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Volumn 25, Issue 11, 2014, Pages 1469-1472

Synthesis and biological activities of dithiocarbamates containing 1,2,3-triazoles group

Author keywords

1 2 3 Trizaoles; Antitumor activity; Dithiocarbamates; Synthesis

Indexed keywords


EID: 84908458261     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2014.05.022     Document Type: Article
Times cited : (30)

References (38)
  • 1
    • 28844502837 scopus 로고    scopus 로고
    • Synthetic approaches towards 2-iminothiazolidines: An overview
    • M. Dhooghe, and N. de Kime Synthetic approaches towards 2-iminothiazolidines: an overview Tetrahedron 62 2006 513 535
    • (2006) Tetrahedron , vol.62 , pp. 513-535
    • Dhooghe, M.1    De Kime, N.2
  • 2
    • 0034775559 scopus 로고    scopus 로고
    • Determination of dithiocarbamate fungicide residues in food by a spectrophotometric method using a vertical disulfide reaction system
    • E.D. Caldas, M.H. Conceicüa, M.C.C. Miranda, L. Souza, and J.F. Lima Determination of dithiocarbamate fungicide residues in food by a spectrophotometric method using a vertical disulfide reaction system J. Agric. Food Chem. 49 2001 4521 4525
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 4521-4525
    • Caldas, E.D.1    Conceicüa, M.H.2    Miranda, M.C.C.3    Souza, L.4    Lima, J.F.5
  • 3
    • 0037060918 scopus 로고    scopus 로고
    • Benzamide-based thiolcarbamates: A new class of HIV-1 NCp7 inhibitors
    • A. Goel, S.J. Mazur, and R.J. Fattah Benzamide-based thiolcarbamates: a new class of HIV-1 NCp7 inhibitors Bioorg. Med. Chem. Lett. 12 2002 767 770
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 767-770
    • Goel, A.1    Mazur, S.J.2    Fattah, R.J.3
  • 4
    • 33845238663 scopus 로고    scopus 로고
    • Straightforward and highly efficient catalyst-free one-pot synthesis of dithiocarbamates under solvent-free conditions
    • N. Azizi, F. Aryanasab, and M.R. Saidi Straightforward and highly efficient catalyst-free one-pot synthesis of dithiocarbamates under solvent-free conditions Org. Lett. 8 2006 5275 5277
    • (2006) Org. Lett. , vol.8 , pp. 5275-5277
    • Azizi, N.1    Aryanasab, F.2    Saidi, M.R.3
  • 5
    • 0033661964 scopus 로고    scopus 로고
    • Synthesis and antifungal activity of novel bisdithiocarbamate derivatives of carbohydrates against Fusarium oxysporum f. sp. Lini
    • C. Rafin, E. Veignie, and M. Sancholle Synthesis and antifungal activity of novel bisdithiocarbamate derivatives of carbohydrates against Fusarium oxysporum f. sp. Lini J. Agric. Food Chem. 48 2000 5283 5287
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 5283-5287
    • Rafin, C.1    Veignie, E.2    Sancholle, M.3
  • 6
    • 0025999174 scopus 로고
    • Facile synthesis of S-alkyl thiocarbamates through reaction of carbamoyl lithium with elemental sulfur
    • T. Mizuno, I. Nishiguchi, T. Okushi, and T. Hirashima Facile synthesis of S-alkyl thiocarbamates through reaction of carbamoyl lithium with elemental sulfur Tetrahedron Lett. 32 1991 6867 6868
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6867-6868
    • Mizuno, T.1    Nishiguchi, I.2    Okushi, T.3    Hirashima, T.4
  • 8
    • 54949113317 scopus 로고    scopus 로고
    • One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: High diastereoselectivity achieved for vinyl dithiocarbamates
    • S. Bhadra, A. Saha, and B.C. Ranu One-pot copper nanoparticle-catalyzed synthesis of S-aryl- and S-vinyl dithiocarbamates in water: high diastereoselectivity achieved for vinyl dithiocarbamates Green Chem. 10 2008 1224 1230
    • (2008) Green Chem. , vol.10 , pp. 1224-1230
    • Bhadra, S.1    Saha, A.2    Ranu, B.C.3
  • 9
    • 31544461215 scopus 로고    scopus 로고
    • Dithiocarbamates: Functional and versatile linkers for the formation of self-assembled monolayers
    • P. Morf, F. Raimondi, and H.G. Nothofer Dithiocarbamates: functional and versatile linkers for the formation of self-assembled monolayers Langmuir 22 2006 658 663
    • (2006) Langmuir , vol.22 , pp. 658-663
    • Morf, P.1    Raimondi, F.2    Nothofer, H.G.3
  • 10
    • 14944342626 scopus 로고    scopus 로고
    • Facile synthesis of novel ionic liquids containing dithiocarbamate
    • D. Zhang, J. Chen, Y. Liang, and H. Zhou Facile synthesis of novel ionic liquids containing dithiocarbamate Synth. Commun. 35 2005 521 526
    • (2005) Synth. Commun. , vol.35 , pp. 521-526
    • Zhang, D.1    Chen, J.2    Liang, Y.3    Zhou, H.4
  • 11
    • 33644855554 scopus 로고    scopus 로고
    • Gold(III) dithiocarbamate derivatives for the treatment of cancer: Solution chemistry, DNA binding, and hemolytic properties
    • L. Ronconi, C. Marzano, and P. Zanello Gold(III) dithiocarbamate derivatives for the treatment of cancer: solution chemistry, DNA binding, and hemolytic properties J. Med. Chem. 49 2006 1648 1657
    • (2006) J. Med. Chem. , vol.49 , pp. 1648-1657
    • Ronconi, L.1    Marzano, C.2    Zanello, P.3
  • 13
    • 0034805605 scopus 로고    scopus 로고
    • Synthesis and chemistry of dithiols
    • G.H. Elgemeie, and S.H. Sayed Synthesis and chemistry of dithiols Synthesis 12 2001 1747 1771
    • (2001) Synthesis , vol.12 , pp. 1747-1771
    • Elgemeie, G.H.1    Sayed, S.H.2
  • 15
    • 0035150482 scopus 로고    scopus 로고
    • Rufinamide: A double-blind, placebo-controlled proof of principle trial in patients with epilepsy
    • S. Palhagen, R. Canger, and O. Henriksen Rufinamide: a double-blind, placebo-controlled proof of principle trial in patients with epilepsy Epilepsy Res. 43 2001 115 124
    • (2001) Epilepsy Res. , vol.43 , pp. 115-124
    • Palhagen, S.1    Canger, R.2    Henriksen, O.3
  • 16
    • 31544472391 scopus 로고    scopus 로고
    • Rapid synthesis of triazole-modified resveratrol analogues via click chemistry
    • F. Pagliai, T. Pirali, and E.D. Grosso Rapid synthesis of triazole-modified resveratrol analogues via click chemistry J. Med. Chem. 49 2006 467 470
    • (2006) J. Med. Chem. , vol.49 , pp. 467-470
    • Pagliai, F.1    Pirali, T.2    Grosso, E.D.3
  • 17
    • 74849096124 scopus 로고    scopus 로고
    • Synthesis and antiprotozoal activity of cationic 1,4-diphenyl-1H-1,2,3-triazoles
    • S.A. Bakunov, S.M. Bakunova, and T. Wenzler Synthesis and antiprotozoal activity of cationic 1,4-diphenyl-1H-1,2,3-triazoles J. Med. Chem. 53 2010 254 272
    • (2010) J. Med. Chem. , vol.53 , pp. 254-272
    • Bakunov, S.A.1    Bakunova, S.M.2    Wenzler, T.3
  • 18
    • 0028063421 scopus 로고
    • 1,2,3-Triazole-[2,5-bis-O-(tert-butyldimethylsilyl)-beta-d-ribofuranosyl]-3′-spiro-5″-(4″-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) analogs: Synthesis and anti-HIV-1 activity
    • R. Alvarez, S. Velazquez, and A. San-Felix 1,2,3-Triazole-[2,5-bis-O-(tert-butyldimethylsilyl)-beta-d-ribofuranosyl]-3′-spiro-5″-(4″-amino-1″,2″-oxathiole 2″,2″-dioxide) (TSAO) analogs: synthesis and anti-HIV-1 activity J. Med. Chem. 37 1994 4185 4194
    • (1994) J. Med. Chem. , vol.37 , pp. 4185-4194
    • Alvarez, R.1    Velazquez, S.2    San-Felix, A.3
  • 19
    • 0034624685 scopus 로고    scopus 로고
    • Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis
    • M.J. Genin, D.A. Allwine, and D.J. Anderson Substituent effects on the antibacterial activity of nitrogen-carbon-linked (azolylphenyl)oxazolidinones with expanded activity against the fastidious gram-negative organisms Haemophilus influenzae and Moraxella catarrhalis J. Med. Chem. 43 2000 953 970
    • (2000) J. Med. Chem. , vol.43 , pp. 953-970
    • Genin, M.J.1    Allwine, D.A.2    Anderson, D.J.3
  • 20
    • 33947301041 scopus 로고
    • Decomposition and addition reactions of organic azides
    • G. L'abbe Decomposition and addition reactions of organic azides Chem. Rev. 69 1969 345 363
    • (1969) Chem. Rev. , vol.69 , pp. 345-363
    • L'Abbe, G.1
  • 22
    • 11544346529 scopus 로고    scopus 로고
    • Asymmetric 1,3-dipolar cycloaddition reactions
    • K.V. Gothelf, and K.A. Jgensen Asymmetric 1,3-dipolar cycloaddition reactions Chem. Rev. 98 1998 863 910
    • (1998) Chem. Rev. , vol.98 , pp. 863-910
    • Gothelf, K.V.1    Jgensen, K.A.2
  • 23
    • 33747608618 scopus 로고    scopus 로고
    • Preparation of alumina supported copper nanoparticles and their application in the synthesis of 1,2,3-triazoles
    • M.L. Kantam, V.S. Jaya, B. Sreedhar, M.M. Rao, and B.M. Choudary Preparation of alumina supported copper nanoparticles and their application in the synthesis of 1,2,3-triazoles J. Mol. Catal. A: Chem. 256 2006 273 277
    • (2006) J. Mol. Catal. A: Chem. , vol.256 , pp. 273-277
    • Kantam, M.L.1    Jaya, V.S.2    Sreedhar, B.3    Rao, M.M.4    Choudary, B.M.5
  • 24
    • 50249135519 scopus 로고    scopus 로고
    • A redox-switchable α-cyclodextrin-based[2]rotaxane
    • Y.L. Zhao, W.R. Dichtel, and A. Trabolsi A redox-switchable α-cyclodextrin-based[2]rotaxane J. Am. Chem. Soc. 130 2008 11294 11296
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11294-11296
    • Zhao, Y.L.1    Dichtel, W.R.2    Trabolsi, A.3
  • 25
    • 76349088475 scopus 로고    scopus 로고
    • Preparation of polymer brushes on attapulgite surfaces via a combination of CROP and click reaction
    • J.C. Chen, Y.P. Wang, and H.D. Wang Preparation of polymer brushes on attapulgite surfaces via a combination of CROP and click reaction Chin. Chem. Lett. 21 2010 496 500
    • (2010) Chin. Chem. Lett. , vol.21 , pp. 496-500
    • Chen, J.C.1    Wang, Y.P.2    Wang, H.D.3
  • 26
    • 84555178421 scopus 로고    scopus 로고
    • Synthesis of novel gem-difluoromethylene-containing 1,2,3-triazoles via click reaction
    • W.W. Zhao, H. Li, J. Zhang, and S. Chao Synthesis of novel gem-difluoromethylene-containing 1,2,3-triazoles via click reaction Chin. J. Chem. 29 2011 2763 2768
    • (2011) Chin. J. Chem. , vol.29 , pp. 2763-2768
    • Zhao, W.W.1    Li, H.2    Zhang, J.3    Chao, S.4
  • 27
    • 84879246005 scopus 로고    scopus 로고
    • +-ATPase inhibitory activity of novel triazolyl substituted tetrahydrobenzofuran derivatives via one-pot three-component click reaction
    • +-ATPase inhibitory activity of novel triazolyl substituted tetrahydrobenzofuran derivatives via one-pot three-component click reaction Chin. J. Chem. 6 2013 831 838
    • (2013) Chin. J. Chem. , vol.6 , pp. 831-838
    • Fang, H.B.1    Jin, L.2    Huang, N.Y.3
  • 28
    • 77952170823 scopus 로고    scopus 로고
    • Polymer-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene as polyvalent ligands in the copper-catalyzed huisgen 1,3-dipolar cycloaddition
    • A. Coelho, P. Diz, O. Caamano, and E. Sotelo Polymer-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene as polyvalent ligands in the copper-catalyzed huisgen 1,3-dipolar cycloaddition Adv. Synth. Catal. 352 2010 1179 1192
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 1179-1192
    • Coelho, A.1    Diz, P.2    Caamano, O.3    Sotelo, E.4
  • 29
    • 79952397293 scopus 로고    scopus 로고
    • Synthesis and tunability of abnormal 1,2,3-triazolylidene palladium and rhodium complexes
    • A. Poulain, D. Canseco-Gonzalez, and R. Hynes-Roche Synthesis and tunability of abnormal 1,2,3-triazolylidene palladium and rhodium complexes Organometallics 30 2011 1021 1029
    • (2011) Organometallics , vol.30 , pp. 1021-1029
    • Poulain, A.1    Canseco-Gonzalez, D.2    Hynes-Roche, R.3
  • 30
    • 79952477717 scopus 로고    scopus 로고
    • 2O acting as a robust catalyst in CuAAC reactions: Water is the required medium
    • 2O acting as a robust catalyst in CuAAC reactions: water is the required medium Green Chem. 13 2011 562 565
    • (2011) Green Chem. , vol.13 , pp. 562-565
    • Wang, K.1    Bi, X.H.2    Xing, S.X.3
  • 31
    • 84857863338 scopus 로고    scopus 로고
    • A highly active magnetically recoverable nano ferrite-glutathione-copper (nano-FGT-Cu) catalyst for Huisgen 1,3-dipolar cycloadditions
    • R.B.N. Baig, and R.S. Varma A highly active magnetically recoverable nano ferrite-glutathione-copper (nano-FGT-Cu) catalyst for Huisgen 1,3-dipolar cycloadditions Green Chem. 14 2012 625 632
    • (2012) Green Chem. , vol.14 , pp. 625-632
    • Baig, R.B.N.1    Varma, R.S.2
  • 32
    • 84864029761 scopus 로고    scopus 로고
    • 4 nano particles catalyzed multicomponent synthesis of 1,4-disubstituted 1,2,3-triazoles in tap water using 'click chemistry'
    • 4 nano particles catalyzed multicomponent synthesis of 1,4-disubstituted 1,2,3-triazoles in tap water using 'click chemistry' Tetrahedron Lett. 53 2012 4595 4599
    • (2012) Tetrahedron Lett. , vol.53 , pp. 4595-4599
    • Kumar, B.S.P.A.1    Reddy, K.H.V.2    Madhav, B.3    Ramesh, K.4    Nageswar, Y.V.D.5
  • 33
    • 34548262318 scopus 로고    scopus 로고
    • Peptidomimetics via copper-catalyzed azide-alkyne cycloadditions
    • Y.L. Angell, and K. Burgess Peptidomimetics via copper-catalyzed azide-alkyne cycloadditions Chem. Soc. Rev. 36 2007 1674 1689
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1674-1689
    • Angell, Y.L.1    Burgess, K.2
  • 34
    • 34547482973 scopus 로고    scopus 로고
    • Clicking polymers: A straightforward approach to novel macromolecular architectures
    • D. Fournier, R. Hoogen-boom, and U.S. Schubert Clicking polymers: a straightforward approach to novel macromolecular architectures Chem. Soc. Rev. 36 2007 1369 1380
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1369-1380
    • Fournier, D.1    Hoogen-Boom, R.2    Schubert, U.S.3
  • 35
    • 34547272503 scopus 로고    scopus 로고
    • The growing applications of click chemistry
    • J.E. Moses, and A.D. Moorhouse The growing applications of click chemistry Chem. Soc. Rev. 36 2007 1249 1262
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1249-1262
    • Moses, J.E.1    Moorhouse, A.D.2
  • 36
    • 34247237682 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloadditions of azides and alkynes: A universal ligation tool in polymer and materials science
    • J.F. Lutz 1,3-Dipolar cycloadditions of azides and alkynes: a universal ligation tool in polymer and materials science Angew. Chem. Int. Ed. 46 2007 1018 1025
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1018-1025
    • Lutz, J.F.1
  • 37
    • 34250644208 scopus 로고    scopus 로고
    • Triazole: The keystone in glycosylated molecular architectures constructed by a click reaction
    • A. Dondoni Triazole: the keystone in glycosylated molecular architectures constructed by a click reaction Chem. Asian J. 2 2007 700 708
    • (2007) Chem. Asian J. , vol.2 , pp. 700-708
    • Dondoni, A.1
  • 38
    • 84865189591 scopus 로고    scopus 로고
    • Highly efficient catalyst-free one-pot synthesis of dithiocarbamates under solvent-free conditions
    • (in Chinese)
    • S.R. Guo, Y.Q. Yuan, and C.N. Zhang Highly efficient catalyst-free one-pot synthesis of dithiocarbamates under solvent-free conditions Chin. J. Org. Chem. 32 2012 907 914 (in Chinese)
    • (2012) Chin. J. Org. Chem. , vol.32 , pp. 907-914
    • Guo, S.R.1    Yuan, Y.Q.2    Zhang, C.N.3


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