Synthesis and biological activities of new 1H-1,2,4-triazole alcohol derivatives containing a ferrocenyl moiety
Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C N...
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Published in | Applied organometallic chemistry Vol. 22; no. 4; pp. 237 - 241 |
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Chichester, UK
John Wiley & Sons, Ltd
01.04.2008
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Abstract | Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. Copyright © 2008 John Wiley & Sons, Ltd.
Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. |
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AbstractList | Fourteen new 1H-1,2,4-triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. Copyright © 2008 John Wiley & Sons, Ltd. Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. |
Author | Dai, Hong Fang, Jianxin Li, Lichun Liu, Jianbing |
Author_xml | – sequence: 1 givenname: Jianbing surname: Liu fullname: Liu, Jianbing organization: State Key Laboratory and Institute of Elemento-Organic Chemistry, NanKai University, Weijin Road 94, Tianjin 300071, People's Republic of China – sequence: 2 givenname: Lichun surname: Li fullname: Li, Lichun organization: State Key Laboratory and Institute of Elemento-Organic Chemistry, NanKai University, Weijin Road 94, Tianjin 300071, People's Republic of China – sequence: 3 givenname: Hong surname: Dai fullname: Dai, Hong organization: State Key Laboratory and Institute of Elemento-Organic Chemistry, NanKai University, Weijin Road 94, Tianjin 300071, People's Republic of China – sequence: 4 givenname: Jianxin surname: Fang fullname: Fang, Jianxin email: fjx@nankai.edu.cn organization: State Key Laboratory and Institute of Elemento-Organic Chemistry, NanKai University, Weijin Road 94, Tianjin 300071, People's Republic of China |
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References | Eweiss NF, Bahajaj AA, Elsherbini EA. J. Heterocyclic Chem. 1986; 23: 1451 b) Buchenauer H. Proc. Br. Crop. Protect. Conf. 1977; 2: 699 Buchenauer H. J. Plant. Dis. Protect. 1979; 10: 341 Liu JB, Li LC, Dai H, Liu T, Fang JX. J. Organomet. Chem. 2006; 691: 2686. Liu JB, Dai H, Li LC, Tao WF, Fang JX. Acta Crystallogr. 2005; 61: m2166. f) Fang JX, Jin Z, Liu T, Liu W. J. Organomet. Chem. 2003; 674: 1. g) Manas MM, Arredondo Y, Pleixats R, Teixido M, Haga MM, Palacin C, Castello JM, Oritizz JA. J. Heterocyclic Chem. 1992; 29: 1557 b) Gasztonyi M, Josepovits G. Pestic. Sci. 1984; 15: 48 Chu CH, Hui XP, Sun L, Zhang Y, Zhang Z, Li ZC, Liao RA. J. Chin. Chem. Soc. 2001; 8: 121 b) Allardyce CS, Dorcier A, Scolaro C, Dyson PJ. Appl. Organomental. Chem. 2005; 9: 1 Tang J. Synthetic Commun. 2000; 30: 1657. h) Rhaimini AE, Mornet R. Indian. J. Heterocyclic Chem. 1992; 29: 1561. b) Widman O. Ber. 1991; 44: 2605. f) Emilsson H, Salender H, Gaarder J. Eur. J. Med. Chem. Chim. Ther. 1985; 21: 333 c) Fang JX, Jin Z, Liu T, Liu W. Appl. Organomental. Chem. 2003; 17: 145 b) Takano H, Oguri Y, Kato T. J. Pestic. Sci. 1983; 8: 572 c) Izumi K, Yamaguchi I, wada A, Oshio H, Takahashi N. Plant Cell Physiol. 1984; 25: 611. d) Jin Z, Huo AH, Liu T, Hu Y, Liu JB, Fang JX. J. Organomet. Chem. 2005; 690: 1226 e) Demirbs N, Demirbas AU. Bioorg. Med. Chem. 2002; 10: 3717 Hill GA. J. Am. Chem. Soc. 1993; 55: 2509 Motohashi N, Meyer R, Gollapudi SR. J. Organomet. Chem. 1990; 398: 205 Gasztonyi M, Josepovits G. Pestic. Sci. 1979; 10: 57. c) Hui XP, Zhang Y, Xu PF, Wang Q, Zhang ZY. Chin. J. Org. Chem. 2005; 25: 700. c) Ikizler AA, Ucar F, Demirbas N, Yasa I, Ikizler A, Genzer T. Indian J. Het. Chem. 1999; 61: 271 d) Walser A, Flynn T, Mason C. J. Het. Chem. 1991; 28: 1121 2006; 691 1993 1991; 55 44 2005; 61 1986 1984 1999 1991 2002 1985 1992 1992; 23 15 61 28 10 21 29 29 1979; 10 1979 1977 2005; 10 2 25 2000; 30 2001 1983 1984; 8 8 25 1990 2005 2003 2005 1991 2003; 398 9 17 690 674 |
References_xml | – volume: 55 44 start-page: 2509 2605 year: 1993 1991 publication-title: J. Am. Chem. Soc. Ber. – volume: 23 15 61 28 10 21 29 29 start-page: 1451 48 271 1121 3717 333 1557 1561 year: 1986 1984 1999 1991 2002 1985 1992 1992 publication-title: J. Heterocyclic Chem. Pestic. Sci. Indian J. Het. Chem. J. Het. Chem. Bioorg. Med. Chem. Eur. J. Med. Chem. Chim. Ther. J. Heterocyclic Chem. Indian. J. Heterocyclic Chem. – volume: 10 2 25 start-page: 341 699 700 year: 1979 1977 2005 publication-title: J. Plant. Dis. Protect. Proc. Br. Crop. Protect. Conf. Chin. J. Org. Chem. – volume: 10 start-page: 57 year: 1979 publication-title: Pestic. Sci. – volume: 8 8 25 start-page: 121 572 611 year: 2001 1983 1984 publication-title: J. Chin. Chem. Soc. J. Pestic. Sci. Plant Cell Physiol. – volume: 398 9 17 690 674 start-page: 205 1 145 1226 1 year: 1990 2005 2003 2005 1991 2003 publication-title: J. Organomet. Chem. Appl. Organomental. Chem. Appl. Organomental. Chem. J. Organomet. Chem. J. Organomet. Chem. – volume: 61 start-page: m2166 year: 2005 publication-title: Acta Crystallogr. – volume: 30 start-page: 1657 year: 2000 publication-title: Synthetic Commun. – volume: 691 start-page: 2686 year: 2006 publication-title: J. Organomet. Chem. |
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Snippet | Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the... Fourteen new 1H-1,2,4-triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the... |
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Title | Synthesis and biological activities of new 1H-1,2,4-triazole alcohol derivatives containing a ferrocenyl moiety |
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