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Volumn 39, Issue 4, 2009, Pages 702-715

Iodine-catalyzed synthesis of 3-arylbenzoquinoline derivatives by three-component reactions

Author keywords

Acetone; Acetophenone; Benzo f quinoline; Iodine; Synthesis

Indexed keywords

1 (4 BROMOPHENYL) 3 (2,4 DICHLOROPHENYL)BENZO[F]QUINOLINE; 1 (4 BROMOPHENYL) 3 (3 CHLOROPHENYL)BENZO[F]QUINOLINE; 1 (4 BROMOPHENYL) 3 (3 NITROPHENYL)BENZO[F]QUINOLINE; 1 (4 BROMOPHENYL) 3 (4 FLUOROPHENYL)BENZO[F]QUINOLINE; 1 (4 CHLOROPHENYL) 3 (2,3 DICHLOROPHENYL)BENZO[F]QUINOLINE; 1 METHYL 3 (2 NITROPHENYL)BENZO[F]QUINOLINE; 1 METHYL 3 (2 THIOPHENYL)BENZO[F]QUINOLINE; 1 METHYL 3 (3 NITROPHENYL)BENZO[F]QUINOLINE; 1 METHYL 3 (4 NITROPHENYL)BENZO[F]QUINOLINE; 3 (2,3 DIMETHOXYPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (2,4 DICHLOROPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (3 BROMOPHENYL) 1 (4 FLUOROPHENYL)BENZO[F]QUINOLINE; 3 (3 BROMOPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (3 BROMOPHENYL) 1 PHENYLBENZO[F]QUINOLINE; 3 (3 CHLOROPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (3 NITROPHENYL) 1 (4 NITROPHENYL)BENZO[F]QUINOLINE; 3 (3,4 DICHLOROPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (3,4 DIMETHYLPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (4 BROMOPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (4 CHLOROPHENYL) 1 (4 METHYLPHENYL)BENZO[F]QUINOLINE; 3 (4 CHLOROPHENYL) 1 (4 NITROPHENYL)BENZO[F]QUINOLINE; 3 (4 CHLOROPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (4 FLUOROPHENYL) 1 METHYLBENZO[F]QUINOLINE; 3 (4 METHOXYPHENYL) 1 METHYLBENZO[F]QUINOLINE; ACETONE; ACETOPHENONE; ALDEHYDE DERIVATIVE; AMINE; IODINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 61849100416     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802431081     Document Type: Article
Times cited : (14)

References (43)
  • 1
    • 0001741503 scopus 로고
    • Studies on the rearrangement of tertiarybutylmethylcarbinol (pinacolyl alcohol), I
    • Whitmore, F. C.; Rothrock, H. S. Studies on the rearrangement of tertiarybutylmethylcarbinol (pinacolyl alcohol), I. J. Am. Chem. Soc. 1933, 55, 1106-1109.
    • (1933) J. Am. Chem. Soc , vol.55 , pp. 1106-1109
    • Whitmore, F.C.1    Rothrock, H.S.2
  • 2
    • 61849095267 scopus 로고    scopus 로고
    • Rutherford, K. G.; Mamer, O. A.; Prokipcak, J. M.; Jobin, R. A. A novel synthesis of some mixed arylmethyl-alkyl ethers. Can. J. Chem. 1966, 44, 2337-2339.
    • Rutherford, K. G.; Mamer, O. A.; Prokipcak, J. M.; Jobin, R. A. A novel synthesis of some mixed arylmethyl-alkyl ethers. Can. J. Chem. 1966, 44, 2337-2339.
  • 3
    • 0000745426 scopus 로고
    • Iodine mediated synthesis of alkyl tert-alkyl ethers
    • Jenner, G. Iodine mediated synthesis of alkyl tert-alkyl ethers. Tetrahedron Lett. 1988, 29, 2445-2448.
    • (1988) Tetrahedron Lett , vol.29 , pp. 2445-2448
    • Jenner, G.1
  • 4
    • 0344496783 scopus 로고    scopus 로고
    • Iodine-induced reaction cascades for the rapid construction of variously substituted benzothiophenes
    • Hessian, K. O.; Flynn, B. L. Iodine-induced reaction cascades for the rapid construction of variously substituted benzothiophenes. Org. Lett. 2003, 5, 4377-4380.
    • (2003) Org. Lett , vol.5 , pp. 4377-4380
    • Hessian, K.O.1    Flynn, B.L.2
  • 5
    • 0037463441 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions
    • Bandgar, B. P.; Shaikh, K. A. Molecular iodine-catalyzed efficient and highly rapid synthesis of bis(indolyl)methanes under mild conditions. Tetrahedron Lett. 2003, 44, 1959-1961.
    • (2003) Tetrahedron Lett , vol.44 , pp. 1959-1961
    • Bandgar, B.P.1    Shaikh, K.A.2
  • 6
    • 10044267850 scopus 로고    scopus 로고
    • Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone
    • Sun, J.; Dong, Y.; Cao, L.; Wang, X.; Wang, S.; Hu, Y. Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone. J. Org. Chem. 2004, 69, 8932-8934.
    • (2004) J. Org. Chem , vol.69 , pp. 8932-8934
    • Sun, J.1    Dong, Y.2    Cao, L.3    Wang, X.4    Wang, S.5    Hu, Y.6
  • 7
    • 0037185616 scopus 로고    scopus 로고
    • A mild and efficient method for esterification and transesterification catalyzed by iodine
    • Ramalinga, K.; Vijayalakshimi, P.; Kaimal, T. N. B. A mild and efficient method for esterification and transesterification catalyzed by iodine. Tetrahedron Lett. 2002, 43, 879-882.
    • (2002) Tetrahedron Lett , vol.43 , pp. 879-882
    • Ramalinga, K.1    Vijayalakshimi, P.2    Kaimal, T.N.B.3
  • 8
    • 0346753436 scopus 로고    scopus 로고
    • A simple and efficient method for transesterification of β-keto esters catalyzed by iodine
    • Chavan, S. P.; Kale, R. R.; Shivasankar, K.; Chandake, S. I.; Benjamin, S. B. A simple and efficient method for transesterification of β-keto esters catalyzed by iodine. Synthesis 2003, 2695-2698.
    • (2003) Synthesis , pp. 2695-2698
    • Chavan, S.P.1    Kale, R.R.2    Shivasankar, K.3    Chandake, S.I.4    Benjamin, S.B.5
  • 9
    • 0037164664 scopus 로고    scopus 로고
    • 1,4-Conjugate addition of allyltrimethylsilane to α,β-unsaturated ketones
    • (a) Yadav, J. S.; Reddy, B. V. S.; Sadasiv, K.; Satheesh, G. 1,4-Conjugate addition of allyltrimethylsilane to α,β-unsaturated ketones. Tetrahedron Lett. 2002, 43, 9695-9697;
    • (2002) Tetrahedron Lett , vol.43 , pp. 9695-9697
    • Yadav, J.S.1    Reddy, B.V.S.2    Sadasiv, K.3    Satheesh, G.4
  • 10
    • 0346749663 scopus 로고    scopus 로고
    • The Michael addition of indole to α,β-unsaturated ketones catalyzed by iodine at room temperature
    • (b) Wang, S. Y.; Ji, S. J.; Loh, T. P. The Michael addition of indole to α,β-unsaturated ketones catalyzed by iodine at room temperature. Synlett 2003, 2377-2379.
    • (2003) Synlett , pp. 2377-2379
    • Wang, S.Y.1    Ji, S.J.2    Loh, T.P.3
  • 11
    • 19944423788 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed imine activation for three-component nucleophilic addition reactions
    • (a) Lee, B. S.; Mahajan, S.; Janda, K. D. Molecular iodine-catalyzed imine activation for three-component nucleophilic addition reactions. Synlett 2005, 1325-1327;
    • (2005) Synlett , pp. 1325-1327
    • Lee, B.S.1    Mahajan, S.2    Janda, K.D.3
  • 12
    • 2442698919 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed highly rapid synthesis of 1,5-benzodiazepine derivatives under mild conditions
    • (b) Bandgar, B. P.; Bettigeri, S. V.; Joshi, N. S. Molecular iodine-catalyzed highly rapid synthesis of 1,5-benzodiazepine derivatives under mild conditions. Synth. Commun. 2004, 34, 1447-1453;
    • (2004) Synth. Commun , vol.34 , pp. 1447-1453
    • Bandgar, B.P.1    Bettigeri, S.V.2    Joshi, N.S.3
  • 13
    • 1842585835 scopus 로고    scopus 로고
    • Mukaiyama aldol reactions of silylenolates catalyzed by iodine
    • (c) Phukan, P. Mukaiyama aldol reactions of silylenolates catalyzed by iodine. Synth Commun. 2004, 34, 1065-1070;
    • (2004) Synth Commun , vol.34 , pp. 1065-1070
    • Phukan, P.1
  • 14
    • 0001721447 scopus 로고    scopus 로고
    • Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes
    • (d) Deka, N.; Kalita, D. J.; Borah, R. Sarma, J. C. Iodine as acetylation catalyst in the preparation of 1,1-diacetates from aldehydes. J. Org. Chem. 1997, 62, 1563-1564.
    • (1997) J. Org. Chem , vol.62 , pp. 1563-1564
    • Deka, N.1    Kalita, D.J.2    Borah, R.3    Sarma, J.C.4
  • 15
    • 0348147693 scopus 로고    scopus 로고
    • Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes
    • (a) Vijjay, N. C.; Rajesh, A. U.; Vinod, S.; Bindu, A. R.; Sreekanth, J. S.; Lakshmi, B. Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes. Acc. Chem. Res. 2003, 36, 899-907;
    • (2003) Acc. Chem. Res , vol.36 , pp. 899-907
    • Vijjay, N.C.1    Rajesh, A.U.2    Vinod, S.3    Bindu, A.R.4    Sreekanth, J.S.5    Lakshmi, B.6
  • 16
    • 0033855773 scopus 로고    scopus 로고
    • Nickel-catalyzed intermolecular domino reactions
    • (b) Shin-Ichi, I. Nickel-catalyzed intermolecular domino reactions. Acc Chem Res. 2000, 33, 511-519;
    • (2000) Acc Chem Res , vol.33 , pp. 511-519
    • Shin-Ichi, I.1
  • 17
    • 7044235263 scopus 로고    scopus 로고
    • Domino reactions in organic synthesis
    • (c) Tietze, L. F. Domino reactions in organic synthesis. Chem. Rev. 1996, 96, 115-136;
    • (1996) Chem. Rev , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 18
    • 0028879573 scopus 로고
    • Recent advances in the use of tandem reactions for organic synthesis
    • (d)Bunce, R. A. Recent advances in the use of tandem reactions for organic synthesis. Tetrahedron 1995, 51, 13103-13159;
    • (1995) Tetrahedron , vol.51 , pp. 13103-13159
    • Bunce, R.A.1
  • 20
    • 4544237117 scopus 로고    scopus 로고
    • Synthesis of some new 2-[3-(2-chloroquinolinyl)]-3-aryl-4-thiazolidinones as potent antibacterial agents
    • (a) Selvi, G.; Rajendran, S. P. Synthesis of some new 2-[3-(2-chloroquinolinyl)]-3-aryl-4-thiazolidinones as potent antibacterial agents. Asian J. Chem. 2004, 16, 1017-1022;
    • (2004) Asian J. Chem , vol.16 , pp. 1017-1022
    • Selvi, G.1    Rajendran, S.P.2
  • 21
    • 0342940303 scopus 로고
    • Synthesis and antibacterial activity of some novel substituted arylsulfonylbenzo[f]quinolines
    • (b) Bahuguna, R. P.; Joshi, B. C. Synthesis and antibacterial activity of some novel substituted arylsulfonylbenzo[f]quinolines. Indian J. Heterocycl. Chem. 1994, 3, 265-268.
    • (1994) Indian J. Heterocycl. Chem , vol.3 , pp. 265-268
    • Bahuguna, R.P.1    Joshi, B.C.2
  • 22
    • 0031753598 scopus 로고    scopus 로고
    • Drug-metabolizing enzyme induction by 2,2′-dipyridyl, 1,7-phenanthroline, 7,8-benzoquinoline, and oltipraz in mouse
    • (a) Carr, B. A.; Franklin, M. R. Drug-metabolizing enzyme induction by 2,2′-dipyridyl, 1,7-phenanthroline, 7,8-benzoquinoline, and oltipraz in mouse. Xenobiotica 1998, 28, 949-956;
    • (1998) Xenobiotica , vol.28 , pp. 949-956
    • Carr, B.A.1    Franklin, M.R.2
  • 23
    • 0030323835 scopus 로고    scopus 로고
    • Drug metabolizing enzyme induction by benzoquinolines, acridine, and quinacrine: Tricyclic aromatic molecules containing a single heterocyclic nitrogen
    • (b) Le, H. T.; Lamb, J. G.; Franklin, M. R. Drug metabolizing enzyme induction by benzoquinolines, acridine, and quinacrine: Tricyclic aromatic molecules containing a single heterocyclic nitrogen. J. Biochem. Toxic. 1996, 11, 297-303.
    • (1996) J. Biochem. Toxic , vol.11 , pp. 297-303
    • Le, H.T.1    Lamb, J.G.2    Franklin, M.R.3
  • 24
    • 0028305603 scopus 로고
    • Preparative chiral HPLC separation of all possible stereoisomers of LY191704 and LY266111 and their in vitro inhibition of human types 1 and 2 steroid 5a-reductases
    • Abell, A. D.; Erhard, K. F.; Yen, H. K.; Yamashita, D. S.; Brandt, M.; Mohammed, H.; Levy, M. A.; Holt, D. A. Preparative chiral HPLC separation of all possible stereoisomers of LY191704 and LY266111 and their in vitro inhibition of human types 1 and 2 steroid 5a-reductases. Bioorg. Med. Chem. Lett. 1994, 4, 1365-1368.
    • (1994) Bioorg. Med. Chem. Lett , vol.4 , pp. 1365-1368
    • Abell, A.D.1    Erhard, K.F.2    Yen, H.K.3    Yamashita, D.S.4    Brandt, M.5    Mohammed, H.6    Levy, M.A.7    Holt, D.A.8
  • 25
    • 36749062648 scopus 로고
    • Studies on benzoquinoline derivatives: Preparation and antimicrobial activity of azo-derivatives of arylthiobenzo[f]quinoline
    • Bahuguna, R. P.; Joshi, B. C.; Mangal, H. N. Studies on benzoquinoline derivatives: Preparation and antimicrobial activity of azo-derivatives of arylthiobenzo[f]quinoline. J. Indian Chem. Soc. 1992, 69, 401-402.
    • (1992) J. Indian Chem. Soc , vol.69 , pp. 401-402
    • Bahuguna, R.P.1    Joshi, B.C.2    Mangal, H.N.3
  • 27
    • 61849180876 scopus 로고    scopus 로고
    • Szmuszkovicz, J, Darlington, W. H, Von Voigtlander, P. F. Preparation and formulation of antipsychotic aminopolyhydrobenz(iso)quinolines and intermediates. WO 8804292 A1, 1988. Chem. Abstr. 1988, 110, 75335
    • Szmuszkovicz, J.; Darlington, W. H.; Von Voigtlander, P. F. Preparation and formulation of antipsychotic aminopolyhydrobenz(iso)quinolines and intermediates. WO 8804292 A1, 1988. Chem. Abstr. 1988, 110, 75335.
  • 28
    • 0025297215 scopus 로고    scopus 로고
    • Cannon, J. G.; Walker, K. A.; Montanari, A.; Long, J. P.; Flynn, J. R. Monomethyl ether derivatives of 7,8-dihydroxy- and 8,9-dihydroxy-4-propyl-1,2,3, 4,4a,5,6,10b-octahydrobenzo [f]quinolines as possible products of metabolism by catechol-O-methyltransferase. J. Med. Chem. 1990, 33, 2000-2006.
    • Cannon, J. G.; Walker, K. A.; Montanari, A.; Long, J. P.; Flynn, J. R. Monomethyl ether derivatives of 7,8-dihydroxy- and 8,9-dihydroxy-4-propyl-1,2,3, 4,4a,5,6,10b-octahydrobenzo [f]quinolines as possible products of metabolism by catechol-O-methyltransferase. J. Med. Chem. 1990, 33, 2000-2006.
  • 29
    • 61849084156 scopus 로고
    • Reaction of 3-[(N-2-naphthyl)formimidoyl]pyridine with substituted acetophenones
    • Russian
    • (a) Kozlov, N. S.; Mikhalevskaya, S. V.; Serzhanina, V. A. Reaction of 3-[(N-2-naphthyl)formimidoyl]pyridine with substituted acetophenones. Khim. Geterotsikl. Soedin. 1989, 351-354 (Russian);
    • (1989) Khim. Geterotsikl. Soedin , pp. 351-354
    • Kozlov, N.S.1    Mikhalevskaya, S.V.2    Serzhanina, V.A.3
  • 30
    • 61849173474 scopus 로고
    • Synthesis and spectral characteristics of acenaphthene derivatives of benzo[f]quinoline
    • Russian
    • (b) Kozlov, N. S.; Shmanai, G. S.; Dang, N. T. Synthesis and spectral characteristics of acenaphthene derivatives of benzo[f]quinoline. Khim. Geterotsikl. Soedin. 1986, 1102-1106 (Russian);
    • (1986) Khim. Geterotsikl. Soedin , pp. 1102-1106
    • Kozlov, N.S.1    Shmanai, G.S.2    Dang, N.T.3
  • 31
    • 36749064657 scopus 로고
    • Synthesis and spectra of 1-ethyl- and 1,2-dimethyl-3-(p-nitrophenyl) benzo[f] quinolines, their salts and dyes
    • (c) Kozlov, N. S.; Zhikhareva, O. D.; Stremok, I. P. Synthesis and spectra of 1-ethyl- and 1,2-dimethyl-3-(p-nitrophenyl) benzo[f] quinolines, their salts and dyes. Dokl. Akad. Nauk BSSR 1977, 21, 425-428;
    • (1977) Dokl. Akad. Nauk BSSR , vol.21 , pp. 425-428
    • Kozlov, N.S.1    Zhikhareva, O.D.2    Stremok, I.P.3
  • 32
    • 61849174000 scopus 로고
    • Synthesis and spectral characteristics of 1-(3-pyridyl)-3-aryl-8-nitro(amino) benzo[f] quinolines
    • (d) Kozlov, N. S.; Gladchenko, L. F.; Sauts, R. D.; Serzhanina, V. A. Synthesis and spectral characteristics of 1-(3-pyridyl)-3-aryl-8-nitro(amino) benzo[f] quinolines. Khim. Geterotsikl. Soedin. 1978, 1646-1649.
    • (1978) Khim. Geterotsikl. Soedin , pp. 1646-1649
    • Kozlov, N.S.1    Gladchenko, L.F.2    Sauts, R.D.3    Serzhanina, V.A.4
  • 33
    • 33749301104 scopus 로고
    • Photochemical synthesis of benzo[f]quinolines
    • (a) Beller, N. R.; Neckers, D. C.; Papadopoulos, E. P. Photochemical synthesis of benzo[f]quinolines. J. Org. Chem. 1977, 42, 3514-3518;
    • (1977) J. Org. Chem , vol.42 , pp. 3514-3518
    • Beller, N.R.1    Neckers, D.C.2    Papadopoulos, E.P.3
  • 34
    • 0034164284 scopus 로고    scopus 로고
    • Synthesis of benzo[f]quinoline derivatives by condensation of arylmethylene-2- naphthylamines with ethyl acetoacetate
    • (b)Kozlov, N. G.; Sauts, R. D.; Gusak, K. N. Synthesis of benzo[f]quinoline derivatives by condensation of arylmethylene-2- naphthylamines with ethyl acetoacetate. Russ. J. Org. Chem. 2000, 36, 531-538;
    • (2000) Russ. J. Org. Chem , vol.36 , pp. 531-538
    • Kozlov, N.G.1    Sauts, R.D.2    Gusak, K.N.3
  • 35
    • 0001803901 scopus 로고    scopus 로고
    • Aryl radical endo cyclization of enamidines: Selective preparation of trans and cis fused octahydrobenzo[f]quinolines
    • (c) Ripa, L.; Hallberg, A. Aryl radical endo cyclization of enamidines: Selective preparation of trans and cis fused octahydrobenzo[f]quinolines. J. Org. Chem. 1998, 63, 84-91;
    • (1998) J. Org. Chem , vol.63 , pp. 84-91
    • Ripa, L.1    Hallberg, A.2
  • 36
    • 46649106341 scopus 로고
    • Synthesis of tetrahydrobenzo[f]quinoline
    • (d) Stetsenko, A. V.; Fursii, F. A. Synthesis of tetrahydrobenzo[f]quinoline. Ukr. Khim. Zh. 1986, 52, 755-759;
    • (1986) Ukr. Khim. Zh , vol.52 , pp. 755-759
    • Stetsenko, A.V.1    Fursii, F.A.2
  • 37
    • 0002405305 scopus 로고
    • Synthesis of substituted thioaryl and aryl sulfonyl benzo[f]quinolines
    • (e) Bahuguna, R. P.; Joshi, B. C. Synthesis of substituted thioaryl and aryl sulfonyl benzo[f]quinolines. Egypt. J. Chem. 1988, 31, 89-96;
    • (1988) Egypt. J. Chem , vol.31 , pp. 89-96
    • Bahuguna, R.P.1    Joshi, B.C.2
  • 38
    • 0343607521 scopus 로고    scopus 로고
    • Synthetic studies of the octahydrobenzo[f]quinoline system
    • (f) Tagmatarchis, N.; Katerinopoulos, H. E. Synthetic studies of the octahydrobenzo[f]quinoline system. J. Heterocycl. Chem. 1996, 33, 983-985;
    • (1996) J. Heterocycl. Chem , vol.33 , pp. 983-985
    • Tagmatarchis, N.1    Katerinopoulos, H.E.2
  • 39
    • 0342940303 scopus 로고
    • Synthesis and antibacterial activity of some novel substituted arylsulfonylbenzo[f]quinolines
    • (g) Bahuguna, R. P.; Joshi, B. C. Synthesis and antibacterial activity of some novel substituted arylsulfonylbenzo[f]quinolines. Indian J. Heterocycl. Chem. 1994, 3, 265-268.
    • (1994) Indian J. Heterocycl. Chem , vol.3 , pp. 265-268
    • Bahuguna, R.P.1    Joshi, B.C.2
  • 40
    • 1642491885 scopus 로고    scopus 로고
    • Synthesis of new 3-aryl-1- methylbenzo[f] quinolines
    • Kozlov, N. G.; Basalaeva, L. I. Synthesis of new 3-aryl-1- methylbenzo[f] quinolines. Russ. J. Org. Chem. 2003, 39, 718-722.
    • (2003) Russ. J. Org. Chem , vol.39 , pp. 718-722
    • Kozlov, N.G.1    Basalaeva, L.I.2
  • 41
    • 33645879237 scopus 로고    scopus 로고
    • Molecular iodine-catalyzed one-pot synthesis of substituted quinolines from imines and aldehydes
    • Lin, X. F.; Cui, S. L.; Wang, Y. G. Molecular iodine-catalyzed one-pot synthesis of substituted quinolines from imines and aldehydes. Tetrahedron Lett. 2006, 47, 3127-3130.
    • (2006) Tetrahedron Lett , vol.47 , pp. 3127-3130
    • Lin, X.F.1    Cui, S.L.2    Wang, Y.G.3
  • 42
    • 33845968052 scopus 로고    scopus 로고
    • An improved and benign synthesis of 9,10-diarylacridine-1,8- dione and indenoquinoline derivatives from 3-anilino-5,5-dimethylcyclohex-2- enones, benzaldehydes, and 1,3-dicarbonyl compounds in an ionic liquid medium
    • (a) Wang, X. S.; Zhang, M. M.; Jiang, H.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M. An improved and benign synthesis of 9,10-diarylacridine-1,8- dione and indenoquinoline derivatives from 3-anilino-5,5-dimethylcyclohex-2- enones, benzaldehydes, and 1,3-dicarbonyl compounds in an ionic liquid medium. Synthesis 2006, 4187-4199;
    • (2006) Synthesis , pp. 4187-4199
    • Wang, X.S.1    Zhang, M.M.2    Jiang, H.3    Shi, D.Q.4    Tu, S.J.5    Wei, X.Y.6    Zong, Z.M.7
  • 43
    • 34247130916 scopus 로고    scopus 로고
    • 4]: Reactions of arylaldehyde, 3-arylamino-5,5- dimethylcyclohex-2-enone, and active methylene compounds
    • 4]: Reactions of arylaldehyde, 3-arylamino-5,5- dimethylcyclohex-2-enone, and active methylene compounds. Tetrahedron 2007, 63, 4439-4449.
    • (2007) Tetrahedron , vol.63 , pp. 4439-4449
    • Wang, X.S.1    Zhang, M.M.2    Jiang, H.3    Yao, C.S.4    Tu, S.J.5


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