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Volumn 214, Issue 2-3, 2010, Pages 135-144

The synthesis, X-ray crystal structure and optical properties of novel 5-aryl-1-arylthiazolyl-3-ferrocenyl-pyrazoline derivatives

Author keywords

Ferrocene; Fluorescence; Pyrazoline; Thiazole; UV absorption; X ray

Indexed keywords


EID: 77956058773     PISSN: 10106030     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jphotochem.2010.06.017     Document Type: Article
Times cited : (31)

References (50)
  • 2
    • 65449125022 scopus 로고    scopus 로고
    • Microwave assisted synthesis of new indophenazine 1,3,5-trisubstruted pyrazoline derivatives of benzofuran and their antimicrobial activity
    • K. Manna, and Y.K. Agrawal Microwave assisted synthesis of new indophenazine 1,3,5-trisubstruted pyrazoline derivatives of benzofuran and their antimicrobial activity Bioorg. Med. Chem. Lett. 19 2009 2688 2692
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 2688-2692
    • Manna, K.1    Agrawal, Y.K.2
  • 3
    • 64249130496 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of 1-(benzofuran-2-yl)-4-nitro-3- arylbutan-1-ones and 3-(benzofuran-2-yl)-4,5-dihydro-5-aryl-1-[4-(aryl)-1,3- thiazol-2-yl]-1H-pyrazoles
    • B.F. Abdel-Wahab, H.A. Abdel-Aziz, and E.M. Ahmed Synthesis and antimicrobial evaluation of 1-(benzofuran-2-yl)-4-nitro-3-arylbutan-1-ones and 3-(benzofuran-2-yl)-4,5-dihydro-5-aryl-1-[4-(aryl)-1,3-thiazol-2-yl] -1H-pyrazoles Eur. J. Med. Chem. 44 2009 2632 2635
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 2632-2635
    • Abdel-Wahab, B.F.1    Abdel-Aziz, H.A.2    Ahmed, E.M.3
  • 4
    • 63149126903 scopus 로고    scopus 로고
    • C-Furyl glycosides, II: Synthesis and antimicrobial evaluation of C-furyl glycosides bearing pyrazolines, isoxazolines, and 5,6-dihydropyrimidine-2(1H)- thiones
    • W.A. El-Sayed, I.F. Nassar, and A.A.-H. Abdel-Rahman C-Furyl glycosides, II: synthesis and antimicrobial evaluation of C-furyl glycosides bearing pyrazolines, isoxazolines, and 5,6-dihydropyrimidine-2(1H)-thiones Monatshefte für Chemie 140 2009 365 370
    • (2009) Monatshefte für Chemie , vol.140 , pp. 365-370
    • El-Sayed, W.A.1    Nassar, I.F.2    Abdel-Rahman, A.A.-H.3
  • 5
    • 77956058841 scopus 로고    scopus 로고
    • Synthesis and antimicrobial studies of some novel pyrazoline and isoxazoline derivatives
    • S.B Jadhav, R.A. Shastri, K.V. Gaikwad, and S.V. Gaikwad Synthesis and antimicrobial studies of some novel pyrazoline and isoxazoline derivatives E.-J. Chem. 6 S1 2009 S183 S188
    • (2009) E.-J. Chem. , vol.6 , Issue.S1
    • Jadhav, S.B.1    Shastri, R.A.2    Gaikwad, K.V.3    Gaikwad, S.V.4
  • 6
    • 57949101849 scopus 로고    scopus 로고
    • Synthesis, spectral studies and antiamoebic activity of new 1-N-substituted thiocarbamoyl-3-phenyl-2-pyrazolines
    • M. Abid, A.R. Bhat, F. Athar, and A. Azam Synthesis, spectral studies and antiamoebic activity of new 1-N-substituted thiocarbamoyl-3-phenyl-2- pyrazolines Eur. J. Med. Chem. 44 2009 417 425
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 417-425
    • Abid, M.1    Bhat, A.R.2    Athar, F.3    Azam, A.4
  • 7
    • 60549115097 scopus 로고    scopus 로고
    • Synthesis of new 2-(5-substituted-3-phenyl-2-pyrazolinyl)-1,3- thiazolino[5,4-b]quinoxaline derivatives and evaluation of their antiamoebic activity
    • A. Budakoti, A.R. Bhat, and A. Azam Synthesis of new 2-(5-substituted-3- phenyl-2-pyrazolinyl)-1,3-thiazolino[5,4-b]quinoxaline derivatives and evaluation of their antiamoebic activity Eur. J. Med. Chem. 44 2009 1317 1325
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 1317-1325
    • Budakoti, A.1    Bhat, A.R.2    Azam, A.3
  • 9
    • 61349169067 scopus 로고    scopus 로고
    • Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and evaluation of their anticancer activity
    • D. Havrylyuk, B. Zimenkovsky, O. Vasylenko, L. Zaprutko, and R. Lesyk Synthesis of novel thiazolone-based compounds containing pyrazoline moiety and evaluation of their anticancer activity Eur. J. Med. Chem. 44 2009 1396 1404
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 1396-1404
    • Havrylyuk, D.1    Zimenkovsky, B.2    Vasylenko, O.3    Zaprutko, L.4    Lesyk, R.5
  • 10
    • 58549107997 scopus 로고    scopus 로고
    • New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity
    • N. Gökhan-Keleki, S. Koyunolu, and S. Yabanolu New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity Bioorg. Med. Chem. 17 2009 675 689
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 675-689
    • Gökhan-Keleki, N.1    Koyunolu, S.2    Yabanolu, S.3
  • 11
    • 70349560117 scopus 로고    scopus 로고
    • Effects of some 1,3,5-trisubstitued-2-pyrazoline derivatives on depression and anxiety parameters of mice
    • Ö.D. Can, Ü.D. Ozkay, Z.A. Kaplancikli, and Y. Öztürk Effects of some 1,3,5-trisubstitued-2-pyrazoline derivatives on depression and anxiety parameters of mice Arch. Pharm. Res. 32 2009 1293 1299
    • (2009) Arch. Pharm. Res. , vol.32 , pp. 1293-1299
    • Can, Ö.D.1    Ozkay, Ü.D.2    Kaplancikli, Z.A.3    Öztürk, Y.4
  • 12
    • 33646023681 scopus 로고    scopus 로고
    • Novel bis(1-acyl-2-pyrazolines) of potential anti-inflammatory and molluscicidal properties
    • F.F. Barsoum, H.M. Hosni, and A.S. Girgis Novel bis(1-acyl-2-pyrazolines) of potential anti-inflammatory and molluscicidal properties Bioorg. Med. Chem. 14 2006 3929 3937
    • (2006) Bioorg. Med. Chem. , vol.14 , pp. 3929-3937
    • Barsoum, F.F.1    Hosni, H.M.2    Girgis, A.S.3
  • 13
    • 38849119065 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents
    • M. Amir, H. Kumar, and S.A. Khan Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents Bioorg. Med. Chem. Lett. 18 2008 918 922
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 918-922
    • Amir, M.1    Kumar, H.2    Khan, S.A.3
  • 14
    • 57849134109 scopus 로고    scopus 로고
    • Antiinflammatory activity of some new 1,3,5-trisubstituted pyrazolines bearing benzene sulfonamide
    • I.G. Rathish, K. Javed, S. Ahmad, S. Bano, and Synthesis Antiinflammatory activity of some new 1,3,5-trisubstituted pyrazolines bearing benzene sulfonamide Bioorg. Med. Chem. Lett. 19 2009 255 258
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 255-258
    • Rathish, I.G.1    Javed, K.2    Ahmad, S.3    Bano, S.4    Synthesis5
  • 15
    • 62549116959 scopus 로고    scopus 로고
    • Facile synthesis of bis(4,5-dihydro-1H-pyrazole-1-carboxamides) and their thio-analogues of potential PGE2 inhibitory properties
    • F.F. Barsoum, and A.S. Girgis Facile synthesis of bis(4,5-dihydro-1H- pyrazole-1-carboxamides) and their thio-analogues of potential PGE2 inhibitory properties Eur. J. Med. Chem. 44 2009 2172 2177
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 2172-2177
    • Barsoum, F.F.1    Girgis, A.S.2
  • 16
    • 61349181828 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of a novel series of 5-(substituted) aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agents
    • S. Khode, V. Maddi, P. Aragade, M. Palkar, P.K. Ronad, S. Mamledesai, A.H.M. Thippeswamy, and D. Satyanarayana Synthesis and pharmacological evaluation of a novel series of 5-(substituted) aryl-3-(3-coumarinyl)-1-phenyl- 2-pyrazolines as novel anti-inflammatory and analgesic agents Eur. J. Med. Chem. 44 2009 1682 1688
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 1682-1688
    • Khode, S.1    Maddi, V.2    Aragade, P.3    Palkar, M.4    Ronad, P.K.5    Mamledesai, S.6    Thippeswamy, A.H.M.7    Satyanarayana, D.8
  • 17
    • 67349227426 scopus 로고    scopus 로고
    • Synthesis and investigation of anti-inflammatory activity and gastric ulcerogenicity of novel nitric oxide-donating pyrazoline derivatives
    • M.E. Shoman, M. Abdel-Aziz, O.M. Aly, H.H. Farag, and M.A. Morsy Synthesis and investigation of anti-inflammatory activity and gastric ulcerogenicity of novel nitric oxide-donating pyrazoline derivatives Eur. J. Med. Chem. 44 2009 3068 3076
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 3068-3076
    • Shoman, M.E.1    Abdel-Aziz, M.2    Aly, O.M.3    Farag, H.H.4    Morsy, M.A.5
  • 18
    • 33846890851 scopus 로고    scopus 로고
    • Synthesis of novel light-emitting calix[4]arene derivatives and their luminescent properties
    • X.Q. Wei, G. Yang, J.B. Cheng, Z.Y. Lu, and M.G. Xie Synthesis of novel light-emitting calix[4]arene derivatives and their luminescent properties Opt. Mater. 29 2007 936 940
    • (2007) Opt. Mater. , vol.29 , pp. 936-940
    • Wei, X.Q.1    Yang, G.2    Cheng, J.B.3    Lu, Z.Y.4    Xie, M.G.5
  • 21
    • 27944479027 scopus 로고    scopus 로고
    • Synthesis and fluorescent property of some novel benzothiazoyl pyrazoline derivatives containing aromatic heterocycle
    • S.J. Ji, and H.B. Shi Synthesis and fluorescent property of some novel benzothiazoyl pyrazoline derivatives containing aromatic heterocycle Dyes Pigments 70 2006 246 250
    • (2006) Dyes Pigments , vol.70 , pp. 246-250
    • Ji, S.J.1    Shi, H.B.2
  • 22
    • 34548531695 scopus 로고    scopus 로고
    • Synthesis and fluorescent property of some novel bischromophore compounds containing pyrazoline and naphthalimide groups
    • B. Bian, S.J. Ji, and H.B. Shi Synthesis and fluorescent property of some novel bischromophore compounds containing pyrazoline and naphthalimide groups Dyes Pigments 76 2008 348 352
    • (2008) Dyes Pigments , vol.76 , pp. 348-352
    • Bian, B.1    Ji, S.J.2    Shi, H.B.3
  • 23
    • 34147098969 scopus 로고    scopus 로고
    • Synthesis and spectrum characteristic of four new organic fluorescent dyes of pyrazoline compounds
    • G. Bai, J.F. Li, D.X. Li, C. Dong, X.Y. Han, and P.H. Lin Synthesis and spectrum characteristic of four new organic fluorescent dyes of pyrazoline compounds Dyes Pigments 75 2007 93 98
    • (2007) Dyes Pigments , vol.75 , pp. 93-98
    • Bai, G.1    Li, J.F.2    Li, D.X.3    Dong, C.4    Han, X.Y.5    Lin, P.H.6
  • 24
    • 33750150209 scopus 로고    scopus 로고
    • Studies on transition metal ions recognition properties of 1-(2-benzothiazole)-3-(2-thiophene)-2-pyrazoline derivatives
    • H.B. Shi, S.J. Ji, and B. Bian Studies on transition metal ions recognition properties of 1-(2-benzothiazole)-3-(2-thiophene)-2-pyrazoline derivatives Dyes Pigments 73 2007 394 396
    • (2007) Dyes Pigments , vol.73 , pp. 394-396
    • Shi, H.B.1    Ji, S.J.2    Bian, B.3
  • 25
    • 34548273074 scopus 로고    scopus 로고
    • Study on the fluorescence properties of a new intramolecular charge transfer compound 1,5-diphenyl-3-(N-ethylcarbazole-3-yl)-2-pyrazoline
    • J.F. Li, B. Guan, D.X. Li, and C. Dong Study on the fluorescence properties of a new intramolecular charge transfer compound 1,5-diphenyl-3-(N- ethylcarbazole-3-yl)-2-pyrazoline Spectrochim. Acta A 68 2007 404 408
    • (2007) Spectrochim. Acta A , vol.68 , pp. 404-408
    • Li, J.F.1    Guan, B.2    Li, D.X.3    Dong, C.4
  • 26
    • 58149492760 scopus 로고    scopus 로고
    • Synthesis and spectral characteristics of two novel intramolecular charge transfer fluorescent dyes
    • S.M. Song, D. Ju, J.F. Li, D.X. Li, Y.L. Wei, C. Dong, P.H. Lin, and S.M. Shuang Synthesis and spectral characteristics of two novel intramolecular charge transfer fluorescent dyes Talanta 77 2009 1707 1714
    • (2009) Talanta , vol.77 , pp. 1707-1714
    • Song, S.M.1    Ju, D.2    Li, J.F.3    Li, D.X.4    Wei, Y.L.5    Dong, C.6    Lin, P.H.7    Shuang, S.M.8
  • 27
    • 56249112630 scopus 로고    scopus 로고
    • New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes
    • D.A. Svechkarev, I.V. Bukatich, and A.O. Doroshenko New 1,3,5-triphenyl-2-pyrazoline-containing 3-hydroxychromones as highly solvatofluorochromic ratiometric polarity probes J. Photochem. Photobiol. A 200 2008 426 431
    • (2008) J. Photochem. Photobiol. A , vol.200 , pp. 426-431
    • Svechkarev, D.A.1    Bukatich, I.V.2    Doroshenko, A.O.3
  • 28
    • 55949100400 scopus 로고    scopus 로고
    • The synthesis, structure and spectroscopic properties of novel oxazolone-, pyrazolone- and pyrazoline-containing heterocycle chromophores
    • Y.F. Sun, and Y.P. Cui The synthesis, structure and spectroscopic properties of novel oxazolone-, pyrazolone- and pyrazoline-containing heterocycle chromophores Dyes Pigments 81 2009 27 34
    • (2009) Dyes Pigments , vol.81 , pp. 27-34
    • Sun, Y.F.1    Cui, Y.P.2
  • 29
    • 70350521280 scopus 로고    scopus 로고
    • Synthesis and spectrum of novel pyrazoline fluorescent compounds
    • Q Liu, L. Gao, L. Wang, Z. Xie, and D. Li Synthesis and spectrum of novel pyrazoline fluorescent compounds Spectroscopy Spec. Anal. 29 2009 2810 2814
    • (2009) Spectroscopy Spec. Anal. , vol.29 , pp. 2810-2814
    • Liu, Q.1    Gao, L.2    Wang, L.3    Xie, Z.4    Li, D.5
  • 30
    • 70349490323 scopus 로고    scopus 로고
    • Stable blue-emitting molecular material derived from calix[4]arene and pyrazoline: Synthesis, optical and electrochemical properties
    • Q. Peng, J. Zou, G. Zeng, Z. Wen, and W. Zheng Stable blue-emitting molecular material derived from calix[4]arene and pyrazoline: synthesis, optical and electrochemical properties Synth. Met. 159 2009 1944 1949
    • (2009) Synth. Met. , vol.159 , pp. 1944-1949
    • Peng, Q.1    Zou, J.2    Zeng, G.3    Wen, Z.4    Zheng, W.5
  • 31
    • 67349208236 scopus 로고    scopus 로고
    • Comparative study on two 2-pyrazoline derivatives with experimental and theoretical methods
    • P.S Zhao, R.Q. Li, X.J. Sun, H.M. Guo, and F.F. Jian Comparative study on two 2-pyrazoline derivatives with experimental and theoretical methods Struct. Chem. 20 2009 443 451
    • (2009) Struct. Chem. , vol.20 , pp. 443-451
    • Zhao, P.S.1    Li, R.Q.2    Sun, X.J.3    Guo, H.M.4    Jian, F.F.5
  • 32
    • 67649289774 scopus 로고    scopus 로고
    • Photoinduced intermolecular and intramolecular charge transfer in the mixed coaggregates of pyrazoline and dicyanonaphthalene
    • Y. Li, S. Liu, M. Chen, and F. Ma Photoinduced intermolecular and intramolecular charge transfer in the mixed coaggregates of pyrazoline and dicyanonaphthalene J. Photochem. Photobiol. A 205 2009 139 144
    • (2009) J. Photochem. Photobiol. A , vol.205 , pp. 139-144
    • Li, Y.1    Liu, S.2    Chen, M.3    Ma, F.4
  • 33
    • 57349195027 scopus 로고    scopus 로고
    • Synthesis of a novel calix[4]arene-based fluorescent ionophore and its metal ions recognition properties
    • Q. Peng, and X.H. Tang Synthesis of a novel calix[4]arene-based fluorescent ionophore and its metal ions recognition properties Chin. Chem. Lett. 20 2009 13 16
    • (2009) Chin. Chem. Lett. , vol.20 , pp. 13-16
    • Peng, Q.1    Tang, X.H.2
  • 34
    • 67349253517 scopus 로고    scopus 로고
    • Synthesis of 1-phenyl-3-biphenyl-5-(N-ethylcarbazole-3-yl)-2-pyrazoline and its use as DNA probe
    • J.F. Li, D.X. Li, Y.Y. Han, S.M. Shuang, and C. Dong Synthesis of 1-phenyl-3-biphenyl-5-(N-ethylcarbazole-3-yl)-2-pyrazoline and its use as DNA probe Spectrochim. Acta A 73 2009 221 225
    • (2009) Spectrochim. Acta A , vol.73 , pp. 221-225
    • Li, J.F.1    Li, D.X.2    Han, Y.Y.3    Shuang, S.M.4    Dong, C.5
  • 36
    • 58949092972 scopus 로고    scopus 로고
    • Site-specific covalent labeling of proteins inside live cells using small molecule probes
    • S. Chattopadhaya, R. Srinivasan, D.S.Y. Yeo, G.Y.J. Chen, and S.Q. Yao Site-specific covalent labeling of proteins inside live cells using small molecule probes Bioorg. Med. Chem. 17 2009 981 989
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 981-989
    • Chattopadhaya, S.1    Srinivasan, R.2    Yeo, D.S.Y.3    Chen, G.Y.J.4    Yao, S.Q.5
  • 37
    • 67649422279 scopus 로고    scopus 로고
    • Synthesis of novel ribavirin hydrazone derivatives and anti-proliferative activity against A549 lung cancer cells
    • W.Y. Liu, H.Y. Li, B.X. Zhao, D.S. Shin, S. Lian, and J.Y. Miao Synthesis of novel ribavirin hydrazone derivatives and anti-proliferative activity against A549 lung cancer cells Carbohydr. Res. 344 2009 1270 1275
    • (2009) Carbohydr. Res. , vol.344 , pp. 1270-1275
    • Liu, W.Y.1    Li, H.Y.2    Zhao, B.X.3    Shin, D.S.4    Lian, S.5    Miao, J.Y.6
  • 38
    • 61349184617 scopus 로고    scopus 로고
    • Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells
    • L.W. Zheng, L.L. Wu, B.X. Zhao, W.L. Dong, and J.Y. Miao Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells Bioorg. Med. Chem. 17 2009 1957 1962
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 1957-1962
    • Zheng, L.W.1    Wu, L.L.2    Zhao, B.X.3    Dong, W.L.4    Miao, J.Y.5
  • 39
    • 56349098902 scopus 로고    scopus 로고
    • Synthesis and preliminary biological evaluation of novel pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives as potential agents against A549 lung cancer cells
    • J.H. Zhang, C.D. Fan, B.X. Zhao, D.S. Shin, W.L. Dong, Y.S. Xie, and J.Y. Miao Synthesis and preliminary biological evaluation of novel pyrazolo[1,5-a]pyrazin-4(5H)-one derivatives as potential agents against A549 lung cancer cells Bioorg. Med. Chem. 16 2008 10165 10171
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 10165-10171
    • Zhang, J.H.1    Fan, C.D.2    Zhao, B.X.3    Shin, D.S.4    Dong, W.L.5    Xie, Y.S.6    Miao, J.Y.7
  • 40
    • 43049115718 scopus 로고    scopus 로고
    • Synthesis and discovery of a novel pyrazole derivative as an inhibitor of apoptosis through modulating integrin β4, ROS and p53 levels in vascular endothelial cells
    • B.X. Zhao, L. Zhang, X.S. Zhu, M.S. Wan, J. Zhao, Y. Zhang, S.L. Zhang, and J.Y. Miao Synthesis and discovery of a novel pyrazole derivative as an inhibitor of apoptosis through modulating integrin β4, ROS and p53 levels in vascular endothelial cells Bioorg. Med. Chem. 16 2008 5171 5180
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 5171-5180
    • Zhao, B.X.1    Zhang, L.2    Zhu, X.S.3    Wan, M.S.4    Zhao, J.5    Zhang, Y.6    Zhang, S.L.7    Miao, J.Y.8
  • 41
    • 40649085969 scopus 로고    scopus 로고
    • Synthesis, structure characterization and preliminary biological evaluation of novel 5-alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H) -one derivatives, J
    • Y.S. Xie, X.H. Pan, B.X. Zhao, J.T. Liu, D.S. Shin, J.H. Zhang, L.W. Zheng, J. Zhao, and J.Y. Miao Synthesis, structure characterization and preliminary biological evaluation of novel 5-alkyl-2-ferrocenyl-6,7- dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives, J Organomet. Chem. 693 2008 1367 1374
    • (2008) Organomet. Chem. , vol.693 , pp. 1367-1374
    • Xie, Y.S.1    Pan, X.H.2    Zhao, B.X.3    Liu, J.T.4    Shin, D.S.5    Zhang, J.H.6    Zheng, L.W.7    Zhao, J.8    Miao, J.Y.9
  • 42
    • 54049104981 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer cells
    • Y. Xia, C.D. Fan, B.X. Zhao, J. Zhao, D.S. Shin, and J.Y. Miao Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5- carbohydrazide hydrazone derivatives as potential agents against A549 lung cancer cells Eur. J. Med. Chem. 43 2008 2347 2353
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 2347-2353
    • Xia, Y.1    Fan, C.D.2    Zhao, B.X.3    Zhao, J.4    Shin, D.S.5    Miao, J.Y.6
  • 43
    • 72249097935 scopus 로고    scopus 로고
    • The synthesis, X-ray crystal structure and optical properties of novel 1,3,5-triaryl pyrazoline derivatives
    • Z.L. Gong, L.W. Zheng, B.X. Zhao, D.Z. Yang, H.S. Lv, W.Y. Liu, and S. Lian The synthesis, X-ray crystal structure and optical properties of novel 1,3,5-triaryl pyrazoline derivatives J. Photochem. Photobiol. A 209 2010 49 55
    • (2010) J. Photochem. Photobiol. A , vol.209 , pp. 49-55
    • Gong, Z.L.1    Zheng, L.W.2    Zhao, B.X.3    Yang, D.Z.4    Lv, H.S.5    Liu, W.Y.6    Lian, S.7
  • 44
    • 70350512016 scopus 로고    scopus 로고
    • Ferrocenyl pyrazolines: Preparation, structure, redox properties and DFT study on regioselective ring-closure
    • V. Zsoldos-Mády, O. Ozohanics, A. Csámpai, V. Kudar, D. Frigyes, and P. Sohár Ferrocenyl pyrazolines: preparation, structure, redox properties and DFT study on regioselective ring-closure J. Organomet. Chem. 694 2009 4185 4195
    • (2009) J. Organomet. Chem. , vol.694 , pp. 4185-4195
    • Zsoldos-Mády, V.1    Ozohanics, O.2    Csámpai, A.3    Kudar, V.4    Frigyes, D.5    Sohár, P.6
  • 45
    • 33750397051 scopus 로고    scopus 로고
    • Synthesis, structure, and in vitro antitumor activity of some glycoside derivatives of ferrocenyl-chalcones and ferrocenyl-pyrazolines
    • V. Zsoldos-Mády, A. Csámpai, R. Szabó, E. Mészáros-Alapi, J. Pásztor, F. Hudecz, and P. Sohár Synthesis, structure, and in vitro antitumor activity of some glycoside derivatives of ferrocenyl-chalcones and ferrocenyl-pyrazolines ChemMedChem 1 2006 1119 1125
    • (2006) ChemMedChem , vol.1 , pp. 1119-1125
    • Zsoldos-Mády, V.1    Csámpai, A.2    Szabó, R.3    Mészáros-Alapi, E.4    Pásztor, J.5    Hudecz, F.6    Sohár, P.7
  • 46
    • 38349051969 scopus 로고    scopus 로고
    • Ferrocenyl chalcones containing anthracenyl group: Synthesis, X-ray crystal structures and electrochemical properties
    • Y.J Jung, K.I. Son, Y.E. Oh, and D.Y. Noh Ferrocenyl chalcones containing anthracenyl group: synthesis, X-ray crystal structures and electrochemical properties Polyhedron 27 2008 861 867
    • (2008) Polyhedron , vol.27 , pp. 861-867
    • Jung, Y.J.1    Son, K.I.2    Oh, Y.E.3    Noh, D.Y.4
  • 47
    • 0037009255 scopus 로고    scopus 로고
    • Antimalarial activity of ferrocenyl chalcones
    • X. Wu, P. Wilairat, and M.L. Go Antimalarial activity of ferrocenyl chalcones Bioorg. Med. Chem. Lett. 12 2002 2299 2302
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 2299-2302
    • Wu, X.1    Wilairat, P.2    Go, M.L.3
  • 48
    • 34748924353 scopus 로고    scopus 로고
    • Zinc mediated selective acylation of ferrocene under solvent-free conditions
    • V.H. Purecha, N.S. Nandurkar, B.M. Bhanage, and J.M. Nagarkar Zinc mediated selective acylation of ferrocene under solvent-free conditions J. Chem. Res. S 7 2007 426 428
    • (2007) J. Chem. Res. S , vol.7 , pp. 426-428
    • Purecha, V.H.1    Nandurkar, N.S.2    Bhanage, B.M.3    Nagarkar, J.M.4
  • 49
    • 0347757182 scopus 로고    scopus 로고
    • Facile synthesis of ferrocenylenones in free solvent at room temperature
    • S.J. Ji, S.Y. Wang, Z.L. Shen, and M.F. Zhou Facile synthesis of ferrocenylenones in free solvent at room temperature Chin. Chem. Lett. 14 2003 1246 1248
    • (2003) Chin. Chem. Lett. , vol.14 , pp. 1246-1248
    • Ji, S.J.1    Wang, S.Y.2    Shen, Z.L.3    Zhou, M.F.4
  • 50
    • 77956059083 scopus 로고
    • Ferrocenyl analogs of chalcones, Dopovidi Akademi nauk Ukrans'ko RSR
    • I.G. Marchenko, A.V. Turov, and V.P. Khilya Ferrocenyl analogs of chalcones, Dopovidi Akademi nauk Ukrans'ko RSR Seriia B 1 1979 43 46
    • (1979) Seriia B , vol.1 , pp. 43-46
    • Marchenko, I.G.1    Turov, A.V.2    Khilya, V.P.3


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