j.catcom.2007.10.002, PII S1566736707004384
    • 3 in aqueous medium Catal Commun 9 1017 1020 10.1016/j.catcom.2007.10.002 10.1016/j.catcom.2007.10.002 (Pubitemid 351264804)
    • (2008) Catalysis Communications , vol.9 , Issue.6 , pp. 1017-1020
    • Ren, Y.-M.1    Cai, C.2
  • 28
    • 40549094672 scopus 로고    scopus 로고
    • DABCO-catalyzed efficient synthesis of naphthopyran derivatives via one-pot three-component condensation reaction at room temperature
    • DOI 10.1080/00397910701862865, PII 791370440
    • S Balalaie S Ramezanpour M Bararjanian JH Gross 2008 DABCO-Catalyzed efficient synthesis of naphthopyran derivatives via one-pot three-component condensation reaction at room temperature Synth Commun 38 1078 1089 10.1080/00397910701862865 1:CAS:528:DC%2BD1cXjtVeksL8%3D 10.1080/ 00397910701862865 (Pubitemid 351364149)
    • (2008) Synthetic Communications , vol.38 , Issue.7 , pp. 1078-1089
    • Balalaie, S.1    Ramezanpour, S.2    Bararjanian, M.3    Gross, J.H.4
  • 29
    • 59349119894 scopus 로고    scopus 로고
    • Mechanochemical solvent-free and catalyst-free one-pot synthesis of pyrano[2,3-d]pyrimidine-2,4(1H,3H)-diones with quantitative yields
    • 10.3390/molecules14010474 1:CAS:528:DC%2BD1MXht1Slt7s%3D 10.3390/molecules14010474 19158656
    • S Mashkouri MR Naimi-Jamal 2009 Mechanochemical solvent-free and catalyst-free one-pot synthesis of pyrano[2,3-d]pyrimidine-2,4(1H,3H)-diones with quantitative yields Molecules 14 1 474 479 10.3390/molecules14010474 1:CAS:528:DC%2BD1MXht1Slt7s%3D 10.3390/molecules14010474 19158656
    • (2009) Molecules , vol.14 , Issue.1 , pp. 474-479
    • Mashkouri, S.1    Naimi-Jamal, M.R.2
  • 30
    • 0038737165 scopus 로고    scopus 로고
    • Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield
    • DOI 10.1016/S0040-4020(03)00554-4
    • G Kaupp MR Naimi-Jamal J Schmeyers 2003 Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield Tetrahedron 59 3753 3760 10.1016/S0040-4020(03)00554-4 1:CAS:528:DC%2BD3sXjsVGltrg%3D 10.1016/S0040-4020(03)00554-4 (Pubitemid 36556085)
    • (2003) Tetrahedron , vol.59 , Issue.21 , pp. 3753-3760
    • Kaupp, G.1    Naimi-Jamal, M.R.2    Schmeyers, J.3
  • 32
    • 0033771354 scopus 로고    scopus 로고
    • Solvent-free preparation of monoacylaminals assisted by microwave irradiation
    • 10.3184/030823400103167813 10.3184/030823400103167813
    • A Sharifi F Mohsenzadeh MR Naimi-Jamal 2000 Solvent-free preparation of monoacylaminals assisted by microwave irradiation J Chem Res 8 394 396 10.3184/030823400103167813 10.3184/030823400103167813
    • (2000) J Chem Res , vol.8 , pp. 394-396
    • Sharifi, A.1    Mohsenzadeh, F.2    Naimi-Jamal, M.R.3
  • 33
    • 33748846784 scopus 로고    scopus 로고
    • One-pot solvent-free preparation of 2-phenyl-1,3,2-aryldioxaborins on acidic alumina
    • DOI 10.1080/00397910600764741, PII N708707223R27852
    • MR Naimi-Jamal M Mirzaei M Bolourtchian A Sharifi 2006 One-pot solvent-free preparation of 2-phenyl-1,3,2-aryldioxaborins on acidic alumina Synth Commun 36 18 2711 2717 10.1080/00397910600764741 1:CAS:528: DC%2BD28XhtV2ht7bE 10.1080/00397910600764741 (Pubitemid 44423109)
    • (2006) Synthetic Communications , vol.36 , Issue.18 , pp. 2711-2717
    • Naimi-Jamal, M.R.1    Mirzaei, M.2    Bolourtchian, M.3    Sharifi, A.4
  • 34
    • 31344454349 scopus 로고    scopus 로고
    • Modified Glaser reaction of terminal alkynes on KF/Alumina
    • DOI 10.1007/s00706-005-0416-6
    • A Sharifi M Mirzaei MR Naimi-Jamal 2006 Modified Glaser reaction of terminal alkynes on KF/Alumina Monatshefte fur Chemie 137 2 213 217 10.1007/s00706-005-0416-6 1:CAS:528:DC%2BD28XotF2rtw%3D%3D 10.1007/s00706-005- 0416-6 (Pubitemid 43139128)
    • (2006) Monatshefte fur Chemie , vol.137 , Issue.2 , pp. 213-217
    • Sharifi, A.1    Mirzaei, M.2    Reza Naimi-Jamal, M.3
  • 35
    • 85129355616 scopus 로고    scopus 로고
    • Microwave assisted Mannich reaction of terminal alkynes on alumina
    • 10.1007/s706-002-8251-8 1:CAS:528:DC%2BD38XivFGrs7o%3D
    • A Sharifi H Farhangian F Mohsenzadeh MR Naimi-Jamal 2002 Microwave assisted Mannich reaction of terminal alkynes on alumina Monatshefte fur Chemie 133 2 199 204 10.1007/s706-002-8251-8 1:CAS:528:DC%2BD38XivFGrs7o%3D
    • (2002) Monatshefte fur Chemie , vol.133 , Issue.2 , pp. 199-204
    • Sharifi, A.1    Farhangian, H.2    Mohsenzadeh, F.3    Naimi-Jamal, M.R.4
  • 36
    • 4043158392 scopus 로고    scopus 로고
    • Synthesis of hydroxyquinoline derivatives, aminohydroxychromene, aminocoumarin and their anti-bacterial activities
    • 10.3987/COM-04-10089 1:CAS:528:DC%2BD2cXmslOjs70%3D 10.3987/COM-04-10089
    • AS Abd-El-Aziz AM El-Agrody AH Bedair TC Corkery A Ata 2004 Synthesis of hydroxyquinoline derivatives, aminohydroxychromene, aminocoumarin and their anti-bacterial activities Heterocycles 63 8 1793 1812 10.3987/COM-04-10089 1:CAS:528:DC%2BD2cXmslOjs70%3D 10.3987/COM-04-10089
    • (2004) Heterocycles , vol.63 , Issue.8 , pp. 1793-1812
    • Abd-El-Aziz, A.S.1    El-Agrody, A.M.2    Bedair, A.H.3    Corkery, T.C.4    Ata, A.5
  • 37
    • 34047202588 scopus 로고    scopus 로고
    • Novel and efficient catalysts for the one-pot synthesis of 3,4-dihydropyrano[c]chromene derivatives in aqueous media
    • DOI 10.1016/j.tetlet.2007.02.135, PII S0040403907004352
    • S Abdolmohammadi S Balalaie 2007 Novel and efficient catalysts for the one-pot synthesis of 3,4-dihydropyrano[c]chromene derivatives in aqueous media Tetrahedron Lett 48 3299 3303 10.1016/j.tetlet.2007.02.135 1:CAS:528: DC%2BD2sXjvF2rt7w%3D 10.1016/j.tetlet.2007.02.135 (Pubitemid 46533987)
    • (2007) Tetrahedron Letters , vol.48 , Issue.18 , pp. 3299-3303
    • Abdolmohammadi, S.1    Balalaie, S.2


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