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Volumn 17, Issue 6, 2013, Pages 594-609

Metal catalyzed click chemistry for molecular imaging probes

Author keywords

3 dipolar cycloaddition (CuAAC); Bioorthgonal reaction; Click chemistry; Cu(I) catalyzed azide alkyne 1; Molecular imaging probe

Indexed keywords

BIOIMAGING; CATALYSIS; CELL MEMBRANES; COPPER COMPOUNDS; CYCLOADDITION; HYDROCARBONS; MOLECULAR IMAGING; MOLECULES; PROBES; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 84877766616     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/1385272811317060005     Document Type: Review
Times cited : (9)

References (102)
  • 1
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C.; Finn, M. G.; Sharpless, K. B., Click chemistry: diverse chemical function from a few good reactions. Angew. Chem. Int. Ed., 2001, 40(11), 2004-2021.
    • (2001) Angew. Chem. Int. Ed , vol.40 , Issue.11 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 2
    • 37549026429 scopus 로고    scopus 로고
    • Bioorthogonal click chemistry: Covalent labeling in living systems
    • Baskin J. M.; Bertozzi, C. R. Bioorthogonal click chemistry: covalent labeling in living systems. QSAR Comb. Sci., 2007, 26(11-12), 1211-1219.
    • (2007) QSAR Comb. Sci , vol.26 , Issue.11-12 , pp. 1211-1219
    • Baskin, J.M.1    Bertozzi, C.R.2
  • 3
    • 76449094187 scopus 로고    scopus 로고
    • Bioorthogonal chemistry: A covalent strategy for the study of biological systems
    • Lim Reyna, K. V.; Lin, Q., Bioorthogonal chemistry: a covalent strategy for the study of biological systems. Sci. China Chem., 2010, 53(1), 61-70.
    • (2010) Sci. China Chem , vol.53 , Issue.1 , pp. 61-70
    • Lim Reyna, K.V.1    Lin, Q.2
  • 4
    • 79959397926 scopus 로고    scopus 로고
    • Alkynes as an eco-compatible on-call functionality orthogonal to biological conditions in water
    • Uhlig, N.; Li, C., Alkynes as an eco-compatible on-call functionality orthogonal to biological conditions in water. Chem. Sci., 2011, (2), 1241-1249.
    • (2011) Chem. Sci
    • Uhlig, N.1    Li, C.2
  • 5
    • 80052583041 scopus 로고    scopus 로고
    • Reliable and efficient procedures for the conjugation of biomolecules through Huisgen azide-alkyne cycloadditions
    • Lallana, E.; Riguera, R.; Fernandez-Megia, E., Reliable and efficient procedures for the conjugation of biomolecules through Huisgen azide-alkyne cycloadditions. Angew. Chem. Int. Ed., 2011, 50(38), 8794-8804.
    • (2011) Angew. Chem. Int. Ed , vol.50 , Issue.38 , pp. 8794-8804
    • Lallana, E.1    Riguera, R.2    Fernandez-Megia, E.3
  • 6
    • 80053031240 scopus 로고    scopus 로고
    • Biomedical applications of tetrazine cycloadditions
    • Devaraj, N. K.; Weissleder, R., Biomedical applications of tetrazine cycloadditions. Acc. Chem. Res., 2011, 44(9), 816-827.
    • (2011) Acc. Chem. Res , vol.44 , Issue.9 , pp. 816-827
    • Devaraj, N.K.1    Weissleder, R.2
  • 7
    • 80053028238 scopus 로고    scopus 로고
    • Photoinducible bioorthogonal chemistry: A spatiotemporally controllable tool to visualize and perturb proteins in live cells
    • Lim Reyna, K. V.; Lin, Q., Photoinducible bioorthogonal chemistry: A spatiotemporally controllable tool to visualize and perturb proteins in live cells. Acc. Chem. Res., 2011, 44(9), 828-839.
    • (2011) Acc. Chem. Res , vol.44 , Issue.9 , pp. 828-839
    • Lim Reyna, K.V.1    Lin, Q.2
  • 8
    • 80053015717 scopus 로고    scopus 로고
    • Exploiting bioorthogonal chemistry to elucidate protein-lipid binding interactions and other biological roles of phospholipids
    • Best, M. D.; Meng, M. R.; Heidi, E. B., Exploiting bioorthogonal chemistry to elucidate protein-lipid binding interactions and other biological roles of phospholipids. Acc. Chem. Res., 2011, 44(9), 686-698.
    • (2011) Acc. Chem. Res , vol.44 , Issue.9 , pp. 686-698
    • Best, M.D.1    Meng, M.R.2    Heidi, E.B.3
  • 9
    • 80055060816 scopus 로고    scopus 로고
    • The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) click reaction and its applications. An overview
    • Liang, L.; Astruc, D., The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) click reaction and its applications. An overview. Coord. Chem. Rev., 2011, (255), 2933-2945.
    • (2011) Coord. Chem. Rev , Issue.255 , pp. 2933-2945
    • Liang, L.1    Astruc, D.2
  • 10
    • 0034677879 scopus 로고    scopus 로고
    • Cell surface engineering by a modified Staudinger reaction
    • Saxon, E.; Bertozzi, C. R., Cell surface engineering by a modified Staudinger reaction. Science, 2000, 287(5460), 2007-2010.
    • (2000) Science , vol.287 , Issue.5460 , pp. 2007-2010
    • Saxon, E.1    Bertozzi, C.R.2
  • 11
    • 80052588424 scopus 로고    scopus 로고
    • Staudinger ligation as a method for bioconjugation
    • Berkel, S. S.; Eldijk, M. B.; Hest, J. C. M., Staudinger ligation as a method for bioconjugation. Angew. Chem. Int. Ed. 2011, 50(38), 8806-8827.
    • (2011) Angew. Chem. Int. Ed , vol.50 , Issue.38 , pp. 8806-8827
    • Berkel, S.S.1    Eldijk, M.B.2    Hest, J.C.M.3
  • 12
    • 0037099395 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. Angew. Chem. Int. Ed. 2002, 41(14), 2596-2599.
    • (2002) Angew. Chem. Int. Ed , vol.41 , Issue.14 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 13
    • 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
    • Tornoe, 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. J. Org. Chem. 2002, 67(9), 3057-3064.
    • (2002) J. Org. Chem , vol.67 , Issue.9 , pp. 3057-3064
    • Tornoe, C.W.1    Christensen, C.2    Meldal, M.3
  • 14
    • 77953886288 scopus 로고
    • Zur existenz niedergliedriger cycloalkine 1
    • Wittig, G.; Krebs, A. Zur existenz niedergliedriger cycloalkine 1. Chem. Ber. Recl. 1961, 94, 3260-3275.
    • (1961) Chem. Ber. Recl , vol.94 , pp. 3260-3275
    • Wittig, G.1    Krebs, A.2
  • 15
    • 9344227358 scopus 로고    scopus 로고
    • A strain-promoted [3+2] azidealkyne cycloaddition for covalent modification of blomolecules in living systems
    • Agard, N. J.; Prescher, J. A.; Bertozzi, C. R., A strain-promoted [3+2] azidealkyne cycloaddition for covalent modification of blomolecules in living systems. J. Am. Chem. Soc. 2004, 126(46), 15046-15047.
    • (2004) J. Am. Chem. Soc , vol.126 , Issue.46 , pp. 15046-15047
    • Agard, N.J.1    Prescher, J.A.2    Bertozzi, C.R.3
  • 16
    • 70349769688 scopus 로고    scopus 로고
    • Click chemistry beyond metal-catalyzed cycloaddition
    • Becer C. R.; Hoogenboom, R.; Schubert, U. S., Click chemistry beyond metal-catalyzed cycloaddition. Angew. Chem. Int. Ed. 2009, 48(27), 4900-4908.
    • (2009) Angew. Chem. Int. Ed , vol.48 , Issue.27 , pp. 4900-4908
    • Becer, C.R.1    Hoogenboom, R.2    Schubert, U.S.3
  • 17
    • 53849105464 scopus 로고    scopus 로고
    • Tetrazine ligation: Fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity
    • Blackman, M. L.; Royzen, M.; Fox, J. M., Tetrazine ligation: Fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity. J. Am. Chem. Soc., 2008, 130(41), 13518-13519.
    • (2008) J. Am. Chem. Soc , vol.130 , Issue.41 , pp. 13518-13519
    • Blackman, M.L.1    Royzen, M.2    Fox, J.M.3
  • 18
    • 42249110717 scopus 로고    scopus 로고
    • A photoinducible 1,3-dipolar cycloaddition reaction for rapid, selective modification of tetrazolecontaining proteins
    • Song, W.; Wang, Y.; Qu, J.; Madden, M. M.; Lin, Q., A photoinducible 1,3-dipolar cycloaddition reaction for rapid, selective modification of tetrazolecontaining proteins. Angew. Chem. Int. Ed., 2008, 47(15), 2832-2835.
    • (2008) Angew. Chem. Int. Ed , vol.47 , Issue.15 , pp. 2832-2835
    • Song, W.1    Wang, Y.2    Qu, J.3    Madden, M.M.4    Lin, Q.5
  • 20
    • 0001427691 scopus 로고
    • 1.3-Dipolare cycloadditionen-Ruckschau und ausblick
    • Huisgen, R., 1.3-Dipolare cycloadditionen-Ruckschau und ausblick. Angew. Chem., Int. Ed. Engl., 1963, 604.
    • (1963) Angew. Chem., Int. Ed. Engl , pp. 604
    • Huisgen, R.1
  • 21
    • 84858043626 scopus 로고    scopus 로고
    • Heterogeneous azide-alkyne click chemistry: Towards metal-free end products
    • Dervaux, B.; Du Prez, F. E., Heterogeneous azide-alkyne click chemistry: towards metal-free end products. Chem. Sci., 2012, (3), 959-966.
    • (2012) Chem. Sci , Issue.3 , pp. 959-966
    • Dervaux, B.1    du Prez, F.E.2
  • 22
    • 84867726453 scopus 로고    scopus 로고
    • Cu-I-catalyzed alkyneazide click cycloadditions from a mechanistic and synthetic perspective
    • Bock, V. D.; Hiemstra, H.; van Maarseveen, J.H., Cu-I-catalyzed alkyneazide click cycloadditions from a mechanistic and synthetic perspective. Eur. J. Org. Chem. 2006, 2006(1), 51-68.
    • (2006) Eur. J. Org. Chem , vol.2006 , Issue.1 , pp. 51-68
    • Bock, V.D.1    Hiemstra, H.2    van Maarseveen, J.H.3
  • 23
    • 77949796395 scopus 로고    scopus 로고
    • Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: New reactivity of copper(I) acetylides
    • Hein, J.E.; Fokin, V. V., Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(I) acetylides. Chem. Soc. Rev., 2010, 39(4), 1302-1315.
    • (2010) Chem. Soc. Rev , vol.39 , Issue.4 , pp. 1302-1315
    • Hein, J.E.1    Fokin, V.V.2
  • 24
    • 33646444425 scopus 로고    scopus 로고
    • Reusable polymer-supported catalyst for the [3+2] Huisgen cycloaddition in automation protocols
    • Girard, C.; Önen, E.; Aufort, M.; Beauvière, S.; Samson, E.; Herscovici, J., Reusable polymer-supported catalyst for the [3+2] Huisgen cycloaddition in automation protocols. Org. Lett., 2006, 8(8), 1689-1692.
    • (2006) Org. Lett , vol.8 , Issue.8 , pp. 1689-1692
    • Girard, C.1    Önen, E.2    Aufort, M.3    Beauvière, S.4    Samson, E.5    Herscovici, J.6
  • 25
    • 79959608349 scopus 로고    scopus 로고
    • Insights into supported copper(II)-catalyzed azide-alkyne cycloaddition in water
    • Wang, Y.; Liu, J.; Xia, C., Insights into supported copper(II)-catalyzed azide-alkyne cycloaddition in water. Adv. Synth. Catal. 2011, 353(9), 1534-1542.
    • (2011) Adv. Synth. Catal , vol.353 , Issue.9 , pp. 1534-1542
    • Wang, Y.1    Liu, J.2    Xia, C.3
  • 27
    • 33947099937 scopus 로고    scopus 로고
    • Click chemistry in Cu-I-zeolites: The Huisgen [3+2]-cycloaddition
    • Chassaing, S.; Kumarraja, M.; Sido, A. S. S.; Pale, P.; Sommer, J., Click chemistry in Cu-I-zeolites: The Huisgen [3+2]-cycloaddition. Org. Lett., 2007, 9(5), 883-886.
    • (2007) Org. Lett , vol.9 , Issue.5 , pp. 883-886
    • Chassaing, S.1    Kumarraja, M.2    Sido, A.S.S.3    Pale, P.4    Sommer, J.5
  • 28
    • 53849092694 scopus 로고    scopus 로고
    • Click Chemistry in zeolites: Copper(I) zeolites as new heterogeneous and ligand-free catalysts for the Huisgen [3+2] cycloaddition
    • Chassaing, S.; Sido, A. S. S.; Alix, A.; Kumarraja, M.; Pale, P.; Sommer, J., Click Chemistry in zeolites: Copper(I) zeolites as new heterogeneous and ligand-free catalysts for the Huisgen [3+2] cycloaddition. Chem. Eur. J. 2008, 14(22), 6713-6721.
    • (2008) Chem. Eur. J , vol.14 , Issue.22 , pp. 6713-6721
    • Chassaing, S.1    Sido, A.S.S.2    Alix, A.3    Kumarraja, M.4    Pale, P.5    Sommer, J.6
  • 29
    • 77149126696 scopus 로고    scopus 로고
    • Mechanistic insights into Copper(I)-catalyzed azide-alkyne cycloadditions using continuous flow conditions
    • Fuchs, M.; Goessler, W.; Pilger, C.; Kappe, C. O. Mechanistic insights into Copper(I)-catalyzed azide-alkyne cycloadditions using continuous flow conditions. Adv. Synth. Catal., 2010, 352(2-3), 323-328.
    • (2010) Adv. Synth. Catal , vol.352 , Issue.2-3 , pp. 323-328
    • Fuchs, M.1    Goessler, W.2    Pilger, C.3    Kappe, C.O.4
  • 30
    • 68949195821 scopus 로고    scopus 로고
    • Synthesis and characterization of isomeric vinyl-1,2,3-triazole materials by azide-alkyne click chemistry
    • Nulwala, H.; Takizawa, K.; Odukale, A.; Khan, A.; Thibault, R. J.; Taft B. R.; Lipshutz, B. H.; Hawker, C. J., Synthesis and characterization of isomeric vinyl-1,2,3-triazole materials by azide-alkyne click chemistry. Macromolecules, 2009, 42(16), 6068-6074.
    • (2009) Macromolecules , vol.42 , Issue.16 , pp. 6068-6074
    • Nulwala, H.1    Takizawa, K.2    Odukale, A.3    Khan, A.4    Thibault, R.J.5    Taft, B.R.6    Lipshutz, B.H.7    Hawker, C.J.8
  • 31
    • 78650194189 scopus 로고    scopus 로고
    • A click procedure with heterogeneous copper to tether technetium-99m chelating agents and rhenium complexes. Evaluation of the chelating properties and biodistribution of the new radiolabelled glucose conjugates
    • Benoist E.; Coulais, Y.; Almant, M.; Kovensky, J.; Moreau, V.; Lesur, D.; Artigau, M.; Picard, C.; Galaup, C.; Gouin, S. G., A click procedure with heterogeneous copper to tether technetium-99m chelating agents and rhenium complexes. Evaluation of the chelating properties and biodistribution of the new radiolabelled glucose conjugates. Carbohydr. Res., 2011, 346(1), 26-34.
    • (2011) Carbohydr. Res , vol.346 , Issue.1 , pp. 26-34
    • Benoist, E.1    Coulais, Y.2    Almant, M.3    Kovensky, J.4    Moreau, V.5    Lesur, D.6    Artigau, M.7    Picard, C.8    Galaup, C.9    Gouin, S.G.10
  • 32
    • 58549087740 scopus 로고    scopus 로고
    • Copper nanoparticles on charcoal for multicomponent catalytic synthesis of 1,2,3-triazole derivatives from benzyl halides or alkyl halides, terminal alkynes and sodium azide in water as a Green solvent
    • Sharghi, H.; Khalifeh, R.; Doroodmand, M. M., Copper nanoparticles on charcoal for multicomponent catalytic synthesis of 1,2,3-triazole derivatives from benzyl halides or alkyl halides, terminal alkynes and sodium azide in water as a Green solvent. Adv. Synth. Catal., 2009, 351(1-2), 207-218.
    • (2009) Adv. Synth. Catal , vol.351 , Issue.1-2 , pp. 207-218
    • Sharghi, H.1    Khalifeh, R.2    Doroodmand, M.M.3
  • 33
    • 33845754525 scopus 로고    scopus 로고
    • Heterogeneous copper-in-charcoal-catalyzed click chemistry
    • Lipshutz, B. H.; Taft, B. R., Heterogeneous copper-in-charcoal-catalyzed click chemistry. Angew. Chem., Int. Ed., 2006, 45(48), 8235-8238.
    • (2006) Angew. Chem., Int. Ed , vol.45 , Issue.48 , pp. 8235-8238
    • Lipshutz, B.H.1    Taft, B.R.2
  • 34
    • 70350602433 scopus 로고    scopus 로고
    • Immobilization of porphyrinatocopper nanoparticles onto activated multiwalled carbon nanotubes and a study of its catalytic cctivity as an efficient heterogeneous catalyst for a click approach to the three-component synthesis of 1,2,3-Triazoles in Water
    • Sharghi, H.; Beyzavi, M. H.; Safavi, A.; Doroodmand M. M.; Khalifeh, R., Immobilization of porphyrinatocopper nanoparticles onto activated multiwalled carbon nanotubes and a study of its catalytic cctivity as an efficient heterogeneous catalyst for a click approach to the three-component synthesis of 1,2,3-Triazoles in Water. Adv. Synth. Catal., 2009, 351(14-15), 2391-2410.
    • (2009) Adv. Synth. Catal , vol.351 , Issue.14-15 , pp. 2391-2410
    • Sharghi, H.1    Beyzavi, M.H.2    Safavi, A.3    Doroodmand, M.M.4    Khalifeh, R.5
  • 35
    • 62249176210 scopus 로고    scopus 로고
    • Copper nanoparticles in ionic liquids: Recyclable and efficient catalytic system for 1,3-dipolar cycloaddition reaction
    • Raut, D.; Wankhede, K.; Vaidya, V.; Bhilare, S.; Darwatkar, N.; Deorukhkar, A.; Trivedi, G.; Salunkhe, M., Copper nanoparticles in ionic liquids: Recyclable and efficient catalytic system for 1,3-dipolar cycloaddition reaction. Catal. Commun., 2009, 10(8), 1240-1243.
    • (2009) Catal. Commun , vol.10 , Issue.8 , pp. 1240-1243
    • Raut, D.1    Wankhede, K.2    Vaidya, V.3    Bhilare, S.4    Darwatkar, N.5    Deorukhkar, A.6    Trivedi, G.7    Salunkhe, M.8
  • 36
    • 33746849010 scopus 로고    scopus 로고
    • Cu/Cu-oxide nanoparticles as catalyst in the click azide-alkyne cycloaddition
    • Molteni, G.; Bianchi, C. L.; Marinoni, G.; Santo, N.; Ponti, A., Cu/Cu-oxide nanoparticles as catalyst in the click azide-alkyne cycloaddition. New J. Chem., 2006, 30(8), 1137-1139.
    • (2006) New J. Chem , vol.30 , Issue.8 , pp. 1137-1139
    • Molteni, G.1    Bianchi, C.L.2    Marinoni, G.3    Santo, N.4    Ponti, A.5
  • 37
    • 20044388373 scopus 로고    scopus 로고
    • Click chemistry: Copper clusters catalyse the cycloaddition of azides with terminal alkynes
    • Pachón, L. D.; van Maarseveen, J. H.; Rothenberg, G., Click chemistry: Copper clusters catalyse the cycloaddition of azides with terminal alkynes. Adv. Synth. Catal., 2005, 347(6), 811-815.
    • (2005) Adv. Synth. Catal , vol.347 , Issue.6 , pp. 811-815
    • Pachón, L.D.1    van Maarseveen, J.H.2    Rothenberg, G.3
  • 38
    • 78650836598 scopus 로고    scopus 로고
    • Rapid synthesis of block and cyclic copolymers via click chemistry in the presence of copper nanoparticles
    • Pressly, E. D.; Amir, R. J.; Hawker, C. J., Rapid synthesis of block and cyclic copolymers via click chemistry in the presence of copper nanoparticles. J. Polym. Sci., Part A: Polym. Chem., 2011, 49(3), 814-819.
    • (2011) J. Polym. Sci., Part A: Polym. Chem , vol.49 , Issue.3 , pp. 814-819
    • Pressly, E.D.1    Amir, R.J.2    Hawker, C.J.3
  • 39
    • 9444260351 scopus 로고    scopus 로고
    • A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction
    • Appukkuttan, P.; Dehaen, W.; Fokin, V. V.; Van der Eycken, E., A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction. Org. Lett., 2004, 6(23), 4223-4225.
    • (2004) Org. Lett , vol.6 , Issue.23 , pp. 4223-4225
    • Appukkuttan, P.1    Dehaen, W.2    Fokin, V.V.3    van der Eycken, E.4
  • 40
    • 77749324895 scopus 로고    scopus 로고
    • Alkyne-azide click reaction catalyzed by metallic copper under ultrasound
    • Cintas, P.; Barge, A.; Tagliapietra, S.; Boffa, L.; Cravotto, G., Alkyne-azide click reaction catalyzed by metallic copper under ultrasound. Nat. Protocol., 2010, (5), 607-616.
    • (2010) Nat. Protocol , Issue.5 , pp. 607-616
    • Cintas, P.1    Barge, A.2    Tagliapietra, S.3    Boffa, L.4    Cravotto, G.5
  • 41
    • 75649094445 scopus 로고    scopus 로고
    • CuO hollow nanostructures catalyze [3 + 2] cycloaddition of azides with terminal alkynes
    • Kim, J. Y.; Park, J. C.; Kang, H.; Song, H.; Park, K. H., CuO hollow nanostructures catalyze [3 + 2] cycloaddition of azides with terminal alkynes. Chem. Commun., 2010, 46(3), 439-441.
    • (2010) Chem. Commun , vol.46 , Issue.3 , pp. 439-441
    • Kim, J.Y.1    Park, J.C.2    Kang, H.3    Song, H.4    Park, K.H.5
  • 42
    • 53449092625 scopus 로고    scopus 로고
    • 2-NHC-Cu(I): An efficient and reusable catalyst for [3+2] cycloaddition of organic azides and terminal alkynes under solvent-free reaction conditions at room temperature
    • 2-NHC-Cu(I): an efficient and reusable catalyst for [3+2] cycloaddition of organic azides and terminal alkynes under solvent-free reaction conditions at room temperature. Tetrahedron, 2008, 64, 10825-10830.
    • (2008) Tetrahedron , vol.64 , pp. 10825-10830
    • Li, P.H.1    Wang, L.2    Zhang, Y.C.3
  • 43
    • 78650355374 scopus 로고    scopus 로고
    • Non-magnetic and magnetic supported copper(I) chelating adsorbents as efficient heterogeneous catalysts and copper scavengers for click chemistry
    • Megia-Fernandez, A.; Ortega-Muńoz, M.; Lopez-Jaramillo, J.; Hernandez-Mateo, F.; Santoyo-Gonzalez, F., Non-magnetic and magnetic supported copper(I) chelating adsorbents as efficient heterogeneous catalysts and copper scavengers for click chemistry. Adv. Synth. Catal., 2010, 352(18), 3306-3320.
    • (2010) Adv. Synth. Catal , vol.352 , Issue.18 , pp. 3306-3320
    • Megia-Fernandez, A.1    Ortega-Muńoz, M.2    Lopez-Jaramillo, J.3    Hernandez-Mateo, F.4    Santoyo-Gonzalez, F.5
  • 45
    • 61349130803 scopus 로고    scopus 로고
    • A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes
    • Katayama, T.; Kamata K.; Yamaguchi, K.; Mizuno, N., A supported copper hydroxide as an efficient, ligand-free, and heterogeneous precatalyst for 1,3-dipolar cycloadditions of organic azides to terminal alkynes. ChemSusChem, 2009, 2(1), 59-62.
    • (2009) ChemSusChem , vol.2 , Issue.1 , pp. 59-62
    • Katayama, T.1    Kamata, K.2    Yamaguchi, K.3    Mizuno, N.4
  • 46
    • 77956377240 scopus 로고    scopus 로고
    • Cu-Mn bimetallic catalyst for Huisgen [3+2]-cycloaddition
    • Yousuf, S. K.; Mukherjee D.; Singh, B.; Maity, S.; Taneja, S. C., Cu-Mn bimetallic catalyst for Huisgen [3+2]-cycloaddition. Green Chem., 2010, 12(9), 1568-1572.
    • (2010) Green Chem , vol.12 , Issue.9 , pp. 1568-1572
    • Yousuf, S.K.1    Mukherjee, D.2    Singh, B.3    Maity, S.4    Taneja, S.C.5
  • 47
    • 53549115052 scopus 로고    scopus 로고
    • Copper (I)-doped Wyoming's montmorillonite for the synthesis of disubstituted 1, 2, 3-triazoles
    • Jlalia, I.; Elamari, H.; Meganem, F.; Herscovici, J.; Girard, C., Copper (I)-doped Wyoming's montmorillonite for the synthesis of disubstituted 1, 2, 3-triazoles. Tetrahedron Lett., 2008, 49(48), 6756-6758.
    • (2008) Tetrahedron Lett , vol.49 , Issue.48 , pp. 6756-6758
    • Jlalia, I.1    Elamari, H.2    Meganem, F.3    Herscovici, J.4    Girard, C.5
  • 48
    • 77956676713 scopus 로고    scopus 로고
    • On the reactivity of activated alkynes in copper and solvent-free Huisgen's reaction
    • Elamari, H.; Jlalia, I.; Louet, C.; Herscovici, J.; Meganem, F.; Girard, C.; On the reactivity of activated alkynes in copper and solvent-free Huisgen's reaction. Tetrahedron: Asymmetry, 2010, 21(9-10), 1179-1183.
    • (2010) Tetrahedron: Asymmetry , vol.21 , Issue.9-10 , pp. 1179-1183
    • Elamari, H.1    Jlalia, I.2    Louet, C.3    Herscovici, J.4    Meganem, F.5    Girard, C.6
  • 49
    • 84863296504 scopus 로고    scopus 로고
    • Magnetic copper-iron nanoparticles as simple heterogeneous catalysts for the azide-alkyne click reaction in water
    • Hudson, R.; Li, C.-J.; Moores, A., Magnetic copper-iron nanoparticles as simple heterogeneous catalysts for the azide-alkyne click reaction in water. Green chem., 2012, 14(3), 622-624.
    • (2012) Green Chem , vol.14 , Issue.3 , pp. 622-624
    • Hudson, R.1    Li, C.-J.2    Moores, A.3
  • 50
    • 84857863338 scopus 로고    scopus 로고
    • A highly active magnetically recoverable nano ferrite-glutathione-copper (nano-FGT-Cu) catalyst for Huisgen 1,3-dipolar cycloadditions
    • Nasir Baig, R. B.; Varma, R. S., A highly active magnetically recoverable nano ferrite-glutathione-copper (nano-FGT-Cu) catalyst for Huisgen 1,3-dipolar cycloadditions. Green Chem., 2012, 14(3), 625-632.
    • (2012) Green Chem , vol.14 , Issue.3 , pp. 625-632
    • Nasir Baig, R.B.1    Varma, R.S.2
  • 51
    • 81255214589 scopus 로고    scopus 로고
    • Hydroxyapatite-supported copper(II)-catalyzed azide-allcyne [3+2] cycloaddition with neither reducing agents nor bases in water
    • Masuyama, Y.; Yoshikawa, K.; Suzuki, N.; Hara, K.; Fukuoka A., Hydroxyapatite-supported copper(II)-catalyzed azide-allcyne [3+2] cycloaddition with neither reducing agents nor bases in water. Tetrahedron Lett., 2011, 52(51), 6916-6918.
    • (2011) Tetrahedron Lett , vol.52 , Issue.51 , pp. 6916-6918
    • Masuyama, Y.1    Yoshikawa, K.2    Suzuki, N.3    Hara, K.4    Fukuoka, A.5
  • 52
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed azide-alkyne cycloaddition
    • Meldal, M.; Tornøe, C. W., Cu-catalyzed azide-alkyne cycloaddition. Chem. Rev., 2008, 108(8), 2952-3015.
    • (2008) Chem. Rev , vol.108 , Issue.8 , pp. 2952-3015
    • Meldal, M.1    Tornøe, C.W.2
  • 53
    • 35548939058 scopus 로고    scopus 로고
    • Ligand-accelerated Cu-catalyzed azide-alkyne cycloaddition: A mechanistic report
    • Rodionov, V. O.; Presolski, V.I.; Diaz, D. D.; Fokin, V. V.; Finn, M.G., Ligand-accelerated Cu-catalyzed azide-alkyne cycloaddition: A mechanistic report. J. Am. Chem. Soc., 2007, 129(42), 12705-12712.
    • (2007) J. Am. Chem. Soc , vol.129 , Issue.42 , pp. 12705-12712
    • Rodionov, V.O.1    Presolski, V.I.2    Diaz, D.D.3    Fokin, V.V.4    Finn, M.G.5
  • 54
    • 77949812304 scopus 로고    scopus 로고
    • Marrying click chemistry with polymerization: Expanding the scope of polymeric materials
    • Golas, P. L.; Matyjaszewski, K., Marrying click chemistry with polymerization: expanding the scope of polymeric materials. Chem. Soc. Rev., 2010, 39(4), 1338-1354.
    • (2010) Chem. Soc. Rev , vol.39 , Issue.4 , pp. 1338-1354
    • Golas, P.L.1    Matyjaszewski, K.2
  • 55
    • 27944488746 scopus 로고    scopus 로고
    • Accelerated bioorthogonal conjugation: A practical method for the Ligation of diverse functional molecules to a polyvalent virus scaffold
    • Gupta, S. S.; Kuzelka, J.; Singh, P.; Lewis, W. G.; Manchester, M.; Finn, M. G., Accelerated bioorthogonal conjugation: A practical method for the Ligation of diverse functional molecules to a polyvalent virus scaffold. Bioconjugate Chem., 2005, 16(6), 1572-1579.
    • (2005) Bioconjugate Chem , vol.16 , Issue.6 , pp. 1572-1579
    • Gupta, S.S.1    Kuzelka, J.2    Singh, P.3    Lewis, W.G.4    Manchester, M.5    Finn, M.G.6
  • 56
    • 84859112267 scopus 로고    scopus 로고
    • A water soluble Cu-I-NHC for CuAAC ligation of unprotected peptides under open air conditions
    • Gaulier, C.; Hospital, A.; Legeret, B.; Delmas, A. F.; Aucagne, V.; Cisnettia, F.; Gautier A., A water soluble Cu-I-NHC for CuAAC ligation of unprotected peptides under open air conditions. Chem. Commun., 2012, 48(33), 4005-4007.
    • (2012) Chem. Commun , vol.48 , Issue.33 , pp. 4005-4007
    • Gaulier, C.1    Hospital, A.2    Legeret, B.3    Delmas, A.F.4    Aucagne, V.5    Cisnettia, F.6    Gautier, A.7
  • 57
    • 79953187599 scopus 로고    scopus 로고
    • [CuBr(PPh3)(3)] for Azide-Allkyne Cycloaddition Reactions under Strict Click Conditions
    • Lal, S.; Diez-Gonzales, S., [CuBr(PPh3)(3)] for Azide-Allkyne Cycloaddition Reactions under Strict Click Conditions. J. Org. Chem., 2011, 76(7), 2367-2373.
    • (2011) J. Org. Chem , vol.76 , Issue.7 , pp. 2367-2373
    • Lal, S.1    Diez-Gonzales, S.2
  • 58
    • 0343177218 scopus 로고
    • On new organic phosphorus bonding III Phosphine methylene derivatives and phosphinimine
    • Staudinger, H., Meyer, J., On new organic phosphorus bonding III Phosphine methylene derivatives and phosphinimine. Helv. Chim. Acta., 1919, 2, 635-646.
    • (1919) Helv. Chim. Acta , vol.2 , pp. 635-646
    • Staudinger, H.1    Meyer, J.2
  • 59
    • 77957896219 scopus 로고    scopus 로고
    • Carboxylic Acid-Promoted Copper(I)-Catalyzed Azide-Alkyne Cycloaddition
    • Shao, C.; Wang, X.; Xu, J.; Zhao, J.; Zhang, Q.; Hu, Y.; Carboxylic Acid-Promoted Copper(I)-Catalyzed Azide-Alkyne Cycloaddition. J. Org. Chem., 2010, 75(20), 7002-7005.
    • (2010) J. Org. Chem , vol.75 , Issue.20 , pp. 7002-7005
    • Shao, C.1    Wang, X.2    Xu, J.3    Zhao, J.4    Zhang, Q.5    Hu, Y.6
  • 60
    • 83455201281 scopus 로고    scopus 로고
    • Quick and highly efficient copper-catalyzed cycloaddition of organic azides with terminal alkynes
    • Wang, D.; Zhao, M.-M.; Liu, X.; Chen, Y.-X.; Li, N.; Chen, B.-H., Quick and highly efficient copper-catalyzed cycloaddition of organic azides with terminal alkynes. Org. Biomol. Chem., 2012, 10(2), 229-231.
    • (2012) Org. Biomol. Chem , vol.10 , Issue.2 , pp. 229-231
    • Wang, D.1    Zhao, M.-M.2    Liu, X.3    Chen, Y.-X.4    Li, N.5    Chen, B.-H.6
  • 61
    • 84860206602 scopus 로고    scopus 로고
    • Copper-catalyzed azide-alkyne cycloaddition reaction in water using cyclodextrin as a phase transfer catalyst
    • Shin, J.-A.; Lim, Y.-G.; Lee, K.-H., Copper-catalyzed azide-alkyne cycloaddition reaction in water using cyclodextrin as a phase transfer catalyst. J. Org. Chem., 2012, 77(8), 4117-4122.
    • (2012) J. Org. Chem , vol.77 , Issue.8 , pp. 4117-4122
    • Shin, J.-A.1    Lim, Y.-G.2    Lee, K.-H.3
  • 62
    • 18244371903 scopus 로고    scopus 로고
    • Efficient synthesis of water-soluble calixarenes using click chemistry
    • Ryu, E. H.; Zhao, Y., Efficient synthesis of water-soluble calixarenes using click chemistry. Org. Lett., 2005, 7(6), 1035-1037.
    • (2005) Org. Lett , vol.7 , Issue.6 , pp. 1035-1037
    • Ryu, E.H.1    Zhao, Y.2
  • 63
  • 64
    • 84857356071 scopus 로고    scopus 로고
    • Unusual Cu(I)-catalyzed 1,3-dipolar cycloaddition of acetylenic amides: Formation of bistriazoles
    • Kwon, M.; Jang, Y.; Yoon, S.; Yang, D.; Jeon, H. B., Unusual Cu(I)-catalyzed 1,3-dipolar cycloaddition of acetylenic amides: formation of bistriazoles. Tetrahedron Lett., 2012, 53(13), 1606-1609.
    • (2012) Tetrahedron Lett , vol.53 , Issue.13 , pp. 1606-1609
    • Kwon, M.1    Jang, Y.2    Yoon, S.3    Yang, D.4    Jeon, H.B.5
  • 66
    • 68949195821 scopus 로고    scopus 로고
    • Synthesis and Characterization of Isomeric Vinyl-1,2,3-triazole Materials by Azide-Alkyne Click Chemistry
    • Hunaid, N.; Kenichi, T.; Anika O., Synthesis and Characterization of Isomeric Vinyl-1,2,3-triazole Materials by Azide-Alkyne Click Chemistry. Macromolecules, 2009, 42(16), 6068-6074.
    • (2009) Macromolecules , vol.42 , Issue.16 , pp. 6068-6074
    • Hunaid, N.1    Kenichi, T.2    Anika, O.3
  • 67
    • 77958182047 scopus 로고    scopus 로고
    • Labeling live cells by Copper-catalyzed alkyne-azide click chemistry
    • Hong, V.; Steinmetz, N. F.; Manchester, M.; Finn, M. G., Labeling live cells by Copper-catalyzed alkyne-azide click chemistry. Bioconjugate Chem., 2010, 21(10), 1912-1916.
    • (2010) Bioconjugate Chem , vol.21 , Issue.10 , pp. 1912-1916
    • Hong, V.1    Steinmetz, N.F.2    Manchester, M.3    Finn, M.G.4
  • 72
    • 84855756802 scopus 로고    scopus 로고
    • Synthesis of a biologically active triazolecontaining analogue of cystatin a through successive peptidomimetic alkyneazide ligations
    • Ibai, E. V.; Fabien, L.; Gilles, L., Synthesis of a biologically active triazolecontaining analogue of cystatin a through successive peptidomimetic alkyneazide ligations. Angew. Chem. Int. Ed., 2012, 51(3), 718-722.
    • (2012) Angew. Chem. Int. Ed , vol.51 , Issue.3 , pp. 718-722
    • Ibai, E.V.1    Fabien, L.2    Gilles, L.3
  • 74
    • 33847303014 scopus 로고    scopus 로고
    • Alkynyl sugar analogs for the labeling and visualization of glycoconjugates in cells
    • Hsu, T.-L.; Hanson, S. R.; Kishikawa, K.; Wang, S.-K.; Sawa, M.; Wong, C.-H., Alkynyl sugar analogs for the labeling and visualization of glycoconjugates in cells. Proc. Natl. Acad. Sci., 2007, 104(8), 2614-2619.
    • (2007) Proc. Natl. Acad. Sci , vol.104 , Issue.8 , pp. 2614-2619
    • Hsu, T.-L.1    Hanson, S.R.2    Kishikawa, K.3    Wang, S.-K.4    Sawa, M.5    Wong, C.-H.6
  • 75
    • 84855517711 scopus 로고    scopus 로고
    • Dynamic metabolic labeling of DNA in vivo with arabinosyl nucleosides
    • Neef, A. B.; Luedtke, N. W., Dynamic metabolic labeling of DNA in vivo with arabinosyl nucleosides. Proc. Natl. Acad. Sci., 2011, 108 (51), 20404-20409.
    • (2011) Proc. Natl. Acad. Sci , vol.108 , Issue.51 , pp. 20404-20409
    • Neef, A.B.1    Luedtke, N.W.2
  • 76
    • 84858785499 scopus 로고    scopus 로고
    • Clickmediated labeling of bacterial membranes through metabolic modification of the lipopolysaccharide inner core
    • Dumont, A.; Malleron, A.; Awwad, M.; Dukan, S.; Vauzeilles, B. Clickmediated labeling of bacterial membranes through metabolic modification of the lipopolysaccharide inner core. Angew. Chem. Int. Ed. 2012, 51(13), 3143-3146.
    • (2012) Angew. Chem. Int. Ed , vol.51 , Issue.13 , pp. 3143-3146
    • Dumont, A.1    Malleron, A.2    Awwad, M.3    Dukan, S.4    Vauzeilles, B.5
  • 79
    • 33748609388 scopus 로고    scopus 로고
    • Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA
    • Gierlich, J.; Burley, G. A.; Gramlich, P. M. E.; Hammond, D. M.; Carell, T., Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA. Org. Lett., 2006, 8(17), 3639-3642.
    • (2006) Org. Lett , vol.8 , Issue.17 , pp. 3639-3642
    • Gierlich, J.1    Burley, G.A.2    Gramlich, P.M.E.3    Hammond, D.M.4    Carell, T.5
  • 81
    • 63749116659 scopus 로고    scopus 로고
    • Comparison of a nucleosidic vs non-nucleosidic postsynthetic Click modification of DNA with base-labile fluorescent probes
    • Berndl, S.; Herzig, N.; Kele, P.; Lachmann, D.; Li, X. H.; Wolfbeis, O. S.; Wagenknecht, H. A., Comparison of a nucleosidic vs non-nucleosidic postsynthetic Click modification of DNA with base-labile fluorescent probes. Bioconjugate Chem., 2009, 20(3), 558-564.
    • (2009) Bioconjugate Chem , vol.20 , Issue.3 , pp. 558-564
    • Berndl, S.1    Herzig, N.2    Kele, P.3    Lachmann, D.4    Li, X.H.5    Wolfbeis, O.S.6    Wagenknecht, H.A.7
  • 82
    • 0037462409 scopus 로고    scopus 로고
    • Click chemistry to construct fluorescent oligonucleotides for DNA sequencing
    • Seo, T. S.; Li, Z.; Ruparel, H.; Ju, J. J., Click chemistry to construct fluorescent oligonucleotides for DNA sequencing. J. Org. Chem., 2003, 68(2), 609-612.
    • (2003) J. Org. Chem , vol.68 , Issue.2 , pp. 609-612
    • Seo, T.S.1    Li, Z.2    Ruparel, H.3    Ju, J.J.4
  • 83
    • 36049013740 scopus 로고    scopus 로고
    • An efficient reagent for 5'-azido oligonucleotide synthesis
    • Lietard, J.; Meyer, A.; Vasseur, J.-J.; Morvan, F., An efficient reagent for 5'-azido oligonucleotide synthesis. Tetrahedron Lett., 2007, 48(50), 8795-8798.
    • (2007) Tetrahedron Lett , vol.48 , Issue.50 , pp. 8795-8798
    • Lietard, J.1    Meyer, A.2    Vasseur, J.-J.3    Morvan, F.4
  • 84
    • 79954513077 scopus 로고    scopus 로고
    • Chemical synthesis of site-specifically 2'-azido-modified RNA and potential applications for bioconjugation and RNA interference
    • Aigner, M.; Hartl, M.; Fauster, K.; Steger, J.; Bister, K.; Micura, R., Chemical synthesis of site-specifically 2'-azido-modified RNA and potential applications for bioconjugation and RNA interference. ChemBioChem., 2011, 12(1), 47-51.
    • (2011) ChemBioChem , vol.12 , Issue.1 , pp. 47-51
    • Aigner, M.1    Hartl, M.2    Fauster, K.3    Steger, J.4    Bister, K.5    Micura, R.6
  • 85
    • 77957569799 scopus 로고    scopus 로고
    • Efficient access to nonhydrolyzable initiator tRNA based on the synthesis of 3'-azido-3 '-deoxyadenosine RNA
    • Steger, J.; Graber, D.; Moroder, H.; Geiermann, A. S.; Aigner, M.; Micura, R., Efficient access to nonhydrolyzable initiator tRNA based on the synthesis of 3'-azido-3 '-deoxyadenosine RNA. Angew. Chem. Int. Ed., 2010, 49(41), 7470-7472.
    • (2010) Angew. Chem. Int. Ed , vol.49 , Issue.41 , pp. 7470-7472
    • Steger, J.1    Graber, D.2    Moroder, H.3    Geiermann, A.S.4    Aigner, M.5    Micura, R.6
  • 86
    • 83555173453 scopus 로고    scopus 로고
    • Efficient reverse click labeling of azide oligonucleotides with multiple alkynyl Cy-Dyes applied to the synthesis of HyBeacon probes for genetic analysis
    • Gerowska, M.; Hall, L.; Richardson, J.; Shelbourne, M.; Brown, T., Efficient reverse click labeling of azide oligonucleotides with multiple alkynyl Cy-Dyes applied to the synthesis of HyBeacon probes for genetic analysis. Tetrahedron, 2012, 68(3), 857-864.
    • (2012) Tetrahedron , vol.68 , Issue.3 , pp. 857-864
    • Gerowska, M.1    Hall, L.2    Richardson, J.3    Shelbourne, M.4    Brown, T.5
  • 87
    • 77955575354 scopus 로고    scopus 로고
    • Orthogonal Alkynyl Amino Acid Reporter for Selective Labeling of Bacterial Proteomes during Infection
    • Grammel, M.; Zhang, M. M.; Hang, H. C., Orthogonal Alkynyl Amino Acid Reporter for Selective Labeling of Bacterial Proteomes during Infection. Angew. Chem., Int. Ed., 2010, 49(34), 5970-5974.
    • (2010) Angew. Chem., Int. Ed , vol.49 , Issue.34 , pp. 5970-5974
    • Grammel, M.1    Zhang, M.M.2    Hang, H.C.3
  • 89
    • 84861361764 scopus 로고    scopus 로고
    • Two-strain, cell-selective protein labeling in mixed bacterial cultures
    • Truong, F.; Yoo, T. H.; Lampo, J. T.; Tirrell, A. D. Two-strain, cell-selective protein labeling in mixed bacterial cultures. J. Am. Chem. Soc., 2012, 134(20), 8551-8556.
    • (2012) J. Am. Chem. Soc , vol.134 , Issue.20 , pp. 8551-8556
    • Truong, F.1    Yoo, T.H.2    Lampo, J.T.3    Tirrell, A.D.4
  • 90
    • 84855643309 scopus 로고    scopus 로고
    • Cell-selective labeling of bacterial proteomes with an orthogonal phenylalanine amino acid reporter
    • Grammel, M.; Dossa, D. P.; Taylor-Salmon E.; Hang, C. H. Cell-selective labeling of bacterial proteomes with an orthogonal phenylalanine amino acid reporter. Chem. Commun., 2012, 48(10), 1473-1474.
    • (2012) Chem. Commun , vol.48 , Issue.10 , pp. 1473-1474
    • Grammel, M.1    Dossa, D.P.2    Taylor-Salmon, E.3    Hang, C.H.4
  • 91
    • 0024379967 scopus 로고
    • Acid pH in tumors and its potential for therapeutic exploitation
    • Tannock, I. F.; Rotin, D., Acid pH in tumors and its potential for therapeutic exploitation. Cancer Res., 1989, 49(16), 4373-4384.
    • (1989) Cancer Res , vol.49 , Issue.16 , pp. 4373-4384
    • Tannock, I.F.1    Rotin, D.2
  • 92
    • 84858700347 scopus 로고    scopus 로고
    • Determination of intracellular pH using sensitive, clickable fluorescent probes
    • Yapici, N. B.; Mandalapu, S. R.; Chew, T.-L.; Khuon, S.; Bi, L., Determination of intracellular pH using sensitive, clickable fluorescent probes. Bioorg. Med. Chem. Lett., 2012, 22(7), 2440-2443.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.7 , pp. 2440-2443
    • Yapici, N.B.1    Mandalapu, S.R.2    Chew, T.-L.3    Khuon, S.4    Bi, L.5
  • 93
    • 84862573729 scopus 로고    scopus 로고
    • Acid-labile traceless click linker for protein transduction
    • Maier, K.; Wagner, E. Acid-labile traceless click linker for protein transduction. J. Am. Chem. Soc., 2012, 134(24), 10169-10173.
    • (2012) J. Am. Chem. Soc , vol.134 , Issue.24 , pp. 10169-10173
    • Maier, K.1    Wagner, E.2
  • 94
    • 70349316698 scopus 로고    scopus 로고
    • Comparative analysis of nanoparticle-antibody conjugations: Carbodiimide versus click chemistry
    • Thorek, D. L. J.; Elias, D. R.; Tsourkas, A., Comparative analysis of nanoparticle-antibody conjugations: carbodiimide versus click chemistry. Molecular Imaging, 2009, 8(4), 221-229.
    • (2009) Molecular Imaging , vol.8 , Issue.4 , pp. 221-229
    • Thorek, D.L.J.1    Elias, D.R.2    Tsourkas, A.3
  • 95
    • 77951045250 scopus 로고    scopus 로고
    • Polyvalent oligonucleotide Iron oxide nanoparticle Click conjugates
    • Cutler, J. I.; Zheng, D.; Xu, X.; Giljohann, D. A.; Mirkin, C. A., Polyvalent oligonucleotide Iron oxide nanoparticle Click conjugates. Nano Lett., 2010, 10(4), 1477-1480.
    • (2010) Nano Lett , vol.10 , Issue.4 , pp. 1477-1480
    • Cutler, J.I.1    Zheng, D.2    Xu, X.3    Giljohann, D.A.4    Mirkin, C.A.5
  • 96
    • 61849100392 scopus 로고    scopus 로고
    • Click chemistry functionalized polymeric nanoparticles target corneal epithelial cells through RGD-cell surface receptors
    • Lu, J.; Shi, M.; Shoichet, M. S., Click chemistry functionalized polymeric nanoparticles target corneal epithelial cells through RGD-cell surface receptors. Bioconjugate Chem., 2009, 20(1), 87-94.
    • (2009) Bioconjugate Chem , vol.20 , Issue.1 , pp. 87-94
    • Lu, J.1    Shi, M.2    Shoichet, M.S.3
  • 97
    • 78349283455 scopus 로고    scopus 로고
    • An intein-mediated site-specific click conjugation strategy for improved tumor targeting of nanoparticle systems
    • Elias, D. R.; Cheng, Z.; Tsourkas, A., An intein-mediated site-specific click conjugation strategy for improved tumor targeting of nanoparticle systems. Small, 2010, 6(21), 2460-2468.
    • (2010) Small , vol.6 , Issue.21 , pp. 2460-2468
    • Elias, D.R.1    Cheng, Z.2    Tsourkas, A.3
  • 98
    • 84855595270 scopus 로고    scopus 로고
    • Polyvalent DNA-graphene nanosheets click conjugates
    • Wang, Z.; Ge, Z.; Zheng, X.; Chen, N.; Peng, C., Fan, C.; Huang, Q., Polyvalent DNA-graphene nanosheets click conjugates. Nanoscale, 2012, 4(2), 394-399.
    • (2012) Nanoscale , vol.4 , Issue.2 , pp. 394-399
    • Wang, Z.1    Ge, Z.2    Zheng, X.3    Chen, N.4    Peng, C.5    Fan, C.6    Huang, Q.7
  • 99
    • 70350304285 scopus 로고    scopus 로고
    • A Click Chemistry approach to the efficient synthesis of multiple imaging probes derived from a single precursor
    • Mindt, T. L.; Muller, C.; Stuker, F.; Salazar, J.-F.; Hohn, A.; Mueggler, T.; Rudin, M.; Schibli, R., A Click Chemistry approach to the efficient synthesis of multiple imaging probes derived from a single precursor. Bioconjugate Chem., 2009, 20(10), 1940-1949.
    • (2009) Bioconjugate Chem , vol.20 , Issue.10 , pp. 1940-1949
    • Mindt, T.L.1    Muller, C.2    Stuker, F.3    Salazar, J.-F.4    Hohn, A.5    Mueggler, T.6    Rudin, M.7    Schibli, R.8
  • 100
    • 84863077449 scopus 로고    scopus 로고
    • Synthesis and evaluation of 18F-labeled styryltriazole and resveratrol derivatives for betaamyloid plaque imaging
    • Lee, I.; Choe, Y. S.; Choi, J. Y.; Lee, K.-H.; Kim, B.-T., Synthesis and evaluation of 18F-labeled styryltriazole and resveratrol derivatives for betaamyloid plaque imaging. J. Med. Chem., 2012, 55(2), 883-892.
    • (2012) J. Med. Chem , vol.55 , Issue.2 , pp. 883-892
    • Lee, I.1    Choe, Y.S.2    Choi, J.Y.3    Lee, K.-H.4    Kim, B.-T.5
  • 101
    • 84860472658 scopus 로고    scopus 로고
    • Synthesis, properties and nearinfrared imaging evaluation of glucose conjugated zinc phthalocyanine via click reaction
    • Lv, F.; He, X.; Lu, L.; Wu, L.; Liu, T., Synthesis, properties and nearinfrared imaging evaluation of glucose conjugated zinc phthalocyanine via click reaction. J. Porphyr. and Phthal., 2012, 16(1), 77-84.
    • (2012) J. Porphyr. and Phthal , vol.16 , Issue.1 , pp. 77-84
    • Lv, F.1    He, X.2    Lu, L.3    Wu, L.4    Liu, T.5
  • 102
    • 84859356662 scopus 로고    scopus 로고
    • A phthalocyanine-peptide conjugate with high In vitro photodynamic activity and enhanced in vivo tumor-retention property
    • Ke, M.-R.; Yeung, S.-L.; Fong, W.-P.; Ng, D. K. P.; Lo, P.-C., A phthalocyanine-peptide conjugate with high In vitro photodynamic activity and enhanced in vivo tumor-retention property. Chem. Eur. J., 2012, 18(14), 4225-4233.
    • (2012) Chem. Eur. J , vol.18 , Issue.14 , pp. 4225-4233
    • Ke, M.-R.1    Yeung, S.-L.2    Fong, W.-P.3    Ng, D.K.P.4    Lo, P.-C.5


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