메뉴 건너뛰기




Volumn 20, Issue 5, 2015, Pages 9263-9294

Recent advances in click chemistry applied to dendrimer synthesis

Author keywords

Click; Dendrimer; Dendron; Diels Alder; H isgen cycloaddition; Thiol ene; Thiol yne

Indexed keywords

DENDRIMER;

EID: 84942782300     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules20059263     Document Type: Review
Times cited : (135)

References (219)
  • 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, 2004-2021.
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 3
    • 77951519941 scopus 로고    scopus 로고
    • Click" methodologies: Efficient, simple and greener routes to design dendrimers
    • Franc, G.; Kakkar, A.K. "Click" methodologies: Efficient, simple and greener routes to design dendrimers. Chem. Soc. Rev. 2010, 39, 1536-1544.
    • (2010) Chem. Soc. Rev , vol.39 , pp. 1536-1544
    • Franc, G.1    Kakkar, A.K.2
  • 4
    • 1342328015 scopus 로고    scopus 로고
    • Hyperbranched polymers: From synthesis to applications
    • Gao, C.; Yan, D. Hyperbranched polymers: From synthesis to applications. Prog. Polym. Sci. 2004, 29, 183-275.
    • (2004) Prog. Polym. Sci , vol.29 , pp. 183-275
    • Gao, C.1    Yan, D.2
  • 6
    • 0035781094 scopus 로고    scopus 로고
    • Polymers with complex architecture by living anionic Polymerization
    • Hadjichristidis, N.; Pitsikalis, M.; Pispas, S.; Iatrou, H. Polymers with Complex Architecture by Living Anionic Polymerization. Chem. Rev. 2001, 101, 3747-3792.
    • (2001) Chem. Rev , vol.101 , pp. 3747-3792
    • Hadjichristidis, N.1    Pitsikalis, M.2    Pispas, S.3    Iatrou, H.4
  • 11
    • 78650316044 scopus 로고    scopus 로고
    • Biomedical applications of dendrimers: A tutorial
    • Mintzer, M.A.; Grinstaff, M.W. Biomedical applications of dendrimers: A tutorial. Chem. Soc. Rev. 2011, 40, 173-190.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 173-190
    • Mintzer, M.A.1    Grinstaff, M.W.2
  • 13
    • 79954579637 scopus 로고    scopus 로고
    • Design of biocompatible dendrimers for cancer diagnosis and therapy: Current status and future perspectives
    • Cheng, Y.; Zhao, L.; Li, Y.; Xu, T. Design of biocompatible dendrimers for cancer diagnosis and therapy: Current status and future perspectives. Chem. Soc. Rev. 2011, 40, 2673-2703.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 2673-2703
    • Cheng, Y.1    Zhao, L.2    Li, Y.3    Xu, T.4
  • 14
    • 0002524543 scopus 로고    scopus 로고
    • Designing dendrimers based on transition-metal complexes. Light-harvesting properties and predetermined redox patterns
    • Balzani, V.; Campagna, S.; Denti, G.; Juris, A.; Serroni, S.; Venturi, M. Designing Dendrimers Based on Transition-Metal Complexes. Light-Harvesting Properties and Predetermined Redox Patterns. Acc. Chem. Res. 1998, 31, 26-34.
    • (1998) Acc. Chem. Res , vol.31 , pp. 26-34
    • Balzani, V.1    Campagna, S.2    Denti, G.3    Juris, A.4    Serroni, S.5    Venturi, M.6
  • 16
    • 84877836111 scopus 로고    scopus 로고
    • Dendritic catalysis-Basic concepts and recent trends
    • Wang, D.; Astruc, D. Dendritic catalysis-Basic concepts and recent trends. Coord. Chem. Rev. 2013, 257, 2317-2334.
    • (2013) Coord. Chem. Rev , vol.257 , pp. 2317-2334
    • Wang, D.1    Astruc, D.2
  • 19
    • 73249130570 scopus 로고    scopus 로고
    • Applications of orthogonal click" chemistries in the synthesis of Functional Soft Materials
    • Iha, R.K.; Wooley, K.L.; Nyström, A.M.; Burke, D.J.; Kade, M.J.; Hawker, C.J. Applications of Orthogonal "Click" Chemistries in the Synthesis of Functional Soft Materials. Chem. Rev. 2009, 109, 5620-5686.
    • (2009) Chem. Rev , vol.109 , pp. 5620-5686
    • Iha, R.K.1    Wooley, K.L.2    Nyström, A.M.3    Burke, D.J.4    Kade, M.J.5    Hawker, C.J.6
  • 20
    • 84861859210 scopus 로고    scopus 로고
    • Synthesis and functionalization of nanoengineered materials using click chemistry
    • Such, G.K.; Johnston, A.P.R.; Liang, K.; Caruso, F. Synthesis and functionalization of nanoengineered materials using click chemistry. Prog. Polym. Sci. 2012, 37, 985-1003.
    • (2012) Prog. Polym. Sci , vol.37 , pp. 985-1003
    • Such, G.K.1    Johnston, A.P.R.2    Liang, K.3    Caruso, F.4
  • 21
    • 0037099395 scopus 로고    scopus 로고
    • 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, 2596-2599.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.A.4
  • 22
    • 73349124811 scopus 로고    scopus 로고
    • Copper-catalyzed azide-Alkyne cycloaddition: Regioselective Synthesis of 1, 4, 5-Trisubstituted 1, 2, 3-Triazoles
    • Spiteri, C.; Moses, J.E. Copper-Catalyzed Azide-Alkyne Cycloaddition: Regioselective Synthesis of 1, 4, 5-Trisubstituted 1, 2, 3-Triazoles. Angew. Chem. Int. Ed. 2010, 49, 31-33.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 31-33
    • Spiteri, C.1    Moses, J.E.2
  • 23
    • 84867726453 scopus 로고    scopus 로고
    • Cui-catalyzed alkyne-Azide click" cycloadditions from a Mechanistic and Synthetic Perspective
    • Bock, V.D.; Hiemstra, H.; van Maarseveen, J.H. CuI-Catalyzed Alkyne-Azide "Click" Cycloadditions from a Mechanistic and Synthetic Perspective. Eur. J. Org. Chem. 2006, 2006, 51-68.
    • (2006) Eur. J. Org. Chem , vol.2006 , pp. 51-68
    • Bock, V.D.1    Hiemstra, H.2    Van Maarseveen, J.H.3
  • 24
    • 84890519070 scopus 로고    scopus 로고
    • Advancements in the mechanistic understanding of the copper-catalyzed azide-Alkyne cycloaddition
    • Berg, R.; Straub, B.F. Advancements in the mechanistic understanding of the copper-catalyzed azide-Alkyne cycloaddition. Beilstein J. Org. Chem. 2013, 9, 2715-2750.
    • (2013) Beilstein J. Org. Chem , vol.9 , pp. 2715-2750
    • Berg, R.1    Straub, B.F.2
  • 25
    • 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, 1302-1315.
    • (2010) Chem. Soc. Rev , vol.39 , pp. 1302-1315
    • Hein, J.E.1    Fokin, V.V.2
  • 26
    • 80052737264 scopus 로고    scopus 로고
    • Synthesis of a controlled three-faced PAMAM particle
    • Arseneault, M.; Dufour, P.; Levesque, I.; Morin, J.-F. Synthesis of a controlled three-faced PAMAM particle. Polym. Chem. 2011, 2, 2293-2298.
    • (2011) Polym. Chem , vol.2 , pp. 2293-2298
    • Arseneault, M.1    Dufour, P.2    Levesque, I.3    Morin, J.-F.4
  • 27
    • 84867851102 scopus 로고    scopus 로고
    • Convergent synthesis of PAMAM dendrimers containing tetra(ethylene oxide) at core using click chemistry
    • Han, S.C.; Kim, J.H.; Lee, J.W. Convergent synthesis of PAMAM dendrimers containing tetra(ethylene oxide) at core using click chemistry. Bull. Korean Chem. Soc. 2012, 33, 3501-3504.
    • (2012) Bull. Korean Chem. Soc , vol.33 , pp. 3501-3504
    • Han, S.C.1    Kim, J.H.2    Lee, J.W.3
  • 28
    • 84858056314 scopus 로고    scopus 로고
    • Diazo transfer and Click chemistry in the solid phase syntheses of lysine-based glycodendrimers as antagonists against Escherichia coli FimH
    • Papadopoulos, A.; Shiao, T.C.; Roy, R. Diazo transfer and Click chemistry in the solid phase syntheses of lysine-based glycodendrimers as antagonists against Escherichia coli FimH. Mol. Pharm. 2012, 9, 394-403.
    • (2012) Mol. Pharm , vol.9 , pp. 394-403
    • Papadopoulos, A.1    Shiao, T.C.2    Roy, R.3
  • 29
    • 77952682147 scopus 로고    scopus 로고
    • Synthesis of DOTA-Conjugated Multimeric [Tyr3]Octreotide Peptides via a Combination of Cu(I)-Catalyzed Click" Cycloaddition and thio acid/sulfonyl azide "sulfo-click" amidation and their in vivo evaluation
    • Yim, C.-B.; Dijkgraaf, I.; Merkx, R.; Versluis, C.; Eek, A.; Mulder, G.E.; Rijkers, D.T.S.; Boerman, O.C.; Liskamp, R.M.J. Synthesis of DOTA-Conjugated Multimeric [Tyr3]Octreotide Peptides via a Combination of Cu(I)-Catalyzed "Click" Cycloaddition and Thio Acid/Sulfonyl Azide "Sulfo-Click" Amidation and Their in Vivo Evaluation. J. Med. Chem. 2010, 53, 3944-3953.
    • (2010) J. Med. Chem , vol.53 , pp. 3944-3953
    • Yim, C.-B.1    Dijkgraaf, I.2    Merkx, R.3    Versluis, C.4    Eek, A.5    Mulder, G.E.6    Rijkers, D.T.S.7    Boerman, O.C.8    Liskamp, R.M.J.9
  • 30
    • 79952735252 scopus 로고    scopus 로고
    • Water-soluble glycodendrimers: Synthesis and stabilization of catalytically active Pd and Pt nanoparticles
    • Gatard, S.; Liang, L.; Salmon, L.; Ruiz, J.; Astruc, D.; Bouquillon, S. Water-soluble glycodendrimers: Synthesis and stabilization of catalytically active Pd and Pt nanoparticles. Tetrahedron Lett. 2011, 52, 1842-1846.
    • (2011) Tetrahedron Lett , vol.52 , pp. 1842-1846
    • Gatard, S.1    Liang, L.2    Salmon, L.3    Ruiz, J.4    Astruc, D.5    Bouquillon, S.6
  • 31
    • 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, 2460-2468.
    • (2010) Small , vol.6 , pp. 2460-2468
    • Elias, D.R.1    Cheng, Z.2    Tsourkas, A.3
  • 32
    • 80055000209 scopus 로고    scopus 로고
    • Synthesis of [3]-rotaxane dendrimers by host-mediated click chemistry
    • Han, S.C.; Yoon, J.; Oh, J.; Lee, J.W. Synthesis of [3]-rotaxane dendrimers by host-mediated click chemistry. Bull. Korean Chem. Soc. 2011, 32, 3809-3812.
    • (2011) Bull. Korean Chem. Soc , vol.32 , pp. 3809-3812
    • Han, S.C.1    Yoon, J.2    Oh, J.3    Lee, J.W.4
  • 33
    • 84945178057 scopus 로고    scopus 로고
    • Efficient synthesis of carbazole core diblock dendrimer by Double Click Chemistry
    • Han, S.C.; Choi, I.-H.; Jin, S.-H.; Lee, J.W. Efficient Synthesis of Carbazole Core Diblock Dendrimer by Double Click Chemistry. Mol. Cryst. Liquid Cryst. 2014, 599, 86-95.
    • (2014) Mol. Cryst. Liquid Cryst , vol.599 , pp. 86-95
    • Han, S.C.1    Choi, I.-H.2    Jin, S.-H.3    Lee, J.W.4
  • 34
    • 17644414186 scopus 로고    scopus 로고
    • Mechanism of the ligand-free cui-catalyzed azide-Alkyne Cycloaddition Reaction
    • Rodionov, V.O.; Fokin, V.V.; Finn, M.G. Mechanism of the Ligand-Free CuI-Catalyzed Azide-Alkyne Cycloaddition Reaction. Angew. Chem. Int. Ed. 2005, 44, 2210-2215.
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 2210-2215
    • Rodionov, V.O.1    Fokin, V.V.2    Finn, M.G.3
  • 35
    • 0034604562 scopus 로고    scopus 로고
    • Acetylenic coupling: A powerful tool in molecular Construction
    • Siemsen, P.; Livingston, R.C.; Diederich, F. Acetylenic Coupling: A Powerful Tool in Molecular Construction. Angew. Chem. Int. Ed. 2000, 39, 2632-2657.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 2632-2657
    • Siemsen, P.1    Livingston, R.C.2    Diederich, F.3
  • 36
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed azide-alkyne cycloaddition
    • Meldal, M.; Tornøe, C.W. Cu-Catalyzed Azide-Alkyne Cycloaddition. Chem. Rev. 2008, 108, 2952-3015.
    • (2008) Chem. Rev , vol.108 , pp. 2952-3015
    • Meldal, M.1    Tornøe, C.W.2
  • 37
    • 84871968844 scopus 로고    scopus 로고
    • Using two simple methods of Ar-ArF self-Assembly and isolation chromophores to further improve the comprehensive performance of NLO dendrimers
    • Wu, W.; Yu, G.; Liu, Y.; Ye, C.; Qin, J.; Li, Z. Using two simple methods of Ar-ArF self-Assembly and isolation chromophores to further improve the comprehensive performance of NLO dendrimers. Chem. Eur. J. 2013, 19, 630-641.
    • (2013) Chem. Eur. J , vol.19 , pp. 630-641
    • Wu, W.1    Yu, G.2    Liu, Y.3    Ye, C.4    Qin, J.5    Li, Z.6
  • 38
    • 84861807036 scopus 로고    scopus 로고
    • Enhancing membrane disruption by targeting and multivalent presentation of antimicrobial peptides
    • Chamorro, C.; Boerman, M.A.; Arnusch, C.J.; Breukink, E.; Pieters, R.J. Enhancing membrane disruption by targeting and multivalent presentation of antimicrobial peptides. Biochim. Biophys. Acta 2012, 1818, 2171-2174.
    • (2012) Biochim. Biophys. Acta , vol.1818 , pp. 2171-2174
    • Chamorro, C.1    Boerman, M.A.2    Arnusch, C.J.3    Breukink, E.4    Pieters, R.J.5
  • 39
    • 78651422155 scopus 로고    scopus 로고
    • Convergent assembly and surface modification of multifunctional dendrimers by three consecutive click reactions
    • Ledin, P.A.; Friscourt, F.; Guo, J.; Boons, G.-J. Convergent Assembly and Surface Modification of Multifunctional Dendrimers by Three Consecutive Click Reactions. Chem. Eur. J. 2011, 17, 839-846.
    • (2011) Chem. Eur. J , vol.17 , pp. 839-846
    • Ledin, P.A.1    Friscourt, F.2    Guo, J.3    Boons, G.-J.4
  • 40
    • 84871931341 scopus 로고    scopus 로고
    • Monitoring surface functionalization of dendrigraft poly-l-lysines via click chemistry by capillary electrophoresis and Taylor dispersion analysis
    • Liu, T.; Oukacine, F.; Collet, H.; Commeyras, A.; Vial, L.; Cottet, H. Monitoring surface functionalization of dendrigraft poly-l-lysines via click chemistry by capillary electrophoresis and Taylor dispersion analysis. J. Chromatogr. A 2013, 1273, 111-116.
    • (2013) J. Chromatogr. A , vol.1273 , pp. 111-116
    • Liu, T.1    Oukacine, F.2    Collet, H.3    Commeyras, A.4    Vial, L.5    Cottet, H.6
  • 41
    • 84875732964 scopus 로고    scopus 로고
    • Convergent synthesis of carbazole core PAMAM dendrimer via click chemistry
    • Lee, J.W.; Han, S.C.; Yun, S.-H.; Jin, S.-H. Convergent synthesis of carbazole core PAMAM dendrimer via click chemistry. Bull. Korean Chem. Soc. 2013, 34, 971-974.
    • (2013) Bull. Korean Chem. Soc , vol.34 , pp. 971-974
    • Lee, J.W.1    Han, S.C.2    Yun, S.-H.3    Jin, S.-H.4
  • 42
    • 80051708651 scopus 로고    scopus 로고
    • Combined covalent and noncovalent functionalization of nanomagnetic carbon surfaces with dendrimers and BODIPY Fluorescent Dye
    • Kainz, Q.M.; Schaetz, A.; Zoepfl, A.; Stark, W.J.; Reiser, O. Combined Covalent and Noncovalent Functionalization of Nanomagnetic Carbon Surfaces with Dendrimers and BODIPY Fluorescent Dye. Chem. Mater. 2011, 23, 3606-3613.
    • (2011) Chem. Mater , vol.23 , pp. 3606-3613
    • Kainz, Q.M.1    Schaetz, A.2    Zoepfl, A.3    Stark, W.J.4    Reiser, O.5
  • 44
    • 84875278349 scopus 로고    scopus 로고
    • Non-ionic dendronized multiamphiphilic polymers as nanocarriers for biomedical applications
    • Gupta, S.; Schade, B.; Kumar, S.; Boettcher, C.; Sharma, S.K.; Haag, R. Non-ionic dendronized multiamphiphilic polymers as nanocarriers for biomedical applications. Small 2013, 9, 894-904.
    • (2013) Small , vol.9 , pp. 894-904
    • Gupta, S.1    Schade, B.2    Kumar, S.3    Boettcher, C.4    Sharma, S.K.5    Haag, R.6
  • 45
    • 77950479226 scopus 로고    scopus 로고
    • High-generation second-order nonlinear optical (NLO) Dendrimers: Convenient synthesis by click chemistry and the increasing trend of NLO Effects
    • Li, Z.A.; Wu, W.; Li, Q.; Yu, G.; Xiao, L.; Liu, Y.; Ye, C.; Qin, J.; Li, Z. High-Generation Second-Order Nonlinear Optical (NLO) Dendrimers: Convenient Synthesis by Click Chemistry and the Increasing Trend of NLO Effects. Angew. Chem. Int. Ed. 2010, 49, 2763-2767.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 2763-2767
    • Li, Z.A.1    Wu, W.2    Li, Q.3    Yu, G.4    Xiao, L.5    Liu, Y.6    Ye, C.7    Qin, J.8    Li, Z.9
  • 46
    • 84915818508 scopus 로고    scopus 로고
    • Dendrimer-Type peptoid-decorated hexaphenylxylenes and tetraphenylmethanes: Synthesis and structure in solution and in the gas phase
    • Peschko, K.; Schade, A.; Vollrath, S.B. L.; Schwarz, U.; Luy, B.; Muhle-Goll, C.; Weis, P.; Braese, S. Dendrimer-Type Peptoid-Decorated Hexaphenylxylenes and Tetraphenylmethanes: Synthesis and Structure in Solution and in the Gas Phase. Chem. Eur. J. 2014, 20, 16273-16278.
    • (2014) Chem. Eur. J , vol.20 , pp. 16273-16278
    • Peschko, K.1    Schade, A.2    Vollrath, S.B.L.3    Schwarz, U.4    Luy, B.5    Muhle-Goll, C.6    Weis, P.7    Braese, S.8
  • 48
    • 77955795023 scopus 로고    scopus 로고
    • Oligonucleotide carbohydrate-centered galactosyl cluster conjugates synthesized by click and phosphoramidite chemistries
    • Pourceau, G.; Meyer, A.; Chevolot, Y.; Souteyrand, E.; Vasseur, J.-J.; Morvan, F. Oligonucleotide Carbohydrate-Centered Galactosyl Cluster Conjugates Synthesized by Click and Phosphoramidite Chemistries. Bioconjugate Chem. 2010, 21, 1520-1529.
    • (2010) Bioconjugate Chem , vol.21 , pp. 1520-1529
    • Pourceau, G.1    Meyer, A.2    Chevolot, Y.3    Souteyrand, E.4    Vasseur, J.-J.5    Morvan, F.6
  • 49
    • 79953187599 scopus 로고    scopus 로고
    • [CuBr(PPh3)3] for azide-alkyne cycloaddition reactions under strict click conditions
    • Lal, S.; Díez-González, S. [CuBr(PPh3)3] for Azide-Alkyne Cycloaddition Reactions under Strict Click Conditions. J. Org. Chem. 2011, 76, 2367-2373.
    • (2011) J. Org. Chem , vol.76 , pp. 2367-2373
    • Lal, S.1    Díez-González, S.2
  • 50
    • 84876676322 scopus 로고    scopus 로고
    • Direct evidence of a dinuclear copper intermediate in Cu(I)-catalyzed azide-Alkyne cycloadditions
    • Worrell, B.T.; Malik, J.A.; Fokin, V.V. Direct Evidence of a Dinuclear Copper Intermediate in Cu(I)-Catalyzed Azide-Alkyne Cycloadditions. Science 2013, 340, 457-460.
    • (2013) Science , vol.340 , pp. 457-460
    • Worrell, B.T.1    Malik, J.A.2    Fokin, V.V.3
  • 51
    • 84910150162 scopus 로고    scopus 로고
    • Alkyne-Azide cycloaddition catalyzed by a dinuclear copper(I) complex
    • Chen, H.-B.; Abeyrathna, N.; Liao, Y. Alkyne-Azide cycloaddition catalyzed by a dinuclear copper(I) complex. Tetrahedron Lett. 2014, 55, 6575-6576.
    • (2014) Tetrahedron Lett , vol.55 , pp. 6575-6576
    • Chen, H.-B.1    Abeyrathna, N.2    Liao, Y.3
  • 52
    • 85027943095 scopus 로고    scopus 로고
    • Dinuclear copper intermediates in copper(I)-Catalyzed Azide-Alkyne cycloaddition directly observed by electrospray ionization mass spectrometry
    • Iacobucci, C.; Reale, S.; Gal, J.-F.; de Angelis, F. Dinuclear Copper Intermediates in Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Directly Observed by Electrospray Ionization Mass Spectrometry. Angew. Chem. Int. Ed. 2015, 54, 3065-3068.
    • (2015) Angew. Chem. Int. Ed , vol.54 , pp. 3065-3068
    • Iacobucci, C.1    Reale, S.2    Gal, J.-F.3    De Angelis, F.4
  • 53
    • 84255187671 scopus 로고    scopus 로고
    • The efficient copper(I) (Hexabenzyl)tren catalyst and dendritic analogues for green Click" Reactions between azides and alkynes in organic solvent and in water: Positive dendritic effects and monometallic mechanism
    • Liang, L.; Ruiz, J.; Astruc, D. The Efficient Copper(I) (Hexabenzyl)tren Catalyst and Dendritic Analogues for Green "Click" Reactions between Azides and Alkynes in Organic Solvent and in Water: Positive Dendritic Effects and Monometallic Mechanism. Adv. Synth. Catal. 2011, 353, 3434-3450.
    • (2011) Adv. Synth. Catal , vol.353 , pp. 3434-3450
    • Liang, L.1    Ruiz, J.2    Astruc, D.3
  • 54
    • 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, 7002-7005.
    • (2010) J. Org. Chem , vol.75 , pp. 7002-7005
    • Shao, C.1    Wang, X.2    Xu, J.3    Zhao, J.4    Zhang, Q.5    Hu, Y.6
  • 55
    • 84892821933 scopus 로고    scopus 로고
    • Synthesis of steroidal dendrimers modified by click" chemistry with PAMAM dendrons as unimolecular micelles
    • Soto-Castro, D.; Magana-Vergara, N.E.; Farfan, N.; Santillan, R. Synthesis of steroidal dendrimers modified by "click" chemistry with PAMAM dendrons as unimolecular micelles. Tetrahedron Lett. 2014, 55, 1014-1019.
    • (2014) Tetrahedron Lett , vol.55 , pp. 1014-1019
    • Soto-Castro, D.1    Magana-Vergara, N.E.2    Farfan, N.3    Santillan, R.4
  • 56
    • 0001288931 scopus 로고
    • 1, 3-Dipolar cycloadditions. Past and Future
    • Huisgen, R. 1, 3-Dipolar Cycloadditions. Past and Future. Angew. Chem. Int. Ed. 1963, 2, 565-598.
    • (1963) Angew. Chem. Int. Ed , vol.2 , pp. 565-598
    • Huisgen, R.1
  • 58
    • 84860169346 scopus 로고    scopus 로고
    • Synthesis of unsymmetrical Frechet-Type dendrimers via double click chemistry
    • Han, S.C.; Kwak, S.H.; Jin, S.-H.; Lee, J.W. Synthesis of unsymmetrical Frechet-Type dendrimers via double click chemistry. Bull. Korean Chem. Soc. 2012, 33, 1393-1396.
    • (2012) Bull. Korean Chem. Soc , vol.33 , pp. 1393-1396
    • Han, S.C.1    Kwak, S.H.2    Jin, S.-H.3    Lee, J.W.4
  • 59
    • 84859820770 scopus 로고    scopus 로고
    • Arginine functionalized peptide dendrimers as potential gene delivery vehicles
    • Luo, K.; Li, C.; Li, L.; She, W.; Wang, G.; Gu, Z. Arginine functionalized peptide dendrimers as potential gene delivery vehicles. Biomaterials 2012, 33, 4917-4927.
    • (2012) Biomaterials , vol.33 , pp. 4917-4927
    • Luo, K.1    Li, C.2    Li, L.3    She, W.4    Wang, G.5    Gu, Z.6
  • 60
    • 77949799806 scopus 로고    scopus 로고
    • Click chemistry under non-classical reaction conditions
    • Kappe, C.O.; Van der Eycken, E. Click chemistry under non-classical reaction conditions. Chem. Soc. Rev. 2010, 39, 1280-1290.
    • (2010) Chem. Soc. Rev , vol.39 , pp. 1280-1290
    • Kappe, C.O.1    Van Der Eycken, E.2
  • 62
    • 84883232243 scopus 로고    scopus 로고
    • Design and Synthesis of a γ1β8-Cyclodextrin Oligomer: A New platform with potential application as a dendrimeric multi-carrier
    • Barge, A.; Caporaso, M.; Cravotto, G.; Martina, K.; Tosco, P.; Aime, S.; Carrera, C.; Gianolio, E.; Pariani, G.; Corpillo, D. Design and Synthesis of a γ1β8-Cyclodextrin Oligomer: A New Platform with Potential Application as a Dendrimeric Multi-carrier. Chem. Eur. J. 2013, 19, 12086-12092.
    • (2013) Chem. Eur. J , vol.19 , pp. 12086-12092
    • Barge, A.1    Caporaso, M.2    Cravotto, G.3    Martina, K.4    Tosco, P.5    Aime, S.6    Carrera, C.7    Gianolio, E.8    Pariani, G.9    Corpillo, D.10
  • 64
    • 0001616346 scopus 로고
    • Characterization of starburst dendrimers by the EPR technique. 1. Copper complexes in water solution
    • Ottaviani, M.F.; Bossmann, S.; Turro, N.J.; Tomalia, D.A. Characterization of starburst dendrimers by the EPR technique. 1. Copper complexes in water solution. J. Am. Chem. Soc. 1994, 116, 661-671.
    • (1994) J. Am. Chem. Soc , vol.116 , pp. 661-671
    • Ottaviani, M.F.1    Bossmann, S.2    Turro, N.J.3    Tomalia, D.A.4
  • 66
    • 79251586889 scopus 로고    scopus 로고
    • Facile synthesis of dendrimer-like star-branched poly(isopropylacrylamide) via combination of click chemistry and atom transfer radical polymerization
    • Wan, X.J.; Xu, J.; Liu, S.Y. Facile synthesis of dendrimer-like star-branched poly(isopropylacrylamide) via combination of click chemistry and atom transfer radical polymerization. Sci. China: Chem. 2010, 53, 2520-2527.
    • (2010) Sci. China: Chem , vol.53 , pp. 2520-2527
    • Wan, X.J.1    Xu, J.2    Liu, S.Y.3
  • 67
    • 77649181022 scopus 로고    scopus 로고
    • Copper toxicity in the general population
    • Brewer, G.J. Copper toxicity in the general population. Clin. Neurophysiol. 2009, 121, 459-460.
    • (2009) Clin. Neurophysiol , vol.121 , pp. 459-460
    • Brewer, G.J.1
  • 68
    • 79952270568 scopus 로고    scopus 로고
    • Differentiating between fluorescence-quenching metal ions with Polyfluorophore Sensors Built on a DNA Backbone
    • Tan, S.S.; Kim, S.J.; Kool, E.T. Differentiating between Fluorescence-Quenching Metal Ions with Polyfluorophore Sensors Built on a DNA Backbone. J. Am. Chem. Soc. 2011, 133, 2664-2671.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 2664-2671
    • Tan, S.S.1    Kim, S.J.2    Kool, E.T.3
  • 69
    • 12744259135 scopus 로고    scopus 로고
    • Dendrimer templates for supported nanoparticle catalysts
    • Springer-Verlag: New York, NY, USA
    • Lang, H; Chandler, B.D. Dendrimer templates for supported nanoparticle catalysts. In Nanotechnology in Catalysis; Springer-Verlag: New York, NY, USA, 2007; Volume 3, pp. 91-113.
    • (2007) Nanotechnology in Catalysis , vol.3 , pp. 91-113
    • Lang, H.1    Chandler, B.D.2
  • 70
    • 84924386685 scopus 로고    scopus 로고
    • Self-Assembling amphiphilic Janus dendrimers: Mesomorphic properties and aggregation in water
    • Fedeli, E.; Lancelot, A.; Serrano, J.L.; Calvo, P.; Sierra, T. Self-Assembling amphiphilic Janus dendrimers: mesomorphic properties and aggregation in water. New J. Chem. 2015, 39, 1960-1967
    • (2015) New J. Chem , vol.39 , pp. 1960-1967
    • Fedeli, E.1    Lancelot, A.2    Serrano, J.L.3    Calvo, P.4    Sierra, T.5
  • 71
    • 79959268068 scopus 로고    scopus 로고
    • GPCR Ligand Dendrimer (GLiDe) Conjugates: Adenosine receptor interactions of a series of multivalent xanthine antagonists
    • Kecskes, A.; Tosh, D.K.; Wei, Q.; Gao, Z.-G.; Jacobson, K.A. GPCR Ligand Dendrimer (GLiDe) Conjugates: Adenosine Receptor Interactions of a Series of Multivalent Xanthine Antagonists. Bioconjugate Chem. 2011, 22, 1115-1127.
    • (2011) Bioconjugate Chem , vol.22 , pp. 1115-1127
    • Kecskes, A.1    Tosh, D.K.2    Wei, Q.3    Gao, Z.-G.4    Jacobson, K.A.5
  • 72
    • 84921416241 scopus 로고    scopus 로고
    • Synthesis and self-Assembly of PAMAM/PAA Janus dendrimers
    • Gao, C.; Liu, M.; Lu, S.; Zhang, X.; Chen, Y. Synthesis and self-Assembly of PAMAM/PAA Janus dendrimers. Mater. Res. Express 2014, 1, 15005-150017.
    • (2014) Mater. Res. Express , vol.1 , pp. 15005-150017
    • Gao, C.1    Liu, M.2    Lu, S.3    Zhang, X.4    Chen, Y.5
  • 73
    • 84906762130 scopus 로고    scopus 로고
    • Recyclable catalytic dendrimer nanoreactor for part-per-Million CuI Catalysis of Click" Chemistry in Water
    • Deraedt, C.; Pinaud, N.; Astruc, D. Recyclable Catalytic Dendrimer Nanoreactor for Part-Per-Million CuI Catalysis of "Click" Chemistry in Water. J. Am. Chem. Soc. 2014, 136, 12092-12098.
    • (2014) J. Am. Chem. Soc , vol.136 , pp. 12092-12098
    • Deraedt, C.1    Pinaud, N.2    Astruc, D.3
  • 74
    • 78549235418 scopus 로고    scopus 로고
    • Polymeric ligands as homogeneous, reusable catalyst systems for copper assisted click chemistry
    • Lammens, M.; Skey, J.; Wallyn, S.; O'Reilly, R.; Du Prez, F. Polymeric ligands as homogeneous, reusable catalyst systems for copper assisted click chemistry. Chem. Commun. 2010, 46, 8719-8721.
    • (2010) Chem. Commun , vol.46 , pp. 8719-8721
    • Lammens, M.1    Skey, J.2    Wallyn, S.3    O'Reilly, R.4    Du Prez, F.5
  • 78
    • 84908018516 scopus 로고    scopus 로고
    • Click hybridization of immune cells and polyamidoamine Dendrimers
    • Xu, L.; Zolotarskaya, O.Y.; Yeudall, W.A.; Yang, H. Click Hybridization of Immune Cells and Polyamidoamine Dendrimers. Adv. Healthcare Mater. 2014, 3, 1430-1438.
    • (2014) Adv. Healthcare Mater , vol.3 , pp. 1430-1438
    • Xu, L.1    Zolotarskaya, O.Y.2    Yeudall, W.A.3    Yang, H.4
  • 79
    • 77949867607 scopus 로고    scopus 로고
    • Strain-promoted alkyne azide cycloaddition for the Functionalization of Poly(amide)-Based Dendrons and Dendrimers
    • Ornelas, C.; Broichhagen, J.; Weck, M. Strain-Promoted Alkyne Azide Cycloaddition for the Functionalization of Poly(amide)-Based Dendrons and Dendrimers. J. Am. Chem. Soc. 2010, 132, 3923-3931.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 3923-3931
    • Ornelas, C.1    Broichhagen, J.2    Weck, M.3
  • 80
    • 84908433183 scopus 로고    scopus 로고
    • Sequential and parallel dual labeling of nanoparticles using click chemistry
    • Zong, H.; Goonewardena, S.N.; Chang, H.-N.; Otis, J.B.; Baker, J.R., Jr. Sequential and parallel dual labeling of nanoparticles using click chemistry. Bioorg. Med. Chem. 2014, 22, 6288-6296.
    • (2014) Bioorg. Med. Chem , vol.22 , pp. 6288-6296
    • Zong, H.1    Goonewardena, S.N.2    Chang, H.-N.3    Otis, J.B.4    Baker, J.R.5
  • 81
    • 84888345447 scopus 로고    scopus 로고
    • PAMAM dendrimers as quantized building blocks for novel nanostructures
    • Van Dongen, M.A.; Vaidyanathan, S.; Banaszak Holl, M.M. PAMAM dendrimers as quantized building blocks for novel nanostructures. Soft Matter 2013, 9, 11188-11196.
    • (2013) Soft Matter , vol.9 , pp. 11188-11196
    • Van Dongen, M.A.1    Vaidyanathan, S.2    Banaszak Holl, M.M.3
  • 83
    • 72549106939 scopus 로고    scopus 로고
    • Cyclooctyne-based reagents for uncatalyzed click chemistry: A computational survey
    • Chenoweth, K.; Chenoweth, D.; Goddard Iii, W.A. Cyclooctyne-based reagents for uncatalyzed click chemistry: A computational survey. Org. Biomol. Chem. 2009, 7, 5255-5258.
    • (2009) Org. Biomol. Chem , vol.7 , pp. 5255-5258
    • Chenoweth, K.1    Chenoweth, D.2    Goddard, W.A.3
  • 86
    • 84860774466 scopus 로고    scopus 로고
    • Efficient and rapid divergent synthesis of ethylene oxide-containing dendrimers through catalyst-free click chemistry
    • Arseneault, M.; Levesque, I.; Morin, J.-F. Efficient and Rapid Divergent Synthesis of Ethylene Oxide-Containing Dendrimers through Catalyst-Free Click Chemistry. Macromolecules 2012, 45, 3687-3694.
    • (2012) Macromolecules , vol.45 , pp. 3687-3694
    • Arseneault, M.1    Levesque, I.2    Morin, J.-F.3
  • 88
    • 84856211636 scopus 로고    scopus 로고
    • Photophysical properties and dye-sensitized solar cell studies on thiadiazole-Triazole-chalcone dendrimers
    • Rajakumar, P.; Thirunarayanan, A.; Raja, S.; Ganesan, S.; Maruthamuthu, P. Photophysical properties and dye-sensitized solar cell studies on thiadiazole-Triazole-chalcone dendrimers. Tetrahedron Lett. 2012, 53, 1139-1143.
    • (2012) Tetrahedron Lett , vol.53 , pp. 1139-1143
    • Rajakumar, P.1    Thirunarayanan, A.2    Raja, S.3    Ganesan, S.4    Maruthamuthu, P.5
  • 89
    • 79959364296 scopus 로고    scopus 로고
    • Charge-shift states in heterometallic, porphyrin-based dendrimers formed via click chemistry
    • Le Pleux, L.; Pellegrin, Y.; Blart, E.; Odobel, F.; Harriman, A. Long-Lived, Charge-Shift States in Heterometallic, Porphyrin-Based Dendrimers Formed via Click Chemistry. J. Phys. Chem. A 2011, 115, 5069-5080.
    • (2011) J. Phys. Chem. A , vol.115 , pp. 5069-5080
    • Le Pleux, L.1    Pellegrin, Y.2    Blart, E.3    Odobel, F.4    Long-Lived, H.A.5
  • 90
    • 84856884679 scopus 로고    scopus 로고
    • Supramolecular dendrimers: Convenient synthesis by programmed self-Assembly and tunable thermoresponsivity
    • Ghosh, P.S.; Hamilton, A.D. Supramolecular Dendrimers: Convenient Synthesis by Programmed Self-Assembly and Tunable Thermoresponsivity. Chem. Eur. J. 2012, 18, 2361-2365.
    • (2012) Chem. Eur. J , vol.18 , pp. 2361-2365
    • Ghosh, P.S.1    Hamilton, A.D.2
  • 91
    • 77952372607 scopus 로고    scopus 로고
    • Thiol-yne chemistry: A powerful tool for creating highly functional materials
    • Hoogenboom, R. Thiol-Yne Chemistry: A Powerful Tool for Creating Highly Functional Materials. Angew. Chem. Int. Ed. 2010, 49, 3415-3417.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 3415-3417
    • Hoogenboom, R.1
  • 92
    • 77949859511 scopus 로고    scopus 로고
    • Thiol-ene click" reactions and recent applications in polymer and materials synthesis
    • Lowe, A.B. Thiol-ene "click" reactions and recent applications in polymer and materials synthesis. Polym. Chem. 2010, 1, 17-36.
    • (2010) Polym. Chem , vol.1 , pp. 17-36
    • Lowe, A.B.1
  • 93
    • 77955683580 scopus 로고    scopus 로고
    • Thiol-based click" chemistries in polymer: Synthesis and Modification
    • Lowe, A.B.; Harvison, M.A. Thiol-Based "Click" Chemistries in Polymer: Synthesis and Modification. Aust. J. Chem. 2010, 63, 1251-1266.
    • (2010) Aust. J. Chem , vol.63 , pp. 1251-1266
    • Lowe, A.B.1    Harvison, M.A.2
  • 94
    • 8344226831 scopus 로고    scopus 로고
    • Thiol-enes chemistry of the past with promise for the future
    • Hoyle, C.E.; Lee, T.Y.; Roper, T. Thiol-enes: Chemistry of the past with promise for the future. J. Polym. Sci. Part A: Polym. Chem. 2004, 42, 5301-5338.
    • (2004) J. Polym. Sci. Part A: Polym. Chem , vol.42 , pp. 5301-5338
    • Hoyle, C.E.1    Lee, T.Y.2    Roper, T.3
  • 95
    • 84914694820 scopus 로고    scopus 로고
    • Synthetic applications of intramolecular thiol-ene Click" Reaction
    • Scanlan E.M.; Corcé V.; Malone, A. Synthetic Applications of Intramolecular Thiol-Ene "Click" Reaction. Molecules 2014, 19, 19137-19151.
    • (2014) Molecules , vol.19 , pp. 19137-19151
    • Scanlan, E.M.1    Corcé, V.2    Malone, A.3
  • 99
    • 84905001198 scopus 로고    scopus 로고
    • Thiol-ene click" reactions and recent applications in polymer and materials synthesis: A first update
    • Lowe, A.B. Thiol-ene "click" reactions and recent applications in polymer and materials synthesis: A first update. Polym. Chem. 2014, 5, 4820-4870.
    • (2014) Polym. Chem , vol.5 , pp. 4820-4870
    • Lowe, A.B.1
  • 100
    • 77954129617 scopus 로고    scopus 로고
    • Photoinduced addition of glycosyl thiols to alkynyl peptides: Use of free-radical thiol-yne coupling for post-Translational double-glycosylation of peptides
    • Lo Conte, M.; Pacifico, S.; Chambery, A.; Marra, A.; Dondoni, A. Photoinduced Addition of Glycosyl Thiols to Alkynyl Peptides: Use of Free-Radical Thiol-Yne Coupling for Post-Translational Double-Glycosylation of Peptides. J. Org. Chem. 2010, 75, 4644-4647.
    • (2010) J. Org. Chem , vol.75 , pp. 4644-4647
    • Lo Conte, M.1    Pacifico, S.2    Chambery, A.3    Marra, A.4    Dondoni, A.5
  • 101
    • 84923242416 scopus 로고    scopus 로고
    • A highly versatile convergent/divergent onion peel" synthetic strategy toward potent multivalent glycodendrimers
    • Sharma, R.; Kottari, N.; Chabre, Y.M.; Abbassi, L.; Shiao, T.C.; Roy, R. A highly versatile convergent/divergent "onion peel" synthetic strategy toward potent multivalent glycodendrimers. Chem. Commun. 2014, 50, 13300-13303.
    • (2014) Chem. Commun , vol.50 , pp. 13300-13303
    • Sharma, R.1    Kottari, N.2    Chabre, Y.M.3    Abbassi, L.4    Shiao, T.C.5    Roy, R.6
  • 102
    • 84902675108 scopus 로고    scopus 로고
    • Onion peel" dendrimers: A straightforward synthetic approach towards highly diversified architectures
    • Sharma, R.; Naresh, K.; Chabre, Y.M.; Rej, R.; Saadeh, N.K.; Roy, R. "Onion peel" dendrimers: A straightforward synthetic approach towards highly diversified architectures. Polym. Chem. 2014, 5, 4321-4331.
    • (2014) Polym. Chem , vol.5 , pp. 4321-4331
    • Sharma, R.1    Naresh, K.2    Chabre, Y.M.3    Rej, R.4    Saadeh, N.K.5    Roy, R.6
  • 103
    • 84905919818 scopus 로고    scopus 로고
    • Facile and efficient synthesis of dendrimers and one-pot preparation of dendritic-linear polymer conjugates via a single chemistry: Utilization of kinetically selective thiol-michael addition reactions
    • Chatani, S.; Podgórski, M.; Wang, C.; Bowman, C.N. Facile and Efficient Synthesis of Dendrimers and One-Pot Preparation of Dendritic-Linear Polymer Conjugates via a Single Chemistry: Utilization of Kinetically Selective Thiol-Michael Addition Reactions. Macromolecules 2014, 47, 4894-4900.
    • (2014) Macromolecules , vol.47 , pp. 4894-4900
    • Chatani, S.1    Podgórski, M.2    Wang, C.3    Bowman, C.N.4
  • 104
    • 77952993294 scopus 로고    scopus 로고
    • Thiol-yne click chemistry: A powerful and versatile methodology for materials synthesis
    • Lowe, A.B.; Hoyle, C.E.; Bowman, C.N. Thiol-yne click chemistry: A powerful and versatile methodology for materials synthesis. J. Mater. Chem. 2010, 20, 4745-4750.
    • (2010) J. Mater. Chem , vol.20 , pp. 4745-4750
    • Lowe, A.B.1    Hoyle, C.E.2    Bowman, C.N.3
  • 105
    • 84875175609 scopus 로고    scopus 로고
    • A polymer network prepared by the thiol-yne photocrosslinking of a liquid crystalline dendrimer
    • Cervera-Procas, R.; Sanchez-Somolinos, C.; Serrano, J.L.; Omenat, A. A Polymer Network Prepared by the Thiol-yne Photocrosslinking of a Liquid Crystalline Dendrimer. Macromol. Rapid Commun. 2013, 34, 498-503.
    • (2013) Macromol. Rapid Commun , vol.34 , pp. 498-503
    • Cervera-Procas, R.1    Sanchez-Somolinos, C.2    Serrano, J.L.3    Omenat, A.4
  • 107
    • 84877794784 scopus 로고    scopus 로고
    • How do multivalent glycodendrimers benefit from sulfur chemistry?
    • Gingras, M.; Chabre, Y.M.; Roy, M.; Roy, R. How do multivalent glycodendrimers benefit from sulfur chemistry? Chem. Soc. Rev. 2013, 42, 4823-4841.
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 4823-4841
    • Gingras, M.1    Chabre, Y.M.2    Roy, M.3    Roy, R.4
  • 108
    • 80052757487 scopus 로고    scopus 로고
    • Diels-Alder click" reactions: Recent applications in polymer and material science
    • Tasdelen, M.A. Diels-Alder "click" reactions: recent applications in polymer and material science. Polym. Chem. 2011, 2, 2133-2145.
    • (2011) Polym. Chem , vol.2 , pp. 2133-2145
    • Tasdelen, M.A.1
  • 109
    • 17044456499 scopus 로고    scopus 로고
    • Dendritic and hyperbranched polyphenylenes via a simple Diels-Alder route
    • Morgenroth, F.; Möllen, K. Dendritic and hyperbranched polyphenylenes via a simple Diels-Alder route. Tetrahedron 1997, 53, 15349-15366.
    • (1997) Tetrahedron , vol.53 , pp. 15349-15366
    • Morgenroth, F.1    Möllen, K.2
  • 110
    • 84956894069 scopus 로고    scopus 로고
    • Fourfold diels-Alder reaction of tetraethynylsilane
    • Geyer, F.L.; Rode, A.; Bunz, U.H.F. Fourfold Diels-Alder Reaction of Tetraethynylsilane. Chem. Eur. J. 2014, 20, 16448-16453.
    • (2014) Chem. Eur. J , vol.20 , pp. 16448-16453
    • Geyer, F.L.1    Rode, A.2    Bunz, U.H.F.3
  • 111
    • 84907821712 scopus 로고    scopus 로고
    • Click" reactions: A versatile toolbox for the synthesis of peptide-conjugates
    • Tang, W.; Becker, M.L. "Click" reactions: A versatile toolbox for the synthesis of peptide-conjugates. Chem. Soc. Rev. 2014, 43, 7013-7039.
    • (2014) Chem. Soc. Rev , vol.43 , pp. 7013-7039
    • Tang, W.1    Becker, M.L.2
  • 112
    • 77949405751 scopus 로고    scopus 로고
    • Combined CuI-catalysed alkyne-Azide cycloaddition and furan-maleimide Diels-Alder click" chemistry approach to thermoresponsive dendrimers
    • Vieyres, A.; Lam, T.; Gillet, R.; Franc, G.; Castonguay, A.; Kakkar, A. Combined CuI-catalysed alkyne-Azide cycloaddition and furan-maleimide Diels-Alder "click" chemistry approach to thermoresponsive dendrimers. Chem. Commun. 2010, 46, 1875-1877.
    • (2010) Chem. Commun , vol.46 , pp. 1875-1877
    • Vieyres, A.1    Lam, T.2    Gillet, R.3    Franc, G.4    Castonguay, A.5    Kakkar, A.6
  • 113
    • 76149146050 scopus 로고    scopus 로고
    • Thermally reversible dendronized step-polymers based on sequential huisgen 1 3-dipolar cycloaddition and diels-Alder click" reactions
    • Polaske, N.W.; McGrath, D.V.; McElhanon, J.R. Thermally Reversible Dendronized Step-Polymers Based on Sequential Huisgen 1, 3-Dipolar Cycloaddition and Diels-Alder "Click" Reactions. Macromolecules 2010, 43, 1270-1276.
    • (2010) Macromolecules , vol.43 , pp. 1270-1276
    • Polaske, N.W.1    McGrath, D.V.2    McElhanon, J.R.3
  • 115
    • 79955658834 scopus 로고    scopus 로고
    • Thermally reversible dendronized linear AB step-polymers via Click" chemistry
    • Polaske, N.W.; McGrath, D.V.; McElhanon, J.R. Thermally reversible dendronized linear AB step-polymers via "Click" chemistry. Macromolecules 2011, 44, 3203-3210.
    • (2011) Macromolecules , vol.44 , pp. 3203-3210
    • Polaske, N.W.1    McGrath, D.V.2    McElhanon, J.R.3
  • 117
    • 84879418205 scopus 로고    scopus 로고
    • Dendron-polymer conjugates via the diels-Alder click" reaction of novel anthracene-based dendrons
    • Gok, O.; Yigit, S.; Merve Kose, M.; Sanyal, R.; Sanyal, A. Dendron-polymer conjugates via the diels-Alder "click" reaction of novel anthracene-based dendrons. J. Polym. Sci. Part. A: Polym. Chem. 2013, 51, 3191-3201.
    • (2013) J. Polym. Sci. Part. A: Polym. Chem , vol.51 , pp. 3191-3201
    • Gok, O.1    Yigit, S.2    Merve Kose, M.3    Sanyal, R.4    Sanyal, A.5
  • 118
    • 84877715753 scopus 로고    scopus 로고
    • PH degradable dendron-functionalized poly(2-ethyl-2-oxazoline) prepared by a cascade Double-click" reaction
    • Kempe, K.; Onbulak, S.; Schubert, U.S.; Sanyal, A.; Hoogenboom, R. pH degradable dendron-functionalized poly(2-ethyl-2-oxazoline) prepared by a cascade "double-click" reaction. Polym. Chem. 2013, 4, 3236-3244.
    • (2013) Polym. Chem , vol.4 , pp. 3236-3244
    • Kempe, K.1    Onbulak, S.2    Schubert, U.S.3    Sanyal, A.4    Hoogenboom, R.5
  • 120
    • 84916878059 scopus 로고    scopus 로고
    • Design strategies for lab-on-A-molecule probes and orthogonal sensing
    • Chen, K.; Shu, Q.; Schmittel, M. Design strategies for lab-on-A-molecule probes and orthogonal sensing. Chem. Soc. Rev. 2015, 44, 136-160.
    • (2015) Chem. Soc. Rev , vol.44 , pp. 136-160
    • Chen, K.1    Shu, Q.2    Schmittel, M.3
  • 121
    • 0036922118 scopus 로고    scopus 로고
    • The specific contribution of phosphorus in dendrimer chemistry
    • Majoral, J.-P.; Caminade, A.-M.; Maraval, V. The specific contribution of phosphorus in dendrimer chemistry. Chem. Commun. 2002, 2929-2942.
    • (2002) Chem. Commun , pp. 2929-2942
    • Majoral, J.-P.1    Caminade, A.-M.2    Maraval, V.3
  • 124
    • 84856008510 scopus 로고    scopus 로고
    • Bioorthogonal reaction pairs enable simultaneous selective multi-Target Imaging Angew
    • Karver, M.R.; Weissleder, R.; Hilderbrand, S.A. Bioorthogonal Reaction Pairs Enable Simultaneous, Selective, Multi-Target Imaging. Angew. Chem. Int. Ed. 2012, 51, 920-922.
    • (2012) Chem. Int. Ed , vol.51 , pp. 920-922
    • Karver, M.R.1    Weissleder, R.2    Hilderbrand, S.A.3
  • 125
    • 84906823958 scopus 로고    scopus 로고
    • Sulfur(VI) fluoride exchange (sufex another good reaction for click chemistry
    • Dong, J.; Krasnova, L.; Finn, M.G.; Sharpless, K.B. Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry. Angew. Chem. Int. Ed. 2014, 53, 9430-9448.
    • (2014) Angew. Chem. Int. Ed , vol.53 , pp. 9430-9448
    • Dong, J.1    Krasnova, L.2    Finn, M.G.3    Sharpless, K.B.4
  • 126
    • 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, 4900-4908.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 4900-4908
    • Becer, C.R.1    Hoogenboom, R.2    Schubert, U.S.3
  • 127
    • 84875461219 scopus 로고    scopus 로고
    • Extending the limits of precision polymer synthesis: Giant polyphenylene dendrimers in the megadalton mass range approaching structural perfection
    • Nguyen, T.-T.-T.; Baumgarten, M.; Rouhanipour, A.; Räder, H.J.; Lieberwirth, I.; Möllen, K. Extending the Limits of Precision Polymer Synthesis: Giant Polyphenylene Dendrimers in the Megadalton Mass Range Approaching Structural Perfection. J. Am. Chem. Soc. 2013, 135, 4183-4186.
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 4183-4186
    • Nguyen, T.-T.-T.1    Baumgarten, M.2    Rouhanipour, A.3    Räder, H.J.4    Lieberwirth, I.5    Möllen, K.6
  • 128
    • 84894647333 scopus 로고    scopus 로고
    • MALDI-TOF mass spectrometry of polyphenylene dendrimers up to the megadalton range. Elucidating structural integrity of macromolecules at unrivaled high molecular weights
    • Räder, H.J.; Nguyen, T.-T.-T.; Möllen, K. MALDI-TOF Mass Spectrometry of Polyphenylene Dendrimers up to the Megadalton Range. Elucidating Structural Integrity of Macromolecules at Unrivaled High Molecular Weights. Macromolecules 2014, 47, 1240-1248.
    • (2014) Macromolecules , vol.47 , pp. 1240-1248
    • Räder, H.J.1    Nguyen, T.-T.-T.2    Möllen, K.3
  • 129
    • 84883743453 scopus 로고    scopus 로고
    • Synthesis of peptide dendrimers with polyhedral oligomeric silsesquioxane cores via click chemistry
    • Pu, Y.-J.; Yuan, H.; Yang, M.; He, B.; Gu, Z.-W. Synthesis of peptide dendrimers with polyhedral oligomeric silsesquioxane cores via click chemistry. Chin. Chem. Lett. 2013, 24, 917-920.
    • (2013) Chin. Chem. Lett , vol.24 , pp. 917-920
    • Pu, Y.-J.1    Yuan, H.2    Yang, M.3    He, B.4    Gu, Z.-W.5
  • 130
    • 84902139093 scopus 로고    scopus 로고
    • Synthesis and evaluation of a targeted nanoglobular dual-modal imaging agent for mr imaging and image-guided surgery of prostate cancer
    • Tan, M.; Ye, Z.; Lindner, D.; Brady-Kalnay, S.M.; Lu, Z.-R. Synthesis and Evaluation of a Targeted Nanoglobular Dual-Modal Imaging Agent for MR Imaging and Image-Guided Surgery of Prostate Cancer. Pharm. Res. 2014, 31, 1469-1476.
    • (2014) Pharm. Res , vol.31 , pp. 1469-1476
    • Tan, M.1    Ye, Z.2    Lindner, D.3    Brady-Kalnay, S.M.4    Lu, Z.-R.5
  • 132
    • 84867527163 scopus 로고    scopus 로고
    • Dendrimer functionalization with a membrane-interacting Domain of Herpes Simplex Virus Type 1: Towards Intracellular Delivery
    • Carberry, T.P.; Tarallo, R.; Falanga, A.; Finamore, E.; Galdiero, M.; Weck, M.; Galdiero, S. Dendrimer Functionalization with a Membrane-Interacting Domain of Herpes Simplex Virus Type 1: Towards Intracellular Delivery. Chem. Eur. J. 2012, 18, 13678-13685.
    • (2012) Chem. Eur. J , vol.18 , pp. 13678-13685
    • Carberry, T.P.1    Tarallo, R.2    Falanga, A.3    Finamore, E.4    Galdiero, M.5    Weck, M.6    Galdiero, S.7
  • 133
    • 77950170337 scopus 로고    scopus 로고
    • Peptide-Targeted nanoglobular Gd-DOTA Monoamide conjugates for magnetic resonance cancer molecular imaging
    • Tan, M.; Wu, X.; Jeong, E.-K.; Chen, Q.; Lu, Z.-R. Peptide-Targeted Nanoglobular Gd-DOTA Monoamide Conjugates for Magnetic Resonance Cancer Molecular Imaging. Biomacromolecules 2010, 11, 754-761.
    • (2010) Biomacromolecules , vol.11 , pp. 754-761
    • Tan, M.1    Wu, X.2    Jeong, E.-K.3    Chen, Q.4    Lu, Z.-R.5
  • 134
    • 84855957721 scopus 로고    scopus 로고
    • Azides in carbohydrate chemistry
    • 1st ed.; Brase, S. Banert, K. Eds.; John Wiley & Sons: New York, NY, USA
    • Beckmann, H.S.G.; Wittmann, V. Azides in carbohydrate chemistry. In Organic Azides: Syntheses and Applications, 1st ed.; Brase, S. Banert, K. Eds.; John Wiley & Sons: New York, NY, USA, 2010; pp. 469-490.
    • (2010) Organic Azides: Syntheses and Applications , pp. 469-490
    • Beckmann, H.S.G.1    Wittmann, V.2
  • 135
    • 84937427454 scopus 로고    scopus 로고
    • Carbohydrate-based dendrimers
    • L'Haridon, L.; Mallet, J.-M. Carbohydrate-based dendrimers. Carbohydr. Chem. 2014, 40, 257-269.
    • (2014) Carbohydr. Chem , vol.40 , pp. 257-269
    • L'Haridon, L.1    Mallet, J.-M.2
  • 136
    • 84886473924 scopus 로고    scopus 로고
    • Click multivalent glycomaterials: Glycoclusters, glycodendrimers, glycopolymers, hybrid glycomaterials, and glycosurfaces
    • John Wiley & Sons, Inc.: New York, NY, USA
    • Mellet, C.O.; Mendez-Ardoy, A.; Fernandez, J.M.G. Click Multivalent Glycomaterials: Glycoclusters, Glycodendrimers, Glycopolymers, Hybrid Glycomaterials, and Glycosurfaces. In Click Chemistry in Glycoscience: New Developments and Strategies; John Wiley & Sons, Inc.: New York, NY, USA, 2013; pp. 143-182.
    • (2013) Click Chemistry in Glycoscience: New Developments and Strategies , pp. 143-182
    • Mellet, C.O.1    Mendez-Ardoy, A.2    Fernandez, J.M.G.3
  • 137
    • 84873122458 scopus 로고    scopus 로고
    • Click reaction in carbohydrate chemistry: Recent developments and future perspective
    • Kushwaha, D.; Dwivedi, P.; Kuanar, S.K.; Tiwari, V.K. Click reaction in carbohydrate chemistry: recent developments and future perspective. Curr. Org. Synth. 2013, 10, 90-135.
    • (2013) Curr. Org. Synth , vol.10 , pp. 90-135
    • Kushwaha, D.1    Dwivedi, P.2    Kuanar, S.K.3    Tiwari, V.K.4
  • 138
    • 84907416726 scopus 로고    scopus 로고
    • Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formation
    • Smadhi, M.; de Bentzmann, S.; Imberty, A.; Gingras, M.; Abderrahim, R.; Goekjian, P.G. Expeditive synthesis of trithiotriazine-cored glycoclusters and inhibition of Pseudomonas aeruginosa biofilm formation. Beilstein J. Org. Chem. 2014, 10, 1981-1990.
    • (2014) Beilstein J. Org. Chem , vol.10 , pp. 1981-1990
    • Smadhi, M.1    De Bentzmann, S.2    Imberty, A.3    Gingras, M.4    Abderrahim, R.5    Goekjian, P.G.6
  • 139
    • 80051579928 scopus 로고    scopus 로고
    • Selection of a synthetic glycan oligomer from a library of DNA-Templated fragments against DC-SIGN and inhibition of HIV gp120 binding to dendritic cells
    • Ciobanu, M.; Huang, K.-T.; Daguer, J.-P.; Barluenga, S.; Chaloin, O.; Schaeffer, E.; Mueller, C.G.; Mitchell, D.A.; Winssinger, N. Selection of a synthetic glycan oligomer from a library of DNA-Templated fragments against DC-SIGN and inhibition of HIV gp120 binding to dendritic cells. Chem. Commun. 2011, 47, 9321-9323.
    • (2011) Chem. Commun , vol.47 , pp. 9321-9323
    • Ciobanu, M.1    Huang, K.-T.2    Daguer, J.-P.3    Barluenga, S.4    Chaloin, O.5    Schaeffer, E.6    Mueller, C.G.7    Mitchell, D.A.8    Winssinger, N.9
  • 140
    • 79955005711 scopus 로고    scopus 로고
    • Multivalent presentation of mannose on hyperbranched polyglycerol and their interaction with concanavalin a lectin
    • Papp, I.; Dernedde, J.; Enders, S.; Riese, S.B.; Shiao, T.C.; Roy, R.; Haag, R. Multivalent Presentation of Mannose on Hyperbranched Polyglycerol and their Interaction with Concanavalin A Lectin. ChemBioChem 2011, 12, 1075-1083.
    • (2011) ChemBioChem , vol.12 , pp. 1075-1083
    • Papp, I.1    Dernedde, J.2    Enders, S.3    Riese, S.B.4    Shiao, T.C.5    Roy, R.6    Haag, R.7
  • 141
    • 84892942743 scopus 로고    scopus 로고
    • Carbohydrate globules: Molecular asterisk-cored dendrimers for carbohydrate presentation
    • Weaver, L.G.; Singh, Y.; Vamvounis, G.; Wyatt, M.F.; Burn, P.L.; Blanchfield, J.T. Carbohydrate globules: molecular asterisk-cored dendrimers for carbohydrate presentation. Polym. Chem. 2014, 5, 1173-1179.
    • (2014) Polym. Chem , vol.5 , pp. 1173-1179
    • Weaver, L.G.1    Singh, Y.2    Vamvounis, G.3    Wyatt, M.F.4    Burn, P.L.5    Blanchfield, J.T.6
  • 142
    • 84855366102 scopus 로고    scopus 로고
    • Recent applications of thiol-ene coupling as a click process for glycoconjugation
    • Dondoni, A.; Marra, A. Recent applications of thiol-ene coupling as a click process for glycoconjugation. Chem. Soc. Rev. 2012, 41, 573-586.
    • (2012) Chem. Soc. Rev , vol.41 , pp. 573-586
    • Dondoni, A.1    Marra, A.2
  • 144
    • 84876952402 scopus 로고    scopus 로고
    • Pyrene and bis-pyrene DNA nucleobase conjugates: Excimer and monomer fluorescence of linear and dendronized cytosine and 7-deazaguanine click adducts
    • Mei, H.; Ingale, S.A.; Seela, F. Pyrene and bis-pyrene DNA nucleobase conjugates: excimer and monomer fluorescence of linear and dendronized cytosine and 7-deazaguanine click adducts. Tetrahedron 2013, 69, 4731-4742.
    • (2013) Tetrahedron , vol.69 , pp. 4731-4742
    • Mei, H.1    Ingale, S.A.2    Seela, F.3
  • 148
    • 79958815062 scopus 로고    scopus 로고
    • Epidermal Growth Factor-PEG Functionalized PAMAM-pentaethylenehexamine dendron for targeted gene delivery produced by click chemistry
    • Yu, H.; Nie, Y.; Dohmen, C.; Li, Y.; Wagner, E. Epidermal Growth Factor-PEG Functionalized PAMAM-Pentaethylenehexamine Dendron for Targeted Gene Delivery Produced by Click Chemistry. Biomacromolecules 2011, 12, 2039-2047.
    • (2011) Biomacromolecules , vol.12 , pp. 2039-2047
    • Yu, H.1    Nie, Y.2    Dohmen, C.3    Li, Y.4    Wagner, E.5
  • 149
    • 84907808562 scopus 로고    scopus 로고
    • Probing the dendritic architecture through AIE: Challenges and successes
    • Arseneault, M.; Leung, N.L. C.; Fung, L.T.; Hu, R.; Morin, J.-F.; Tang, B.Z. Probing the dendritic architecture through AIE: challenges and successes. Polym. Chem. 2014, 5, 6087-6096.
    • (2014) Polym. Chem , vol.5 , pp. 6087-6096
    • Arseneault, M.1    Leung, N.L.C.2    Fung, L.T.3    Hu, R.4    Morin, J.-F.5    Tang, B.Z.6
  • 151
    • 28744443398 scopus 로고    scopus 로고
    • Dendrimers in biomedical applications-Reflections on the field
    • Svenson, S.; Tomalia, D.A. Dendrimers in biomedical applications-Reflections on the field. Adv. Drug. Deliv. Rev 2005 57 2106-2129.
    • (2005) Adv. Drug. Deliv. Rev , vol.57 , pp. 2106-2129
    • Svenson, S.1    Tomalia, D.A.2
  • 155
    • 84873630670 scopus 로고    scopus 로고
    • Janus PEG-based dendrimers for use in combination therapy: Controlled multi-drug loading and sequential release
    • Acton, A.L.; Fante, C.; Flatley, B.; Burattini, S.; Hamley, I.W.; Wang, Z.; Greco, F.; Hayes, W. Janus PEG-Based Dendrimers for Use in Combination Therapy: Controlled Multi-Drug Loading and Sequential Release. Biomacromolecules 2013, 14, 564-574.
    • (2013) Biomacromolecules , vol.14 , pp. 564-574
    • Acton, A.L.1    Fante, C.2    Flatley, B.3    Burattini, S.4    Hamley, I.W.5    Wang, Z.6    Greco, F.7    Hayes, W.8
  • 156
  • 157
    • 79953737215 scopus 로고    scopus 로고
    • Degree of chain branching-dependent assemblies and conducting behavior in ionic liquid crystalline Janus dendrimers
    • Choi, J.-W.; Cho, B.-K. Degree of chain branching-dependent assemblies and conducting behavior in ionic liquid crystalline Janus dendrimers. Soft Matter 2011, 7, 4045-4049.
    • (2011) Soft Matter , vol.7 , pp. 4045-4049
    • Choi, J.-W.1    Cho, B.-K.2
  • 158
    • 80052077544 scopus 로고    scopus 로고
    • Encoded dendrimers with defined chiral composition via click" reaction of enantiopure building blocks
    • Yeniad, B.; Naik, H.; Amir, R.J.; Koning, C.E.; Hawker, C.J.; Heise, A. Encoded dendrimers with defined chiral composition via "click" reaction of enantiopure building blocks. Chem. Commun. 2011, 47, 9870-9872.
    • (2011) Chem. Commun , vol.47 , pp. 9870-9872
    • Yeniad, B.1    Naik, H.2    Amir, R.J.3    Koning, C.E.4    Hawker, C.J.5    Heise, A.6
  • 159
    • 77953133273 scopus 로고    scopus 로고
    • Probe design and synthesis of Galβ(1→3)[NeuAcα(2→6)]GlcNAcβ(1→2)Man motif of N-glycan
    • Bao, G.-m.; Tanaka, K.; Ikenaka, K.; Fukase, K. Probe design and synthesis of Galβ(1→3)[NeuAcα(2→6)]GlcNAcβ(1→2)Man motif of N-glycan. Bioorg. Med. Chem. 2010, 18, 3760-3766.
    • (2010) Bioorg. Med. Chem , vol.18 , pp. 3760-3766
    • Bao, G.-M.1    Tanaka, K.2    Ikenaka, K.3    Fukase, K.4
  • 160
    • 79952152986 scopus 로고    scopus 로고
    • Facile construction of multifunctional nanocarriers using sequential click chemistry for applications in biology
    • Sharma, A.; Neibert, K.; Sharma, R.; Maysinger, D.; Kakkar, A. Facile Construction of Multifunctional Nanocarriers Using Sequential Click Chemistry for Applications in Biology. Macromolecules 2011, 44, 521-529.
    • (2011) Macromolecules , vol.44 , pp. 521-529
    • Sharma, A.1    Neibert, K.2    Sharma, R.3    Maysinger, D.4    Kakkar, A.5
  • 161
    • 79952141052 scopus 로고    scopus 로고
    • Construction of a well-defined multifunctional dendrimer for Theranostics
    • Ornelas, C.; Pennell, R.; Liebes, L.F.; Weck, M. Construction of a Well-Defined Multifunctional Dendrimer for Theranostics. Org. Lett. 2011, 13, 976-979.
    • (2011) Org. Lett , vol.13 , pp. 976-979
    • Ornelas, C.1    Pennell, R.2    Liebes, L.F.3    Weck, M.4
  • 162
    • 84863628087 scopus 로고    scopus 로고
    • Convergent synthesis of dendrimers via the passerini Three-Component Reaction
    • Jee, J.-A.; Spagnuolo, L.A.; Rudick, J.G. Convergent Synthesis of Dendrimers via the Passerini Three-Component Reaction. Org. Lett. 2012, 14, 3292-3295.
    • (2012) Org. Lett , vol.14 , pp. 3292-3295
    • Jee, J.-A.1    Spagnuolo, L.A.2    Rudick, J.G.3
  • 164
    • 84902682931 scopus 로고    scopus 로고
    • Synthesis and characterization of carbazole dendronized coumarin derivatives as solution-processed non-doped emitters and hole-Transporters for electroluminescent devices
    • Prachumrak, N.; Pojanasopa, S.; Tarsang, R.; Namuangruk, S.; Jungsuttiwong, S.; Keawin, T.; Sudyoadsuk, T.; Promarak, V. Synthesis and characterization of carbazole dendronized coumarin derivatives as solution-processed non-doped emitters and hole-Transporters for electroluminescent devices. New J. Chem. 2014, 38, 3282-3294.
    • (2014) New J. Chem , vol.38 , pp. 3282-3294
    • Prachumrak, N.1    Pojanasopa, S.2    Tarsang, R.3    Namuangruk, S.4    Jungsuttiwong, S.5    Keawin, T.6    Sudyoadsuk, T.7    Promarak, V.8
  • 166
    • 0034599146 scopus 로고    scopus 로고
    • Dendronized polymers: Syn thesis, characterization, assembly at interfaces, and manipulation
    • Schlöter, A.D.; Rabe, J.P. Dendronized Polymers: Synthesis, Characterization, Assembly at Interfaces, and Manipulation. Angew. Chem. Int. Ed. 2000, 39, 864-883.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 864-883
    • Schlöter, A.D.1    Rabe, J.P.2
  • 167
    • 18544376102 scopus 로고    scopus 로고
    • Dendronized polymers-building a new bridge from molecules to nanoscopic objects
    • Frauenrath, H. Dendronized polymers-building a new bridge from molecules to nanoscopic objects. Prog. Polym. Sci. 2005, 30, 325-384.
    • (2005) Prog. Polym. Sci , vol.30 , pp. 325-384
    • Frauenrath, H.1
  • 168
    • 82955194462 scopus 로고    scopus 로고
    • Synthesis of first-And second-generation poly(amide)-dendronized polymers via ring-opening metathesis polymerization
    • Jung, H.; Carberry, T.P.; Weck, M. Synthesis of first-And second-generation poly(amide)-dendronized polymers via ring-opening metathesis polymerization. Macromolecules 2011, 44, 9075-9083.
    • (2011) Macromolecules , vol.44 , pp. 9075-9083
    • Jung, H.1    Carberry, T.P.2    Weck, M.3
  • 169
    • 84921273829 scopus 로고    scopus 로고
    • Synthesis of amphiphilic dendronized polymers to study their self-Assembly and transport behavior
    • Kumari, M.; Singh, A.K.; Kumar, S.; Achazi, K.; Gupta, S.; Haag, R.; Sharma, S.K. Synthesis of amphiphilic dendronized polymers to study their self-Assembly and transport behavior. Polym. Adv. Technol. 2014, 25, 1208-1215.
    • (2014) Polym. Adv. Technol , vol.25 , pp. 1208-1215
    • Kumari, M.1    Singh, A.K.2    Kumar, S.3    Achazi, K.4    Gupta, S.5    Haag, R.6    Sharma, S.K.7
  • 170
    • 84861814182 scopus 로고    scopus 로고
    • Synthesis and self-Assembly of amphiphilic brush-dendritic-linear poly[poly(ethylene glycol) methyl ether methacrylate]-bpolyamidoamine-b-poly(ϵ-caprolactone) copolymers
    • He, X.; Zhong, L.; Wu, X.; Cai, X.; Xie, M.; Lin, S.; Yan, D. Synthesis and self-Assembly of amphiphilic brush-dendritic-linear poly[poly(ethylene glycol) methyl ether methacrylate]-bpolyamidoamine-b-poly(ϵ-caprolactone) copolymers. J. Polym. Sci. Part. A: Polym. Chem. 2012, 50, 2841-2853.
    • (2012) J. Polym. Sci. Part. A: Polym. Chem , vol.50 , pp. 2841-2853
    • He, X.1    Zhong, L.2    Wu, X.3    Cai, X.4    Xie, M.5    Lin, S.6    Yan, D.7
  • 171
    • 80052087040 scopus 로고    scopus 로고
    • Synthesis of cyclic dendronized polymers via divergent "graft-from" and convergent click graft-To" routes: Preparation of modular toroidal macromolecules
    • Laurent, B.A.; Grayson, S.M. Synthesis of Cyclic Dendronized Polymers via Divergent "Graft-from" and Convergent Click "Graft-To" Routes: Preparation of Modular Toroidal Macromolecules. J. Am. Chem. Soc. 2011, 133, 13421-13429.
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 13421-13429
    • Laurent, B.A.1    Grayson, S.M.2
  • 172
    • 79955815999 scopus 로고    scopus 로고
    • High temperature synthesis of vinyl terminated polymers based on dendronized acrylates: A detailed product analysis study
    • Zorn, A.-M.; Malkoch, M.; Carlmark, A.; Barner-Kowollik, C. High temperature synthesis of vinyl terminated polymers based on dendronized acrylates: A detailed product analysis study. Polym. Chem. 2011, 2, 1163-1173.
    • (2011) Polym. Chem , vol.2 , pp. 1163-1173
    • Zorn, A.-M.1    Malkoch, M.2    Carlmark, A.3    Barner-Kowollik, C.4
  • 173
    • 77949606752 scopus 로고    scopus 로고
    • Photoresponsive poly(methyl methacrylate)-bazodendron block copolymers prepared by ATRP and click chemistry
    • Del Barrio, J.; Oriol, L.; Alcala, R.; Sanchez, C. Photoresponsive poly(methyl methacrylate)-bazodendron block copolymers prepared by ATRP and click chemistry. J. Polym. Sci. Part A: Polym. Chem. 2010, 48, 1538-1550.
    • (2010) J. Polym. Sci. Part A: Polym. Chem , vol.48 , pp. 1538-1550
    • Del Barrio, J.1    Oriol, L.2    Alcala, R.3    Sanchez, C.4
  • 174
    • 77949414428 scopus 로고    scopus 로고
    • Recognition mediated encapsulation and isolation of flavin-polymer conjugates using dendritic guest moieties
    • Subramani, C.; Yesilbag, G.; Jordan, B.J.; Li, X.; Khorasani, A.; Cooke, G.; Sanyal, A.; Rotello, V.M. Recognition mediated encapsulation and isolation of flavin-polymer conjugates using dendritic guest moieties. Chem. Commun. 2010, 46, 2067-2069.
    • (2010) Chem. Commun , vol.46 , pp. 2067-2069
    • Subramani, C.1    Yesilbag, G.2    Jordan, B.J.3    Li, X.4    Khorasani, A.5    Cooke, G.6    Sanyal, A.7    Rotello, V.M.8
  • 175
    • 79957958713 scopus 로고    scopus 로고
    • Novel macrothiols for the synthesis of a structurally comprehensive dendritic library using thiol-ene click chemistry
    • Walter, M.V.; Lundberg, P.; Hult, A.; Malkoch, M. Novel macrothiols for the synthesis of a structurally comprehensive dendritic library using thiol-ene click chemistry. J. Polym. Sci. Part A: Polym. Chem. 2011, 49, 2990-2995.
    • (2011) J. Polym. Sci. Part A: Polym. Chem , vol.49 , pp. 2990-2995
    • Walter, M.V.1    Lundberg, P.2    Hult, A.3    Malkoch, M.4
  • 178
    • 84879348746 scopus 로고    scopus 로고
    • Modular synthesis of amphiphilic janus glycodendrimers and their self-Assembly into glycodendrimersomes and other complex architectures with bioactivity to biomedically relevant lectins
    • Percec, V.; Leowanawat, P.; Sun, H.-J.; Kulikov, O.; Nusbaum, C.D.; Tran, T.M.; Bertin, A.; Wilson, D.A.; Peterca, M.; Zhang, S.; et al. Modular Synthesis of Amphiphilic Janus Glycodendrimers and Their Self-Assembly into Glycodendrimersomes and Other Complex Architectures with Bioactivity to Biomedically Relevant Lectins. J. Am. Chem. Soc. 2013, 135, 9055-9077.
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 9055-9077
    • Percec, V.1    Leowanawat, P.2    Sun, H.-J.3    Kulikov, O.4    Nusbaum, C.D.5    Tran, T.M.6    Bertin, A.7    Wilson, D.A.8    Peterca, M.9    Zhang, S.10
  • 179
    • 80053547937 scopus 로고    scopus 로고
    • Guest-release control in enzyme-sensitive, amphiphilic-dendrimer-based nanoparticles through photochemical crosslinking
    • Raghupathi, K.R.; Azagarsamy, M.A.; Thayumanavan, S. Guest-Release Control in Enzyme-Sensitive, Amphiphilic-Dendrimer-Based Nanoparticles through Photochemical Crosslinking. Chem. Eur. J. 2011, 17, 11752-11760.
    • (2011) Chem. Eur. J , vol.17 , pp. 11752-11760
    • Raghupathi, K.R.1    Azagarsamy, M.A.2    Thayumanavan, S.3
  • 181
    • 84983452831 scopus 로고    scopus 로고
    • Degradable dendrimers
    • John Wiley & Sons: New York, NY, USA
    • Gingras M. Degradable dendrimers. In Designing Dendrimers; John Wiley & Sons: New York, NY, USA, 2011; pp. 403-462
    • (2011) Designing Dendrimers , pp. 403-462
    • Gingras, M.1
  • 182
    • 62949111143 scopus 로고    scopus 로고
    • Degradable dendrimers divergently synthesized via click chemistry
    • Kohman, R.E.; Zimmerman, S.C. Degradable dendrimers divergently synthesized via click chemistry. Chem. Commun. 2009, 794-796.
    • (2009) Chem. Commun , pp. 794-796
    • Kohman, R.E.1    Zimmerman, S.C.2
  • 183
    • 84903985318 scopus 로고    scopus 로고
    • A responsive hyperbranched polymer not only can self-immolate but also can self-cross-link
    • Yu, Z.-Q.; Xu, X.-M.; Hong, C.-Y.; Wu, D.-C.; You, Y.-Z. A Responsive Hyperbranched Polymer Not Only Can Self-Immolate but Also Can Self-Cross-Link. Macromolecules 2014, 47, 4136-4143.
    • (2014) Macromolecules , vol.47 , pp. 4136-4143
    • Yu, Z.-Q.1    Xu, X.-M.2    Hong, C.-Y.3    Wu, D.-C.4    You, Y.-Z.5
  • 184
    • 84874261653 scopus 로고    scopus 로고
    • Facile synthesis of stable and water-dispersible multihydroxy conjugated polymer nanoparticles with tunable size by dendritic cross-linking
    • Zhou, L.; Geng, J.; Wang, G.; Liu, J.; Liu, B. Facile synthesis of stable and water-dispersible multihydroxy conjugated polymer nanoparticles with tunable size by dendritic cross-linking. ACS Macro Lett. 2012, 1, 927-932.
    • (2012) ACS Macro Lett , vol.1 , pp. 927-932
    • Zhou, L.1    Geng, J.2    Wang, G.3    Liu, J.4    Liu, B.5
  • 185
    • 84882247505 scopus 로고    scopus 로고
    • Dual-purpose PEG scaffolds for the preparation of soft and biofunctional hydrogels: The convergence between CuAAC and thiol-ene reactions
    • Oberg, K.; Hed, Y.; Joelsson Rahmn, I.; Kelly, J.; Lowenhielm, P.; Malkoch, M. Dual-purpose PEG scaffolds for the preparation of soft and biofunctional hydrogels: The convergence between CuAAC and thiol-ene reactions. Chem. Commun. 2013, 49, 6938-6940.
    • (2013) Chem. Commun , vol.49 , pp. 6938-6940
    • Oberg, K.1    Hed, Y.2    Joelsson Rahmn, I.3    Kelly, J.4    Lowenhielm, P.5    Malkoch, M.6
  • 186
    • 80052066359 scopus 로고    scopus 로고
    • Water-soluble dendritic-linear triblock copolymer-modified magnetic nanoparticles: Preparation, characterization and drug release properties
    • Wu, X.; He, X.; Zhong, L.; Lin, S.; Wang, D.; Zhu, X.; Yan, D. Water-soluble dendritic-linear triblock copolymer-modified magnetic nanoparticles: preparation, characterization and drug release properties. J. Mater. Chem. 2011, 21, 13611-13620.
    • (2011) J. Mater. Chem , vol.21 , pp. 13611-13620
    • Wu, X.1    He, X.2    Zhong, L.3    Lin, S.4    Wang, D.5    Zhu, X.6    Yan, D.7
  • 187
    • 84925004535 scopus 로고    scopus 로고
    • Functional porous membranes from amorphous linear dendritic polyester hybrids
    • Mongkhontreerat, S.; Walter, M.V.; Cai, Y.; Brismar, H.; Hult, A.; Malkoch, M. Functional porous membranes from amorphous linear dendritic polyester hybrids. Polym. Chem. 2015, 6, 2390-2395.
    • (2015) Polym. Chem , vol.6 , pp. 2390-2395
    • Mongkhontreerat, S.1    Walter, M.V.2    Cai, Y.3    Brismar, H.4    Hult, A.5    Malkoch, M.6
  • 188
    • 73949090949 scopus 로고    scopus 로고
    • Efficient synthesis of fluorescent squaraine rotaxane Dendrimers
    • Xiao, S.; Fu, N.; Peckham, K.; Smith, B.D. Efficient Synthesis of Fluorescent Squaraine Rotaxane Dendrimers. Org. Lett. 2010, 12, 140-143.
    • (2010) Org. Lett , vol.12 , pp. 140-143
    • Xiao, S.1    Fu, N.2    Peckham, K.3    Smith, B.D.4
  • 189
    • 77955760079 scopus 로고    scopus 로고
    • Pushing the limits for thiol-ene and CuAAC Reactions: Synthesis of a 6th generation dendrimer in a single day
    • Antoni, P.; Robb, M.J.; Campos, L.; Montanez, M.; Hult, A.; Malmstrom, E.; Malkoch, M.; Hawker, C.J. Pushing the Limits for Thiol-Ene and CuAAC Reactions: Synthesis of a 6th Generation Dendrimer in a Single Day. Macromolecules 2010, 43, 6625-6631.
    • (2010) Macromolecules , vol.43 , pp. 6625-6631
    • Antoni, P.1    Robb, M.J.2    Campos, L.3    Montanez, M.4    Hult, A.5    Malmstrom, E.6    Malkoch, M.7    Hawker, C.J.8
  • 190
    • 84862557067 scopus 로고    scopus 로고
    • Simplifying the synthesis of dendrimers: Accelerated approaches
    • Walter, M.V.; Malkoch, M. Simplifying the synthesis of dendrimers: Accelerated approaches. Chem. Soc. Rev. 2012, 41, 4593-4609.
    • (2012) Chem. Soc. Rev , vol.41 , pp. 4593-4609
    • Walter, M.V.1    Malkoch, M.2
  • 191
    • 84903771326 scopus 로고    scopus 로고
    • Synthesis of UV-curable hyperbranched polyurethane (meth)acrylate oligomers via thiol-eneclick" chemistry
    • Han, W.; Lin, B.; Yang, H.; Zhang, X. Synthesis of UV-curable hyperbranched polyurethane (meth)acrylate oligomers via thiol-ene "click" chemistry. J. Appl. Polym. Sci. 2013, 128, 4261-4270.
    • (2013) J. Appl. Polym. Sci , vol.128 , pp. 4261-4270
    • Han, W.1    Lin, B.2    Yang, H.3    Zhang, X.4
  • 192
    • 80052776105 scopus 로고    scopus 로고
    • Exhaustive glycosylation, pegylation, and glutathionylation of a [G4]-ene48 dendrimer via photoinduced thiol-ene coupling
    • Conte, M.L.; Robb, M.J.; Hed, Y.; Marra, A.; Malkoch, M.; Hawker, C.J.; Dondoni, A. Exhaustive glycosylation, pegylation, and glutathionylation of a [G4]-ene48 dendrimer via photoinduced thiol-ene coupling. J. Polym. Sci. Part A: Polym. Chem. 2011, 49, 4468-4475.
    • (2011) J. Polym. Sci. Part A: Polym. Chem , vol.49 , pp. 4468-4475
    • Conte, M.L.1    Robb, M.J.2    Hed, Y.3    Marra, A.4    Malkoch, M.5    Hawker, C.J.6    Dondoni, A.7
  • 193
    • 84983420885 scopus 로고    scopus 로고
    • Facile access to internally functionalized denderimers by using efficient and orthogonal click reactions
    • Kang, T.; Khan, A.; Ohshimizu, K.; Hunt, J.N.; Sivanandan, K.; Amir, R.J.; Ueda, M.; Hawker, C.J. Facile access to internally functionalized denderimers by using efficient and orthogonal click reactions. Polym. Prepr. 2010, 51, 533-534.
    • (2010) Polym. Prepr , vol.51 , pp. 533-534
    • Kang, T.1    Khan, A.2    Ohshimizu, K.3    Hunt, J.N.4    Sivanandan, K.5    Amir, R.J.6    Ueda, M.7    Hawker, C.J.8
  • 194
    • 84872112972 scopus 로고    scopus 로고
    • Facile synthesis of polyester dendrimers as drug Delivery Carriers
    • Ma, X.; Zhou, Z.; Jin, E.; Sun, Q.; Zhang, B.; Tang, J.; Shen, Y. Facile Synthesis of Polyester Dendrimers as Drug Delivery Carriers. Macromolecules 2013, 46, 37-42.
    • (2013) Macromolecules , vol.46 , pp. 37-42
    • Ma, X.1    Zhou, Z.2    Jin, E.3    Sun, Q.4    Zhang, B.5    Tang, J.6    Shen, Y.7
  • 195
    • 85027921589 scopus 로고    scopus 로고
    • Fluoride-promoted esterification with imidazolide-Activated compounds: A modular and sustainable approach to dendrimers
    • García-Gallego, S.; Hult, D.; Olsson, J.V.; Malkoch, M. Fluoride-Promoted Esterification with Imidazolide-Activated Compounds: A Modular and Sustainable Approach to Dendrimers. Angew. Chem. Int. Ed. 2015, 54, 2416-2419.
    • (2015) Angew. Chem. Int. Ed , vol.54 , pp. 2416-2419
    • García-Gallego, S.1    Hult, D.2    Olsson, J.V.3    Malkoch, M.4
  • 197
    • 84905833610 scopus 로고    scopus 로고
    • Heterofunctionalized carbosilane dendritic systems: Bifunctionalized dendrons as building blocks versus statistically decorated dendrimers
    • Galan, M.; Fuentes-Paniagua, E.; de la Mata, F.J.; Gomez, R. Heterofunctionalized carbosilane dendritic systems: Bifunctionalized dendrons as building blocks versus statistically decorated dendrimers. Organometallics 2014, 33, 3977-3989.
    • (2014) Organometallics , vol.33 , pp. 3977-3989
    • Galan, M.1    Fuentes-Paniagua, E.2    De La Mata, F.J.3    Gomez, R.4
  • 198
    • 66349103061 scopus 로고    scopus 로고
    • Application of thiol-ene chemistry to the preparation of carbosilane-Thioether dendrimers
    • Rissing, C.; Son, D.Y. Application of thiol-ene chemistry to the preparation of carbosilane-Thioether dendrimers. Organometallics 2009, 28, 3167-3172.
    • (2009) Organometallics , vol.28 , pp. 3167-3172
    • Rissing, C.1    Son, D.Y.2
  • 199
    • 84983407513 scopus 로고    scopus 로고
    • Thiol-ene chemistry for the synthesis and modification of branched organosilicon polymers
    • Son, D.Y.; Rissing, C.; Chen, L.; Andersson, T.E. Thiol-ene chemistry for the synthesis and modification of branched organosilicon polymers. Polym. Prepr. 2010, 51, 730-731.
    • (2010) Polym. Prepr , vol.51 , pp. 730-731
    • Son, D.Y.1    Rissing, C.2    Chen, L.3    Andersson, T.E.4
  • 200
    • 79955142251 scopus 로고    scopus 로고
    • Nitrone-mediated radical coupling reactions: A new synthetic tool exemplified on dendrimer synthesis
    • Wong, E.H. H.; Altintas, O.; Stenzel, M.H.; Barner-Kowollik, C.; Junkers, T. Nitrone-mediated radical coupling reactions: A new synthetic tool exemplified on dendrimer synthesis. Chem. Commun. 2011, 47, 5491-5493.
    • (2011) Chem. Commun , vol.47 , pp. 5491-5493
    • Wong, E.H.H.1    Altintas, O.2    Stenzel, M.H.3    Barner-Kowollik, C.4    Junkers, T.5
  • 201
  • 202
    • 77954314881 scopus 로고    scopus 로고
    • Designing dendritic frameworks using versatile building blocks suitable for CuI-catalyzed alkyne azide click" chemistry
    • Hourani, R.; Sharma, A.; Kakkar, A. Designing dendritic frameworks using versatile building blocks suitable for CuI-catalyzed alkyne azide "click" chemistry. Tetrahedron Lett. 2010, 51, 3792-3795.
    • (2010) Tetrahedron Lett , vol.51 , pp. 3792-3795
    • Hourani, R.1    Sharma, A.2    Kakkar, A.3
  • 203
    • 84877734053 scopus 로고    scopus 로고
    • From nitro-To sulfonyl-based chromophores: Improvement of the comprehensive performance of nonlinear optical dendrimers
    • Wu, W.; Xu, G.; Li, C.; Yu, G.; Liu, Y.; Ye, C.; Qin, J.; Li, Z. From Nitro-To Sulfonyl-Based Chromophores: Improvement of the Comprehensive Performance of Nonlinear Optical Dendrimers. Chem. Eur. J. 2013, 19, 6874-6888.
    • (2013) Chem. Eur. J , vol.19 , pp. 6874-6888
    • Wu, W.1    Xu, G.2    Li, C.3    Yu, G.4    Liu, Y.5    Ye, C.6    Qin, J.7    Li, Z.8
  • 204
    • 84882758907 scopus 로고    scopus 로고
    • Dendrimers with large nonlinear optical performance by introducing isolation chromophore, utilizing the ar/arf self-Assembly effect, and modifying the topological structure
    • Wu, W.; Ye, C.; Qin, J.; Li, Z. Dendrimers with Large Nonlinear Optical Performance by Introducing Isolation Chromophore, Utilizing the Ar/ArF Self-Assembly Effect, And Modifying the Topological Structure. ACS Appl. Mater. Interfaces 2013, 5, 7033-7041.
    • (2013) ACS Appl. Mater. Interfaces , vol.5 , pp. 7033-7041
    • Wu, W.1    Ye, C.2    Qin, J.3    Li, Z.4
  • 205
    • 84876895589 scopus 로고    scopus 로고
    • Using an isolation chromophore to further improve the comprehensive performance of nonlinear optical (NLO) dendrimers
    • Wu, W.; Huang, Q.; Xu, G.; Wang, C.; Ye, C.; Qin, J.; Li, Z. Using an isolation chromophore to further improve the comprehensive performance of nonlinear optical (NLO) dendrimers. J. Mater. Chem. C 2013, 1, 3226-3234.
    • (2013) J. Mater. Chem C , vol.1 , pp. 3226-3234
    • Wu, W.1    Huang, Q.2    Xu, G.3    Wang, C.4    Ye, C.5    Qin, J.6    Li, Z.7
  • 206
    • 84873497505 scopus 로고    scopus 로고
    • Triazole-based ferrocenyl dendrimers as a medium for encapsulated palladium nanoparticles
    • Rajakumar, P.; Anandhan, R.; Malathi, S.; Balasubramanian, S. Triazole-based ferrocenyl dendrimers as a medium for encapsulated palladium nanoparticles. Synlett 2013, 24, 575-580.
    • (2013) Synlett , vol.24 , pp. 575-580
    • Rajakumar, P.1    Anandhan, R.2    Malathi, S.3    Balasubramanian, S.4
  • 207
    • 84898941340 scopus 로고    scopus 로고
    • Syn thesis photophysical and electrochemical properties of 1, 2, 3-Triazolyl bridged ferrocenyl dendrimers through click chemistry
    • Rajakumar, P.; Kannan, A.; Anandhan, R. Synthesis, photophysical and electrochemical properties of 1, 2, 3-Triazolyl bridged ferrocenyl dendrimers through click chemistry. New J. Chem. 2014, 38, 1594-1600.
    • (2014) New J. Chem , vol.38 , pp. 1594-1600
    • Rajakumar, P.1    Kannan, A.2    Anandhan, R.3
  • 208
    • 77949369376 scopus 로고    scopus 로고
    • Non-planar push-pull chromophores
    • Kato, S.-I.; Diederich, F. Non-planar push-pull chromophores. Chem. Commun. 2010, 46, 1994-2006.
    • (2010) Chem. Commun , vol.46 , pp. 1994-2006
    • Kato, S.-I.1    Diederich, F.2
  • 209
    • 80053477634 scopus 로고    scopus 로고
    • 10 Years of Click Chemistry: Synthesis and Applications of Ferrocene-Derived Triazoles
    • Ganesh, V.; Sudhir, V.S.; Kundu, T.; Chandrasekaran, S. 10 Years of Click Chemistry: Synthesis and Applications of Ferrocene-Derived Triazoles. Chem. Asian J. 2011, 6, 2670-2694.
    • (2011) Chem. Asian J , vol.6 , pp. 2670-2694
    • Ganesh, V.1    Sudhir, V.S.2    Kundu, T.3    Chandrasekaran, S.4
  • 210
    • 78249288765 scopus 로고    scopus 로고
    • Click Syntheses of 1, 2, 3-Triazolylbiferrocenyl Dendrimers and the Selective Roles of the Inner and Outer Ferrocenyl Groups in the Redox Recognition of ATP2- and Pd2+
    • Djeda, R.; Rapakousiou, A.; Liang, L.; Guidolin, N.; Ruiz, J.; Astruc, D. Click Syntheses of 1, 2, 3-Triazolylbiferrocenyl Dendrimers and the Selective Roles of the Inner and Outer Ferrocenyl Groups in the Redox Recognition of ATP2- and Pd2+. Angew. Chem. Int. Ed. 2010, 49, 8152-8156.
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 8152-8156
    • Djeda, R.1    Rapakousiou, A.2    Liang, L.3    Guidolin, N.4    Ruiz, J.5    Astruc, D.6
  • 211
    • 77956012400 scopus 로고    scopus 로고
    • Click" Synthesis of a Heterobifunctional Ferrocenyl Dendrimer with Molecular Recognition Properties and Influence of the Ferrocenyl Redox Potential on the Formation of Gold Nanoparticles
    • Liang, L.; Ruiz, J.; Astruc, D. "Click" Synthesis of a Heterobifunctional Ferrocenyl Dendrimer with Molecular Recognition Properties and Influence of the Ferrocenyl Redox Potential on the Formation of Gold Nanoparticles. J. Inorg. Organomet. Polym. Mater. 2010, 20, 503-510.
    • (2010) J. Inorg. Organomet. Polym. Mater , vol.20 , pp. 503-510
    • Liang, L.1    Ruiz, J.2    Astruc, D.3
  • 212
    • 77954925569 scopus 로고    scopus 로고
    • Click" synthesis of organo-silicon dendrimers
    • Astruc, D.; Ornelas, C.; Ruiz, J. "Click" synthesis of organo-silicon dendrimers. Main Group Chem. 2010, 9, 87-100.
    • (2010) Main Group Chem , vol.9 , pp. 87-100
    • Astruc, D.1    Ornelas, C.2    Ruiz, J.3
  • 214
    • 84867700330 scopus 로고    scopus 로고
    • 1, 2, 3-Triazole ferrocenyldendrimers through click chemistry approach and their optical and electrochemical properties
    • Rajakumar, P.; Anandhan, R.; Kannan, A. 1, 2, 3-Triazole Ferrocenyldendrimers Through Click Chemistry Approach and their Optical and Electrochemical Properties. Aust. J. Chem. 2012, 65, 1457-1462.
    • (2012) Aust. J. Chem , vol.65 , pp. 1457-1462
    • Rajakumar, P.1    Anandhan, R.2    Kannan, A.3
  • 215
    • 84859898418 scopus 로고    scopus 로고
    • Click dendrimers triazole-related aspects catalysts, mechanism, syn thesis, and functions. A bridge between dendritic architectures and nanomaterials
    • Astruc, D.; Liang, L.; Rapakousiou, A.; Ruiz, J. Click Dendrimers and Triazole-Related Aspects: Catalysts, Mechanism, Synthesis, and Functions. A Bridge between Dendritic Architectures and Nanomaterials. Acc. Chem. Res. 2012, 45, 630-640.
    • (2012) Acc. Chem. Res , vol.45 , pp. 630-640
    • Astruc, D.1    Liang, L.2    Rapakousiou, A.3    Ruiz, J.4
  • 216
    • 84878633333 scopus 로고    scopus 로고
    • Click" synthesis and redox properties of triazolyl cobalticinium dendrimers
    • Rapakousiou, A.; Wang, Y.; Belin, C.; Pinaud, N.; Ruiz, J.; Astruc, D. "Click" Synthesis and Redox Properties of Triazolyl Cobalticinium Dendrimers. Inorg. Chem. 2013, 52, 6685-6693.
    • (2013) Inorg. Chem , vol.52 , pp. 6685-6693
    • Rapakousiou, A.1    Wang, Y.2    Belin, C.3    Pinaud, N.4    Ruiz, J.5    Astruc, D.6
  • 217
    • 77649301782 scopus 로고    scopus 로고
    • Encapsulation and stabilization of gold nanoparticles withclick" polyethyleneglycol dendrimers
    • Boisselier, E.; Diallo, A.K.; Salmon, L.; Ornelas, C.; Ruiz, J.; Astruc, D. Encapsulation and Stabilization of Gold Nanoparticles with "Click" Polyethyleneglycol Dendrimers. J. Am. Chem. Soc. 2010, 132, 2729-2742.
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 2729-2742
    • Boisselier, E.1    Diallo, A.K.2    Salmon, L.3    Ornelas, C.4    Ruiz, J.5    Astruc, D.6
  • 218
    • 68349136859 scopus 로고    scopus 로고
    • Drug-drug interactions of triazole antifungal agents in multimorbid patients and implications for patient care
    • Nivoix, Y.; Ubeaud-Sequier, G.; Engel, P.; Levêque, D.; Herbrecht, R. Drug-drug interactions of triazole antifungal agents in multimorbid patients and implications for patient care. Curr. Drug. Metab. 2009, 10, 395-409.
    • (2009) Curr. Drug. Metab , vol.10 , pp. 395-409
    • Nivoix, Y.1    Ubeaud-Sequier, G.2    Engel, P.3    Levêque, D.4    Herbrecht, R.5
  • 219
    • 82955169573 scopus 로고    scopus 로고
    • Triazole antifungal agents in invasive fungal infections: A comparative review
    • Lass-Floerl, C. Triazole antifungal agents in invasive fungal infections: A comparative review. Drugs 2011, 71, 2405-2419.
    • (2011) Drugs , vol.71 , pp. 2405-2419
    • Lass-Floerl, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.