50th Anniversary Perspective: Polymer Functionalization

Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696

Cu-Catalyzed Azide−Alkyne Cycloaddition

Meldal, M., & Tornøe, C. W. (2008) · Chemical Reviews · doi:10.1021/cr0783479 · Cited by 4,628

Thiol–Ene Click Chemistry

Hoyle, C. E., & Bowman, C. N. (2010) · Angewandte Chemie International Edition · doi:10.1002/anie.200903924 · Cited by 4,182

Multicomponent Reactions with Isocyanides

Dömling, A., & Ugi, I. (2000) · Angewandte Chemie · doi:10.1002/1521-3773(20000915)39:18<3168::aid-anie3168>3.0.co;2-u · Cited by 4,077

Controlled/living radical polymerization: Features, developments, and perspectives

Braunecker, W. A., & Matyjaszewski, K. (2007) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2006.11.002 · Cited by 3,202

A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems

Agard, N. J., Prescher, J. A., & Bertozzi, C. R. (2004) · Journal of the American Chemical Society · doi:10.1021/ja044996f · Cited by 3,017

A Thermally Re-mendable Cross-Linked Polymeric Material

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Controlled Ring-Opening Polymerization of Lactide and Glycolide

Dechy-Cabaret, O., Martin-Vaca, B., & Bourissou, D. (2004) · Chemical Reviews · doi:10.1021/cr040002s · Cited by 2,257

Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(i) acetylides

Hein, J. E., & Fokin, V. V. (2010) · Chemical Society Reviews · doi:10.1039/b904091a · Cited by 2,198

Amide bond formation and peptide coupling

Montalbetti, C. A. G. N., & Falque, V. (2005) · Tetrahedron · doi:10.1016/j.tet.2005.08.031 · Cited by 1,786

Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis

Hoyle, C. E., Lowe, A. B., & Bowman, C. N. (2010) · Chemical Society Reviews · doi:10.1039/b901979k · Cited by 1,639

The Thiol-Michael Addition Click Reaction: A Powerful and Widely Used Tool in Materials Chemistry

Nair, D. P., Podgórski, M., Chatani, S., Gong, T., Xi, W., Fenoli, C. R., & Bowman, C. N. (2014) · Chemistry of Materials · doi:10.1021/cm402180t · Cited by 1,596

Thiol-ene “click” reactions and recent applications in polymer and materials synthesis

Lowe, A. B. (2010) · Polym. Chem. · doi:10.1039/b9py00216b · Cited by 1,563

Organocatalytic Ring-Opening Polymerization

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Thiol–enes: Chemistry of the past with promise for the future

Hoyle, C. E., Lee, T. Y., & Roper, T. (2004) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.20366 · Cited by 1,457

Sulfur(VI) Fluoride Exchange (SuFEx): Another Good Reaction for Click Chemistry

Dong, J., Krasnova, L., Finn, M. G., & Sharpless, K. B. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201309399 · Cited by 1,390

Sequence-Controlled Polymers

Lutz, J.-F., Ouchi, M., Liu, D. R., & Sawamoto, M. (2013) · Science · doi:10.1126/science.1238149 · Cited by 1,381

The Use of Esters of N-Hydroxysuccinimide in Peptide Synthesis

Anderson, G. W., Zimmerman, J. E., & Callahan, F. M. (1964) · Journal of the American Chemical Society · doi:10.1021/ja01063a037 · Cited by 1,240

100 years of the biginelli dihydropyrimidine synthesis

Oliver Kappe, C. (1993) · Tetrahedron · doi:10.1016/s0040-4020(01)87971-0 · Cited by 1,228

Borylation and Silylation of C–H Bonds: A Platform for Diverse C–H Bond Functionalizations

Hartwig, J. F. (2012) · Accounts of Chemical Research · doi:10.1021/ar200206a · Cited by 1,074

A Robust and Versatile Photoinduced Living Polymerization of Conjugated and Unconjugated Monomers and Its Oxygen Tolerance

Xu, J., Jung, K., Atme, A., Shanmugam, S., & Boyer, C. (2014) · Journal of the American Chemical Society · doi:10.1021/ja501745g · Cited by 990

Click Chemistry beyond Metal‐Catalyzed Cycloaddition

Becer, C. R., Hoogenboom, R., & Schubert, U. S. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900755 · Cited by 866

Marrying click chemistry with polymerization: expanding the scope of polymeric materials

Golas, P. L., & Matyjaszewski, K. (2010) · Chem. Soc. Rev. · doi:10.1039/b901978m · Cited by 863

The power of thiol‐ene chemistry

Kade, M. J., Burke, D. J., & Hawker, C. J. (2010) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.23824 · Cited by 853

Control of a Living Radical Polymerization of Methacrylates by Light

Fors, B. P., & Hawker, C. J. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201203639 · Cited by 820

Clicking polymers: a straightforward approach to novel macromolecular architectures

Fournier, D., Hoogenboom, R., & Schubert, U. S. (2007) · Chemical Society Reviews · doi:10.1039/b700809k · Cited by 774

Thiol–ene “click” reactions and recent applications in polymer and materials synthesis: a first update

Lowe, A. B. (2014) · Polym. Chem. · doi:10.1039/c4py00339j · Cited by 768

Multicomponent reactions for the synthesis of pyrroles

Estévez, V., Villacampa, M., & Menéndez, J. C. (2010) · Chemical Society Reviews · doi:10.1039/b917644f · Cited by 744

Aziridines and Epoxides in Organic Synthesis

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Macromolecular Engineering through Click Chemistry and Other Efficient Transformations

Sumerlin, B. S., & Vogt, A. P. (2010) · Macromolecules · doi:10.1021/ma901447e · Cited by 701

“Clicking” Polymers or Just Efficient Linking: What Is the Difference?

Barner‐Kowollik, C., Du Prez, F. E., Espeel, P., Hawker, C. J., Junkers, T., Schlaad, H., & Van Camp, W. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201003707 · Cited by 632

End group removal and modification of RAFT polymers

Willcock, H., & O'Reilly, R. K. (2010) · Polym. Chem. · doi:10.1039/b9py00340a · Cited by 607

Synthesis of Neoglycopolymers by a Combination of “Click Chemistry” and Living Radical Polymerization

Ladmiral, V., Mantovani, G., Clarkson, G. J., Cauet, S., Irwin, J. L., & Haddleton, D. M. (2006) · Journal of the American Chemical Society · doi:10.1021/ja058364k · Cited by 586

Diels–Alder “click” reactions: recent applications in polymer and material science

Tasdelen, M. A. (2011) · Polymer Chemistry · doi:10.1039/c1py00041a · Cited by 582

PEG- and Peptide-Grafted Aliphatic Polyesters by Click Chemistry

Parrish, B., Breitenkamp, R. B., & Emrick, T. (2005) · Journal of the American Chemical Society · doi:10.1021/ja050310n · Cited by 579

Post-polymerization functionalization of polyolefins

Boaen, N. K., & Hillmyer, M. A. (2005) · Chemical Society Reviews · doi:10.1039/b311405h · Cited by 563

Modular synthesis of block copolymers via cycloaddition of terminal azide and alkyne functionalized polymers

Opsteen, J. A., & van Hest, J. C. M. (2005) · Chemical Communications · doi:10.1039/b412930j · Cited by 516

Activated Ester Containing Polymers: Opportunities and Challenges for the Design of Functional Macromolecules

Das, A., & Theato, P. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00291 · Cited by 483

Highly Efficient One-Pot Synthesis of N-Sulfonylamidines by Cu-Catalyzed Three-Component Coupling of Sulfonyl Azide, Alkyne, and Amine

Bae, I., Han, H., & Chang, S. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0432968 · Cited by 479

Development of Thermal and Photochemical Strategies for Thiol−Ene Click Polymer Functionalization

Campos, L. M., Killops, K. L., Sakai, R., Paulusse, J. M. J., Damiron, D., Drockenmuller, E., Messmore, B. W., & Hawker, C. J. (2008) · Macromolecules · doi:10.1021/ma801630n · Cited by 461

Highly Efficient “Click” Functionalization of Poly(3-azidopropyl methacrylate) Prepared by ATRP

Sumerlin, B. S., Tsarevsky, N. V., Louche, G., Lee, R. Y., & Matyjaszewski, K. (2005) · Macromolecules · doi:10.1021/ma0511245 · Cited by 452

Synthesis of Star Polymers by a Combination of ATRP and the “Click” Coupling Method

Gao, H., & Matyjaszewski, K. (2006) · Macromolecules · doi:10.1021/ma060926c · Cited by 449

Chemical modification of polyethersulfone nanofiltration membranes: A review

Van der Bruggen, B. (2009) · Journal of Applied Polymer Science · doi:10.1002/app.30578 · Cited by 440

Boronic Acid-Based Hydrogels Undergo Self-Healing at Neutral and Acidic pH

Deng, C. C., Brooks, W. L. A., Abboud, K. A., & Sumerlin, B. S. (2015) · ACS Macro Letters · doi:10.1021/acsmacrolett.5b00018 · Cited by 438

Step-Growth “Click” Coupling of Telechelic Polymers Prepared by Atom Transfer Radical Polymerization

Tsarevsky, N. V., Sumerlin, B. S., & Matyjaszewski, K. (2005) · Macromolecules · doi:10.1021/ma050370d · Cited by 427

Click chemistry in materials synthesis. 1. Adhesive polymers from copper‐catalyzed azide‐alkyne cycloaddition

Díaz, D. D., Punna, S., Holzer, P., McPherson, A. K., Sharpless, K. B., Fokin, V. V., & Finn, M. G. (2004) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.20330 · Cited by 424

Thio-Click Modification of Poly[2-(3-butenyl)-2-oxazoline]

Gress, A., Völkel, A., & Schlaad, H. (2007) · Macromolecules · doi:10.1021/ma071357r · Cited by 417

Well-Defined Protein−Polymer Conjugates via in Situ RAFT Polymerization

Boyer, C., Bulmus, V., Liu, J., Davis, T. P., Stenzel, M. H., & Barner-Kowollik, C. (2007) · Journal of the American Chemical Society · doi:10.1021/ja070956a · Cited by 411

Thiol−Yne Photopolymerizations: Novel Mechanism, Kinetics, and Step-Growth Formation of Highly Cross-Linked Networks

Fairbanks, B. D., Scott, T. F., Kloxin, C. J., Anseth, K. S., & Bowman, C. N. (2009) · Macromolecules · doi:10.1021/ma801903w · Cited by 405

Design and Synthesis of N-Maleimido-Functionalized Hydrophilic Polymers via Copper-Mediated Living Radical Polymerization: A Suitable Alternative to PEGylation Chemistry

Mantovani, G., Lecolley, F., Tao, L., Haddleton, D. M., Clerx, J., Cornelissen, J. J. L. M., & Velonia, K. (2005) · Journal of the American Chemical Society · doi:10.1021/ja0430999 · Cited by 394

Click chemistry under non-classical reaction conditions

Kappe, C. O., & Van der Eycken, E. (2010) · Chem. Soc. Rev. · doi:10.1039/b901973c · Cited by 390

Introducing Multicomponent Reactions to Polymer Science: Passerini Reactions of Renewable Monomers

Kreye, O., Tóth, T., & Meier, M. A. R. (2011) · Journal of the American Chemical Society · doi:10.1021/ja1113003 · Cited by 375

Iterative exponential growth of stereo- and sequence-controlled polymers

Barnes, J. C., Ehrlich, D. J. C., Gao, A. X., Leibfarth, F. A., Jiang, Y., Zhou, E., Jamison, T. F., & Johnson, J. A. (2015) · Nature Chemistry · doi:10.1038/nchem.2346 · Cited by 361

Polymer “Clicking” by CuAAC Reactions

Meldal, M. (2008) · Macromolecular Rapid Communications · doi:10.1002/marc.200800159 · Cited by 360

Problems and Possibilities of the Free‐Radical Addition of Thiols to Unsaturated Compounds

Griesbaum, K. (1970) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197002731 · Cited by 357

Triazolinediones enable ultrafast and reversible click chemistry for the design of dynamic polymer systems

Billiet, S., De Bruycker, K., Driessen, F., Goossens, H., Van Speybroeck, V., Winne, J. M., & Du Prez, F. E. (2014) · Nature Chemistry · doi:10.1038/nchem.2023 · Cited by 356

“Clicking” on/with polymers: a rapidly expanding field for the straightforward preparation of novel macromolecular architectures

Kempe, K., Krieg, A., Becer, C. R., & Schubert, U. S. (2012) · Chem. Soc. Rev. · doi:10.1039/c1cs15107j · Cited by 353

Reliable and Efficient Procedures for the Conjugation of Biomolecules through Huisgen Azide–Alkyne Cycloadditions

Lallana, E., Riguera, R., & Fernandez‐Megia, E. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101019 · Cited by 328

Copper‐Free Azide–Alkyne Cycloadditions: New Insights and Perspectives

Lutz, J. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200705365 · Cited by 326

RAFT and click chemistry: A versatile approach to well-defined block copolymers

Quémener, D., Davis, T. P., Barner-Kowollik, C., & Stenzel, M. H. (2006) · Chem. Commun. · doi:10.1039/b611224b · Cited by 300

Iridium‐Catalyzed Intermolecular Azide–Alkyne Cycloaddition of Internal Thioalkynes under Mild Conditions

Ding, S., Jia, G., & Sun, J. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201309855 · Cited by 300

Hyperbranched Polymers by Thiol−Yne Chemistry: From Small Molecules to Functional Polymers

Konkolewicz, D., Gray-Weale, A., & Perrier, S. (2009) · Journal of the American Chemical Society · doi:10.1021/ja908206a · Cited by 298

Thiol-yne ‘click’/coupling chemistry and recent applications in polymer and materials synthesis and modification

Lowe, A. B. (2014) · Polymer · doi:10.1016/j.polymer.2014.08.015 · Cited by 296

Adaptable Hetero Diels–Alder Networks for Fast Self‐Healing under Mild Conditions

Oehlenschlaeger, K. K., Mueller, J. O., Brandt, J., Hilf, S., Lederer, A., Wilhelm, M., Graf, R., Coote, M. L., Schmidt, F. G., & Barner‐Kowollik, C. (2014) · Advanced Materials · doi:10.1002/adma.201306258 · Cited by 295

Graft Copolymers by a Combination of ATRP and Two Different Consecutive Click Reactions

Tsarevsky, N. V., Bencherif, S. A., & Matyjaszewski, K. (2007) · Macromolecules · doi:10.1021/ma070705m · Cited by 292

Synthesis of well‐defined polymeric activated esters

Theato, P. (2008) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.22994 · Cited by 287

Sequence Control in Polymer Chemistry through the Passerini Three‐Component Reaction

Solleder, S. C., & Meier, M. A. R. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201308960 · Cited by 268

Thiol−Ene Modification of 1,2-Polybutadiene Using UV Light or Sunlight

ten Brummelhuis, N., Diehl, C., & Schlaad, H. (2008) · Macromolecules · doi:10.1021/ma802047w · Cited by 252

Metal-Free Ring-Opening Metathesis Polymerization

Ogawa, K. A., Goetz, A. E., & Boydston, A. J. (2015) · Journal of the American Chemical Society · doi:10.1021/ja512073m · Cited by 252

“Click”-Inspired Chemistry in Macromolecular Science: Matching Recent Progress and User Expectations

Espeel, P., & Du Prez, F. E. (2015) · Macromolecules · doi:10.1021/ma501386v · Cited by 249

One-Pot Multistep Reactions Based on Thiolactones: Extending the Realm of Thiol−Ene Chemistry in Polymer Synthesis

Espeel, P., Goethals, F., & Du Prez, F. E. (2011) · Journal of the American Chemical Society · doi:10.1021/ja1098098 · Cited by 231

Materials Science and Technology: A Comprehensive Treatment

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Photo-reversible dimerisation reactions and their applications in polymeric systems

Kaur, G., Johnston, P., & Saito, K. (2014) · Polym. Chem. · doi:10.1039/c3py01234d · Cited by 230

End group transformations of RAFT‐generated polymers with bismaleimides: Functional telechelics and modular block copolymers

Li, M., De, P., Gondi, S. R., & Sumerlin, B. S. (2008) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.22837 · Cited by 228

Ultrafast Click Conjugation of Macromolecular Building Blocks at Ambient Temperature

Inglis, A. J., Sinnwell, S., Stenzel, M. H., & Barner‐Kowollik, C. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200805993 · Cited by 224

Versatile Pathway to Functional Telechelics via RAFT Polymerization and Click Chemistry

Gondi, S. R., Vogt, A. P., & Sumerlin, B. S. (2007) · Macromolecules · doi:10.1021/ma061959v · Cited by 222

Macromolecular metamorphosis via stimulus-induced transformations of polymer architecture

Sun, H., Kabb, C. P., Dai, Y., Hill, M. R., Ghiviriga, I., Bapat, A. P., & Sumerlin, B. S. (2017) · Nature Chemistry · doi:10.1038/nchem.2730 · Cited by 220

Sequential thiol‐ene/thiol‐ene and thiol‐ene/thiol‐yne reactions as a route to well‐defined mono and bis end‐functionalized poly(N‐isopropylacrylamide)

Yu, B., Chan, J. W., Hoyle, C. E., & Lowe, A. B. (2009) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.23436 · Cited by 218

RAFT Polymerization of Pentafluorophenyl Methacrylate: Preparation of Reactive Linear Diblock Copolymers

Eberhardt, M., & Théato, P. (2005) · Macromolecular Rapid Communications · doi:10.1002/marc.200500390 · Cited by 209

RAFT Polymerization and Thiol Chemistry: A Complementary Pairing for Implementing Modern Macromolecular Design

Roth, P. J., Boyer, C., Lowe, A. B., & Davis, T. P. (2011) · Macromolecular Rapid Communications · doi:10.1002/marc.201100127 · Cited by 205

One-pot tandem living radical polymerisation–Huisgens cycloaddition process (“click”) catalysed by N-alkyl-2-pyridylmethanimine/Cu(i)Br complexes

Mantovani, G., Ladmiral, V., Tao, L., & Haddleton, D. M. (2005) · Chem. Commun. · doi:10.1039/b500558b · Cited by 202

Combining Ring-Opening Metathesis Polymerization (ROMP) with Sharpless-Type “Click” Reactions: An Easy Method for the Preparation of Side Chain Functionalized Poly(oxynorbornenes)

Binder, W. H., & Kluger, C. (2004) · Macromolecules · doi:10.1021/ma0480087 · Cited by 199

Functionalization of poly(methyl methacrylate) (PMMA) as a substrate for DNA microarrays

Fixe, F. (2004) · Nucleic Acids Research · doi:10.1093/nar/gng157 · Cited by 197

Synthesis and characterization of telechelic polymethacrylates via RAFT polymerization

Lima, V., Jiang, X., Brokken‐Zijp, J., Schoenmakers, P. J., Klumperman, B., & Van Der Linde, R. (2005) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.20558 · Cited by 191

Triazole: a unique building block for the construction of functional materials

Juríček, M., Kouwer, P. H. J., & Rowan, A. E. (2011) · Chemical Communications · doi:10.1039/c1cc10685f · Cited by 190

Synthesis of thiol-linked neoglycopolymers and thermo-responsive glycomicelles as potential drug carrier

Chen, G., Amajjahe, S., & Stenzel, M. H. (2009) · Chemical Communications · doi:10.1039/b900215d · Cited by 187

Generic Concept to Program the Time Domain of Self-Assemblies with a Self-Regulation Mechanism

Heuser, T., Steppert, A.-K., Molano Lopez, C., Zhu, B., & Walther, A. (2015) · Nano Letters · doi:10.1021/nl5039506 · Cited by 185

Visible Light Photocatalytic Thiol–Ene Reaction: An Elegant Approach for Fast Polymer Postfunctionalization and Step-Growth Polymerization

Xu, J., & Boyer, C. (2015) · Macromolecules · doi:10.1021/ma502460t · Cited by 183

Synthesis of well‐defined azido and amino end‐functionalized polystyrene by atom transfer radical polymerization

Matyjaszewski, K., Nakagawa, Y., & Gaynor, S. G. (1997) · Macromolecular Rapid Communications · doi:10.1002/marc.1997.030181209 · Cited by 180

Versatile Precursors of Functional RAFT Agents. Application to the Synthesis of Bio-Related End-Functionalized Polymers

Bathfield, M., D'Agosto, F., Spitz, R., Charreyre, M.-T., & Delair, T. (2006) · Journal of the American Chemical Society · doi:10.1021/ja057481c · Cited by 180

Simultaneous and Reversible Functionalization of Copolymers for Biological Applications

Ghosh, S., Basu, S., & Thayumanavan, S. (2006) · Macromolecules · doi:10.1021/ma061420x · Cited by 177

The Thiol−Isocyanate Click Reaction: Facile and Quantitative Access to ω-End-Functional Poly(N,N-diethylacrylamide) Synthesized by RAFT Radical Polymerization

Li, H., Yu, B., Matsushima, H., Hoyle, C. E., & Lowe, A. B. (2009) · Macromolecules · doi:10.1021/ma9010878 · Cited by 168

Bringing Efficiency to Materials Synthesis: The Philosophy of Click Chemistry

Hawker, C. J., Fokin, V. V., Finn, M. G., & Sharpless, K. B. (2007) · Australian Journal of Chemistry · doi:10.1071/ch07107 · Cited by 167

Efficient Usage of Thiocarbonates for Both the Production and the Biofunctionalization of Polymers

Boyer, C., Bulmus, V., & Davis, T. P. (2009) · Macromolecular Rapid Communications · doi:10.1002/marc.200800708 · Cited by 164

A Scalable and High‐Yield Strategy for the Synthesis of Sequence‐Defined Macromolecules

Solleder, S. C., Zengel, D., Wetzel, K. S., & Meier, M. A. R. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201509398 · Cited by 164

Hydrophobically Modified Sulfobetaine Copolymers with Tunable Aqueous UCST through Postpolymerization Modification of Poly(pentafluorophenyl acrylate)

Woodfield, P. A., Zhu, Y., Pei, Y., & Roth, P. J. (2014) · Macromolecules · doi:10.1021/ma402391a · Cited by 162

Direct Synthesis of Well-Defined Heterotelechelic Polymers for Bioconjugations

Boyer, C. A., Liu, J., Bulmuş, V., Davis, T. P., Barner‐Kowollik, C., & Stenzel, M. H. (2008) · Macromolecules · doi:10.1021/ma800289u · Cited by 161

Rhodium-Catalyzed, Regiospecific Functionalization of Polyolefins in the Melt

Kondo, Y., García-Cuadrado, D., Hartwig, J. F., Boaen, N. K., Wagner, N. L., & Hillmyer, M. A. (2002) · Journal of the American Chemical Society · doi:10.1021/ja016763j · Cited by 160

Conjugation of RAFT-generated polymers to proteins by two consecutive thiol–ene reactions

Li, M., De, P., Li, H., & Sumerlin, B. S. (2010) · Polymer Chemistry · doi:10.1039/c0py00025f · Cited by 158

Imine Hydrogels with Tunable Degradability for Tissue Engineering

Boehnke, N., Cam, C., Bat, E., Segura, T., & Maynard, H. D. (2015) · Biomacromolecules · doi:10.1021/acs.biomac.5b00519 · Cited by 158

Cycloadditions in Modern Polymer Chemistry

Delaittre, G., Guimard, N. K., & Barner‐Kowollik, C. (2015) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5b00075 · Cited by 157

Recent advances in the preparation of functionalized polysulfones

Dızman, C., Taşdelen, M. A., & Yağcı, Y. (2013) · Polymer International · doi:10.1002/pi.4525 · Cited by 155

Rapid Bonding/Debonding on Demand: Reversibly Cross-Linked Functional Polymers via Diels−Alder Chemistry

Inglis, A. J., Nebhani, L., Altintas, O., Schmidt, F. G., & Barner‐Kowollik, C. (2010) · Macromolecules · doi:10.1021/ma100945b · Cited by 153

Facile Synthesis of Clickable, Water-Soluble, and Degradable Polyphosphoesters

Zhang, S., Li, A., Zou, J., Lin, L. Y., & Wooley, K. L. (2012) · ACS Macro Letters · doi:10.1021/mz200226m · Cited by 151

Multicomponent Combinatorial Polymerization via the Biginelli Reaction

Xue, H., Zhao, Y., Wu, H., Wang, Z., Yang, B., Wei, Y., Wang, Z., & Tao, L. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b04425 · Cited by 147

One- pot synthesis and biofunctionalization of glycopolymers via RAFT polymerization and thiol–ene reactions

Boyer, C. A., & Davis, T. P. (2009) · Chemical Communications · doi:10.1039/b910296e · Cited by 145

Thiol–yne and Thiol–ene “Click” Chemistry as a Tool for a Variety of Platinum Drug Delivery Carriers, from Statistical Copolymers to Crosslinked Micelles

Huynh, V. T., Chen, G., SOUZA, P. D., & Stenzel, M. H. (2011) · Biomacromolecules · doi:10.1021/bm200135e · Cited by 139

Iterative Exponential Growth Synthesis and Assembly of Uniform Diblock Copolymers

Jiang, Y., Golder, M. R., Nguyen, H. V. ‐., Wang, Y., Zhong, M., Barnes, J. C., Ehrlich, D. C., & Johnson, J. A. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b04964 · Cited by 139

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