메뉴 건너뛰기




Volumn 11, Issue 5, 2014, Pages 701-731

Recent applications of doebner, Doebner-von Miller and Knoevenagel-Doebner reactions in organic syntheses

Author keywords

Doebner reaction; Doebner von miller; Heterocyclic syntheses; Knoevenagel reaction; Quinolines

Indexed keywords


EID: 84922722196     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/1570179411666140426003616     Document Type: Article
Times cited : (43)

References (184)
  • 1
    • 85064407458 scopus 로고
    • Total synthesis of(±)-virantmycin and determination of its stereochemistry
    • Morimot, Y.; Matsuda, F.; Shirahama, H. Total synthesis of(±)-virantmycin and determination of its stereochemistry. Synlett 1991, 1991(3), 202-203.
    • (1991) Synlett , vol.1991 , Issue.3 , pp. 202-203
    • Morimot, Y.1    Matsuda, F.2    Shirahama, H.3
  • 3
    • 0031449261 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • Michael, J.P. Quinoline, quinazoline and acridone alkaloids Nat. Prod. Rep. 1997, 14, 605-618.
    • (1997) Nat. Prod. Rep , vol.14 , pp. 605-618
    • Michael, J.P.1
  • 4
    • 0014750166 scopus 로고
    • Antiprotozoal 4-aryloxy-2- aminoquinolines and related compounds
    • Markees, D.G.; Dewey, V.C.; Kidder, G.W. Antiprotozoal 4-aryloxy-2- aminoquinolines and related compounds. J. Med. Chem. 1970, 13, 324-326.
    • (1970) J. Med. Chem , vol.13 , pp. 324-326
    • Markees, D.G.1    Dewey, V.C.2    Kidder, G.W.3
  • 5
    • 0022397488 scopus 로고
    • Design, synthesis and pharmacological activities of 2-substituted 4-phenylquinolines as potential antidepressant drugs
    • Alhaider, A.A.; Abdelkader, M.A.; Lien, E.J. Design, synthesis and pharmacological activities of 2-substituted 4-phenylquinolines as potential antidepressant drugs. J. Med. Chem. 1985, 28, 1394-1398.
    • (1985) J. Med. Chem , vol.28 , pp. 1394-1398
    • Alhaider, A.A.1    Abdelkader, M.A.2    Lien, E.J.3
  • 6
    • 0023936336 scopus 로고
    • 2, 4-Diamino-6, 7- dimethoxyquinoline derivatives as. alpha. 1-adrenoceptor antagonists and antihypertensive agents
    • Campbell, S.F.; Hardstone, J.D.; Palmer, M.J. 2, 4-Diamino-6, 7- dimethoxyquinoline derivatives as. alpha. 1-adrenoceptor antagonists and antihypertensive agents. J. Med. Chem. 1988, 31, 1031-1035.
    • (1988) J. Med. Chem , vol.31 , pp. 1031-1035
    • Campbell, S.F.1    Hardstone, J.D.2    Palmer, M.J.3
  • 7
    • 33645893172 scopus 로고    scopus 로고
    • Docking studies and development of novel 5- heteroarylamino-2, 4-diamino-8-chloropyrimido-[4,5-b] quinolines as potential antimalarials
    • Joshi, A.A.; Viswanathan, C. Docking studies and development of novel 5- heteroarylamino-2, 4-diamino-8-chloropyrimido-[4,5-b] quinolines as potential antimalarials. Bioorg. Med. Chem. Lett. 2006, 16(10), 2613-2617.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , Issue.10 , pp. 2613-2617
    • Joshi, A.A.1    Viswanathan, C.2
  • 8
    • 33845321975 scopus 로고    scopus 로고
    • Synthesis, antituberculosis activity, and 3D-QSAR study of 4-(adamantan-1-yl)-2- substituted quinolines
    • Nayyar, A.; Monga, V.; Malde, A.; Coutinho, E.; Jain, R. Synthesis, antituberculosis activity, and 3D-QSAR study of 4-(adamantan-1-yl)-2- substituted quinolines. Bioorg. Med. Chem. 2007, 15(2), 626-640.
    • (2007) Bioorg. Med. Chem , vol.15 , Issue.2 , pp. 626-640
    • Nayyar, A.1    Monga, V.2    Malde, A.3    Coutinho, E.4    Jain, R.5
  • 9
    • 0035664024 scopus 로고    scopus 로고
    • Synthesis and pharmacological activity of 1, 2, 4-triazolo [4,3- a] quinolines
    • Savini, L.; Chiasserini, L.; Pellerano, C.; Filippelli, W.; Falcone, G. Synthesis and pharmacological activity of 1, 2, 4-triazolo [4,3- a] quinolines. Farmaco 2001, 56(12), 939-945.
    • (2001) Farmaco , vol.56 , Issue.12 , pp. 939-945
    • Savini, L.1    Chiasserini, L.2    Pellerano, C.3    Filippelli, W.4    Falcone, G.5
  • 10
    • 78649500865 scopus 로고    scopus 로고
    • Design, synthesis, and preclinical evaluation of new 5, 6-(or 6, 7-) disubstituted-2-(fluorophenyl) quinolin-4-one derivatives as potent antitumor agents
    • Chou, L.-C.; Tsai, M.-T.; Hsu, M.-H.; Wang, S.-H.; Way, T.-D.; Huang, C.- H.; Lin, H.-Y.; Qian, K.; Dong, Y.; Lee, K.-H. Design, synthesis, and preclinical evaluation of new 5, 6-(or 6, 7-) disubstituted-2-(fluorophenyl) quinolin-4-one derivatives as potent antitumor agents. J. Med. Chem. 2010, 53(22), 8047-8058.
    • (2010) J. Med. Chem , vol.53 , Issue.22 , pp. 8047-8058
    • Chou, L.-C.1    Tsai, M.-T.2    Hsu, M.-H.3    Wang, S.-H.4    Way, T.-D.5    Huang, C.-H.6    Lin, H.-Y.7    Qian, K.8    Dong, Y.9    Lee, K.-H.10
  • 11
    • 0034698708 scopus 로고    scopus 로고
    • Synthesis and evaluation of quinoline carboxyguanidines as antidiabetic agents
    • Edmont, D.; Rocher, R.; Plisson, C.; Chenault, J. Synthesis and evaluation of quinoline carboxyguanidines as antidiabetic agents. Bioorg. Med. Chem. Lett. 2000, 10(16), 1831-1834.
    • (2000) Bioorg. Med. Chem. Lett , vol.10 , Issue.16 , pp. 1831-1834
    • Edmont, D.1    Rocher, R.2    Plisson, C.3    Chenault, J.4
  • 13
    • 21644444324 scopus 로고    scopus 로고
    • Synthesis, anticonvulsant and antihypertensive activities of 8- substituted quinoline derivatives
    • Muruganantham, N.; Sivakumar, R.; Anbalagan, N.; Gunasekaran, V.; Leonard, J.T. Synthesis, anticonvulsant and antihypertensive activities of 8- substituted quinoline derivatives. Biol. Pharm. Bull. 2004, 27(10), 1683- 1687.
    • (2004) Biol. Pharm. Bull , vol.27 , Issue.10 , pp. 1683-1687
    • Muruganantham, N.1    Sivakumar, R.2    Anbalagan, N.3    Gunasekaran, V.4    Leonard, J.T.5
  • 14
    • 0035924211 scopus 로고    scopus 로고
    • Synthesis, in vitro pharmacology, and molecular modeling of syn-huprines as acetylcholinesterase inhibitors
    • Camps, P.; Gómez, E.; Muñoz-Torrero, D.; Badia, A.; Vivas, N.M.; Barril, X.; Orozco, M.; Luque, F.J. Synthesis, in vitro pharmacology, and molecular modeling of syn-huprines as acetylcholinesterase inhibitors. J. Med. Chem. 2001, 44(26), 4733-4736.
    • (2001) J. Med. Chem , vol.44 , Issue.26 , pp. 4733-4736
    • Camps, P.1    Gómez, E.2    Muñoz-Torrero, D.3    Badia, A.4    Vivas, N.M.5    Barril, X.6    Orozco, M.7    Luque, F.J.8
  • 17
    • 0028243048 scopus 로고
    • A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives
    • Maguire, M.P.; Sheets, K.R.; McVety, K.; Spada, A.P.; Zilberstein, A. A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives. J. Med. Chem. 1994, 37(14), 2129-2137.
    • (1994) J. Med. Chem , vol.37 , Issue.14 , pp. 2129-2137
    • Maguire, M.P.1    Sheets, K.R.2    McVety, K.3    Spada, A.P.4    Zilberstein, A.5
  • 18
    • 0032560231 scopus 로고    scopus 로고
    • Synthesis and Structure-Activity Relationships of Carboxyflavones as Structurally Rigid CysLT 1(LTD4) Receptor Antagonists
    • Zwaagstra, M.E.; Timmerman, H.; van de Stolpe, A.C.; de Kanter, F.J.; Tamura, M.; Wada, Y.; Zhang, M.-Q. Synthesis and Structure-Activity Relationships of Carboxyflavones as Structurally Rigid CysLT 1(LTD4) Receptor Antagonists. J. Med. Chem. 1998, 41(9), 1428-1438.
    • (1998) J. Med. Chem , vol.41 , Issue.9 , pp. 1428-1438
    • Zwaagstra, M.E.1    Timmerman, H.2    van de Stolpe, A.C.3    de Kanter, F.J.4    Tamura, M.5    Wada, Y.6    Zhang, M.-Q.7
  • 19
    • 74949112775 scopus 로고    scopus 로고
    • Novel ratiometric fluorescent sensor for silver ions
    • Wang, H.-H.; Xue, L.; Qian, Y.-Y.; Jiang, H. Novel ratiometric fluorescent sensor for silver ions. Org. Lett. 2009, 12(2), 292-295.
    • (2009) Org. Lett , vol.12 , Issue.2 , pp. 292-295
    • Wang, H.-H.1    Xue, L.2    Qian, Y.-Y.3    Jiang, H.4
  • 20
    • 0010609309 scopus 로고
    • Eine Synthese des Chinolins
    • Skraup, Z.H. Eine Synthese des Chinolins. Monatsh. Chem. 1880, 1(1), 316- 318.
    • (1880) Monatsh. Chem , vol.1 , Issue.1 , pp. 316-318
    • Skraup, Z.H.1
  • 21
  • 22
    • 84889644736 scopus 로고    scopus 로고
    • Recent developments of the Stille reaction as a revolutionized method in total synthesis
    • Heravi, M.M.; Hashemi, E.; Azimian, F. Recent developments of the Stille reaction as a revolutionized method in total synthesis. Tetrahedron 2014, 70(1), 7-21.
    • (2014) Tetrahedron , vol.70 , Issue.1 , pp. 7-21
    • Heravi, M.M.1    Hashemi, E.2    Azimian, F.3
  • 23
    • 84898788499 scopus 로고    scopus 로고
    • Negishi coupling: An easy progress for C-C bond construction in total synthesis
    • Heravi, M.; Hashemi, E.; Nazari, N. Negishi coupling: an easy progress for C-C bond construction in total synthesis. Mol. Divers. 2014, 18(2), 441-472.
    • (2014) Mol. Divers , vol.18 , Issue.2 , pp. 441-472
    • Heravi, M.1    Hashemi, E.2    Nazari, N.3
  • 24
    • 84885448415 scopus 로고    scopus 로고
    • Oxazolidinones as chiral auxiliaries in asymmetric aldol reactions applied to total synthesis
    • Heravi, M.M.; Zadsirjan, V. Oxazolidinones as chiral auxiliaries in asymmetric aldol reactions applied to total synthesis. Tetrahedron: Asymmetry 2013, 24(19), 1149-1188.
    • (2013) Tetrahedron: Asymmetry , vol.24 , Issue.19 , pp. 1149-1188
    • Heravi, M.M.1    Zadsirjan, V.2
  • 25
    • 85039884924 scopus 로고    scopus 로고
    • Recent advances in C-heteroatom bond forming by asymmetric Michael addition
    • Heravi, M.M.; Hajiabbasi, P. Recent advances in C-heteroatom bond forming by asymmetric Michael addition. Mol. Divers 2013, 1-29.
    • (2013) Mol. Divers , pp. 1-29
    • Heravi, M.M.1    Hajiabbasi, P.2
  • 26
    • 84880698534 scopus 로고    scopus 로고
    • Recent progress in asymmetric Biginelli reaction
    • Heravi, M.M.; Asadi, S.; Lashkariani, B. Recent progress in asymmetric Biginelli reaction. Mol. Divers. 2013, 17(2), 389-407.
    • (2013) Mol. Divers , vol.17 , Issue.2 , pp. 389-407
    • Heravi, M.M.1    Asadi, S.2    Lashkariani, B.3
  • 27
    • 84866742794 scopus 로고    scopus 로고
    • Recent applications of the Suzuki reaction in total synthesis
    • Heravi, M.M.; Hashemi, E. Recent applications of the Suzuki reaction in total synthesis. Tetrahedron 2012, 68(45), 9145-9178.
    • (2012) Tetrahedron , vol.68 , Issue.45 , pp. 9145-9178
    • Heravi, M.M.1    Hashemi, E.2
  • 28
    • 84861347636 scopus 로고    scopus 로고
    • Recent advances in application of intramolecular Suzuki cross-coupling in cyclization and heterocyclization
    • Heravi, M.M.; Hashemi, E. Recent advances in application of intramolecular Suzuki cross-coupling in cyclization and heterocyclization. Monatsh. Chem. 2012, 143(6), 861-880.
    • (2012) Monatsh. Chem , vol.143 , Issue.6 , pp. 861-880
    • Heravi, M.M.1    Hashemi, E.2
  • 29
    • 84870371379 scopus 로고    scopus 로고
    • Recent advances in Kumada-Tamao-Corriu cross-coupling reaction catalyzed by different ligands
    • Heravi, M.M.; Hajiabbasi, P. Recent advances in Kumada-Tamao-Corriu cross-coupling reaction catalyzed by different ligands. Monatsh. Chem. 2012, 143(12), 1575-1592.
    • (2012) Monatsh. Chem , vol.143 , Issue.12 , pp. 1575-1592
    • Heravi, M.M.1    Hajiabbasi, P.2
  • 30
    • 84867499517 scopus 로고    scopus 로고
    • McMurry Coupling of Aldehydes and Ketones for the Formation of Heterocyles Via Olefination
    • Heravi, M.M.; Faghihi, Z. McMurry Coupling of Aldehydes and Ketones for the Formation of Heterocyles Via Olefination. Curr. Org. Chem. 2012, 16(18), 2097-2123.
    • (2012) Curr. Org. Chem , vol.16 , Issue.18 , pp. 2097-2123
    • Heravi, M.M.1    Faghihi, Z.2
  • 31
    • 84868583459 scopus 로고    scopus 로고
    • Recent applications of organocatalysts in asymmetric aldol reactions
    • Heravi, M.M.; Asadi, S. Recent applications of organocatalysts in asymmetric aldol reactions. Tetrahedron: Asymmetry 2012, 23, 1431-1465.
    • (2012) Tetrahedron: Asymmetry , vol.23 , pp. 1431-1465
    • Heravi, M.M.1    Asadi, S.2
  • 32
    • 84857584240 scopus 로고    scopus 로고
    • Application of Nanomaterials in Heterocylic Chemistry
    • Heravi, M.M.; Alishiri, T. Application of Nanomaterials in Heterocylic Chemistry. Heterocycles 2011, 85(3), 545-586.
    • (2011) Heterocycles , vol.85 , Issue.3 , pp. 545-586
    • Heravi, M.M.1    Alishiri, T.2
  • 33
    • 79751478802 scopus 로고    scopus 로고
    • Recent Advances in the Application of the Heck Reaction in the Synthesis of Heterocyclic Compounds
    • Heravi, M.M.; Fazeli, A. Recent Advances in the Application of the Heck Reaction in the Synthesis of Heterocyclic Compounds. Heterocycles 2010, 81(9), 1979-2026.
    • (2010) Heterocycles , vol.81 , Issue.9 , pp. 1979-2026
    • Heravi, M.M.1    Fazeli, A.2
  • 34
    • 65449165027 scopus 로고    scopus 로고
    • Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis
    • Heravi, M.M.; Sadjadi, S. Recent developments in use of heteropolyacids, their salts and polyoxometalates in organic synthesis. J. Iran. Chem. Soc. 2009, 6(1), 1-54.
    • (2009) J. Iran. Chem. Soc , vol.6 , Issue.1 , pp. 1-54
    • Heravi, M.M.1    Sadjadi, S.2
  • 35
    • 68449100165 scopus 로고    scopus 로고
    • Recent advances in the application of the Sonogashira method in the synthesis of heterocyclic compounds
    • Heravi, M.M.; Sadjadi, S. Recent advances in the application of the Sonogashira method in the synthesis of heterocyclic compounds. Tetrahedron 2009, 65(37), 7761-7775.
    • (2009) Tetrahedron , vol.65 , Issue.37 , pp. 7761-7775
    • Heravi, M.M.1    Sadjadi, S.2
  • 36
    • 70349971948 scopus 로고    scopus 로고
    • Application of sulfamic acid in organic synthesis-A short review
    • Heravi, M.M.; Baghernejad, B.; Oskooie, H.A. Application of sulfamic acid in organic synthesis-A short review. Curr. Org. Chem. 2009, 13(10), 1002-1014.
    • (2009) Curr. Org. Chem , vol.13 , Issue.10 , pp. 1002-1014
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3
  • 37
    • 7744242263 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • Michael, J.P. Quinoline, quinazoline and acridone alkaloids. Nat. Prod. Rep. 2004, 21(5), 650-668.
    • (2004) Nat. Prod. Rep , vol.21 , Issue.5 , pp. 650-668
    • Michael, J.P.1
  • 38
    • 26844495371 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • Michael, J.P. Quinoline, quinazoline and acridone alkaloids. Nat. Prod. Rep. 2005, 22(5), 627-646.
    • (2005) Nat. Prod. Rep , vol.22 , Issue.5 , pp. 627-646
    • Michael, J.P.1
  • 40
    • 1542626885 scopus 로고
    • Fluorine-containing analogs of 4- hydroxypropiophenone
    • Hoi, N.P.B.; Xuong, N.D.; Lavit, D. Fluorine-containing analogs of 4- hydroxypropiophenone. J. Org. Chem. 1953, 18, 910-915.
    • (1953) J. Org. Chem , vol.18 , pp. 910-915
    • Hoi, N.P.B.1    Xuong, N.D.2    Lavit, D.3
  • 41
    • 0024582632 scopus 로고
    • Potential antitumor agents. 57. 2- Phenylquinoline-8-carboxamides as minimal DNA-intercalating antitumor agents with in vivo solid tumor activity
    • Atwell, G.J.; Baguley, B.C.; Denny, W.A. Potential antitumor agents. 57. 2- Phenylquinoline-8-carboxamides as minimal DNA-intercalating antitumor agents with in vivo solid tumor activity. J. Med. Chem. 1989, 32, 396-401.
    • (1989) J. Med. Chem , vol.32 , pp. 396-401
    • Atwell, G.J.1    Baguley, B.C.2    Denny, W.A.3
  • 42
    • 84862293494 scopus 로고
    • Doebner, O. Ann. 1887, 242, 265-289.
    • (1887) Ann , vol.242 , pp. 265-289
    • Doebner, O.1
  • 43
    • 33947459553 scopus 로고
    • 2-Aminopyridine and the doebner reaction
    • Allen, C.F.H.; Spangler, F.W.; Webster, E.R. 2-Aminopyridine and the doebner reaction. J. Org. Chem. 1951, 16(1), 17-20.
    • (1951) J. Org. Chem , vol.16 , Issue.1 , pp. 17-20
    • Allen, C.F.H.1    Spangler, F.W.2    Webster, E.R.3
  • 44
    • 33947339318 scopus 로고
    • 2-Phenylquinoline-4-carboxylic acid-6-arsonic acid
    • Johnson, J.R.; Adams, R. 2-Phenylquinoline-4-carboxylic acid-6-arsonic acid. J. Am. Chem. Soc. 1921, 43, 2255-2257.
    • (1921) J. Am. Chem. Soc , vol.43 , pp. 2255-2257
    • Johnson, J.R.1    Adams, R.2
  • 45
    • 33745411481 scopus 로고
    • Ueber ɑ-Alkylcinchoninsäuren
    • Doebner, O. Ueber ɑ-Alkylcinchoninsäuren. Ber. Dtsch. Chem. Ges. 1887, 20, 277-281.
    • (1887) Ber. Dtsch. Chem. Ges , vol.20 , pp. 277-281
    • Doebner, O.1
  • 46
    • 0005846141 scopus 로고
    • The synthesis of substituted 5,6- benzocinchoninic acids by the Doebner and by the Pfitzinger reactions
    • Robinson, E.A.; Bogert, M.T. The synthesis of substituted 5,6- benzocinchoninic acids by the Doebner and by the Pfitzinger reactions. J. Org. Chem. 1936, 01(1), 65-75.
    • (1936) J. Org. Chem , vol.1 , Issue.1 , pp. 65-75
    • Robinson, E.A.1    Bogert, M.T.2
  • 47
    • 33947441022 scopus 로고
    • Failure of the Doebner Reaction with 2-Chloro-5- aminopyridine. Synthesis of a Pyrrolidine Derivative1
    • Weiss, M.J.; Hauser, C.R. Failure of the Doebner Reaction with 2-Chloro-5- aminopyridine. Synthesis of a Pyrrolidine Derivative1. J. Am. Chem. Soc. 1946, 68(4), 722-723.
    • (1946) J. Am. Chem. Soc , vol.68 , Issue.4 , pp. 722-723
    • Weiss, M.J.1    Hauser, C.R.2
  • 48
    • 0004944419 scopus 로고
    • Cyclization of 2-Aminopyridine Derivatives. I. Substituted Ethyl 2-Pyridylaminomethylenemalonates1,2
    • Lappin, G.R. Cyclization of 2-Aminopyridine Derivatives. I. Substituted Ethyl 2-Pyridylaminomethylenemalonates1,2. J. Am. Chem. Soc. 1948, 70(10), 3348-3350.
    • (1948) J. Am. Chem. Soc , vol.70 , Issue.10 , pp. 3348-3350
    • Lappin, G.R.1
  • 49
    • 0010439264 scopus 로고
    • Cyclization of 2-aminopyridine derivatives. ii. the reaction of substituted 2-aminopyridines with ethyl malonate1
    • Lappin, G.R.; Petersen, Q.R.; Wheeler, C.E. Cyclization of 2-aminopyridine derivatives. ii. the reaction of substituted 2-aminopyridines with ethyl malonate1. J. Org. Chem. 1950, 15(2), 377-380.
    • (1950) J. Org. Chem , vol.15 , Issue.2 , pp. 377-380
    • Lappin, G.R.1    Petersen, Q.R.2    Wheeler, C.E.3
  • 50
    • 62649173577 scopus 로고    scopus 로고
    • One-pot synthesis of quinoline-4-carboxylic acid derivatives in water: Ytterbium perfluorooctanoate catalyzed Doebner reaction
    • Wang, L.M.; Hu, L.; Chen, H.J.; Sui, Y.Y.; Shen, W. One-pot synthesis of quinoline-4-carboxylic acid derivatives in water: Ytterbium perfluorooctanoate catalyzed Doebner reaction. J. Fluorine Chem. 2009, 130(4), 406-409.
    • (2009) J. Fluorine Chem , vol.130 , Issue.4 , pp. 406-409
    • Wang, L.M.1    Hu, L.2    Chen, H.J.3    Sui, Y.Y.4    Shen, W.5
  • 51
    • 0034570227 scopus 로고    scopus 로고
    • Some biological properties of new quinoline-4-carboxylic acid and quinoline-4- carboxamide derivatives
    • Strigášová, J.; Hudecová, D.; Vareška, L.; Lásiková, A.; Végh, D. Some biological properties of new quinoline-4-carboxylic acid and quinoline-4- carboxamide derivatives. Folia Microbiol. 2000, 45(4), 305-309.
    • (2000) Folia Microbiol , vol.45 , Issue.4 , pp. 305-309
    • Strigášová, J.1    Hudecová, D.2    Vareška, L.3    Lásiková, A.4    Végh, D.5
  • 52
    • 77953430555 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of schiff bases of cinchophen as antimicrobial agents
    • Wadher, S.J.; Karande, N.A.; Borkar, D.S.; Yeole, P.G. Synthesis and biological evaluation of schiff bases of cinchophen as antimicrobial agents. Int. J. Chem. Tech. Res. 2009, 1(4), 1297-1302.
    • (2009) Int. J. Chem. Tech. Res , vol.1 , Issue.4 , pp. 1297-1302
    • Wadher, S.J.1    Karande, N.A.2    Borkar, D.S.3    Yeole, P.G.4
  • 54
    • 27744450163 scopus 로고    scopus 로고
    • Rapid synthesis of quinoline-4-carboxylic acid derivatives from arylimines and 2-substituted acrylates or acrylamides under indium(iii) chloride and microwave activations. Scope and limitations of the reaction
    • Duvelleroy, D.; Perrio, C.; Parisel, O.; Lasne, M.-C. Rapid synthesis of quinoline-4-carboxylic acid derivatives from arylimines and 2-substituted acrylates or acrylamides under indium(iii) chloride and microwave activations. Scope and limitations of the reaction. Org. Biomol. Chem. 2005, 3(20), 3794-3804.
    • (2005) Org. Biomol. Chem , vol.3 , Issue.20 , pp. 3794-3804
    • Duvelleroy, D.1    Perrio, C.2    Parisel, O.3    Lasne, M.-C.4
  • 55
    • 2942642146 scopus 로고    scopus 로고
    • A new insight into the Pfitzinger reaction. A facile synthesis of 6- sulfamoylquinoline-4-carboxylic acids
    • Ivachtchenko, A.V.; Khvat, A.V.; Kobak, V.V.; Kysil, V.M.; Williams, C.T. A new insight into the Pfitzinger reaction. A facile synthesis of 6- sulfamoylquinoline-4-carboxylic acids. Tetrahedron Lett. 2004, 45(28), 5473-5476.
    • (2004) Tetrahedron Lett , vol.45 , Issue.28 , pp. 5473-5476
    • Ivachtchenko, A.V.1    Khvat, A.V.2    Kobak, V.V.3    Kysil, V.M.4    Williams, C.T.5
  • 56
    • 33646056650 scopus 로고    scopus 로고
    • New potential biologically active compounds: Design and an efficient synthesis of N-substituted 4-aryl-4,6,7,8-tetrahydroquinoline- 2,5(1H,3H)-diones under microwave irradiation
    • Tu, S.; Zhu, X.; Zhang, J.; Xu, J.; Zhang, Y.; Wang, Q.; Jia, R.; Jiang, B.; Zhang, J.; Yao, C. New potential biologically active compounds: Design and an efficient synthesis of N-substituted 4-aryl-4,6,7,8-tetrahydroquinoline- 2,5(1H,3H)-diones under microwave irradiation. Bioorg. Med. Chem. Lett. 2006, 16(11), 2925-2928.
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , Issue.11 , pp. 2925-2928
    • Tu, S.1    Zhu, X.2    Zhang, J.3    Xu, J.4    Zhang, Y.5    Wang, Q.6    Jia, R.7    Jiang, B.8    Zhang, J.9    Yao, C.10
  • 57
    • 0024582632 scopus 로고
    • Potential antitumor agents. 57. 2- Phenylquinoline-8-carboxamides as minimal DNA-intercalating antitumor agents with in vivo solid tumor activity
    • Atwell, G.J.; Baguley, B.C.; Denny, W.A. Potential antitumor agents. 57. 2- Phenylquinoline-8-carboxamides as minimal DNA-intercalating antitumor agents with in vivo solid tumor activity. J. Med. Chem. 1989, 32(2), 396-401.
    • (1989) J. Med. Chem , vol.32 , Issue.2 , pp. 396-401
    • Atwell, G.J.1    Baguley, B.C.2    Denny, W.A.3
  • 58
    • 0019252702 scopus 로고
    • Structure-activity relationships of antibacterial 6,7- and 7,8-disubstituted 1-alkyl-1,4-dihydro- 4-oxoquinoline-3-carboxylic acids
    • Koga, H.; Itoh, A.; Murayama, S.; Suzue, S.; Irikura, T. Structure-activity relationships of antibacterial 6,7- and 7,8-disubstituted 1-alkyl-1,4-dihydro- 4-oxoquinoline-3-carboxylic acids. J. Med. Chem. 1980, 23(12), 1358-1363.
    • (1980) J. Med. Chem , vol.23 , Issue.12 , pp. 1358-1363
    • Koga, H.1    Itoh, A.2    Murayama, S.3    Suzue, S.4    Irikura, T.5
  • 59
    • 77954087193 scopus 로고    scopus 로고
    • Microwave-irradiated synthesis and antimicrobial activity of 2-phenyl-7-substitutedalkyl/arylaminoquinoline-4- carboxylic acid derivatives
    • Bhatt, H.G.; Agrawal, Y.K. Microwave-irradiated synthesis and antimicrobial activity of 2-phenyl-7-substitutedalkyl/arylaminoquinoline-4- carboxylic acid derivatives. Med. Chem. Res. 2010, 19(4), 392-402.
    • (2010) Med. Chem. Res , vol.19 , Issue.4 , pp. 392-402
    • Bhatt, H.G.1    Agrawal, Y.K.2
  • 60
    • 33745381902 scopus 로고    scopus 로고
    • Macrocycles via Doebner reaction followed by macrolactonization
    • Henkel, B.; Lis, M.; Illgen, K.; Eckl, R. Macrocycles via Doebner reaction followed by macrolactonization. Synlett 2006, (9), 1315-1318.
    • (2006) Synlett , Issue.9 , pp. 1315-1318
    • Henkel, B.1    Lis, M.2    Illgen, K.3    Eckl, R.4
  • 61
    • 85163161435 scopus 로고
    • Über Pyrazo-pyrrolidone
    • Dohrn, M.; Thiele, A. Über Pyrazo-pyrrolidone. Ber. Dtsch. Chem. Ges. B 1931, 64(11), 2863-2865.
    • (1931) Ber. Dtsch. Chem. Ges. B , vol.64 , Issue.11 , pp. 2863-2865
    • Dohrn, M.1    Thiele, A.2
  • 63
    • 33644552576 scopus 로고
    • A modification of the skraup synthesis of quinoline
    • Cohn, B.E.; Gustavson, R.G. A modification of the skraup synthesis of quinoline. J. Am. Chem. Soc. 1928, 50, 2709-2711.
    • (1928) J. Am. Chem. Soc , vol.50 , pp. 2709-2711
    • Cohn, B.E.1    Gustavson, R.G.2
  • 64
    • 0010062736 scopus 로고
    • A modification of the skraup synthesis of quinoline
    • Cohn, E.W. A modification of the skraup synthesis of quinoline. J. Am. Chem. Soc. 1930, 52, 3685-3688.
    • (1930) J. Am. Chem. Soc , vol.52 , pp. 3685-3688
    • Cohn, E.W.1
  • 67
    • 34250544782 scopus 로고
    • Über Chinin und Chinidin
    • Skraup, Z.H. Über Chinin und Chinidin. Monatsh. Chem. 1881, 2(1), 587-609.
    • (1881) Monatsh. Chem , vol.2 , Issue.1 , pp. 587-609
    • Skraup, Z.H.1
  • 68
    • 0010607133 scopus 로고
    • Synthetische Versuche in der Chinolinreihe
    • Skraup, Z.H. Synthetische Versuche in der Chinolinreihe. Monatsh. Chem. 1881, 2(1), 139-170.
    • (1881) Monatsh. Chem , vol.2 , Issue.1 , pp. 139-170
    • Skraup, Z.H.1
  • 69
    • 84979140792 scopus 로고
    • Ueber eine dem Chinolin homologe Base
    • Doebner, O.; Miller, W.V. Ueber eine dem Chinolin homologe Base. Ber. Dtsh. Chem. Ges. 1881, 14, 2812-2817.
    • (1881) Ber. Dtsh. Chem. Ges , vol.14 , pp. 2812-2817
    • Doebner, O.1    Miller, W.V.2
  • 70
    • 84987551773 scopus 로고
    • Unusual Friedel- Crafts Reactions; 41. Synthesis of 2, 4-Diphenyl-2-methyl-1, 2- dihydroquinolines from Anilines and Phenylacetylene
    • Arduini, A.; Bigi, F.; Casiraghi, G.; Casnati, G.; Sartori, G. Unusual Friedel- Crafts Reactions; 41. Synthesis of 2, 4-Diphenyl-2-methyl-1, 2- dihydroquinolines from Anilines and Phenylacetylene. Synthesis 1981, 975- 977.
    • (1981) Synthesis , pp. 975-977
    • Arduini, A.1    Bigi, F.2    Casiraghi, G.3    Casnati, G.4    Sartori, G.5
  • 71
    • 0038505775 scopus 로고
    • Rocz
    • Glinka, J. Rocz. Chem. 1965, 39, 885-893.
    • (1965) Chem , vol.39 , pp. 885-893
    • Glinka, J.1
  • 73
    • 0037140878 scopus 로고    scopus 로고
    • Novel facile synthesis of 2,2,4 substituted 1,2-dihydroquinolines via a modified Skraup reaction
    • Theoclitou, M.-E.; Robinson, L.A. Novel facile synthesis of 2,2,4 substituted 1,2-dihydroquinolines via a modified Skraup reaction. Tetrahedron Lett. 2002, 43(21), 3907-3910.
    • (2002) Tetrahedron Lett , vol.43 , Issue.21 , pp. 3907-3910
    • Theoclitou, M.-E.1    Robinson, L.A.2
  • 74
    • 33644539496 scopus 로고    scopus 로고
    • On the mechanism of the Skraup-Doebner- Von Miller quinoline synthesis
    • Denmark, S.E.; Venkatraman, S. On the mechanism of the Skraup-Doebner- Von Miller quinoline synthesis. J. Org. Chem. 2006, 71(4), 1668-1676.
    • (2006) J. Org. Chem , vol.71 , Issue.4 , pp. 1668-1676
    • Denmark, S.E.1    Venkatraman, S.2
  • 75
    • 33747435799 scopus 로고    scopus 로고
    • Skraup-Doebner-Von Miller quinoline synthesis revisited: Reversal of the regiochemistry for ɑ- aryl-β,γ-unsaturated ɑ-ketoesters
    • Wu, Y.C.; Liu, L.; Li, H.J.; Wang, D.; Chen, Y.J. Skraup-Doebner-Von Miller quinoline synthesis revisited: Reversal of the regiochemistry for ɑ- aryl-β,γ-unsaturated ɑ-ketoesters. J. Org. Chem. 2006, 71(17), 6592-6595.
    • (2006) J. Org. Chem , vol.71 , Issue.17 , pp. 6592-6595
    • Wu, Y.C.1    Liu, L.2    Li, H.J.3    Wang, D.4    Chen, Y.J.5
  • 76
    • 84858626101 scopus 로고    scopus 로고
    • Unexpected 5,6,7,8,9,10- hexahydro-6,6-pentamethylenephenanthridines and 2,3,4,5-tetrahydro-4,4- tetramethylene-1 H -cyclopenta[ c ]quinolines from skraup-doebner-von miller quinoline synthesis and their implications for the mechanism of that reaction
    • Fotie, J.; Kemami Wangun, H.V.; Fronczek, F.R.; Massawe, N.; Bhattarai, B.T.; Rhodus, J.L.; Singleton, T.A.; Bohle, D.S. Unexpected 5,6,7,8,9,10- hexahydro-6,6-pentamethylenephenanthridines and 2,3,4,5-tetrahydro-4,4- tetramethylene-1 H -cyclopenta[ c ]quinolines from skraup-doebner-von miller quinoline synthesis and their implications for the mechanism of that reaction. J. Org. Chem. 2012, 77(6), 2784-2790.
    • (2012) J. Org. Chem , vol.77 , Issue.6 , pp. 2784-2790
    • Fotie, J.1    Kemami Wangun, H.V.2    Fronczek, F.R.3    Massawe, N.4    Bhattarai, B.T.5    Rhodus, J.L.6    Singleton, T.A.7    Bohle, D.S.8
  • 79
    • 78650718580 scopus 로고    scopus 로고
    • Ruthenium-catalysed synthesis of 2- and 3- substituted quinolines from anilines and 1,3-diols
    • Monrad, R.N.; Madsen, R. Ruthenium-catalysed synthesis of 2- and 3- substituted quinolines from anilines and 1,3-diols. Org. Biomol. Chem. 2011, 9(2), 610-615.
    • (2011) Org. Biomol. Chem , vol.9 , Issue.2 , pp. 610-615
    • Monrad, R.N.1    Madsen, R.2
  • 80
    • 72249084943 scopus 로고    scopus 로고
    • Synthesis of novel annelated systems based on the interaction and reactivity estimation of amino-1,5- benzodiazepin-2-ones with dimethyl-2-oxoglutaconate
    • Janciene, R.; Stumbreviciute, Z.; Vektariene, A.; Kosychova, L.; Klimavicius, A.; Palaima, A.; Puodziunaite, B. Synthesis of novel annelated systems based on the interaction and reactivity estimation of amino-1,5- benzodiazepin-2-ones with dimethyl-2-oxoglutaconate. J. Heterocycl. Chem. 2009, 46(6), 1339-1345.
    • (2009) J. Heterocycl. Chem , vol.46 , Issue.6 , pp. 1339-1345
    • Janciene, R.1    Stumbreviciute, Z.2    Vektariene, A.3    Kosychova, L.4    Klimavicius, A.5    Palaima, A.6    Puodziunaite, B.7
  • 81
    • 0020721792 scopus 로고
    • Efficient homogeneous acid catalysis of heteropoly acid and its characterization through ether cleavage reactions
    • Izumi, Y.; Matsuo, K.; Urabe, K. Efficient homogeneous acid catalysis of heteropoly acid and its characterization through ether cleavage reactions. J. Mol. Catal. 1983, 18, 299-314.
    • (1983) J. Mol. Catal , vol.18 , pp. 299-314
    • Izumi, Y.1    Matsuo, K.2    Urabe, K.3
  • 84
    • 32244445946 scopus 로고    scopus 로고
    • Synthesis of quinaldines and lepidines by a Doebner-Miller reaction under thermal and microwave irradiation conditions using phosphotungstic acid
    • Sivaprasad, G.; Rajesh, R.; Perumal, P.T. Synthesis of quinaldines and lepidines by a Doebner-Miller reaction under thermal and microwave irradiation conditions using phosphotungstic acid. Tetrahedron Lett. 2006, 47(11), 1783-1785.
    • (2006) Tetrahedron Lett , vol.47 , Issue.11 , pp. 1783-1785
    • Sivaprasad, G.1    Rajesh, R.2    Perumal, P.T.3
  • 85
    • 77958529214 scopus 로고    scopus 로고
    • Limitations of the two-phase doebner-miller reaction for the synthesis of quinolines
    • Reynolds, K.A.; Young, D.J.; Loughlin, W.A. Limitations of the two-phase doebner-miller reaction for the synthesis of quinolines. Synthesis 2010, (21), 3645-3648.
    • (2010) Synthesis , Issue.21 , pp. 3645-3648
    • Reynolds, K.A.1    Young, D.J.2    Loughlin, W.A.3
  • 86
    • 84858079543 scopus 로고    scopus 로고
    • Unusual open chain quinolinyl peroxol and its alcohol counterpart obtained through a modified Skraup-Doebner-Von Miller quinoline synthesis: Theoretical studies and complete 1H- and 13C-NMR assignments
    • Fotie, J.; Kemami Wangun, H.V.; Dreux, K.; Sommerfeld, T.; Pittman, J. Unusual open chain quinolinyl peroxol and its alcohol counterpart obtained through a modified Skraup-Doebner-Von Miller quinoline synthesis: Theoretical studies and complete 1H- and 13C-NMR assignments. Magn. Reson. Chem. 2012, 50(1), 68-73.
    • (2012) Magn. Reson. Chem , vol.50 , Issue.1 , pp. 68-73
    • Fotie, J.1    Kemami Wangun, H.V.2    Dreux, K.3    Sommerfeld, T.4    Pittman, J.5
  • 87
    • 84869502149 scopus 로고    scopus 로고
    • C-N Coupling of 1,2-Dihydro- 2,2,4-trimethylquinoline Derivatives via a Silver(I)-Catalyzed Direct Functionalization of a C-H Bond
    • Fotie, J.; Rhodus, J.L.; Taha, H.A.; Reid, C.S. C-N Coupling of 1,2-Dihydro- 2,2,4-trimethylquinoline Derivatives via a Silver(I)-Catalyzed Direct Functionalization of a C-H Bond. Heteroatom Chem. 2012, 23(6), 598-604.
    • (2012) Heteroatom Chem , vol.23 , Issue.6 , pp. 598-604
    • Fotie, J.1    Rhodus, J.L.2    Taha, H.A.3    Reid, C.S.4
  • 88
    • 84870927313 scopus 로고    scopus 로고
    • An Expedient Phase Transfer Catalyst- Mediated Synthesis of 2-Alkyl/Aryl-1,8-phenanthrolines
    • Chakrabarty, M.; Mukherji, A. An Expedient Phase Transfer Catalyst- Mediated Synthesis of 2-Alkyl/Aryl-1,8-phenanthrolines. J. Heterocycl. Chem. 2012, 49(6), 1443-1446.
    • (2012) J. Heterocycl. Chem , vol.49 , Issue.6 , pp. 1443-1446
    • Chakrabarty, M.1    Mukherji, A.2
  • 90
    • 34249892223 scopus 로고    scopus 로고
    • Synthesis and Fluorescence Properties of 5,7-Diphenylquinoline and 2,5,7-Triphenylquinoline Derived from m-Terphenylamine
    • Qi, S.; Shi, K.; Gao, H.; Liu, Q.; Wang, H. Synthesis and Fluorescence Properties of 5,7-Diphenylquinoline and 2,5,7-Triphenylquinoline Derived from m-Terphenylamine. Molecules 2007, 12(5), 988-996.
    • (2007) Molecules , vol.12 , Issue.5 , pp. 988-996
    • Qi, S.1    Shi, K.2    Gao, H.3    Liu, Q.4    Wang, H.5
  • 92
    • 70449587604 scopus 로고    scopus 로고
    • A Review on High Burden of Malaria during Pregnancy: Need of Social Science
    • Priohit, B.; Mahapatra, A. A Review on High Burden of Malaria during Pregnancy: Need of Social Science. Stud. Ethno-Med. 2009, 3, 33-38.
    • (2009) Stud. Ethno-Med , vol.3 , pp. 33-38
    • Priohit, B.1    Mahapatra, A.2
  • 95
    • 58249097269 scopus 로고    scopus 로고
    • The Ammosamides: Structures of Cell Cycle Modulators from a Marine- Derived Streptomyces Species
    • Hughes, C.C.; MacMillan, J.B.; Gaudêncio, S.P.; Jensen, P.R.; Fenical, W. The Ammosamides: Structures of Cell Cycle Modulators from a Marine- Derived Streptomyces Species. Angew. Chem. Int. Ed. 2009, 48, 725-727.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 725-727
    • Hughes, C.C.1    MacMillan, J.B.2    Gaudêncio, S.P.3    Jensen, P.R.4    Fenical, W.5
  • 97
    • 77955847907 scopus 로고    scopus 로고
    • Short and straightforward total synthesis of Ammosamide B
    • Wu, Q.; Jiao, X.; Wang, L.; Xiao, Q.; Liu, X.; Xie, P. Short and straightforward total synthesis of Ammosamide B. Tetrahedron Lett. 2010, 51(37), 4806-4807.
    • (2010) Tetrahedron Lett , vol.51 , Issue.37 , pp. 4806-4807
    • Wu, Q.1    Jiao, X.2    Wang, L.3    Xiao, Q.4    Liu, X.5    Xie, P.6
  • 98
    • 1842502954 scopus 로고    scopus 로고
    • Synthesis of Imidazolo Analogues of the Oxidation-Reduction Cofactor Pyrroloquinoline Quinone(PQQ)
    • Fouchard, D.M.D.; Tillekeratne, L.M.V.; Hudson, R.A. Synthesis of Imidazolo Analogues of the Oxidation-Reduction Cofactor Pyrroloquinoline Quinone(PQQ). J. Org. Chem. 2004, 69(7), 2626-2629.
    • (2004) J. Org. Chem , vol.69 , Issue.7 , pp. 2626-2629
    • Fouchard, D.M.D.1    Tillekeratne, L.M.V.2    Hudson, R.A.3
  • 99
    • 0000692011 scopus 로고
    • Total synthesis of the quinonoid alcohol dehydrogenase coenzyme(1) of methylotrophic bacteria
    • Corey E.J.; Tra-montano A. Total synthesis of the quinonoid alcohol dehydrogenase coenzyme(1) of methylotrophic bacteria. J. Am. Chem. Soc. 1981, 103(18), 5599-5600.
    • (1981) J. Am. Chem. Soc , vol.103 , Issue.18 , pp. 5599-5600
    • Corey, E.J.1    Tra-Montano, A.2
  • 100
    • 4544341583 scopus 로고    scopus 로고
    • Novel analogues of sydnone: Synthesis, characterization and antibacterial evaluation
    • Moustafa, M.A.; Gineinah, M.M.; Nasr, M.N.; Bayoumi, W.A. Novel analogues of sydnone: Synthesis, characterization and antibacterial evaluation. Arch. Pharm. 2004, 337(8), 427-433.
    • (2004) Arch. Pharm , vol.337 , Issue.8 , pp. 427-433
    • Moustafa, M.A.1    Gineinah, M.M.2    Nasr, M.N.3    Bayoumi, W.A.4
  • 101
    • 0242493882 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents
    • Dunkley, C.S.; Thoman, C.J. Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents. Bioorg. Med. Chem. Lett. 2003, 13(17), 2899-2901.
    • (2003) Bioorg. Med. Chem. Lett , vol.13 , Issue.17 , pp. 2899-2901
    • Dunkley, C.S.1    Thoman, C.J.2
  • 103
    • 33745150008 scopus 로고    scopus 로고
    • Synthesis and pharmacological screening of 5- methyl-3-[P-(6'-aryl-2'-thioxo-1', 2', 5', 6'-tetrahydro-pyrimidin-4'-yl)- phenyl]-3 H-2-oxo-D4-1, 3, 4-oxadiazoles
    • Kamble, R.; Sudha, B. Synthesis and pharmacological screening of 5- methyl-3-[P-(6'-aryl-2'-thioxo-1', 2', 5', 6'-tetrahydro-pyrimidin-4'-yl)- phenyl]-3 H-2-oxo-D4-1, 3, 4-oxadiazoles. Indian J. Pharm. Sci. 2006, 68(2), 249.
    • (2006) Indian J. Pharm. Sci , vol.68 , Issue.2 , pp. 249
    • Kamble, R.1    Sudha, B.2
  • 105
    • 84984082864 scopus 로고
    • Mesoionic Ψ-oxatriazoles as hypotensive agents
    • Kier, L.R.; Al-Shamma, A.; Hahn, R.; Tye, A. Mesoionic Ψ-oxatriazoles as hypotensive agents. J. Pharm. Sci. 1966, 55(12), 1467-1468.
    • (1966) J. Pharm. Sci , vol.55 , Issue.12 , pp. 1467-1468
    • Kier, L.R.1    Al-Shamma, A.2    Hahn, R.3    Tye, A.4
  • 106
    • 0033856652 scopus 로고    scopus 로고
    • 1,5-Benzodiazepine derivatives of 3- arylsydnones: Synthesis and antimicrobial activity of 3-aryl-4-[2′-aryl- 2′,4′,6′,7′-tetrahydro-(1′H)-1′,5′-benzodiazepine-4′-yl]sydnones
    • Kavali, J.R.; Badami, B.V. 1,5-Benzodiazepine derivatives of 3- arylsydnones: synthesis and antimicrobial activity of 3-aryl-4-[2′-aryl- 2′,4′,6′,7′-tetrahydro-(1′H)-1′,5′-benzodiazepine-4′-yl]sydnones. Il Farmaco 2000, 55(5), 406-409.
    • (2000) Il Farmaco , vol.55 , Issue.5 , pp. 406-409
    • Kavali, J.R.1    Badami, B.V.2
  • 107
    • 79961138965 scopus 로고    scopus 로고
    • Synthesis and characterisation of 3-hydroxy-4, 5-dihydro[1,2,3] oxadiazolo [3,4- a]quinolin-10-ium and its fluoro derivative
    • Chandrasekhar, R.; Gopalan, B.; Nanjan, M.J. Synthesis and characterisation of 3-hydroxy-4, 5-dihydro[1,2,3] oxadiazolo [3,4- a]quinolin-10-ium and its fluoro derivative. Int. J. ChemTech. Res. 2011, 3(3), 1125-1128.
    • (2011) Int. J. ChemTech. Res , vol.3 , Issue.3 , pp. 1125-1128
    • Chandrasekhar, R.1    Gopalan, B.2    Nanjan, M.J.3
  • 108
    • 55349097854 scopus 로고    scopus 로고
    • A new enone-containing triglyceride derivative as precursor of thermosets from renewable resources
    • Montero de Espinosa, L.; Ronda, J.; Galià, M.; Cádiz, V. A new enone-containing triglyceride derivative as precursor of thermosets from renewable resources. J. Polym. Sci. Part A: Polym. Chem. 2008, 46(20), 6843-6850.
    • (2008) J. Polym. Sci. Part A: Polym. Chem , vol.46 , Issue.20 , pp. 6843-6850
    • de Montero Espinosa, L.1    Ronda, J.2    Galià, M.3    Cádiz, V.4
  • 109
    • 77956354249 scopus 로고    scopus 로고
    • Quinoline-containing networks from enone and aldehyde triglyceride derivatives
    • De Espinosa, L.M.; Ronda, J.C.; Galià, M.; Cádiz, V. Quinoline-containing networks from enone and aldehyde triglyceride derivatives. J. Polym. Sci. A 2010, 48(4), 869-878.
    • (2010) J. Polym. Sci. A , vol.48 , Issue.4 , pp. 869-878
    • De Espinosa, L.M.1    Ronda, J.C.2    Galià, M.3    Cádiz, V.4
  • 110
    • 17644363353 scopus 로고    scopus 로고
    • Fracture toughness and impact strength of anhydride-cured biobased epoxy
    • Miyagawa, H.; Misra, M.; Drzal, L.T.; Mohanty, A.K. Fracture toughness and impact strength of anhydride-cured biobased epoxy. Polym. Eng. Sci. 2005, 45(4), 487-495.
    • (2005) Polym. Eng. Sci , vol.45 , Issue.4 , pp. 487-495
    • Miyagawa, H.1    Misra, M.2    Drzal, L.T.3    Mohanty, A.K.4
  • 111
    • 84870927539 scopus 로고    scopus 로고
    • Phosphorylated 3-Heteroarylcoumarins and Their Use in Fluorescence Microscopy and Nanoscopy
    • Nizamov, S.; Willig, K.I.; Sednev, M.V.; Belov, V.N.; Hell, S.W. Phosphorylated 3-Heteroarylcoumarins and Their Use in Fluorescence Microscopy and Nanoscopy. Chem. Eur. J. 2012, 18(51), 16339-16348.
    • (2012) Chem. Eur. J , vol.18 , Issue.51 , pp. 16339-16348
    • Nizamov, S.1    Willig, K.I.2    Sednev, M.V.3    Belov, V.N.4    Hell, S.W.5
  • 112
    • 84981750119 scopus 로고
    • Condensation von Malonsäure mit aromatischen Aldehyden durch Ammoniak und Amine
    • Knoevenagel, E. Condensation von Malonsäure mit aromatischen Aldehyden durch Ammoniak und Amine. Ber. Dtsch. Chem. Ges. 1898, 31, 2596-2619.
    • (1898) Ber. Dtsch. Chem. Ges , vol.31 , pp. 2596-2619
    • Knoevenagel, E.1
  • 113
    • 0032998392 scopus 로고    scopus 로고
    • Solvent-Free Microwave Enhanced Knoevenagel Condensation of Ethyl Cyanoacetate with Aldehydes
    • Mitra, A.K.; De, A.; Karchaudhuri, N. Solvent-Free Microwave Enhanced Knoevenagel Condensation of Ethyl Cyanoacetate with Aldehydes. Synth. Commun. 1999, 29(16), 2731-2739.
    • (1999) Synth. Commun , vol.29 , Issue.16 , pp. 2731-2739
    • Mitra, A.K.1    De, A.2    Karchaudhuri, N.3
  • 114
    • 0033805239 scopus 로고    scopus 로고
    • Synthesis of Cinnamic Acid Derivatives Using Ethanol as Solvent or Microwave Assisted Method
    • Pellón, R.F.; Mamposo, T.; González, E.; Calderón, O. Synthesis of Cinnamic Acid Derivatives Using Ethanol as Solvent or Microwave Assisted Method. Synth. Commun. 2000, 30(20), 3769-3774.
    • (2000) Synth. Commun , vol.30 , Issue.20 , pp. 3769-3774
    • Pellón, R.F.1    Mamposo, T.2    González, E.3    Calderón, O.4
  • 115
    • 79960438220 scopus 로고
    • Ueber die der Sorbinsäure homologen, ungesättigten Säuren mit zwei Doppelbindungen
    • Doebner O. Ueber die der Sorbinsäure homologen, ungesättigten Säuren mit zwei Doppelbindungen. Ber. Dtsch. Chem. Ges. 1902, 35, 1136-1147.
    • (1902) Ber. Dtsch. Chem. Ges , vol.35 , pp. 1136-1147
    • Doebner, O.1
  • 116
    • 84889342346 scopus 로고    scopus 로고
    • John Wiley & Sons Ltd.: Volkswagen AG, Wolfsburg, Germany
    • Laue, T.; Planges, A. Named Organic Reactions. John Wiley & Sons Ltd.: Volkswagen AG, Wolfsburg, Germany, 2005; pp. 176-179.
    • (2005) Named Organic Reactions , pp. 176-179
    • Laue, T.1    Planges, A.2
  • 117
    • 77953433363 scopus 로고    scopus 로고
    • Bismuth(III) Chloride-Mediated, Efficient, Solvent-Free, MWI-Enhanced Doebner Condensation for the Synthesis of(E)-Cinnamic Acids
    • Suresh; Kumar, D.; Sandhu, J.S. Bismuth(III) Chloride-Mediated, Efficient, Solvent-Free, MWI-Enhanced Doebner Condensation for the Synthesis of(E)-Cinnamic Acids. Synth. Commun. 2010, 40(13), 1915-1919.
    • (2010) Synth. Commun , vol.40 , Issue.13 , pp. 1915-1919
    • Suresh, S.1    Kumar, D.2    Sandhu, J.S.3
  • 118
    • 59349108245 scopus 로고    scopus 로고
    • Doebner condensation in ionic liquids [Bmim]BF4 and [Bpy]BF4 to synthesize ɑ, β-unsaturated carboxylic acid
    • Jiang, D.; Wang, Y.Y.; Xu, Y.N.; Dai, L.Y. Doebner condensation in ionic liquids [Bmim]BF4 and [Bpy]BF4 to synthesize ɑ, β-unsaturated carboxylic acid. Chin. Chem. Lett. 2009, 20(3), 279-282.
    • (2009) Chin. Chem. Lett , vol.20 , Issue.3 , pp. 279-282
    • Jiang, D.1    Wang, Y.Y.2    Xu, Y.N.3    Dai, L.Y.4
  • 119
    • 9044235171 scopus 로고
    • Tilden Lecture. Applications of microwave dielectric heating effects to synthetic problems in chemistry
    • Mingos, D.M.P.; Baghurst, D.R. Tilden Lecture. Applications of microwave dielectric heating effects to synthetic problems in chemistry. Chem. Soc. Rev. 1991, 20(1), 1-47.
    • (1991) Chem. Soc. Rev , vol.20 , Issue.1 , pp. 1-47
    • Mingos, D.M.P.1    Baghurst, D.R.2
  • 121
    • 34447552438 scopus 로고    scopus 로고
    • Solvent free microwave assisted Doebner reaction: A green method for the preparation of cinnamic acids
    • Khabazzadeh, H.; Nejad, R.M.; Sheibani, H.; Saidi, K. Solvent free microwave assisted Doebner reaction: A green method for the preparation of cinnamic acids. Catal. Commun. 2007, 8(9), 1411-1413.
    • (2007) Catal. Commun , vol.8 , Issue.9 , pp. 1411-1413
    • Khabazzadeh, H.1    Nejad, R.M.2    Sheibani, H.3    Saidi, K.4
  • 122
    • 36849069431 scopus 로고    scopus 로고
    • gem-dibromomethylarenes: A convenient substitute for noncommercial aldehydes in the Knoevenagel-Doebner reaction for the synthesis of ɑ,β- unsaturated carboxylic acids
    • Augustine, J.K.; Naik, Y.A.; Mandal, A.B.; Chowdappa, N.; Praveen, V.B. gem-dibromomethylarenes: A convenient substitute for noncommercial aldehydes in the Knoevenagel-Doebner reaction for the synthesis of ɑ,β- unsaturated carboxylic acids. J. Org. Chem. 2007, 72(25), 9854-9856.
    • (2007) J. Org. Chem , vol.72 , Issue.25 , pp. 9854-9856
    • Augustine, J.K.1    Naik, Y.A.2    Mandal, A.B.3    Chowdappa, N.4    Praveen, V.B.5
  • 123
    • 0032578889 scopus 로고    scopus 로고
    • The ultrasound promoted Knoevenagel condensation of aromatic aldehydes
    • McNulty, J.; Steere, J.A.; Wolf, S. The ultrasound promoted Knoevenagel condensation of aromatic aldehydes. Tetrahedron Lett. 1998, 39(44), 8013- 8016.
    • (1998) Tetrahedron Lett , vol.39 , Issue.44 , pp. 8013-8016
    • McNulty, J.1    Steere, J.A.2    Wolf, S.3
  • 124
    • 0038737165 scopus 로고    scopus 로고
    • Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield
    • Kaupp, G.; Reza Naimi-Jamal, M.; Schmeyers, J. Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield. Tetrahedron 2003, 59(21), 3753-3760.
    • (2003) Tetrahedron , vol.59 , Issue.21 , pp. 3753-3760
    • Kaupp, G.1    Reza Naimi-Jamal, M.2    Schmeyers, J.3
  • 125
    • 28944451360 scopus 로고    scopus 로고
    • A Practical, efficient, and atom economic alternative to the Wittig and Horner-Wadsworth-Emmons reactions for the synthesis of(E)-ɑ,β- unsaturated esters from aldehydes
    • List, B.; Doehring, A.; Hechavarria Fonseca, M.T.; Job, A.; Rios Torres, R. A Practical, efficient, and atom economic alternative to the Wittig and Horner-Wadsworth-Emmons reactions for the synthesis of(E)-ɑ,β- unsaturated esters from aldehydes. Tetrahedron 2006, 62(2-3), 476-482.
    • (2006) Tetrahedron , vol.62 , Issue.2-3 , pp. 476-482
    • List, B.1    Doehring, A.2    Hechavarria Fonseca, M.T.3    Job, A.4    Rios Torres, R.5
  • 126
    • 84961979098 scopus 로고    scopus 로고
    • Mechanism of the organocatalyzed decarboxylative Knoevenagel-Doebner reaction. A theoretical study
    • Bermúdez, E.; Ventura, O.N.; Méndez, P.S. Mechanism of the organocatalyzed decarboxylative Knoevenagel-Doebner reaction. A theoretical study. J. Phys. Chem. A 2010, 114(50), 13086-13092.
    • (2010) J. Phys. Chem. A , vol.114 , Issue.50 , pp. 13086-13092
    • Bermúdez, E.1    Ventura, O.N.2    Méndez, P.S.3
  • 128
    • 79955449980 scopus 로고    scopus 로고
    • First bovine serum albumin-promoted synthesis of enones, cinnamic acids and coumarins in ionic liquid: An insight into the role of protein impurities in porcine pancreas lipase for olefinic bond formation
    • Sharma, N.; Sharma, U.K.; Kumar, R.; Katoch, N.; Sinha, A.K. First bovine serum albumin-promoted synthesis of enones, cinnamic acids and coumarins in ionic liquid: An insight into the role of protein impurities in porcine pancreas lipase for olefinic bond formation. Adv. Synth. Catal. 2011, 353(6), 871-878.
    • (2011) Adv. Synth. Catal , vol.353 , Issue.6 , pp. 871-878
    • Sharma, N.1    Sharma, U.K.2    Kumar, R.3    Katoch, N.4    Sinha, A.K.5
  • 129
    • 79960281863 scopus 로고    scopus 로고
    • Organocatalytic decarboxylative Doebner-Knoevenagel reactions between arylaldehydes and monoethyl malonate mediated by a bifunctional polymeric catalyst
    • Lu, J.; Toy, P.H. Organocatalytic decarboxylative Doebner-Knoevenagel reactions between arylaldehydes and monoethyl malonate mediated by a bifunctional polymeric catalyst. Synlett 2011, (12), 1723-1726.
    • (2011) Synlett , Issue.12 , pp. 1723-1726
    • Lu, J.1    Toy, P.H.2
  • 130
    • 80054702904 scopus 로고    scopus 로고
    • Alum [KA1(S0 4) 2. 12H 20]: An efficient, novel, clean, catalyst for Doebner Knoevenagel reaction for the efficient production of ɑβ-unsaturated acids
    • Suresh, D.K.; Sandhu, J.S. Alum [KA1(S0 4) 2. 12H 20]: An efficient, novel, clean, catalyst for Doebner Knoevenagel reaction for the efficient production of ɑβ-unsaturated acids. Indian J. Chem. Sect. B 2011, 50(10), 1479-1483.
    • (2011) Indian J. Chem. Sect. B , vol.50 , Issue.10 , pp. 1479-1483
    • Suresh, D.K.1    Sandhu, J.S.2
  • 131
    • 84862925036 scopus 로고    scopus 로고
    • β- alanine-DBU: A highly efficient catalytic system for knoevenagel-doebner reaction under mild conditions
    • Zhu, L.; Lei, N.; Miao, Z.; Sheng, C.; Zhuang, C.; Yao, J.; Zhang, W. β- alanine-DBU: A highly efficient catalytic system for knoevenagel-doebner reaction under mild conditions. Chin. J. Chem. 2012, 30(1), 139-143.
    • (2012) Chin. J. Chem , vol.30 , Issue.1 , pp. 139-143
    • Zhu, L.1    Lei, N.2    Miao, Z.3    Sheng, C.4    Zhuang, C.5    Yao, J.6    Zhang, W.7
  • 132
    • 53849125438 scopus 로고    scopus 로고
    • Practical synthesis of(E)-ɑ,β- unsaturated carboxylic acids using a one-pot hydroformylation/decarboxylative Knoevenagel reaction sequence
    • Kemme, S.T.; Šmejkal, T.; Breita, B. Practical synthesis of(E)-ɑ,β- unsaturated carboxylic acids using a one-pot hydroformylation/decarboxylative Knoevenagel reaction sequence. Adv. Synth. Catal. 2008, 350(7-8), 989-994.
    • (2008) Adv. Synth. Catal , vol.350 , Issue.7-8 , pp. 989-994
    • Kemme, S.T.1    Šmejkal, T.2    Breita, B.3
  • 133
    • 27544514442 scopus 로고    scopus 로고
    • Bidentate Ligands by Self- Assembly through Hydrogen Bonding: A General Room Temperature/Ambient Pressure Regioselective Hydroformylation of Terminal Alkenes
    • Seiche, W.; Schuschkowski, A.; Breit, B. Bidentate Ligands by Self- Assembly through Hydrogen Bonding: A General Room Temperature/Ambient Pressure Regioselective Hydroformylation of Terminal Alkenes. Adv. Synth. Catal. 2005, 347(11-13), 1488-1494.
    • (2005) Adv. Synth. Catal , vol.347 , Issue.11-13 , pp. 1488-1494
    • Seiche, W.1    Schuschkowski, A.2    Breit, B.3
  • 134
    • 0038547968 scopus 로고    scopus 로고
    • Hydrogen Bonding as a Construction Element for Bidentate Donor Ligands in Homogeneous Catalysis:β Regioselective Hydroformylation of Terminal Alkenes
    • Breit, B.; Seiche, W. Hydrogen Bonding as a Construction Element for Bidentate Donor Ligands in Homogeneous Catalysis:β Regioselective Hydroformylation of Terminal Alkenes. J. Am. Chem. Soc. 2003, 125(22), 6608-6609.
    • (2003) J. Am. Chem. Soc , vol.125 , Issue.22 , pp. 6608-6609
    • Breit, B.1    Seiche, W.2
  • 135
    • 0001065518 scopus 로고
    • Condensed O-, Nheterocycles by the transformation of azidoacrylates
    • Krutosikova, A.; Dandarova, M.; Chylova, J.; Vegh, D. Condensed O-, Nheterocycles by the transformation of azidoacrylates. Monatsh. Chem. 1992, 123(8-9), 807-815.
    • (1992) Monatsh. Chem , vol.123 , Issue.8-9 , pp. 807-815
    • Krutosikova, A.1    Dandarova, M.2    Chylova, J.3    Vegh, D.4
  • 136
    • 0000426566 scopus 로고
    • Substituted vinyl azides in the synthesis of condensed nitrogen heterocycles
    • Krutošíková, A.; Dandárová, M.; Alföldi, J. Substituted vinyl azides in the synthesis of condensed nitrogen heterocycles. Chem. Pap. 1994, 48(4), 268- 273.
    • (1994) Chem. Pap , vol.48 , Issue.4 , pp. 268-273
    • Krutošíková, A.1    Dandárová, M.2    Alföldi, J.3
  • 137
    • 21844502033 scopus 로고
    • Synthesis of pyrrolo[2′,3′:4,5]furo[3,2- c]pyridines
    • Bencková, M.; Krutošíková, A. Synthesis of pyrrolo[2′,3′:4,5]furo[3,2- c]pyridines. Monatsh. Chem. 1995, 126(6-7), 753-758.
    • (1995) Monatsh. Chem , vol.126 , Issue.6-7 , pp. 753-758
    • Bencková, M.1    Krutošíková, A.2
  • 138
    • 21844501039 scopus 로고
    • Synthesis and reactions of 2,3- dimethylfuro[3,2-c]pyridines
    • Bobošík, V.; Krutošíková, A.; Jordis, U. Synthesis and reactions of 2,3- dimethylfuro[3,2-c]pyridines. Monatsh. Chem. 1995, 126(6-7), 747-752.
    • (1995) Monatsh. Chem , vol.126 , Issue.6-7 , pp. 747-752
    • Bobošík, V.1    Krutošíková, A.2    Jordis, U.3
  • 139
    • 0030360750 scopus 로고    scopus 로고
    • Synthesis of 2-arylfuro [3, 2-c] pyridines and their derivatives
    • Krutošíková, A.; Sleziak, R. Synthesis of 2-arylfuro [3, 2-c] pyridines and their derivatives. Collect. Czech. Chem. Commun. 1996, 61(11), 1627-1636.
    • (1996) Collect. Czech. Chem. Commun , vol.61 , Issue.11 , pp. 1627-1636
    • Krutošíková, A.1    Sleziak, R.2
  • 140
    • 0009274905 scopus 로고    scopus 로고
    • Synthesis of Pyrrolo [2', 3': 4, 5] Furo [3, 2- c] Pyridine-2-Carboxylic Acids
    • Bencková, M.; Krutošíková, A. Synthesis of Pyrrolo [2', 3': 4, 5] Furo [3, 2- c] Pyridine-2-Carboxylic Acids. Molecules 1997, 1(10), 163-165.
    • (1997) Molecules , vol.1 , Issue.10 , pp. 163-165
    • Bencková, M.1    Krutošíková, A.2
  • 141
    • 0040708672 scopus 로고    scopus 로고
    • 5-Aminofuro [3, 2-c] pyridinium tosylates and substituted furo [3, 2-c] pyridine N-oxides: Synthesis and reactions
    • Bencková, M.; Krutošíková, A. 5-Aminofuro [3, 2-c] pyridinium tosylates and substituted furo [3, 2-c] pyridine N-oxides: Synthesis and reactions. Collect. Czech. Chem. Commun. 1999, 64(3), 539-547.
    • (1999) Collect. Czech. Chem. Commun , vol.64 , Issue.3 , pp. 539-547
    • Bencková, M.1    Krutošíková, A.2
  • 143
    • 46649114772 scopus 로고    scopus 로고
    • Synthesis and reactions of 2-[3-(trifluoromethyl)phenyl]furo[3,2-c]pyridine
    • Bradiaková, I.; Prónayová, N.; Gatial, A.; Krutošíková, A. Synthesis and reactions of 2-[3-(trifluoromethyl)phenyl]furo[3,2-c]pyridine. Chem. Pap. 2008, 62(4), 428-434.
    • (2008) Chem. Pap , vol.62 , Issue.4 , pp. 428-434
    • Bradiaková, I.1    Prónayová, N.2    Gatial, A.3    Krutošíková, A.4
  • 144
    • 62349089364 scopus 로고    scopus 로고
    • [1]Benzofuro[3,2-c]pyridine synthesis and coordination reactions
    • Mojumdar, S.C.; Šimon, P.; Krutošíková, A. [1]Benzofuro[3,2-c]pyridine synthesis and coordination reactions. J. Therm. Anal. Calorim. 2009, 96(1), 103-109.
    • (2009) J. Therm. Anal. Calorim , vol.96 , Issue.1 , pp. 103-109
    • Mojumdar, S.C.1    Šimon, P.2    Krutošíková, A.3
  • 145
    • 0043136369 scopus 로고    scopus 로고
    • Cinacalcet HCl: A calcimimetic agent for the management of primary and secondary hyperparathyroidism
    • Franceschini, N.; Joy, M.S.; Kshirsagar, A. Cinacalcet HCl: a calcimimetic agent for the management of primary and secondary hyperparathyroidism. Expert Opin. Invest. Drugs 2003, 12(8), 1413-1421.
    • (2003) Expert Opin. Invest. Drugs , vol.12 , Issue.8 , pp. 1413-1421
    • Franceschini, N.1    Joy, M.S.2    Kshirsagar, A.3
  • 146
    • 0031733696 scopus 로고    scopus 로고
    • Clinical epidemiology of cardiovascular disease in chronic renal disease
    • Foley, R.N.; Parfrey, P.S.; Sarnak, M.J. Clinical epidemiology of cardiovascular disease in chronic renal disease. Am. J. Kidney Dis. 1998, 32(5), S112-S119.
    • (1998) Am. J. Kidney Dis , vol.32 , Issue.5 , pp. 112-119
    • Foley, R.N.1    Parfrey, P.S.2    Sarnak, M.J.3
  • 147
  • 148
    • 0017246498 scopus 로고
    • Gaschromatographischmassenspektrometrische Untersuchungen über die Bildung von Phenolen und aromatischen Kohlenwasserstoffen in Lebensmitteln
    • Tressl, R.; Kossa, T.; Renner, R.; Köppler, H. Gaschromatographischmassenspektrometrische Untersuchungen über die Bildung von Phenolen und aromatischen Kohlenwasserstoffen in Lebensmitteln. Z. Lebensm.-Unters.- Forsch. 1976, 162(2), 123-130.
    • (1976) Z. Lebensm.-Unters.- Forsch , vol.162 , Issue.2 , pp. 123-130
    • Tressl, R.1    Kossa, T.2    Renner, R.3    Köppler, H.4
  • 149
    • 0018107687 scopus 로고
    • Simple Phenol and Phenolic Compounds in Food Flavor
    • Maga, J.A. Simple Phenol and Phenolic Compounds in Food Flavor. Crit. Rev. Food Sci. Nutr. 1978, 10, 323-372.
    • (1978) Crit. Rev. Food Sci. Nutr , vol.10 , pp. 323-372
    • Maga, J.A.1
  • 152
    • 0028458785 scopus 로고
    • Epoxidation of styrene and substituted styrenes by whole cells of Mycobacterium sp. M156
    • Stuart, R.R.; Colette, S.M.; David, J.L. Epoxidation of styrene and substituted styrenes by whole cells of Mycobacterium sp. M156. Bioorg. Med. Chem. 1994, 2, 553-556.
    • (1994) Bioorg. Med. Chem , vol.2 , pp. 553-556
    • Stuart, R.R.1    Colette, S.M.2    David, J.L.3
  • 153
    • 0033536252 scopus 로고    scopus 로고
    • Carbonylation reactions: 7. Regioselective synthesis of 2-arylpropionic acids by catalytic carbonylation of styrene derivatives in the presence of palladium compounds: The critical role of the counter anion
    • Michel, C.B.; Adriano, L.M.; Igor, T. Carbonylation reactions: 7. Regioselective synthesis of 2-arylpropionic acids by catalytic carbonylation of styrene derivatives in the presence of palladium compounds: the critical role of the counter anion. J. Mol. Catal. A: Chem. 1999, 143, 131-136.
    • (1999) J. Mol. Catal. A: Chem , vol.143 , pp. 131-136
    • Michel, C.B.1    Adriano, L.M.2    Igor, T.3
  • 154
    • 0034606911 scopus 로고    scopus 로고
    • One-pot selective synthesis of β- nitrostyrenes from styrenes, promoted by Cu(II)
    • Campos, P.J.; Garcia, B.; Rodriguez, M.A. One-pot selective synthesis of β- nitrostyrenes from styrenes, promoted by Cu(II). Tetrahedron Lett. 2000, 41, 979-982.
    • (2000) Tetrahedron Lett , vol.41 , pp. 979-982
    • Campos, P.J.1    Garcia, B.2    Rodriguez, M.A.3
  • 155
    • 0028479742 scopus 로고
    • Photocrosslinking of Poly(4- hydroxystyrene) via Electrophilic Aromatic Substitution: Use of Polyfunctional Benzylic Alcohols in the Design of Chemically Amplified Resist Materials with Tunable Sensitivities
    • Lee, S.M.; Frechet, J.M.J.; Willson, C.G. Photocrosslinking of Poly(4- hydroxystyrene) via Electrophilic Aromatic Substitution: Use of Polyfunctional Benzylic Alcohols in the Design of Chemically Amplified Resist Materials with Tunable Sensitivities. Macromolecules 1994, 27, 5154- 5159.
    • (1994) Macromolecules , vol.27 , pp. 5154-5159
    • Lee, S.M.1    Frechet, J.M.J.2    Willson, C.G.3
  • 156
    • 0032099157 scopus 로고    scopus 로고
    • Anionic polymerization of 3,5-(2,4-)dimethoxystyrene and 2,4,6-trimethoxystyrene and functionalization of the resulting polymers by lithiation
    • Atsushi, T.; Atsushi, M.; Takeo, K.; Yoshinobu, I. Anionic polymerization of 3,5-(2,4-)dimethoxystyrene and 2,4,6-trimethoxystyrene and functionalization of the resulting polymers by lithiation. React. Funct. Polym. 1998, 37, 39-47.
    • (1998) React. Funct. Polym , vol.37 , pp. 39-47
    • Atsushi, T.1    Atsushi, M.2    Takeo, K.3    Yoshinobu, I.4
  • 157
    • 0030186848 scopus 로고    scopus 로고
    • Phenolic and other metabolites of Phellinus pini, a fungus pathogenic to pine
    • William, A.A.; David, J.M.; Priyotosh, C. Phenolic and other metabolites of Phellinus pini, a fungus pathogenic to pine. Phytochemistry 1996, 42, 1321- 1324.
    • (1996) Phytochemistry , vol.42 , pp. 1321-1324
    • William, A.A.1    David, J.M.2    Priyotosh, C.3
  • 158
    • 3142581964 scopus 로고    scopus 로고
    • Antioxidative and antimutagenic activities of 4-vinyl- 2, 6-dimethoxyphenol(canolol) isolated from canola oil
    • Kuwahara, H.; Kanazawa, A.; Wakamatu, D.; Morimura, S.; Kida, K.; Akaike, T.; Maeda, H. Antioxidative and antimutagenic activities of 4-vinyl- 2, 6-dimethoxyphenol(canolol) isolated from canola oil. J. Agric. Food Chem. 2004, 52, 4380-4387.
    • (2004) J. Agric. Food Chem , vol.52 , pp. 4380-4387
    • Kuwahara, H.1    Kanazawa, A.2    Wakamatu, D.3    Morimura, S.4    Kida, K.5    Akaike, T.6    Maeda, H.7
  • 159
    • 11144219950 scopus 로고    scopus 로고
    • Impact of isolation method on the antioxidant activity of rapeseed meal phenolics
    • Vuorela, S.; Meyer, A.S.; Heinonen, M. Impact of isolation method on the antioxidant activity of rapeseed meal phenolics. J. Agric. Food Chem. 2004, 52, 8202-8207.
    • (2004) J. Agric. Food Chem , vol.52 , pp. 8202-8207
    • Vuorela, S.1    Meyer, A.S.2    Heinonen, M.3
  • 160
    • 0037051266 scopus 로고    scopus 로고
    • Direct synthesis of styrene by rhodium-catalyzed oxidative arylation of ethylene with benzene
    • Matsumoto, T.; Periana, R.A.; Taube, D.J.; Yoshida, H. Direct synthesis of styrene by rhodium-catalyzed oxidative arylation of ethylene with benzene. J. Catal. 2002, 206, 272-280.
    • (2002) J. Catal , vol.206 , pp. 272-280
    • Matsumoto, T.1    Periana, R.A.2    Taube, D.J.3    Yoshida, H.4
  • 161
    • 27744447605 scopus 로고    scopus 로고
    • Microwave-Enhanced Synthesis of NShifted Buflavine Analogues via a Suzuki-Ring-Closing Metathesis Protocol
    • Prasad, A.; Dehaen, W.; Eycken, E.V. Microwave-Enhanced Synthesis of NShifted Buflavine Analogues via a Suzuki-Ring-Closing Metathesis Protocol. Org. Lett. 2005, 7, 2723-2726.
    • (2005) Org. Lett , vol.7 , pp. 2723-2726
    • Prasad, A.1    Dehaen, W.2    Eycken, E.V.3
  • 162
    • 0037067557 scopus 로고    scopus 로고
    • Generation of Substituted Styrenes via Suzuki Cross-Coupling of Aryl Halides with 2,4,6-Trivinylcyclotriboroxane
    • Kerins, F.; O'Shea, D.F. Generation of Substituted Styrenes via Suzuki Cross-Coupling of Aryl Halides with 2,4,6-Trivinylcyclotriboroxane. J. Org. Chem. 2002, 67, 4968-4971.
    • (2002) J. Org. Chem , vol.67 , pp. 4968-4971
    • Kerins, F.1    O'Shea, D.F.2
  • 163
    • 33845436407 scopus 로고    scopus 로고
    • One-pot two-step synthesis of 4- vinylphenols from 4-hydroxy substituted benzaldehydes under microwave irradiation: A new perspective on the classical Knoevenagel-Doebner reaction
    • Sinha, A.K.; Sharma, A.; Joshi, B.P. One-pot two-step synthesis of 4- vinylphenols from 4-hydroxy substituted benzaldehydes under microwave irradiation: a new perspective on the classical Knoevenagel-Doebner reaction. Tetrahedron 2007, 63(4), 960-965.
    • (2007) Tetrahedron , vol.63 , Issue.4 , pp. 960-965
    • Sinha, A.K.1    Sharma, A.2    Joshi, B.P.3
  • 164
    • 34250642402 scopus 로고    scopus 로고
    • Bioinspired metalcatalysed Doebner-Knoevenagel condensations between malonic acid half thioesters and aldehydes
    • Berrué, F.; Antoniotti, S.; Thomas, O.P.; Amade, P. Bioinspired metalcatalysed Doebner-Knoevenagel condensations between malonic acid half thioesters and aldehydes. Eur. J. Org. Chem. 2007, 2007(11), 1743-1748.
    • (2007) Eur. J. Org. Chem , vol.2007 , Issue.11 , pp. 1743-1748
    • Berrué, F.1    Antoniotti, S.2    Thomas, O.P.3    Amade, P.4
  • 165
    • 0034682909 scopus 로고    scopus 로고
    • A New Role for Polyketides
    • Rohr, J. A New Role for Polyketides. Angew. Chem. Int. Ed. 2000, 39(16), 2847-2849.
    • (2000) Angew. Chem. Int. Ed , vol.39 , Issue.16 , pp. 2847-2849
    • Rohr, J.1
  • 166
    • 19744363827 scopus 로고    scopus 로고
    • Catalytic Enantioselective Thioester Aldol reactions that rre compatible with protic functional groups
    • Magdziak, D.; Lalic, G.; Lee, H.M.; Fortner, K.C.; Aloise, A.D.; Shair, M.D. Catalytic Enantioselective Thioester Aldol reactions that rre compatible with protic functional groups. J. Am. Chem. Soc. 2005, 127, 7284-7285.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 7284-7285
    • Magdziak, D.1    Lalic, G.2    Lee, H.M.3    Fortner, K.C.4    Aloise, A.D.5    Shair, M.D.6
  • 167
    • 78649462912 scopus 로고    scopus 로고
    • The knoevenagel-doebner reaction on 1,2-O-(2,2,2-Trichloroethylidene) derivatives of D-Gluco- and D-Mannofuranose
    • Kök, G.; Karayildirim, T.; Ay, K.; Ay, E. The knoevenagel-doebner reaction on 1,2-O-(2,2,2-Trichloroethylidene) derivatives of D-Gluco- and D-Mannofuranose. Molecules 2010, 15(11), 7724-7731.
    • (2010) Molecules , vol.15 , Issue.11 , pp. 7724-7731
    • Kök, G.1    Karayildirim, T.2    Ay, K.3    Ay, E.4
  • 169
    • 0036182796 scopus 로고    scopus 로고
    • Glycodendrimers: Novel glycotope isosteres unmasking sugar coding. Case study with T-antigen markers from breast cancer MUC1 glycoprotein
    • Roy, R.; Baek, M.-G. Glycodendrimers: novel glycotope isosteres unmasking sugar coding. Case study with T-antigen markers from breast cancer MUC1 glycoprotein. Rev. Mol. Biotechnol. 2002, 90(3-4), 291-309.
    • (2002) Rev. Mol. Biotechnol , vol.90 , Issue.3-4 , pp. 291-309
    • Roy, R.1    Baek, M.-G.2
  • 170
    • 0000358206 scopus 로고
    • Carbohydrate-Protein Interactions: Basis of Glycobiology
    • Lee, Y.C.; Lee, R.T. Carbohydrate-Protein Interactions: Basis of Glycobiology. Acc. Chem. Res. 1995, 28(8), 321-327.
    • (1995) Acc. Chem. Res , vol.28 , Issue.8 , pp. 321-327
    • Lee, Y.C.1    Lee, R.T.2
  • 171
    • 0036462602 scopus 로고    scopus 로고
    • The Cluster Glycoside Effect
    • Lundquist, J.J.; Toone, E.J. The Cluster Glycoside Effect. Chem. Rev. 2002, 102(2), 555-578.
    • (2002) Chem. Rev , vol.102 , Issue.2 , pp. 555-578
    • Lundquist, J.J.1    Toone, E.J.2
  • 172
  • 174
    • 84866747276 scopus 로고    scopus 로고
    • Synthesis and properties of macrocyclic diazene switch with binaphthalene unit attached via acrylamide linkers
    • Kicková, A.; Horváth, B.; Kerner, L.; Putala, M. Synthesis and properties of macrocyclic diazene switch with binaphthalene unit attached via acrylamide linkers. Chem. Pap. 2013, 67(1), 101-109.
    • (2013) Chem. Pap , vol.67 , Issue.1 , pp. 101-109
    • Kicková, A.1    Horváth, B.2    Kerner, L.3    Putala, M.4
  • 175
    • 77949304370 scopus 로고    scopus 로고
    • Combined Transition-Metal- and Organocatalysis: An atom economic C3 homologation of alkenes to carbonyl and carboxylic compounds
    • Kemme, S.T.; Šmejkal, T.; Breit, B. Combined Transition-Metal- and Organocatalysis: An atom economic C3 homologation of alkenes to carbonyl and carboxylic compounds. Chem. Eur. J. 2010, 16(11), 3423-3433.
    • (2010) Chem. Eur. J , vol.16 , Issue.11 , pp. 3423-3433
    • Kemme, S.T.1    Šmejkal, T.2    Breit, B.3
  • 176
    • 0035906868 scopus 로고    scopus 로고
    • Domino Hydroformylation/Knoevenagel/Hydrogenation Reactions
    • Breit, B.; Zahn, S.K. Domino Hydroformylation/Knoevenagel/Hydrogenation Reactions. Angew. Chem. Int. Ed. 2001, 40(10), 1910-1913.
    • (2001) Angew. Chem. Int. Ed , vol.40 , Issue.10 , pp. 1910-1913
    • Breit, B.1    Zahn, S.K.2
  • 177
    • 78650884357 scopus 로고    scopus 로고
    • A stereoselective and practical synthesis of (E)-ɑ,β-unsaturated ketones from aldehydes
    • Balducci, E.; Attolino, E.; Taddei, M. A stereoselective and practical synthesis of (E)-ɑ,β-unsaturated ketones from aldehydes. Eur. J. Org. Chem. 2011, 2011(2), 311-318.
    • (2011) Eur. J. Org. Chem , vol.2011 , Issue.2 , pp. 311-318
    • Balducci, E.1    Attolino, E.2    Taddei, M.3
  • 178
    • 33748606917 scopus 로고    scopus 로고
    • Microwaves Make Hydroformylation a Rapid and Easy Process
    • Petricci, E.; Mann, A.; Schoenfelder, A.; Rota, A.; Taddei, M. Microwaves Make Hydroformylation a Rapid and Easy Process. Org. Lett. 2006, 8(17), 3725-3727.
    • (2006) Org. Lett , vol.8 , Issue.17 , pp. 3725-3727
    • Petricci, E.1    Mann, A.2    Schoenfelder, A.3    Rota, A.4    Taddei, M.5
  • 179
    • 77949847412 scopus 로고    scopus 로고
    • Microwave- Assisted Carbonylation and Cyclocarbonylation of Aryl Iodides under Ligand Free Heterogeneous Catalysis
    • Salvadori, J.; Balducci, E.; Zaza, S.; Petricci, E.; Taddei, M. Microwave- Assisted Carbonylation and Cyclocarbonylation of Aryl Iodides under Ligand Free Heterogeneous Catalysis. J. Org. Chem. 2010, 75(6), 1841- 1847.
    • (2010) J. Org. Chem , vol.75 , Issue.6 , pp. 1841-1847
    • Salvadori, J.1    Balducci, E.2    Zaza, S.3    Petricci, E.4    Taddei, M.5
  • 180
    • 77951111748 scopus 로고    scopus 로고
    • Rhodiumcatalyzed multicomponent synthesis of chiral oxazolopiperidines
    • Salvadori, J.; Airiau, E.; Girard, N.; Mann, A.; Taddei, M. Rhodiumcatalyzed multicomponent synthesis of chiral oxazolopiperidines. Tetrahedron 2010, 66(21), 3749-3753.
    • (2010) Tetrahedron , vol.66 , Issue.21 , pp. 3749-3753
    • Salvadori, J.1    Airiau, E.2    Girard, N.3    Mann, A.4    Taddei, M.5
  • 181
    • 0001739879 scopus 로고
    • Amino acid catalysis of the knoevenagel reaction
    • Prout, F.S. Amino acid catalysis of the knoevenagel reaction. J. Org. Chem. 1953, 18(8), 928-933.
    • (1953) J. Org. Chem , vol.18 , Issue.8 , pp. 928-933
    • Prout, F.S.1
  • 182
    • 0347309432 scopus 로고
    • A one-step synthesis of cinnamic acids using malonic acid: The verley-doebner modification of the Knoevenagel condensation
    • Kolb, K.E.; Field, K.W.; Schatz, P.F. A one-step synthesis of cinnamic acids using malonic acid: The verley-doebner modification of the Knoevenagel condensation. J. Chem. Educ. 1990, 67(12), A304.
    • (1990) J. Chem. Educ , vol.67 , Issue.12
    • Kolb, K.E.1    Field, K.W.2    Schatz, P.F.3
  • 183
    • 33749427826 scopus 로고    scopus 로고
    • Reactions of 3-isochromanone with aromatic aldehydes-microwave assisted condensations performed on solid basic inorganic supports
    • Vass, A.; Földesi, A.; Lóránd, T. Reactions of 3-isochromanone with aromatic aldehydes-microwave assisted condensations performed on solid basic inorganic supports. J. Biochem. Biophys. Methods 2006, 69(1-2), 179- 187.
    • (2006) J. Biochem. Biophys. Methods , vol.69 , Issue.1-2 , pp. 179-187
    • Vass, A.1    Földesi, A.2    Lóránd, T.3
  • 184
    • 27944442776 scopus 로고    scopus 로고
    • Knoevenagel reaction of diethylphosphonoacetic acid: A facile route to diethyl(E)-2-arylvinylphosphonates
    • Krawczyk, H.; Albrecht, L. Knoevenagel reaction of diethylphosphonoacetic acid: a facile route to diethyl(E)-2-arylvinylphosphonates. Synthesis 2005, 2887-2896.
    • (2005) Synthesis , pp. 2887-2896
    • Krawczyk, H.1    Albrecht, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.