메뉴 건너뛰기




Volumn 2014, Issue , 2014, Pages

18F-labeling using click cycloadditions

Author keywords

[No Author keywords available]

Indexed keywords

ALKYNE; AZIDE; COPPER; FLUORINE 18; FLUORINE;

EID: 84904115048     PISSN: 23146133     EISSN: 23146141     Source Type: Journal    
DOI: 10.1155/2014/361329     Document Type: Review
Times cited : (42)

References (99)
  • 1
    • 0034241796 scopus 로고    scopus 로고
    • Positron emission tomography provides molecular imaging of biological processes
    • DOI 10.1073/pnas.97.16.9226
    • Phelps M. E., Positron emission tomography provides molecular imaging of biological processes. Proceedings of the National Academy of Sciences of the United States of America 2000 97 16 9226 9233 2-s2.0-0034241796 10.1073/pnas.97.16.9226 (Pubitemid 30627544)
    • (2000) Proceedings of the National Academy of Sciences of the United States of America , vol.97 , Issue.16 , pp. 9226-9233
    • Phelps, M.E.1
  • 3
    • 0024202142 scopus 로고
    • Direct electrophilic radiofluorination of phenylalanine, tyrosine and dopa
    • DOI 10.1016/0883-2889(88)90107-4
    • Coenen H. H., Franken K., Kling P., Stocklin G., Direct electrophilic radiofluorination of phenylalanine, tyrosine and dopa. Applied Radiation and Isotopes 1988 39 12 1243 1250 2-s2.0-0024202142 10.1016/0883-2889(88)90107-4 (Pubitemid 19005344)
    • (1988) Applied Radiation and Isotopes , vol.39 , Issue.12 , pp. 1243-1250
    • Coenen, H.H.1    Franken, K.2    Kling, P.3    Stocklin, G.4
  • 4
    • 0028670748 scopus 로고
    • 18F]-N- succinimidyl 4-(fluoromethyl)benzoate for protein labeling
    • 2-s2.0-0028670748 10.1016/0969-8043(94)90031-0
    • 18F]-N-succinimidyl 4-(fluoromethyl)benzoate for protein labeling. Applied Radiation and Isotopes 1994 45 12 1155 1163 2-s2.0-0028670748 10.1016/0969-8043(94)90031-0
    • (1994) Applied Radiation and Isotopes , vol.45 , Issue.12 , pp. 1155-1163
    • Lang, L.1    Eckelman, W.C.2
  • 5
    • 0001427691 scopus 로고
    • 1.3-dipolare cycloadditionen
    • Huisgen R., 1.3-dipolare cycloadditionen. Angewandte Chemie 1963 13 604 637
    • (1963) Angewandte Chemie , Issue.13 , pp. 604-637
    • Huisgen, R.1
  • 7
    • 80053955813 scopus 로고    scopus 로고
    • Copper-free click chemistry with the short-lived positron emitter fluorine-18
    • 2-s2.0-80053955813 10.1039/c1ob06034a
    • Bouvet V., Wuest M., Wuest F., Copper-free click chemistry with the short-lived positron emitter fluorine-18. Organic & Biomolecular Chemistry 2011 9 21 7393 7399 2-s2.0-80053955813 10.1039/c1ob06034a
    • (2011) Organic & Biomolecular Chemistry , vol.9 , Issue.21 , pp. 7393-7399
    • Bouvet, V.1    Wuest, M.2    Wuest, F.3
  • 9
    • 80255137225 scopus 로고    scopus 로고
    • 18F]ADIBO): A biocompatible radioactive labeling synthon for peptides using catalyst free [3+2] cycloaddition
    • 2-s2.0-80255137225 10.1016/j.bmcl.2011.09.126
    • 18F]ADIBO): a biocompatible radioactive labeling synthon for peptides using catalyst free [3+2] cycloaddition. Bioorganic & Medicinal Chemistry Letters 2011 21 23 6987 6991 2-s2.0-80255137225 10.1016/j.bmcl.2011.09.126
    • (2011) Bioorganic & Medicinal Chemistry Letters , vol.21 , Issue.23 , pp. 6987-6991
    • Arumugam, S.1    Chin, J.2    Schirrmacher, R.3    Popik, V.V.4    Kostikov, A.P.5
  • 10
    • 83455172909 scopus 로고    scopus 로고
    • Copper-free click for PET: Rapid 1,3-dipolar cycloadditions with a fluorine-18 cyclooctyne
    • 2-s2.0-83455172909 10.1021/ml200187j
    • Carpenter R. D., Hausner S. H., Sutcliffe J. L., Copper-free click for PET: rapid 1,3-dipolar cycloadditions with a fluorine-18 cyclooctyne. ACS Medicinal Chemistry Letters 2011 2 12 885 889 2-s2.0-83455172909 10.1021/ml200187j
    • (2011) ACS Medicinal Chemistry Letters , vol.2 , Issue.12 , pp. 885-889
    • Carpenter, R.D.1    Hausner, S.H.2    Sutcliffe, J.L.3
  • 11
    • 84865153140 scopus 로고    scopus 로고
    • F-18-labeling protocol of peptides based on chemically orthogonal strain-promoted cycloaddition under physiologically friendly reaction conditions
    • Sachin K., Jadhav V. H., Kim E.-M., Kim H. L., Lee S. B., Jeong H.-J., Lim S. T., Sohn M.-H., Kim D. W., F-18-labeling protocol of peptides based on chemically orthogonal strain-promoted cycloaddition under physiologically friendly reaction conditions. Bioconjugate Chemistry 2012 23 8 1680 1686
    • (2012) Bioconjugate Chemistry , vol.23 , Issue.8 , pp. 1680-1686
    • Sachin, K.1    Jadhav, V.H.2    Kim, E.-M.3    Kim, H.L.4    Lee, S.B.5    Jeong, H.-J.6    Lim, S.T.7    Sohn, M.-H.8    Kim, D.W.9
  • 17
    • 84864667434 scopus 로고    scopus 로고
    • Advancing tetrazine bioorthogonal reactions through the development of new synthetic tools
    • Devaraj N., Advancing tetrazine bioorthogonal reactions through the development of new synthetic tools. Synlett 2012 23 15 2147 2152
    • (2012) Synlett , vol.23 , Issue.15 , pp. 2147-2152
    • Devaraj, N.1
  • 23
  • 24
    • 77954414562 scopus 로고    scopus 로고
    • The click chemistry approach applied to fluorine-18
    • 2-s2.0-77954414562 10.2174/1874471011003030202
    • Ross T. L., The click chemistry approach applied to fluorine-18. Current Radiopharmaceuticals 2010 3 3 202 223 2-s2.0-77954414562 10.2174/ 1874471011003030202
    • (2010) Current Radiopharmaceuticals , vol.3 , Issue.3 , pp. 202-223
    • Ross, T.L.1
  • 25
    • 84880852328 scopus 로고    scopus 로고
    • Recent trends in bioorthogonal click-radiolabeling reactions using fluorine-18
    • Pretze M., Pietzsch D., Mamat C., Recent trends in bioorthogonal click-radiolabeling reactions using fluorine-18. Molecules 2013 18 7 8618 8665
    • (2013) Molecules , vol.18 , Issue.7 , pp. 8618-8665
    • Pretze, M.1    Pietzsch, D.2    Mamat, C.3
  • 26
    • 33746820191 scopus 로고    scopus 로고
    • I catalyzed 1,3-dipolar cycloaddition
    • DOI 10.1016/j.tetlet.2006.06.176, PII S0040403906013980
    • 18F]fluoropeptides using CuI catalyzed 1,3-dipolar cycloaddition. Tetrahedron Letters 2006 47 37 6681 6684 2-s2.0-33746820191 10.1016/j.tetlet. 2006.06.176 (Pubitemid 44176106)
    • (2006) Tetrahedron Letters , vol.47 , Issue.37 , pp. 6681-6684
    • Marik, J.1    Sutcliffe, J.L.2
  • 28
    • 72149125596 scopus 로고    scopus 로고
    • 18F]fluoro-1-butyne as a radiolabeled synthon for click chemistry with azido compounds
    • 2-s2.0-72149125596 10.1016/j.apradiso.2009.11.003
    • 18F]fluoro- 1-butyne as a radiolabeled synthon for click chemistry with azido compounds. Applied Radiation and Isotopes 2010 68 2 329 333 2-s2.0-72149125596 10.1016/j.apradiso.2009.11.003
    • (2010) Applied Radiation and Isotopes , vol.68 , Issue.2 , pp. 329-333
    • Kim, D.H.1    Choe, Y.S.2    Kim, B.-T.3
  • 31
    • 34347338806 scopus 로고    scopus 로고
    • 18F]fluoroethylazide for positron emission tomography
    • DOI 10.1021/bc060301j
    • 18F]fluoroethylazide for positron emission tomography. Bioconjugate Chemistry 2007 18 3 989 993 2-s2.0-34347338806 10.1021/bc060301j (Pubitemid 47010823)
    • (2007) Bioconjugate Chemistry , vol.18 , Issue.3 , pp. 989-993
    • Glaser, M.1    Arstad, E.2
  • 32
    • 69549123869 scopus 로고    scopus 로고
    • 18F-labelled tyrosine kinase inhibitor for EGFR kinase activity imaging in tumors
    • 2-s2.0-69549123869 10.1016/j.apradiso.2009.07.018
    • 18F-labelled tyrosine kinase inhibitor for EGFR kinase activity imaging in tumors. Applied Radiation and Isotopes 2009 67 11 1977 1984 2-s2.0-69549123869 10.1016/j.apradiso.2009.07.018
    • (2009) Applied Radiation and Isotopes , vol.67 , Issue.11 , pp. 1977-1984
    • Kobus, D.1    Giesen, Y.2    Ullrich, R.3    Backes, H.4    Neumaier, B.5
  • 35
    • 77956341930 scopus 로고    scopus 로고
    • Development of a new epidermal growth factor receptor positron emission tomography imaging agent based on the 3-cyanoquinoline core: Synthesis and biological evaluation
    • 2-s2.0-77956341930 10.1016/j.bmc.2010.08.004
    • Pisaneschi F., Nguyen Q.-D., Shamsaei E., Glaser M., Robins E., Kaliszczak M., Smith G., Spivey A. C., Aboagye E. O., Development of a new epidermal growth factor receptor positron emission tomography imaging agent based on the 3-cyanoquinoline core: synthesis and biological evaluation. Bioorganic and Medicinal Chemistry 2010 18 18 6634 6645 2-s2.0-77956341930 10.1016/j.bmc.2010.08.004
    • (2010) Bioorganic and Medicinal Chemistry , vol.18 , Issue.18 , pp. 6634-6645
    • Pisaneschi, F.1    Nguyen, Q.-D.2    Shamsaei, E.3    Glaser, M.4    Robins, E.5    Kaliszczak, M.6    Smith, G.7    Spivey, A.C.8    Aboagye, E.O.9
  • 42
    • 84863992098 scopus 로고    scopus 로고
    • Radiolabelling and evaluation of novel haloethylsulfoxides as PET imaging agents for tumor hypoxia
    • Laurens E., Yeoh S. D., Rigopoulos A., Radiolabelling and evaluation of novel haloethylsulfoxides as PET imaging agents for tumor hypoxia. Nuclear Medicine and Biology 2012 39 6 871 882
    • (2012) Nuclear Medicine and Biology , vol.39 , Issue.6 , pp. 871-882
    • Laurens, E.1    Yeoh, S.D.2    Rigopoulos, A.3
  • 43
    • 84855199788 scopus 로고    scopus 로고
    • A fluorous and click approach for screening potential PET probes: Evaluation of potential hypoxia biomarkers
    • 2-s2.0-84855199788 10.1016/j.bmc.2011.10.084
    • Bejot R., Carroll L., Bhakoo K., Declerck J., Gouverneur V., A fluorous and click approach for screening potential PET probes: evaluation of potential hypoxia biomarkers. Bioorganic and Medicinal Chemistry 2012 20 1 324 329 2-s2.0-84855199788 10.1016/j.bmc.2011.10.084
    • (2012) Bioorganic and Medicinal Chemistry , vol.20 , Issue.1 , pp. 324-329
    • Bejot, R.1    Carroll, L.2    Bhakoo, K.3    Declerck, J.4    Gouverneur, V.5
  • 44
    • 84861574314 scopus 로고    scopus 로고
    • Radiolabeling of RGD peptide and preliminary biological evaluation in mice bearing U87MG tumors
    • Li J., Shi L., Jia L., Jiang D., Zhou W., Hu W., Qi Y., Zhang L., Radiolabeling of RGD peptide and preliminary biological evaluation in mice bearing U87MG tumors. Bioorganic & Medicinal Chemistry 2012 20 12 3850 3855
    • (2012) Bioorganic & Medicinal Chemistry , vol.20 , Issue.12 , pp. 3850-3855
    • Li, J.1    Shi, L.2    Jia, L.3    Jiang, D.4    Zhou, W.5    Hu, W.6    Qi, Y.7    Zhang, L.8
  • 47
    • 84879177635 scopus 로고    scopus 로고
    • 18F]fluoroethyl), 1H[1,2,3]triazole 4-ethylene] triphenylphosphonium bromide as a potential positron emission tomography tracer for imaging apoptosis
    • 10.1002/jlcr.3024
    • 18F]fluoroethyl),1H[1,2,3]triazole 4-ethylene] triphenylphosphonium bromide as a potential positron emission tomography tracer for imaging apoptosis. Journal of Labelled Compounds and Radiopharmaceuticals 2013 56 6 313 316 10.1002/jlcr.3024
    • (2013) Journal of Labelled Compounds and Radiopharmaceuticals , vol.56 , Issue.6 , pp. 313-316
    • Haslop, A.1    Gee, A.2    Plisson, C.3    Long, N.4
  • 50
    • 34247884233 scopus 로고    scopus 로고
    • An efficient F-18 labeling method for PET study: Huisgen 1,3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds
    • DOI 10.1016/j.tetlet.2007.04.048, PII S0040403907007174
    • Sirion U., Kim H. J., Lee J. H., Seo J. W., Lee B. S., Lee S. J., Oh S. J., Chi D. Y., An efficient F-18 labeling method for PET study: huisgen 1,3-dipolar cycloaddition of bioactive substances and F-18-labeled compounds. Tetrahedron Letters 2007 48 23 3953 3957 2-s2.0-34247884233 10.1016/j.tetlet. 2007.04.048 (Pubitemid 46702266)
    • (2007) Tetrahedron Letters , vol.48 , Issue.23 , pp. 3953-3957
    • Sirion, U.1    Kim, H.J.2    Lee, J.H.3    Seo, J.W.4    Lee, B.S.5    Lee, S.J.6    Oh, S.J.7    Chi, D.Y.8
  • 53
    • 80054808224 scopus 로고    scopus 로고
    • 18F-labeled peptides using the copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition
    • 2-s2.0-80054808224 10.1038/nprot.2011.390
    • 18F-labeled peptides using the copper(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition. Nature Protocols 2011 6 11 1718 1725 2-s2.0-80054808224 10.1038/nprot.2011.390
    • (2011) Nature Protocols , vol.6 , Issue.11 , pp. 1718-1725
    • Gill, H.S.1    Marik, J.2
  • 54
    • 84860523921 scopus 로고    scopus 로고
    • The effect of fluorination of zinc oxide nanoparticles on evaluation of their biodistribution after oral administration
    • 2-s2.0-84860523921 10.1088/0957-4484/23/20/205102 205102
    • Lee C.-M., Jeong H.-J., Kim D. W., Sohn M.-H., Lim S. T., The effect of fluorination of zinc oxide nanoparticles on evaluation of their biodistribution after oral administration. Nanotechnology 2012 23 20 2-s2.0-84860523921 10.1088/0957-4484/23/20/205102 205102
    • (2012) Nanotechnology , vol.23 , Issue.20
    • Lee, C.-M.1    Jeong, H.-J.2    Kim, D.W.3    Sohn, M.-H.4    Lim, S.T.5
  • 56
    • 34248206043 scopus 로고    scopus 로고
    • 18F-labeled neurotensin(8-13) via copper-mediated 1,3-dipolar [3+2]cycloaddition reaction
    • 18F-labeled neurotensin(8-13) via copper-mediated 1,3-dipolar [3+2]cycloaddition reaction. Letters in Drug Design and Discovery 2007 4 4 279 285 2-s2.0-34248206043 10.2174/157018007784619998 (Pubitemid 46708892)
    • (2007) Letters in Drug Design and Discovery , vol.4 , Issue.4 , pp. 279-285
    • Ramenda, T.1    Bergmann, R.2    Wuest, F.3
  • 57
    • 72149091156 scopus 로고    scopus 로고
    • Radiolabelling of proteins with fluorine-18 via click chemistry
    • 2-s2.0-72149091156 10.1039/b916075b
    • Ramenda T., Kniess T., Bergmann R., Steinbach J., Wuest F., Radiolabelling of proteins with fluorine-18 via click chemistry. Chemical Communications 2009 48 7521 7523 2-s2.0-72149091156 10.1039/b916075b
    • (2009) Chemical Communications , Issue.48 , pp. 7521-7523
    • Ramenda, T.1    Kniess, T.2    Bergmann, R.3    Steinbach, J.4    Wuest, F.5
  • 58
    • 84876679552 scopus 로고    scopus 로고
    • 18F]F-SA): A versatile building block for labeling of peptides, proteins and oligonucleotides with fluorine-18 via Cu(I)-mediated click chemistry
    • 18F]F-SA): a versatile building block for labeling of peptides, proteins and oligonucleotides with fluorine-18 via Cu(I)-mediated click chemistry. Amino Acids 2013 44 4 1167 1180
    • (2013) Amino Acids , vol.44 , Issue.4 , pp. 1167-1180
    • Ramenda, T.1    Steinbach, J.2    Wuest, F.3
  • 61
    • 84865125806 scopus 로고    scopus 로고
    • 18F-labeling of large 37-amino-acid pHLIP peptide analogues and their biological evaluation
    • 10.1021/bc3000222
    • 18F-labeling of large 37-amino-acid pHLIP peptide analogues and their biological evaluation. Bioconjugate Chemistry 2012 23 8 1557 1566 10.1021/bc3000222
    • (2012) Bioconjugate Chemistry , vol.23 , Issue.8 , pp. 1557-1566
    • Daumar, P.1    Wanger-Baumann, C.A.2    Pillarsetty, N.3
  • 62
    • 70349295775 scopus 로고    scopus 로고
    • 18F]fluorobenzoate: A putatively more stable prosthetic group for the fluorine-18 labeling of biomolecules via click chemistry
    • 2-s2.0-70349295775 10.2174/1874471010902010063
    • 18F]fluorobenzoate: a putatively more stable prosthetic group for the fluorine-18 labeling of biomolecules via click chemistry. Current Radiopharmaceuticals 2009 2 1 63 74 2-s2.0-70349295775 10.2174/ 1874471010902010063
    • (2009) Current Radiopharmaceuticals , vol.2 , Issue.1 , pp. 63-74
    • Vaidyanathan, G.1    White, B.J.2    Zalutsky, M.R.3
  • 63
    • 84862739115 scopus 로고    scopus 로고
    • 18F]FNPB): A new stable aromatic porosthetic group for efficient labeling of peptides with fluorine-18
    • 18F]FNPB): a new stable aromatic porosthetic group for efficient labeling of peptides with fluorine-18. Journal of Labelled Compounds and Radiopharmaceuticals 2012 55 6 229 234
    • (2012) Journal of Labelled Compounds and Radiopharmaceuticals , vol.55 , Issue.6 , pp. 229-234
    • Li, Y.1    Liu, Y.2    Zhang, L.3    Xu, Y.4
  • 65
    • 78751634809 scopus 로고    scopus 로고
    • General method for labeling siRNA by click chemistry with fluorine-18 for the purpose of PET maging
    • 2-s2.0-78751634809 10.1021/bc100263y
    • Mercier F., Paris J., Kaisin G., Thonon D., Flagothier J., Teller N., Lemaire C., Luxen A., General method for labeling siRNA by click chemistry with fluorine-18 for the purpose of PET maging. Bioconjugate Chemistry 2011 22 1 108 114 2-s2.0-78751634809 10.1021/bc100263y
    • (2011) Bioconjugate Chemistry , vol.22 , Issue.1 , pp. 108-114
    • Mercier, F.1    Paris, J.2    Kaisin, G.3    Thonon, D.4    Flagothier, J.5    Teller, N.6    Lemaire, C.7    Luxen, A.8
  • 66
    • 84862629483 scopus 로고    scopus 로고
    • Synthesis of two new alkyne-bearing linkers used for the preparation of siRNA for labeling by click chemistry with fluorine-18
    • Flagothier J., Kaisin G., Mercier F., Thonon D., Teller N., Wouters J., Luxen A., Synthesis of two new alkyne-bearing linkers used for the preparation of siRNA for labeling by click chemistry with fluorine-18. Applied Radiation and Isotopes 2012 70 8 1549 1557
    • (2012) Applied Radiation and Isotopes , vol.70 , Issue.8 , pp. 1549-1557
    • Flagothier, J.1    Kaisin, G.2    Mercier, F.3    Thonon, D.4    Teller, N.5    Wouters, J.6    Luxen, A.7
  • 67
    • 84865046494 scopus 로고    scopus 로고
    • 18F-labeled click synthons" from azide-functionalized diaryliodonium salts
    • 18F-labeled click synthons" from azide-functionalized diaryliodonium salts. European Journal of Organic Chemistry 2012 2012 24 4541 4547
    • (2012) European Journal of Organic Chemistry , vol.2012 , Issue.24 , pp. 4541-4547
    • Chun, J.-H.1    Pike, V.W.2
  • 68
    • 63549126486 scopus 로고    scopus 로고
    • 18F-labeling and glycosylation by click chemistry
    • 2-s2.0-63549126486 10.1016/j.carres.2009.02.001
    • 18F-labeling and glycosylation by click chemistry. Carbohydrate Research 2009 344 6 753 761 2-s2.0-63549126486 10.1016/j.carres.2009.02.001
    • (2009) Carbohydrate Research , vol.344 , Issue.6 , pp. 753-761
    • Maschauer, S.1    Prante, O.2
  • 70
  • 71
    • 84893333017 scopus 로고    scopus 로고
    • 18F-Glyco-RGD peptides for PET imaging of integrin expression: Efficient radiosynthesis by click chemistry and modulation of biodistribution by glycosylation
    • 18F-Glyco-RGD peptides for PET imaging of integrin expression: efficient radiosynthesis by click chemistry and modulation of biodistribution by glycosylation. Molecular Pharmaceutics 2014 11 2 505 515
    • (2014) Molecular Pharmaceutics , vol.11 , Issue.2 , pp. 505-515
    • Maschauer, S.1    Haubner, R.2    Kuwert, T.3    Prante, O.4
  • 79
    • 79551517797 scopus 로고    scopus 로고
    • Development of new folate-based PET radiotracers: Preclinical evaluation of 68Ga-DOTA-folate conjugates
    • 2-s2.0-79551517797 10.1007/s00259-010-1597-8
    • Fani M., Wang X., Nicolas G., Medina C., Raynal I., Port M., Maecke H. R., Development of new folate-based PET radiotracers: preclinical evaluation of 68Ga-DOTA-folate conjugates. European Journal of Nuclear Medicine and Molecular Imaging 2011 38 1 108 119 2-s2.0-79551517797 10.1007/s00259-010-1597-8
    • (2011) European Journal of Nuclear Medicine and Molecular Imaging , vol.38 , Issue.1 , pp. 108-119
    • Fani, M.1    Wang, X.2    Nicolas, G.3    Medina, C.4    Raynal, I.5    Port, M.6    Maecke, H.R.7
  • 81
    • 0013064237 scopus 로고    scopus 로고
    • A stepwise huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev V. V., Green L. G., Fokin V. V., Sharpless K. B., A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "Ligation" of azides and terminal alkynes. Angewandte Chemie 2002 114 14 2708 2711
    • (2002) Angewandte Chemie , vol.114 , Issue.14 , pp. 2708-2711
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 82
    • 0037012920 scopus 로고    scopus 로고
    • Peptidotriazoles on solid phase: [1,2,3]-Triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides
    • DOI 10.1021/jo011148j
    • Tornøe C. W., Christensen C., Meldal M., Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. Journal of Organic Chemistry 2002 67 9 3057 3064 2-s2.0-0037012920 10.1021/jo011148j (Pubitemid 34457265)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.9 , pp. 3057-3064
    • Tornoe, C.W.1    Christensen, C.2    Meldal, M.3
  • 83
    • 34250353931 scopus 로고    scopus 로고
    • Click chemistry - What's in a name? Triazole synthesis and beyond
    • DOI 10.1055/s-2007-966071
    • Gil M. V., Arévalo M. J., López Ó., Click chemistry-what's in a name? Triazole synthesis and beyond. Synthesis 2007 11 1589 1620 2-s2.0-34250353931 10.1055/s-2007-966071 (Pubitemid 46911512)
    • (2007) Synthesis , Issue.11 , pp. 1589-1620
    • Gil, M.V.1    Arevalo, M.J.2    Lopez, O.3
  • 84
    • 77949810836 scopus 로고    scopus 로고
    • The application of CuAAC "click" chemistry to catenane and rotaxane synthesis
    • 2-s2.0-77949810836 10.1039/b901974j
    • Hänni K. D., Leigh D. A., The application of CuAAC "click" chemistry to catenane and rotaxane synthesis. Chemical Society Reviews 2010 39 4 1240 1251 2-s2.0-77949810836 10.1039/b901974j
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1240-1251
    • Hänni, K.D.1    Leigh, D.A.2
  • 85
    • 77949818761 scopus 로고    scopus 로고
    • Click chemistry generates privileged CH hydrogen-bonding triazoles: The latest addition to anion supramolecular chemistry
    • 2-s2.0-77949818761 10.1039/b818033b
    • Hua Y., Flood A. H., Click chemistry generates privileged CH hydrogen-bonding triazoles: the latest addition to anion supramolecular chemistry. Chemical Society Reviews 2010 39 4 1262 1271 2-s2.0-77949818761 10.1039/b818033b
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1262-1271
    • Hua, Y.1    Flood, A.H.2
  • 86
    • 77949799806 scopus 로고    scopus 로고
    • Click chemistry under non-classical reaction conditions
    • 2-s2.0-77949799806 10.1039/b901973c
    • Kappe C. O., Van Der Eycken E., Click chemistry under non-classical reaction conditions. Chemical Society Reviews 2010 39 4 1280 1290 2-s2.0-77949799806 10.1039/b901973c
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1280-1290
    • Kappe, C.O.1    Van Der Eycken, E.2
  • 87
    • 77949796395 scopus 로고    scopus 로고
    • Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: New reactivity of copper(i) acetylides
    • 2-s2.0-77949796395 10.1039/b904091a
    • Hein J. E., Fokin V. V., Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(i) acetylides. Chemical Society Reviews 2010 39 4 1302 1315 2-s2.0-77949796395 10.1039/b904091a
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1302-1315
    • Hein, J.E.1    Fokin, V.V.2
  • 88
    • 77949786732 scopus 로고    scopus 로고
    • In situ click chemistry: Probing the binding landscapes of biological molecules
    • 2-s2.0-77949786732 10.1039/b901969n
    • Mamidyala S. K., Finn M. G., In situ click chemistry: probing the binding landscapes of biological molecules. Chemical Society Reviews 2010 39 4 1252 1261 2-s2.0-77949786732 10.1039/b901969n
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1252-1261
    • Mamidyala, S.K.1    Finn, M.G.2
  • 89
    • 77949795885 scopus 로고    scopus 로고
    • Electrochemical applications. How click chemistry brought biomimetic models to the next level: Electrocatalysis under controlled rate of electron transfer
    • 2-s2.0-77949795885 10.1039/b901972n
    • Decréau R. A., Collman J. P., Hosseini A., Electrochemical applications. How click chemistry brought biomimetic models to the next level: electrocatalysis under controlled rate of electron transfer. Chemical Society Reviews 2010 39 4 1291 1301 2-s2.0-77949795885 10.1039/b901972n
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1291-1301
    • Decréau, R.A.1    Collman, J.P.2    Hosseini, A.3
  • 90
    • 77949779995 scopus 로고    scopus 로고
    • Click chemistry with DNA
    • 2-s2.0-77949779995 10.1039/b901971p
    • El-Sagheer A. H., Brown T., Click chemistry with DNA. Chemical Society Reviews 2010 39 4 1388 1405 2-s2.0-77949779995 10.1039/b901971p
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1388-1405
    • El-Sagheer, A.H.1    Brown, T.2
  • 91
    • 33846703461 scopus 로고    scopus 로고
    • 'Click' chemistry in polymer and materials science
    • DOI 10.1002/marc.200600625
    • Binder W. H., Sachsenhofer R., "Click" chemistry in polymer and materials science. Macromolecular Rapid Communications 2007 28 1 15 54 2-s2.0-33846703461 10.1002/marc.200600625 (Pubitemid 46192085)
    • (2007) Macromolecular Rapid Communications , vol.28 , Issue.1 , pp. 15-54
    • Binder, W.H.1    Sachsenhofer, R.2
  • 92
    • 77949812304 scopus 로고    scopus 로고
    • Marrying click chemistry with polymerization: Expanding the scope of polymeric materials
    • 2-s2.0-77949812304 10.1039/b901978m
    • Golas P. L., Matyjaszewski K., Marrying click chemistry with polymerization: expanding the scope of polymeric materials. Chemical Society Reviews 2010 39 4 1338 1354 2-s2.0-77949812304 10.1039/b901978m
    • (2010) Chemical Society Reviews , vol.39 , Issue.4 , pp. 1338-1354
    • Golas, P.L.1    Matyjaszewski, K.2
  • 93
    • 0002218143 scopus 로고
    • Über die Einwirkung von Diazobenzolimid auf Acetylendicarbonsä ure-methylester
    • Michael A., Über die Einwirkung von Diazobenzolimid auf Acetylendicarbonsäure-methylester. Journal für Praktische Chemie 1893 48 1 94 95
    • (1893) Journal für Praktische Chemie , vol.48 , Issue.1 , pp. 94-95
    • Michael, A.1
  • 94
    • 84903592008 scopus 로고    scopus 로고
    • 18F-fluoro- glycosylation: A short review
    • 214748 10.1155/2014/214748
    • 18F-fluoro-glycosylation: a short review. BioMed Research International 2014 2014 30 214748 10.1155/2014/214748
    • (2014) BioMed Research International , vol.2014 , pp. 30
    • Maschauer, S.1    Prante, O.2
  • 96
    • 77649181022 scopus 로고    scopus 로고
    • Copper toxicity in the general population
    • 2-s2.0-77649181022 10.1016/j.clinph.2009.12.015
    • Brewer G. J., Copper toxicity in the general population. Clinical Neurophysiology 2010 121 4 459 460 2-s2.0-77649181022 10.1016/j.clinph.2009.12. 015
    • (2010) Clinical Neurophysiology , vol.121 , Issue.4 , pp. 459-460
    • Brewer, G.J.1
  • 97
    • 21844465098 scopus 로고    scopus 로고
    • 18F]SFB)
    • DOI 10.1016/j.apradiso.2005.03.005, PII S0969804305000898
    • 18F]SFB). Applied Radiation and Isotopes 2005 63 3 329 332 2-s2.0-21844465098 10.1016/j.apradiso.2005.03.005 (Pubitemid 40961711)
    • (2005) Applied Radiation and Isotopes , vol.63 , Issue.3 , pp. 329-332
    • Mading, P.1    Fuchtner, F.2    Wust, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.