메뉴 건너뛰기




Volumn 62, Issue , 2015, Pages 247-272

One-pot multi-step reactions based on thiolactone chemistry: A powerful synthetic tool in polymer science

Author keywords

Amine thiol ene conjugation; Functionalized polymers; One pot multi step click chemistry; Thiolactone chemistry

Indexed keywords

PHYSICS;

EID: 84919631130     PISSN: 00143057     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.eurpolymj.2014.07.008     Document Type: Review
Times cited : (141)

References (257)
  • 1
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • H.C. Kolb, M.G. Finn, and K.B. Sharpless Click chemistry: diverse chemical function from a few good reactions Angew Chem Int Ed 40 11 2001 2004 2021
    • (2001) Angew Chem Int Ed , vol.40 , Issue.11 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 2
    • 23844451374 scopus 로고    scopus 로고
    • The convergence of synthetic organic and polymer chemistries
    • C.J. Hawker, and K.L. Wooley The convergence of synthetic organic and polymer chemistries Science 309 5738 2005 1200 1205
    • (2005) Science , vol.309 , Issue.5738 , pp. 1200-1205
    • Hawker, C.J.1    Wooley, K.L.2
  • 3
    • 33846703461 scopus 로고    scopus 로고
    • 'Click' chemistry in polymer and materials science
    • W.H. Binder, and R. Sachsenhofer 'Click' chemistry in polymer and materials science Macromol Rapid Commun 28 1 2007 15 54
    • (2007) Macromol Rapid Commun , vol.28 , Issue.1 , pp. 15-54
    • Binder, W.H.1    Sachsenhofer, R.2
  • 4
    • 34250890189 scopus 로고    scopus 로고
    • Bringing efficiency to materials synthesis: The philosophy of click chemistry
    • C.J. Hawker, V.V. Fokin, M.G. Finn, and K.B. Sharpless Bringing efficiency to materials synthesis: the philosophy of click chemistry Aust J Chem 60 6 2007 381 383
    • (2007) Aust J Chem , vol.60 , Issue.6 , pp. 381-383
    • Hawker, C.J.1    Fokin, V.V.2    Finn, M.G.3    Sharpless, K.B.4
  • 5
    • 54749104711 scopus 로고    scopus 로고
    • 'Click' chemistry in polymer and material science: An update
    • W.H. Binder, and R. Sachsenhofer 'Click' chemistry in polymer and material science: an update Macromol Rapid Commun 29 12-13 2008 952 981
    • (2008) Macromol Rapid Commun , vol.29 , Issue.1213 , pp. 952-981
    • Binder, W.H.1    Sachsenhofer, R.2
  • 6
    • 70349769688 scopus 로고    scopus 로고
    • Click chemistry beyond metal-catalyzed cycloaddition
    • C.R. Becer, R. Hoogenboom, and U.S. Schubert Click chemistry beyond metal-catalyzed cycloaddition Angew Chem Int Ed 48 27 2009 4900 4908
    • (2009) Angew Chem Int Ed , vol.48 , Issue.27 , pp. 4900-4908
    • Becer, C.R.1    Hoogenboom, R.2    Schubert, U.S.3
  • 7
    • 34547482973 scopus 로고    scopus 로고
    • Clicking polymers: A straightforward approach to novel macromolecular architectures
    • D. Fournier, R. Hoogenboom, and U.S. Schubert Clicking polymers: a straightforward approach to novel macromolecular architectures Chem Soc Rev 36 8 2007 1369 1380
    • (2007) Chem Soc Rev , vol.36 , Issue.8 , pp. 1369-1380
    • Fournier, D.1    Hoogenboom, R.2    Schubert, U.S.3
  • 8
    • 34548639157 scopus 로고    scopus 로고
    • Click chemistry: Versatility and control in the hands of materials scientists
    • H. Nandivada, X. Jiang, and J. Lahann Click chemistry: versatility and control in the hands of materials scientists Adv Mater 19 17 2007 2197 2208
    • (2007) Adv Mater , vol.19 , Issue.17 , pp. 2197-2208
    • Nandivada, H.1    Jiang, X.2    Lahann, J.3
  • 9
    • 73249130570 scopus 로고    scopus 로고
    • Applications of orthogonal "click" chemistries in the synthesis of functional soft materials
    • R.K. Iha, K.L. Wooley, A.M. Nystrom, D.J. Burke, M.J. Kade, and C.J. Hawker Applications of orthogonal "click" chemistries in the synthesis of functional soft materials Chem Rev 109 11 2009 5620 5686
    • (2009) Chem Rev , vol.109 , Issue.11 , pp. 5620-5686
    • Iha, R.K.1    Wooley, K.L.2    Nystrom, A.M.3    Burke, D.J.4    Kade, M.J.5    Hawker, C.J.6
  • 10
    • 77949812304 scopus 로고    scopus 로고
    • Marrying click chemistry with polymerization: Expanding the scope of polymeric materials
    • P. Golas, and K. Matyjaszewski Marrying click chemistry with polymerization: expanding the scope of polymeric materials Chem Soc Rev 39 4 2010 1338 1354
    • (2010) Chem Soc Rev , vol.39 , Issue.4 , pp. 1338-1354
    • Golas, P.1    Matyjaszewski, K.2
  • 11
    • 73649085447 scopus 로고    scopus 로고
    • Macromolecular engineering through click chemistry and other efficient transformations
    • B.S. Sumerlin, and A.P. Vogt Macromolecular engineering through click chemistry and other efficient transformations Macromolecules 43 1 2010 1 13
    • (2010) Macromolecules , vol.43 , Issue.1 , pp. 1-13
    • Sumerlin, B.S.1    Vogt, A.P.2
  • 13
    • 82955165019 scopus 로고    scopus 로고
    • "clicking" on/with polymers: A rapidly expanding field for the straightforward preparation of novel macromolecular architectures
    • K. Kempe, A. Krieg, C.R. Becer, and U.S. Schubert "Clicking" on/with polymers: a rapidly expanding field for the straightforward preparation of novel macromolecular architectures Chem Soc Rev 41 1 2012 176 191
    • (2012) Chem Soc Rev , vol.41 , Issue.1 , pp. 176-191
    • Kempe, K.1    Krieg, A.2    Becer, C.R.3    Schubert, U.S.4
  • 15
    • 58249116718 scopus 로고    scopus 로고
    • Synthesis of functional polymers by post-polymerization modification
    • M.A. Gauthier, M.I. Gibson, and H.A. Klok Synthesis of functional polymers by post-polymerization modification Angew Chem Int Ed 48 1 2009 48 58
    • (2009) Angew Chem Int Ed , vol.48 , Issue.1 , pp. 48-58
    • Gauthier, M.A.1    Gibson, M.I.2    Klok, H.A.3
  • 17
    • 84870051545 scopus 로고    scopus 로고
    • Standing on the shoulders of Hermann Staudinger: Post-polymerization modification from past to present
    • K.A. Günay, P. Theato, and H.-A. Klok Standing on the shoulders of Hermann Staudinger: post-polymerization modification from past to present J Polym Sci, Part A: Polym Chem 51 1 2013 1 28
    • (2013) J Polym Sci, Part A: Polym Chem , vol.51 , Issue.1 , pp. 1-28
    • Günay, K.A.1    Theato, P.2    Klok, H.-A.3
  • 18
    • 52649137250 scopus 로고    scopus 로고
    • Optimization of click chemistry of ferrocene derivatives on acetylene-functionalized silicon(1 0 0) surfaces
    • S. Ciampi, G. Le Saux, J.B. Harper, and J.J. Gooding Optimization of click chemistry of ferrocene derivatives on acetylene-functionalized silicon(1 0 0) surfaces Electroanalysis 20 14 2008 1513 1519
    • (2008) Electroanalysis , vol.20 , Issue.14 , pp. 1513-1519
    • Ciampi, S.1    Le Saux, G.2    Harper, J.B.3    Gooding, J.J.4
  • 19
    • 72049099826 scopus 로고    scopus 로고
    • Spatially selective functionalization of conducting polymers by "electroclick" chemistry
    • T.S. Hansen, A.E. Daugaard, S. Hvilsted, and N.B. Larsen Spatially selective functionalization of conducting polymers by "electroclick" chemistry Adv Mater 21 44 2009 4483 4486
    • (2009) Adv Mater , vol.21 , Issue.44 , pp. 4483-4486
    • Hansen, T.S.1    Daugaard, A.E.2    Hvilsted, S.3    Larsen, N.B.4
  • 20
    • 64749095964 scopus 로고    scopus 로고
    • Ferrocene and porphyrin monolayers on Si(1 0 0) surfaces: Preparation and effect of linker length on electron transfer
    • K. Huang, F. Duclairoir, T. Pro, J. Buckley, G. Marchand, and E. Martinez Ferrocene and porphyrin monolayers on Si(1 0 0) surfaces: preparation and effect of linker length on electron transfer ChemPhysChem 10 6 2009 963 971
    • (2009) ChemPhysChem , vol.10 , Issue.6 , pp. 963-971
    • Huang, K.1    Duclairoir, F.2    Pro, T.3    Buckley, J.4    Marchand, G.5    Martinez, E.6
  • 21
    • 77949779995 scopus 로고    scopus 로고
    • Click chemistry with DNA
    • A.H. El-Sagheer, and T. Brown Click chemistry with DNA Chem Soc Rev 39 4 2010 1388 1405
    • (2010) Chem Soc Rev , vol.39 , Issue.4 , pp. 1388-1405
    • El-Sagheer, A.H.1    Brown, T.2
  • 22
    • 34547596467 scopus 로고    scopus 로고
    • Conjugates of stimuli-responsive polymers and proteins
    • A.S. Hoffman, and P.S. Stayton Conjugates of stimuli-responsive polymers and proteins Prog Polym Sci 32 8-9 2007 922 932
    • (2007) Prog Polym Sci , vol.32 , Issue.89 , pp. 922-932
    • Hoffman, A.S.1    Stayton, P.S.2
  • 23
    • 34547870488 scopus 로고    scopus 로고
    • Living radical polymerization as a tool for the synthesis of polymer-protein/peptide bioconjugates
    • J. Nicolas, G. Mantovani, and D.M. Haddleton Living radical polymerization as a tool for the synthesis of polymer-protein/peptide bioconjugates Macromol Rapid Commun 28 10 2007 1083 1111
    • (2007) Macromol Rapid Commun , vol.28 , Issue.10 , pp. 1083-1111
    • Nicolas, J.1    Mantovani, G.2    Haddleton, D.M.3
  • 24
    • 37249018985 scopus 로고    scopus 로고
    • Modern trends in polymer bioconjugates design
    • J.-F. Lutz, and H.G. Boerner Modern trends in polymer bioconjugates design Prog Polym Sci 33 1 2008 1 39
    • (2008) Prog Polym Sci , vol.33 , Issue.1 , pp. 1-39
    • Lutz, J.-F.1    Boerner, H.G.2
  • 25
    • 43449108552 scopus 로고    scopus 로고
    • Efficient construction of therapeutics, bioconjugates, biomaterials and bioactive surfaces using azide-alkyne "click" chemistry
    • J.-F. Lutz, and Z. Zarafshani Efficient construction of therapeutics, bioconjugates, biomaterials and bioactive surfaces using azide-alkyne "click" chemistry Adv Drug Des Dev 60 9 2008 958 970
    • (2008) Adv Drug des Dev , vol.60 , Issue.9 , pp. 958-970
    • Lutz, J.-F.1    Zarafshani, Z.2
  • 26
    • 33744544685 scopus 로고    scopus 로고
    • Transition metal catalyzed methods for site-selective protein modification
    • J.M. Antos, and M.B. Francis Transition metal catalyzed methods for site-selective protein modification Curr Opin Chem Biol 10 3 2006 253 262
    • (2006) Curr Opin Chem Biol , vol.10 , Issue.3 , pp. 253-262
    • Antos, J.M.1    Francis, M.B.2
  • 27
    • 37549026429 scopus 로고    scopus 로고
    • Bioorthogonal click chemistry: Covalent labeling in living systems
    • J.M. Baskin, and C.R. Bertozzi Bioorthogonal click chemistry: covalent labeling in living systems QSAR Comb Sci 26 11-12 2007 1211 1219
    • (2007) QSAR Comb Sci , vol.26 , Issue.1112 , pp. 1211-1219
    • Baskin, J.M.1    Bertozzi, C.R.2
  • 28
    • 57749121492 scopus 로고    scopus 로고
    • Chemoselective ligation and modification strategies for peptides and proteins
    • C.P.R. Hackenberger, and D. Schwarzer Chemoselective ligation and modification strategies for peptides and proteins Angew Chem Int Ed 47 52 2008 10030 10074
    • (2008) Angew Chem Int Ed , vol.47 , Issue.52 , pp. 10030-10074
    • Hackenberger, C.P.R.1    Schwarzer, D.2
  • 29
    • 56349111505 scopus 로고    scopus 로고
    • Novel strategies for the site-specific covalent labelling of nucleic acids
    • S.H. Weisbrod, and A. Marx Novel strategies for the site-specific covalent labelling of nucleic acids Chem Commun 44 2008 5675 5685
    • (2008) Chem Commun , vol.44 , pp. 5675-5685
    • Weisbrod, S.H.1    Marx, A.2
  • 30
    • 67650474557 scopus 로고    scopus 로고
    • Click chemistry and bioorthogonal reactions: Unprecedented selectivity in the labeling of biological molecules
    • M.D. Best Click chemistry and bioorthogonal reactions: unprecedented selectivity in the labeling of biological molecules Biochemistry 48 28 2009 6571 6584
    • (2009) Biochemistry , vol.48 , Issue.28 , pp. 6571-6584
    • Best, M.D.1
  • 31
    • 0348109450 scopus 로고    scopus 로고
    • The growing impact of click chemistry on drug discovery
    • H.C. Kolb, and K.B. Sharpless The growing impact of click chemistry on drug discovery Drug Discovery Today 8 24 2003 1128 1137
    • (2003) Drug Discovery Today , vol.8 , Issue.24 , pp. 1128-1137
    • Kolb, H.C.1    Sharpless, K.B.2
  • 32
    • 51649102031 scopus 로고    scopus 로고
    • Click chemistry, a powerful tool for pharmaceutical sciences
    • C.D. Hein, X.-M. Liu, and D. Wang Click chemistry, a powerful tool for pharmaceutical sciences Pharm Res 25 10 2008 2216 2230
    • (2008) Pharm Res , vol.25 , Issue.10 , pp. 2216-2230
    • Hein, C.D.1    Liu, X.-M.2    Wang, D.3
  • 33
    • 71249129936 scopus 로고    scopus 로고
    • Synthesis and applications of biomedical and pharmaceutical polymers via click chemistry methodologies
    • M. van Dijk, D.T.S. Rijkers, R.M.J. Liskamp, C.F. van Nostrum, and W.E. Hennink Synthesis and applications of biomedical and pharmaceutical polymers via click chemistry methodologies Bioconjugate Chem 20 11 2009 2001 2016
    • (2009) Bioconjugate Chem , vol.20 , Issue.11 , pp. 2001-2016
    • Van Dijk, M.1    Rijkers, D.T.S.2    Liskamp, R.M.J.3    Van Nostrum, C.F.4    Hennink, W.E.5
  • 34
    • 76749093968 scopus 로고    scopus 로고
    • Design and fabrication of magnetic nanoparticles for targeted drug delivery and imaging
    • O. Veiseh, J.W. Gunn, and M. Zhang Design and fabrication of magnetic nanoparticles for targeted drug delivery and imaging Adv Drug Des Dev 62 3 2010 284 304
    • (2010) Adv Drug des Dev , vol.62 , Issue.3 , pp. 284-304
    • Veiseh, O.1    Gunn, J.W.2    Zhang, M.3
  • 35
    • 67650309559 scopus 로고    scopus 로고
    • Has click chemistry lead to a paradigm shift in polymer material design?
    • C. Barner-Kowollik, and A.J. Inglis Has click chemistry lead to a paradigm shift in polymer material design? Macromol Chem Phys 210 12 2009 987 992
    • (2009) Macromol Chem Phys , vol.210 , Issue.12 , pp. 987-992
    • Barner-Kowollik, C.1    Inglis, A.J.2
  • 36
    • 84873292926 scopus 로고    scopus 로고
    • Orthogonality in organic, polymer, and supramolecular chemistry: From Merrifield to click chemistry
    • C.-H. Wong, and S.C. Zimmerman Orthogonality in organic, polymer, and supramolecular chemistry: from Merrifield to click chemistry Chem Commun 49 17 2013 1679 1695
    • (2013) Chem Commun , vol.49 , Issue.17 , pp. 1679-1695
    • Wong, C.-H.1    Zimmerman, S.C.2
  • 37
    • 27144512710 scopus 로고    scopus 로고
    • Orthogonal approaches to the simultaneous and cascade functionalization of macromolecules using click chemistry
    • M. Malkoch, R.J. Thibault, E. Drockenmuller, M. Messerschmidt, B. Voit, and T.P. Russell Orthogonal approaches to the simultaneous and cascade functionalization of macromolecules using click chemistry J Am Chem Soc 127 42 2005 14942 14949
    • (2005) J Am Chem Soc , vol.127 , Issue.42 , pp. 14942-14949
    • Malkoch, M.1    Thibault, R.J.2    Drockenmuller, E.3    Messerschmidt, M.4    Voit, B.5    Russell, T.P.6
  • 38
    • 55349112178 scopus 로고    scopus 로고
    • Click assisted one-pot multi-step reactions in polymer science: Accelerated synthetic protocols
    • P. Lundberg, C.J. Hawker, A. Hult, and M. Malkoch Click assisted one-pot multi-step reactions in polymer science: accelerated synthetic protocols Macromol Rapid Commun 29 12-13 2008 998 1015
    • (2008) Macromol Rapid Commun , vol.29 , Issue.1213 , pp. 998-1015
    • Lundberg, P.1    Hawker, C.J.2    Hult, A.3    Malkoch, M.4
  • 39
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • V.V. Rostovtsev, L.G. Green, V.V. Fokin, and K.B. Sharpless A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes Angew Chem Int Ed 41 14 2002 2596 2599
    • (2002) Angew Chem Int Ed , vol.41 , Issue.14 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 40
    • 34247237682 scopus 로고    scopus 로고
    • 1,3-Dipolar cycloadditions of azides and alkynes: A universal ligation tool in polymer and materials science
    • J.F. Lutz 1,3-Dipolar cycloadditions of azides and alkynes: a universal ligation tool in polymer and materials science Angew Chem Int Ed 46 7 2007 1018 1025
    • (2007) Angew Chem Int Ed , vol.46 , Issue.7 , pp. 1018-1025
    • Lutz, J.F.1
  • 41
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed azide-alkyne cycloaddition
    • M. Meldal, and C.W. Tornoe Cu-catalyzed azide-alkyne cycloaddition Chem Rev 108 8 2008 2952 3015
    • (2008) Chem Rev , vol.108 , Issue.8 , pp. 2952-3015
    • Meldal, M.1    Tornoe, C.W.2
  • 42
    • 55049090701 scopus 로고    scopus 로고
    • Polymer, "clicking" by CuAAC reactions
    • M. Meldal Polymer, "clicking" by CuAAC reactions Macromol Rapid Commun 29 12-13 2008 1016 1051
    • (2008) Macromol Rapid Commun , vol.29 , Issue.1213 , pp. 1016-1051
    • Meldal, M.1
  • 43
    • 8344226831 scopus 로고    scopus 로고
    • Thiol-enes: Chemistry of the past with promise for the future
    • C.E. Hoyle, T.Y. Lee, and T. Roper Thiol-enes: chemistry of the past with promise for the future J Polym Sci, Part A: Polym Chem 42 21 2004 5301 5338
    • (2004) J Polym Sci, Part A: Polym Chem , vol.42 , Issue.21 , pp. 5301-5338
    • Hoyle, C.E.1    Lee, T.Y.2    Roper, T.3
  • 44
    • 77955251908 scopus 로고    scopus 로고
    • Nucleophile-initiated thiol-Michael reactions: Effect of organocatalyst, thiol, and ene
    • J.W. Chan, C.E. Hoyle, A.B. Lowe, and M. Bowman Nucleophile-initiated thiol-Michael reactions: effect of organocatalyst, thiol, and ene Macromolecules 43 15 2010 6381 6388
    • (2010) Macromolecules , vol.43 , Issue.15 , pp. 6381-6388
    • Chan, J.W.1    Hoyle, C.E.2    Lowe, A.B.3    Bowman, M.4
  • 45
    • 77949823784 scopus 로고    scopus 로고
    • Thiol-click chemistry: A multifaceted toolbox for small molecule and polymer synthesis
    • C.E. Hoyle Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis Chem Soc Rev 39 4 2010 1355 1387
    • (2010) Chem Soc Rev , vol.39 , Issue.4 , pp. 1355-1387
    • Hoyle, C.E.1
  • 46
    • 77649122695 scopus 로고    scopus 로고
    • Thiol-ene click chemistry
    • C.E. Hoyle, and C.N. Bowman Thiol-ene click chemistry Angew Chem Int Ed 49 9 2010 1540 1573
    • (2010) Angew Chem Int Ed , vol.49 , Issue.9 , pp. 1540-1573
    • Hoyle, C.E.1    Bowman, C.N.2
  • 47
    • 77952372607 scopus 로고    scopus 로고
    • Thiol-yne chemistry: A powerful tool for creating highly functional materials
    • R. Hoogenboom Thiol-yne chemistry: a powerful tool for creating highly functional materials Angew Chem Int Ed 49 20 2011 3415 3417
    • (2011) Angew Chem Int Ed , vol.49 , Issue.20 , pp. 3415-3417
    • Hoogenboom, R.1
  • 48
    • 84892568067 scopus 로고    scopus 로고
    • The thiol-Michael addition click reaction: A powerful and widely used tool in materials chemistry
    • D.P. Nair, M. Podgórski, S. Chatani, T. Gong, W. Xi, and C.R. Fenoli The thiol-Michael addition click reaction: a powerful and widely used tool in materials chemistry Chem Mater 26 1 2013 724 744
    • (2013) Chem Mater , vol.26 , Issue.1 , pp. 724-744
    • Nair, D.P.1    Podgórski, M.2    Chatani, S.3    Gong, T.4    Xi, W.5    Fenoli, C.R.6
  • 49
    • 84886888479 scopus 로고    scopus 로고
    • Kinetic comparison of 13 homogeneous thiol-X reactions
    • L.-T.T. Nguyen, M.T. Gokmen, and F.E. Du Prez Kinetic comparison of 13 homogeneous thiol-X reactions Polym Chem 4 22 2013 5527 5536
    • (2013) Polym Chem , vol.4 , Issue.22 , pp. 5527-5536
    • Nguyen, L.-T.T.1    Gokmen, M.T.2    Du Prez, F.E.3
  • 50
    • 84905001198 scopus 로고    scopus 로고
    • Thiol-ene "click" reactions and recent applications in polymer and materials synthesis: A first update
    • A.B. Lowe Thiol-ene "click" reactions and recent applications in polymer and materials synthesis: a first update Polym Chem 2014
    • (2014) Polym Chem
    • Lowe, A.B.1
  • 51
    • 17644411685 scopus 로고    scopus 로고
    • Synthesis of pentafluorophenyl(meth)acrylate polymers: New precursor polymers for the synthesis of multifunctional materials
    • M. Eberhardt, R. Mruk, R. Zentel, and P. Theato Synthesis of pentafluorophenyl(meth)acrylate polymers: new precursor polymers for the synthesis of multifunctional materials Eur Polym J 41 7 2005 1569 1575
    • (2005) Eur Polym J , vol.41 , Issue.7 , pp. 1569-1575
    • Eberhardt, M.1    Mruk, R.2    Zentel, R.3    Theato, P.4
  • 52
    • 34347333418 scopus 로고    scopus 로고
    • Synthesis and polymerization of active ester monomers based on 4-vinylbenzoic acid
    • K. Nilles, and P. Theato Synthesis and polymerization of active ester monomers based on 4-vinylbenzoic acid Eur Polym J 43 7 2007 2901 2912
    • (2007) Eur Polym J , vol.43 , Issue.7 , pp. 2901-2912
    • Nilles, K.1    Theato, P.2
  • 53
    • 57349185823 scopus 로고    scopus 로고
    • Synthesis of reactive telechelic polymers based on pentafluorophenyl esters
    • P.J. Roth, K.T. Wiss, R. Zentel, and P. Theato Synthesis of reactive telechelic polymers based on pentafluorophenyl esters Macromolecules 41 22 2008 8513 8519
    • (2008) Macromolecules , vol.41 , Issue.22 , pp. 8513-8519
    • Roth, P.J.1    Wiss, K.T.2    Zentel, R.3    Theato, P.4
  • 54
    • 55349142477 scopus 로고    scopus 로고
    • Synthesis of well-defined polymeric activated esters
    • P. Theato Synthesis of well-defined polymeric activated esters J Polym Sci, Part A: Polym Chem 46 20 2008 6677 6687
    • (2008) J Polym Sci, Part A: Polym Chem , vol.46 , Issue.20 , pp. 6677-6687
    • Theato, P.1
  • 55
    • 77956022249 scopus 로고    scopus 로고
    • Sequential conversion of orthogonally functionalized diblock copolymers based on pentafluorophenyl esters
    • K. Nilles, and P. Theato Sequential conversion of orthogonally functionalized diblock copolymers based on pentafluorophenyl esters J Polym Sci, Part A: Polym Chem 48 16 2010 3683 3692
    • (2010) J Polym Sci, Part A: Polym Chem , vol.48 , Issue.16 , pp. 3683-3692
    • Nilles, K.1    Theato, P.2
  • 56
    • 4344659604 scopus 로고    scopus 로고
    • Preparation and characterization of azlactone functionalized polymer supports and their application as scavengers
    • A. Guyomard, D. Fournier, S. Pascual, L. Fontaine, and J.F. Bardeau Preparation and characterization of azlactone functionalized polymer supports and their application as scavengers Eur Polym J 40 10 2004 2343 2348
    • (2004) Eur Polym J , vol.40 , Issue.10 , pp. 2343-2348
    • Guyomard, A.1    Fournier, D.2    Pascual, S.3    Fontaine, L.4    Bardeau, J.F.5
  • 57
    • 33746360243 scopus 로고    scopus 로고
    • Well-defined azlactone-functionalized (Co)polymers on a solid support: Synthesis via supported living radical polymerization and application as nucleophile scavengers
    • D. Fournier, S. Pascual, V. Montembault, D.M. Haddleton, and L. Fontaine Well-defined azlactone-functionalized (Co)polymers on a solid support: synthesis via supported living radical polymerization and application as nucleophile scavengers J Comb Chem 8 4 2006 522 530
    • (2006) J Comb Chem , vol.8 , Issue.4 , pp. 522-530
    • Fournier, D.1    Pascual, S.2    Montembault, V.3    Haddleton, D.M.4    Fontaine, L.5
  • 58
    • 84866100680 scopus 로고    scopus 로고
    • Introducing the azlactone functionality into polymers through controlled radical polymerization: Strategies and recent developments
    • H.T. Ho, M.E. Levere, D. Fournier, V. Montembault, S. Pascual, and L. Fontaine Introducing the azlactone functionality into polymers through controlled radical polymerization: strategies and recent developments Aust J Chem 65 8 2012 970 977
    • (2012) Aust J Chem , vol.65 , Issue.8 , pp. 970-977
    • Ho, H.T.1    Levere, M.E.2    Fournier, D.3    Montembault, V.4    Pascual, S.5    Fontaine, L.6
  • 59
    • 84860787863 scopus 로고    scopus 로고
    • Highly efficient ring-opening reaction of azlactone-based copolymer platforms for the design of functionalized materials
    • A. Laquievre, N.S. Allaway, J. Lyskawa, P. Woisel, J.-M. Lefebvre, and D. Fournier Highly efficient ring-opening reaction of azlactone-based copolymer platforms for the design of functionalized materials Macromol Rapid Commun 33 9 2012 848 855
    • (2012) Macromol Rapid Commun , vol.33 , Issue.9 , pp. 848-855
    • Laquievre, A.1    Allaway, N.S.2    Lyskawa, J.3    Woisel, P.4    Lefebvre, J.-M.5    Fournier, D.6
  • 60
    • 82655175458 scopus 로고    scopus 로고
    • Azlactone-functionalized polymers as reactive platforms for the design of advanced materials: Progress in the last ten years
    • M.E. Buck, and D.M. Lynn Azlactone-functionalized polymers as reactive platforms for the design of advanced materials: progress in the last ten years Polym Chem 3 1 2012 66 80
    • (2012) Polym Chem , vol.3 , Issue.1 , pp. 66-80
    • Buck, M.E.1    Lynn, D.M.2
  • 61
    • 79951527554 scopus 로고    scopus 로고
    • One-pot multistep reactions based on thiolactones: Extending the realm of thiol-ene chemistry in polymer synthesis
    • P. Espeel, F. Goethals, and F.E. Du Prez One-pot multistep reactions based on thiolactones: extending the realm of thiol-ene chemistry in polymer synthesis J Am Chem Soc 133 6 2011 1678 1681
    • (2011) J Am Chem Soc , vol.133 , Issue.6 , pp. 1678-1681
    • Espeel, P.1    Goethals, F.2    Du Prez, F.E.3
  • 63
    • 34250201064 scopus 로고    scopus 로고
    • Synthesis and cleavage of lactones and thiolactones. Applications in organic synthesis. A review
    • Z. Paryzek, and W. Skiera Synthesis and cleavage of lactones and thiolactones. Applications in organic synthesis. A review Org Prep Proced Int 39 3 2007 203 296
    • (2007) Org Prep Proced Int , vol.39 , Issue.3 , pp. 203-296
    • Paryzek, Z.1    Skiera, W.2
  • 64
    • 0028982297 scopus 로고
    • Alpha-thiolactones as novel intermediates in the cysteine conjugate beta-lyase-catalyzed bioactivation of bromine-containing cysteine S-conjugates
    • M.B. Finkelstein, W. Dekant, A.S. Kende, and M.W. Anders Alpha-thiolactones as novel intermediates in the cysteine conjugate beta-lyase-catalyzed bioactivation of bromine-containing cysteine S-conjugates J Am Chem Soc 117 37 1995 9590 9591
    • (1995) J Am Chem Soc , vol.117 , Issue.37 , pp. 9590-9591
    • Finkelstein, M.B.1    Dekant, W.2    Kende, A.S.3    Anders, M.W.4
  • 65
    • 84980189204 scopus 로고
    • Alpha-thiolactones from thioketenes
    • E. Schaumann, and U. Behrens Alpha-thiolactones from thioketenes Angew Chem Int Ed 16 10 1977 722 723
    • (1977) Angew Chem Int Ed , vol.16 , Issue.10 , pp. 722-723
    • Schaumann, E.1    Behrens, U.2
  • 66
    • 8644271256 scopus 로고
    • Acyl-Lacton-Umlagerung. 17. Synthese von Gamma-Tniol-Lactonen und Delta-Thiol-Lactonen und Ihr Ringoffnungsmechanismus
    • F. Korte, and H. Christoph Acyl-Lacton-Umlagerung. 17. Synthese Von Gamma-Tniol-Lactonen Und Delta-Thiol-Lactonen Und Ihr Ringoffnungsmechanismus Chem Ber 94 8 1961 1966 1976
    • (1961) Chem Ber , vol.94 , Issue.8 , pp. 1966-1976
    • Korte, F.1    Christoph, H.2
  • 67
    • 0025804215 scopus 로고
    • Synthesis of 4-thiazolidineacetic acids and beta-homopenicillamine
    • J. Martens, J. Kintscher, and W. Arnold Synthesis of 4-thiazolidineacetic acids and beta-homopenicillamine Synth-Stuttgart 6 1991 497 498
    • (1991) Synth-Stuttgart , vol.6 , pp. 497-498
    • Martens, J.1    Kintscher, J.2    Arnold, W.3
  • 68
    • 0026006708 scopus 로고
    • Synthetic studies towards leinamycin. A concise synthesis of the spiro-fused 1,3-dioxo-1,2-dithiolane moiety
    • G. Pattenden, and A.J. Shuker Synthetic studies towards leinamycin. A concise synthesis of the spiro-fused 1,3-dioxo-1,2-dithiolane moiety Tetrahedron Lett 32 45 1991 6625 6628
    • (1991) Tetrahedron Lett , vol.32 , Issue.45 , pp. 6625-6628
    • Pattenden, G.1    Shuker, A.J.2
  • 69
    • 0026718597 scopus 로고
    • A new convenient method for preparation of condensed aromatic and heterocyclic thiolactones
    • D. Vegh, J. Morel, B. Decroix, and P. Zalupsky A new convenient method for preparation of condensed aromatic and heterocyclic thiolactones Synth Commun 22 14 1992 2057 2061
    • (1992) Synth Commun , vol.22 , Issue.14 , pp. 2057-2061
    • Vegh, D.1    Morel, J.2    Decroix, B.3    Zalupsky, P.4
  • 70
    • 34250083778 scopus 로고
    • Synthesis of alpha-methyl-homocysteinethiolactone
    • J. Hausler Synthesis of alpha-methyl-homocysteinethiolactone Monatshefte Fur Chemie 124 10 1993 1071 1075
    • (1993) Monatshefte fur Chemie , vol.124 , Issue.10 , pp. 1071-1075
    • Hausler, J.1
  • 71
    • 0033017628 scopus 로고    scopus 로고
    • Preparation of carboxythiolactones and their active derivatives
    • B.J. Garbiras, and S. Marburg Preparation of carboxythiolactones and their active derivatives Synth-Stuttgart 2 1999 270 274
    • (1999) Synth-Stuttgart , vol.2 , pp. 270-274
    • Garbiras, B.J.1    Marburg, S.2
  • 72
    • 0036208689 scopus 로고    scopus 로고
    • Temperature dependence of the reduction of phthalic thioanhydrides by NaBH4: Competition between 3-hydroxythiolactone and phthalide formation
    • I. Polec, L. Lutsen, D. Vanderzande, and J. Gelan Temperature dependence of the reduction of phthalic thioanhydrides by NaBH4: competition between 3-hydroxythiolactone and phthalide formation Eur J Org Chem 6 2002 1033 1036
    • (2002) Eur J Org Chem , vol.6 , pp. 1033-1036
    • Polec, I.1    Lutsen, L.2    Vanderzande, D.3    Gelan, J.4
  • 73
    • 0342338586 scopus 로고
    • Formation of peptide bonds by aminolysis of homocysteine thiolactones
    • R. Benesch, and R.E. Benesch Formation of peptide bonds by aminolysis of homocysteine thiolactones J Am Chem Soc 78 8 1956 1597 1599
    • (1956) J Am Chem Soc , vol.78 , Issue.8 , pp. 1597-1599
    • Benesch, R.1    Benesch, R.E.2
  • 74
    • 0000662047 scopus 로고
    • The kinetics of basic hydrolysis of some γ-lactones and γ-thiolactones in aqueous acetone1
    • C.M. Stevens, and D.S. Tarbell The kinetics of basic hydrolysis of some γ-lactones and γ-thiolactones in aqueous acetone1 J Org Chem 19 12 1954 1996 2003
    • (1954) J Org Chem , vol.19 , Issue.12 , pp. 1996-2003
    • Stevens, C.M.1    Tarbell, D.S.2
  • 75
    • 0342411564 scopus 로고
    • Anionic ring-opening polymerization of thiolactones
    • C.G. Overberger, and J.K. Weise Anionic ring-opening polymerization of thiolactones J Am Chem Soc 90 13 1968 3533 3537
    • (1968) J Am Chem Soc , vol.90 , Issue.13 , pp. 3533-3537
    • Overberger, C.G.1    Weise, J.K.2
  • 76
    • 0033355306 scopus 로고    scopus 로고
    • Anionic ring-opening polymerization of ε-thionocaprolactone
    • F. Sanda, D. Jirakanjana, M. Hitomi, and T. Endo Anionic ring-opening polymerization of ε-thionocaprolactone Macromolecules 32 24 1999 8010 8014
    • (1999) Macromolecules , vol.32 , Issue.24 , pp. 8010-8014
    • Sanda, F.1    Jirakanjana, D.2    Hitomi, M.3    Endo, T.4
  • 77
    • 36649017213 scopus 로고    scopus 로고
    • Enzymatic synthesis of polythioester by the ring-opening polymerization of cyclic thioester
    • M. Kato, K. Toshima, and S. Matsumura Enzymatic synthesis of polythioester by the ring-opening polymerization of cyclic thioester Biomacromolecules 8 11 2007 3590 3596
    • (2007) Biomacromolecules , vol.8 , Issue.11 , pp. 3590-3596
    • Kato, M.1    Toshima, K.2    Matsumura, S.3
  • 78
    • 0001607609 scopus 로고
    • A modification of the method for determining methionine in proteins
    • H.D. Baernstein A modification of the method for determining methionine in proteins J Biol Chem 106 2 1934 451 456
    • (1934) J Biol Chem , vol.106 , Issue.2 , pp. 451-456
    • Baernstein, H.D.1
  • 79
    • 0000283376 scopus 로고
    • The isolation of homocysteine and its conversion to a thiolactone
    • B. Riegel, and V. du Vigneaud The isolation of homocysteine and its conversion to a thiolactone J Biol Chem 112 1 1935 149 154
    • (1935) J Biol Chem , vol.112 , Issue.1 , pp. 149-154
    • Riegel, B.1    Du Vigneaud, V.2
  • 80
    • 33750550442 scopus 로고    scopus 로고
    • Mechanism of the condensation of homocysteine thiolactone with aldehydes
    • H. Jakubowski Mechanism of the condensation of homocysteine thiolactone with aldehydes Chem Eur J 12 31 2006 8039 8043
    • (2006) Chem Eur J , vol.12 , Issue.31 , pp. 8039-8043
    • Jakubowski, H.1
  • 81
    • 1542373560 scopus 로고    scopus 로고
    • Molecular basis of homocysteine toxicity in humans
    • H. Jakubowski Molecular basis of homocysteine toxicity in humans Cell Mol Life Sci 61 4 2004 470 487
    • (2004) Cell Mol Life Sci , vol.61 , Issue.4 , pp. 470-487
    • Jakubowski, H.1
  • 82
    • 0026952290 scopus 로고
    • Acidic derivatives of homocysteine thiolactone: Utility as anionic linkers
    • W.J. Leanza, L.S. Chupak, R.L. Tolman, and S. Marburg Acidic derivatives of homocysteine thiolactone: utility as anionic linkers Bioconjugate Chem 3 6 1992 514 518
    • (1992) Bioconjugate Chem , vol.3 , Issue.6 , pp. 514-518
    • Leanza, W.J.1    Chupak, L.S.2    Tolman, R.L.3    Marburg, S.4
  • 83
    • 0028904862 scopus 로고
    • Synthesis of pyrrolo[2,1-c][1,4]benzodiazepines via an intramolecular aza-Wittig reaction. Synthesis of the antibiotic DC-81
    • P. Molina, I. Diaz, and A. Tarraga Synthesis of pyrrolo[2,1-c][1,4]benzodiazepines via an intramolecular aza-Wittig reaction. Synthesis of the antibiotic DC-81 Tetrahedron 51 19 1995 5617 5630
    • (1995) Tetrahedron , vol.51 , Issue.19 , pp. 5617-5630
    • Molina, P.1    Diaz, I.2    Tarraga, A.3
  • 85
    • 79952084312 scopus 로고    scopus 로고
    • Protein reactivity of natural product-derived gamma-butyrolactones
    • M.H. Kunzmann, I. Staub, T. Boettcher, and S.A. Sieber Protein reactivity of natural product-derived gamma-butyrolactones Biochemistry 50 5 2011 910 916
    • (2011) Biochemistry , vol.50 , Issue.5 , pp. 910-916
    • Kunzmann, M.H.1    Staub, I.2    Boettcher, T.3    Sieber, S.A.4
  • 86
    • 0002160677 scopus 로고
    • Amination and acylation reactions by homocysteine thiolactone and N-benzyloxycarbonylhomocysteine thiolactone
    • R. Laliberte, Y. Knobler, and M. Frankel Amination and acylation reactions by homocysteine thiolactone and N-benzyloxycarbonylhomocysteine thiolactone J Chem Soc 1963 2756 2762
    • (1963) J Chem Soc , pp. 2756-2762
    • Laliberte, R.1    Knobler, Y.2    Frankel, M.3
  • 87
    • 0025698245 scopus 로고
    • PH-responsive release of fluorophore from homocysteine-carrying polymerized liposomes
    • H. Kitano, H. Wolf, and N. Ise PH-responsive release of fluorophore from homocysteine-carrying polymerized liposomes Macromolecules 23 7 1990 1958 1961
    • (1990) Macromolecules , vol.23 , Issue.7 , pp. 1958-1961
    • Kitano, H.1    Wolf, H.2    Ise, N.3
  • 88
    • 0038167466 scopus 로고    scopus 로고
    • Library screening for synthetic agonists and antagonists of a Pseudomonas aeruginosa autoinducer
    • K.M. Smith, Y. Bu, and H. Suga Library screening for synthetic agonists and antagonists of a Pseudomonas aeruginosa autoinducer Chem Biol 10 6 2003 563 571
    • (2003) Chem Biol , vol.10 , Issue.6 , pp. 563-571
    • Smith, K.M.1    Bu, Y.2    Suga, H.3
  • 89
    • 39149136153 scopus 로고    scopus 로고
    • Synthesis of S-linked carbohydrate analogues via a Ferrier reaction
    • D. Ellis, S.E. Norman, and H.M.I. Osborn Synthesis of S-linked carbohydrate analogues via a Ferrier reaction Tetrahedron 64 12 2008 2832 2854
    • (2008) Tetrahedron , vol.64 , Issue.12 , pp. 2832-2854
    • Ellis, D.1    Norman, S.E.2    Osborn, H.M.I.3
  • 90
    • 77956609573 scopus 로고    scopus 로고
    • Synthesis of optically active deuterium-labeled homocysteine thiolactone
    • Y. Shinohara, H. Hasegawa, T. Hashimoto, and K. Ichida Synthesis of optically active deuterium-labeled homocysteine thiolactone J Labelled Compd Radiopharm 53 8 2010 552 555
    • (2010) J Labelled Compd Radiopharm , vol.53 , Issue.8 , pp. 552-555
    • Shinohara, Y.1    Hasegawa, H.2    Hashimoto, T.3    Ichida, K.4
  • 91
    • 79961173351 scopus 로고    scopus 로고
    • Thiolactone modulators of quorum sensing revealed through library design and screening
    • C.E. McInnis, and H.E. Blackwell Thiolactone modulators of quorum sensing revealed through library design and screening Bioorg Med Chem 19 16 2011 4820 4828
    • (2011) Bioorg Med Chem , vol.19 , Issue.16 , pp. 4820-4828
    • McInnis, C.E.1    Blackwell, H.E.2
  • 93
    • 0015029667 scopus 로고
    • Vitamin B6 derivatives. 13. Synthesis of tetrahydrothiazine derivatives of vitamin B6 and their biological properties
    • K. Okumura, T. Oda, K. Kondo, I. Inoue, T. Danno, and H. Yamaguchi Vitamin B6 derivatives. 13. Synthesis of tetrahydrothiazine derivatives of vitamin B6 and their biological properties J Med Chem 14 3 1971 226 229
    • (1971) J Med Chem , vol.14 , Issue.3 , pp. 226-229
    • Okumura, K.1    Oda, T.2    Kondo, K.3    Inoue, I.4    Danno, T.5    Yamaguchi, H.6
  • 94
    • 0000163251 scopus 로고
    • X:Y-ZH Systems as potential 1,3-dipoles. Part 22. Cycloaddition reactions of pyridoxal imines. Relevance to α-amino acid racemases and transaminases
    • R. Grigg, S. Thianpatanagul, and J. Kemp X:Y-ZH Systems as potential 1,3-dipoles. Part 22. Cycloaddition reactions of pyridoxal imines. Relevance to α-amino acid racemases and transaminases Tetrahedron 44 23 1988 7283 7292
    • (1988) Tetrahedron , vol.44 , Issue.23 , pp. 7283-7292
    • Grigg, R.1    Thianpatanagul, S.2    Kemp, J.3
  • 95
    • 33748685012 scopus 로고    scopus 로고
    • XY-ZH compounds as potential 1,3-dipoles. Part 63: Silver catalysed azomethine ylide cycloaddition - The synthesis of spiro homoserine lactone analogues
    • R. Grigg, and M.A.B. Sarker XY-ZH compounds as potential 1,3-dipoles. Part 63: Silver catalysed azomethine ylide cycloaddition - the synthesis of spiro homoserine lactone analogues Tetrahedron 62 44 2006 10332 10343
    • (2006) Tetrahedron , vol.62 , Issue.44 , pp. 10332-10343
    • Grigg, R.1    Sarker, M.A.B.2
  • 97
    • 0021682384 scopus 로고
    • Controlled coupling of aminoglycoside antibiotics to proteins for use in homogeneous enzyme immunoassays
    • P. Singh, M. Pirio, D.K. Leung, and Y.G. Tsay Controlled coupling of aminoglycoside antibiotics to proteins for use in homogeneous enzyme immunoassays Can J Chem 62 11 1984 2471 2477
    • (1984) Can J Chem , vol.62 , Issue.11 , pp. 2471-2477
    • Singh, P.1    Pirio, M.2    Leung, D.K.3    Tsay, Y.G.4
  • 98
    • 0018758795 scopus 로고
    • Albumin microspheres as carrier of an inhibitor of leukocyte elastase - Potential therapeutic agent for emphysema
    • R.R. Martodam, D.Y. Twumasi, I.E. Liener, J.C. Powers, N. Nishino, and G. Krejcarek Albumin microspheres as carrier of an inhibitor of leukocyte elastase - potential therapeutic agent for emphysema Proc Natl Acad Sci USA 76 5 1979 2128 2132
    • (1979) Proc Natl Acad Sci USA , vol.76 , Issue.5 , pp. 2128-2132
    • Martodam, R.R.1    Twumasi, D.Y.2    Liener, I.E.3    Powers, J.C.4    Nishino, N.5    Krejcarek, G.6
  • 99
    • 84982507697 scopus 로고
    • Enzyme immobilization by reactive carriers containing maleinimide groups
    • G. Manecke, and H.J. Middeke Enzyme immobilization by reactive carriers containing maleinimide groups Angew Makromol Chem 91 NOV 1980 179 201
    • (1980) Angew Makromol Chem , vol.91 , Issue.NOV , pp. 179-201
    • Manecke, G.1    Middeke, H.J.2
  • 100
    • 7044255111 scopus 로고
    • A thiolation reagent for cell-surface carbohydrate
    • K.E. Taylor, and Y.C. Wu A thiolation reagent for cell-surface carbohydrate Biochem Int 1 4 1980 353 358
    • (1980) Biochem Int , vol.1 , Issue.4 , pp. 353-358
    • Taylor, K.E.1    Wu, Y.C.2
  • 101
    • 0021105782 scopus 로고
    • Methyl beta-glycosides of N-acetyl-6-O-(omega-aminoacyl)muramyl-l-alanyl-d-isoglutamines, and their conjugates with meningococcal group-C polysaccharide
    • M.M. Ponpipom, and K.M. Rupprecht Methyl beta-glycosides of N-acetyl-6-O-(omega-aminoacyl)muramyl-l-alanyl-d-isoglutamines, and their conjugates with meningococcal group-C polysaccharide Carbohydr Res 113 1 1983 45 56
    • (1983) Carbohydr Res , vol.113 , Issue.1 , pp. 45-56
    • Ponpipom, M.M.1    Rupprecht, K.M.2
  • 102
    • 0021961237 scopus 로고
    • Homocysteine thiolactone as precursor of methionine amide - Application to the modification of peptides of the tachykinin family
    • G. Chassaing, S. Lavielle, S. Julien, and A. Marquet Homocysteine thiolactone as precursor of methionine amide - application to the modification of peptides of the tachykinin family Tetrahedron Lett 26 5 1985 623 626
    • (1985) Tetrahedron Lett , vol.26 , Issue.5 , pp. 623-626
    • Chassaing, G.1    Lavielle, S.2    Julien, S.3    Marquet, A.4
  • 103
    • 0024523935 scopus 로고
    • Drug protein conjugates. 18. Detection of antibodies towards the antimalarial amodiaquine and its quinone imine metabolite in man and the rat
    • G. Christie, A.M. Breckenridge, and B.K. Park Drug protein conjugates. 18. Detection of antibodies towards the antimalarial amodiaquine and its quinone imine metabolite in man and the rat Biochem Pharmacol 38 9 1989 1451 1458
    • (1989) Biochem Pharmacol , vol.38 , Issue.9 , pp. 1451-1458
    • Christie, G.1    Breckenridge, A.M.2    Park, B.K.3
  • 104
    • 0007682945 scopus 로고
    • Thiolation of beta-lactoglobulin with N-acetylhomocysteine thiolactone (N-Ahtl) and S-acetylmercaptosuccinic anhydride
    • S.C. Kim, N.F. Olson, and T. Richardson Thiolation of beta-lactoglobulin with N-acetylhomocysteine thiolactone (N-Ahtl) and S-acetylmercaptosuccinic anhydride Milk Sci Int 45 9 1990 580 583
    • (1990) Milk Sci Int , vol.45 , Issue.9 , pp. 580-583
    • Kim, S.C.1    Olson, N.F.2    Richardson, T.3
  • 105
    • 0025914163 scopus 로고
    • A simple method for introducing a thiol-group at the 5′-end of synthetic oligonucleotides
    • 4561
    • A. Kumar, S. Advani, H. Dawar, and G.P. Talwar A simple method for introducing a thiol-group at the 5′-end of synthetic oligonucleotides Nucleic Acids Res 19 16 1991 4561
    • (1991) Nucleic Acids Res , vol.19 , Issue.16
    • Kumar, A.1    Advani, S.2    Dawar, H.3    Talwar, G.P.4
  • 106
    • 0000926798 scopus 로고    scopus 로고
    • Solid-phase enzymatic synthesis of a sialyl Lewis X tetrasaccharide on a sepharose matrix
    • O. Blixt, and T. Norberg Solid-phase enzymatic synthesis of a sialyl Lewis X tetrasaccharide on a sepharose matrix J Org Chem 63 8 1998 2705 2710
    • (1998) J Org Chem , vol.63 , Issue.8 , pp. 2705-2710
    • Blixt, O.1    Norberg, T.2
  • 108
    • 84861611274 scopus 로고    scopus 로고
    • Synthesis and characterization of chitosan-homocysteine thiolactone as a mucoadhesive polymer
    • K. Juntapram, N. Praphairaksit, K. Siraleartmukul, and N. Muangsin Synthesis and characterization of chitosan-homocysteine thiolactone as a mucoadhesive polymer Carbohydr Polym 87 4 2012 2399 2408
    • (2012) Carbohydr Polym , vol.87 , Issue.4 , pp. 2399-2408
    • Juntapram, K.1    Praphairaksit, N.2    Siraleartmukul, K.3    Muangsin, N.4
  • 110
    • 84958689892 scopus 로고
    • Heterocyclic compounds from lactones, lactams and thiollactones. XII. Synthesis of alpha-isocyanato-gamma-thiolbutyrolactone and of functional derivatives and their rearrangement to hydantoins and 1,2,4-triazines
    • U. Kraatz, H. Wamhoff, and F. Korte Heterocyclic compounds from lactones, lactams and thiollactones. XII. Synthesis of alpha-isocyanato-gamma-thiolbutyrolactone and of functional derivatives and their rearrangement to hydantoins and 1,2,4-triazines Justus Liebigs Ann Chem 758 1972 177 184
    • (1972) Justus Liebigs Ann Chem , vol.758 , pp. 177-184
    • Kraatz, U.1    Wamhoff, H.2    Korte, F.3
  • 111
    • 84919643887 scopus 로고    scopus 로고
    • their salts and esters, and pharmaceutical compositions containing them. US Pat. ed. US1982
    • Gonella J. [(2-Oxo-3-tetrahydrothienylcarbamoyl)alkylthio]acetic acids, their salts and esters, and pharmaceutical compositions containing them. US Pat. ed. US1982. p. 13.
    • [(2-Oxo-3-tetrahydrothienylcarbamoyl)alkylthio]acetic Acids , pp. 13
    • Gonella, J.1
  • 112
    • 0029847208 scopus 로고    scopus 로고
    • Erdosteine
    • K.L. Dechant, and S. Noble Erdosteine Drugs 52 6 1996 875 881
    • (1996) Drugs , vol.52 , Issue.6 , pp. 875-881
    • Dechant, K.L.1    Noble, S.2
  • 113
    • 34250160322 scopus 로고
    • New synthesis of S-alkyl-DL-homocysteines
    • H.M. Kolenbrander New synthesis of S-alkyl-DL-homocysteines Can J Chem 47 17 1969 3271 3273
    • (1969) Can J Chem , vol.47 , Issue.17 , pp. 3271-3273
    • Kolenbrander, H.M.1
  • 114
    • 0019820499 scopus 로고
    • Synthesis and evaluation of some stable multisubstrate adducts as inhibitors of catechol O-methyltransferase
    • G.L. Anderson, D.L. Bussolotti, and J.K. Coward Synthesis and evaluation of some stable multisubstrate adducts as inhibitors of catechol O-methyltransferase J Med Chem 24 11 1981 1271 1277
    • (1981) J Med Chem , vol.24 , Issue.11 , pp. 1271-1277
    • Anderson, G.L.1    Bussolotti, D.L.2    Coward, J.K.3
  • 116
    • 0020414302 scopus 로고
    • Carbocyclic analog of 3-deazaadenosine - A novel antiviral agent using S-adenosylhomocysteine hydrolase as a pharmacological target
    • J.A. Montgomery, S.J. Clayton, H.J. Thomas, W.M. Shannon, G. Arnett, and A.J. Bodner Carbocyclic analog of 3-deazaadenosine - a novel antiviral agent using S-adenosylhomocysteine hydrolase as a pharmacological target J Med Chem 25 6 1982 626 629
    • (1982) J Med Chem , vol.25 , Issue.6 , pp. 626-629
    • Montgomery, J.A.1    Clayton, S.J.2    Thomas, H.J.3    Shannon, W.M.4    Arnett, G.5    Bodner, A.J.6
  • 117
    • 84988153961 scopus 로고
    • Preparation of S-(3-indolylmethyl) derivatives of mercaptoamino acids
    • E. Benghiat, and P.A. Crooks Preparation of S-(3-indolylmethyl) derivatives of mercaptoamino acids Synth-Stuttgart 12 1982 1033 1036
    • (1982) Synth-Stuttgart , vol.12 , pp. 1033-1036
    • Benghiat, E.1    Crooks, P.A.2
  • 118
    • 0015894351 scopus 로고
    • Carboxyalkylthioacrylates
    • P.D. Halphen, and T.C. Owen Carboxyalkylthioacrylates J Org Chem 38 20 1973 3507 3510
    • (1973) J Org Chem , vol.38 , Issue.20 , pp. 3507-3510
    • Halphen, P.D.1    Owen, T.C.2
  • 119
    • 84879368636 scopus 로고    scopus 로고
    • One-pot, additive-free preparation of functionalized polyurethanes via amine-thiol-ene conjugation
    • P. Espeel, F. Goethals, F. Driessen, L.-T.T. Nguyen, and F.E. Du Prez One-pot, additive-free preparation of functionalized polyurethanes via amine-thiol-ene conjugation Polym Chem 4 8 2013 2449 2456
    • (2013) Polym Chem , vol.4 , Issue.8 , pp. 2449-2456
    • Espeel, P.1    Goethals, F.2    Driessen, F.3    Nguyen, L.-T.T.4    Du Prez, F.E.5
  • 120
    • 33646760275 scopus 로고    scopus 로고
    • Mechanism of hydrolysis and aminolysis of homocysteine thiolactone
    • J. Garel, and D.S. Tawfik Mechanism of hydrolysis and aminolysis of homocysteine thiolactone Chem Eur J 12 15 2006 4144 4152
    • (2006) Chem Eur J , vol.12 , Issue.15 , pp. 4144-4152
    • Garel, J.1    Tawfik, D.S.2
  • 121
    • 73649130272 scopus 로고    scopus 로고
    • Influence of type of initiation on thiol-ene click chemistry
    • M. Uygun, M.A. Tasdelen, and Y. Yagci Influence of type of initiation on thiol-ene click chemistry Macromol Chem Phys 211 1 2010 103 110
    • (2010) Macromol Chem Phys , vol.211 , Issue.1 , pp. 103-110
    • Uygun, M.1    Tasdelen, M.A.2    Yagci, Y.3
  • 122
    • 0000076537 scopus 로고
    • Homolytic substitution at furan and thiophene - Rate constants for the formation and decay of the radical intermediates
    • T.J. Burkey, D. Griller, L. Lunazzi, and A.S. Nazran Homolytic substitution at furan and thiophene - rate constants for the formation and decay of the radical intermediates J Org Chem 48 21 1983 3704 3707
    • (1983) J Org Chem , vol.48 , Issue.21 , pp. 3704-3707
    • Burkey, T.J.1    Griller, D.2    Lunazzi, L.3    Nazran, A.S.4
  • 123
    • 37049078793 scopus 로고
    • Epr studies of the addition of 1,1-bis(alkoxycarbonyl)alkyl radicals and tris(ethoxycarbonyl)methyl radicals to alkenes and to alkyl isocyanides
    • V. Diart, and B.P. Roberts Epr studies of the addition of 1,1-bis(alkoxycarbonyl)alkyl radicals and tris(ethoxycarbonyl)methyl radicals to alkenes and to alkyl isocyanides J Chem Soc Perkin Trans 2 10 1992 1761 1768
    • (1992) J Chem Soc Perkin Trans , vol.2 , Issue.10 , pp. 1761-1768
    • Diart, V.1    Roberts, B.P.2
  • 125
    • 58149324664 scopus 로고
    • MNDO calculations on the reactivity of furan compounds towards polymeric radicals
    • J.A. Paz, J. Rieumont, L.A. Montero, and J.R. Alvarez MNDO calculations on the reactivity of furan compounds towards polymeric radicals Polymer 36 26 1995 5011 5013
    • (1995) Polymer , vol.36 , Issue.26 , pp. 5011-5013
    • Paz, J.A.1    Rieumont, J.2    Montero, L.A.3    Alvarez, J.R.4
  • 126
    • 0000969806 scopus 로고
    • Free-radical addition of heteroarenethiols and heteroarylmethanethiols to hexyne and phenylacetylene - Chemical behavior of the transient beta-B-sulfanylvinyl radicals
    • L. Benati, L. Capella, P.C. Montevecchi, and P. Spagnolo Free-radical addition of heteroarenethiols and heteroarylmethanethiols to hexyne and phenylacetylene - chemical behavior of the transient beta-B-sulfanylvinyl radicals J Org Chem 60 24 1995 7941 7946
    • (1995) J Org Chem , vol.60 , Issue.24 , pp. 7941-7946
    • Benati, L.1    Capella, L.2    Montevecchi, P.C.3    Spagnolo, P.4
  • 127
    • 33646679654 scopus 로고    scopus 로고
    • Michael addition reactions in macromolecular design for emerging technologies
    • B.D. Mather, K. Viswanathan, K.M. Miller, and T.E. Long Michael addition reactions in macromolecular design for emerging technologies Prog Polym Sci 31 5 2006 487 531
    • (2006) Prog Polym Sci , vol.31 , Issue.5 , pp. 487-531
    • Mather, B.D.1    Viswanathan, K.2    Miller, K.M.3    Long, T.E.4
  • 128
    • 4544234205 scopus 로고    scopus 로고
    • Effects of chemistries of trifunctional amines on mechanisms of Michael addition polymerizations with diacrylates
    • Wu, Y. Liu, He, Chung, and Goh Effects of chemistries of trifunctional amines on mechanisms of Michael addition polymerizations with diacrylates Macromolecules 37 18 2004 6763 6770
    • (2004) Macromolecules , vol.37 , Issue.18 , pp. 6763-6770
    • Wu1    Liu, Y.2    He3    Chung4    Goh5
  • 129
    • 84892586333 scopus 로고    scopus 로고
    • Diversely substituted polyamide structures through thiol ene polymerization of renewable thiolactone building blocks
    • F. Goethals, S. Martens, P. Espeel, O. van den Berg, and F.E. Du Prez Diversely substituted polyamide structures through thiol ene polymerization of renewable thiolactone building blocks Macromolecules 47 1 2014 61 69
    • (2014) Macromolecules , vol.47 , Issue.1 , pp. 61-69
    • Goethals, F.1    Martens, S.2    Espeel, P.3    Van Den Berg, O.4    Du Prez, F.E.5
  • 131
    • 78649702044 scopus 로고    scopus 로고
    • Investigation into thiol-(meth)acrylate Michael addition reactions using amine and phosphine catalysts
    • G.-Z. Li, R.K. Randev, A.H. Soeriyadi, G. Rees, C. Boyer, and Z. Tong Investigation into thiol-(meth)acrylate Michael addition reactions using amine and phosphine catalysts Polym Chem 1 8 2010 1196 1204
    • (2010) Polym Chem , vol.1 , Issue.8 , pp. 1196-1204
    • Li, G.-Z.1    Randev, R.K.2    Soeriyadi, A.H.3    Rees, G.4    Boyer, C.5    Tong, Z.6
  • 132
    • 84872338040 scopus 로고    scopus 로고
    • Synthesis of (bio)-degradable poly(beta-thioester)s via amine catalyzed thiol-ene click polymerization
    • J. Vandenbergh, K. Ranieri, and T. Junkers Synthesis of (bio)-degradable poly(beta-thioester)s via amine catalyzed thiol-ene click polymerization Macromol Chem Phys 213 24 2012 2611 2617
    • (2012) Macromol Chem Phys , vol.213 , Issue.24 , pp. 2611-2617
    • Vandenbergh, J.1    Ranieri, K.2    Junkers, T.3
  • 133
    • 84875224589 scopus 로고    scopus 로고
    • Poly(amide urethane)s with functional/reactive side groups based on a bis-cyclic bio-based monomer/coupling agent
    • H. Keul, S. Mommer, and M. Möller Poly(amide urethane)s with functional/reactive side groups based on a bis-cyclic bio-based monomer/coupling agent Eur Polym J 49 4 2013 853 864
    • (2013) Eur Polym J , vol.49 , Issue.4 , pp. 853-864
    • Keul, H.1    Mommer, S.2    Möller, M.3
  • 134
    • 0037007888 scopus 로고    scopus 로고
    • Catalysts for the living insertion polymerization of alkenes: Access to new polyolefin architectures using Ziegler-Natta chemistry
    • G.W. Coates, P.D. Hustad, and S. Reinartz Catalysts for the living insertion polymerization of alkenes: access to new polyolefin architectures using Ziegler-Natta chemistry Angew Chem Int Ed 41 13 2002 2237 2257
    • (2002) Angew Chem Int Ed , vol.41 , Issue.13 , pp. 2237-2257
    • Coates, G.W.1    Hustad, P.D.2    Reinartz, S.3
  • 135
    • 33847336369 scopus 로고    scopus 로고
    • Anionic vinyl polymerization - 50 years after Michael Szwarc
    • D. Baskaran, and A.H.E. Mueller Anionic vinyl polymerization - 50 years after Michael Szwarc Prog Polym Sci 32 2 2007 173 219
    • (2007) Prog Polym Sci , vol.32 , Issue.2 , pp. 173-219
    • Baskaran, D.1    Mueller, A.H.E.2
  • 136
    • 33846841153 scopus 로고    scopus 로고
    • Controlled/living radical polymerization: Features, developments, and perspectives
    • W.A. Braunecker, and K. Matyjaszewski Controlled/living radical polymerization: features, developments, and perspectives Prog Polym Sci 32 1 2007 93 146
    • (2007) Prog Polym Sci , vol.32 , Issue.1 , pp. 93-146
    • Braunecker, W.A.1    Matyjaszewski, K.2
  • 137
    • 33846653444 scopus 로고    scopus 로고
    • Living alkene polymerization: New methods for the precision synthesis of polyolefins
    • G.J. Domski, J.M. Rose, G.W. Coates, A.D. Bolig, and M. Brookhart Living alkene polymerization: new methods for the precision synthesis of polyolefins Prog Polym Sci 32 1 2007 30 92
    • (2007) Prog Polym Sci , vol.32 , Issue.1 , pp. 30-92
    • Domski, G.J.1    Rose, J.M.2    Coates, G.W.3    Bolig, A.D.4    Brookhart, M.5
  • 138
    • 33847309049 scopus 로고    scopus 로고
    • Living ring-opening polymerizations of heterocyclic monomers
    • S. Penczek, M. Cypryk, A. Duda, P. Kubisa, and S. Slomkowski Living ring-opening polymerizations of heterocyclic monomers Prog Polym Sci 32 2 2007 247 282
    • (2007) Prog Polym Sci , vol.32 , Issue.2 , pp. 247-282
    • Penczek, S.1    Cypryk, M.2    Duda, A.3    Kubisa, P.4    Slomkowski, S.5
  • 139
    • 33846707826 scopus 로고    scopus 로고
    • Chain-growth polycondensation: The living polymerization process in polycondensation
    • T. Yokozawa, and A. Yokoyama Chain-growth polycondensation: the living polymerization process in polycondensation Prog Polym Sci 32 1 2007 147 172
    • (2007) Prog Polym Sci , vol.32 , Issue.1 , pp. 147-172
    • Yokozawa, T.1    Yokoyama, A.2
  • 140
    • 38849114363 scopus 로고    scopus 로고
    • Branched polymer via free radical polymerization of chain transfer monomer: A theoretical and experimental investigation
    • J. Liu, Y. Wang, Q. Fu, X. Zhu, and W. Shi Branched polymer via free radical polymerization of chain transfer monomer: a theoretical and experimental investigation J Polym Sci, Part A: Polym Chem 46 4 2008 1449 1459
    • (2008) J Polym Sci, Part A: Polym Chem , vol.46 , Issue.4 , pp. 1449-1459
    • Liu, J.1    Wang, Y.2    Fu, Q.3    Zhu, X.4    Shi, W.5
  • 141
    • 77955254389 scopus 로고    scopus 로고
    • End group removal and modification of RAFT polymers
    • H. Willcock, and R.K. O'Reilly End group removal and modification of RAFT polymers Polym Chem 1 2 2010 149 157
    • (2010) Polym Chem , vol.1 , Issue.2 , pp. 149-157
    • Willcock, H.1    O'Reilly, R.K.2
  • 142
    • 78650474535 scopus 로고    scopus 로고
    • End-functional polymers, thiocarbonylthio group removal/transformation and reversible addition-fragmentation-chain transfer (RAFT) polymerization
    • G. Moad, E. Rizzardo, and S.H. Thang End-functional polymers, thiocarbonylthio group removal/transformation and reversible addition-fragmentation-chain transfer (RAFT) polymerization Polym Int 60 1 2011 9 25
    • (2011) Polym Int , vol.60 , Issue.1 , pp. 9-25
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 143
    • 73649138205 scopus 로고    scopus 로고
    • Combining thio bromo click chemistry and RAFT polymerization: A powerful tool for preparing functionalized multiblock and hyperbranched polymers
    • J. Xu, L. Tao, C. Boyer, A.B. Lowe, and T.P. Davis Combining thio bromo click chemistry and RAFT polymerization: a powerful tool for preparing functionalized multiblock and hyperbranched polymers Macromolecules 43 1 2010 20 24
    • (2010) Macromolecules , vol.43 , Issue.1 , pp. 20-24
    • Xu, J.1    Tao, L.2    Boyer, C.3    Lowe, A.B.4    Davis, T.P.5
  • 144
    • 33750074183 scopus 로고    scopus 로고
    • Facile and efficient one-pot transformation of RAFT polymer end groups via a mild aminolysis/Michael addition sequence
    • X.P. Qiu, and F.M. Winnik Facile and efficient one-pot transformation of RAFT polymer end groups via a mild aminolysis/Michael addition sequence Macromol Rapid Commun 27 19 2006 1648 1653
    • (2006) Macromol Rapid Commun , vol.27 , Issue.19 , pp. 1648-1653
    • Qiu, X.P.1    Winnik, F.M.2
  • 145
    • 58349108839 scopus 로고    scopus 로고
    • Convergent synthesis of 3-arm star polymers from RAFT-prepared poly(N,N-diethylacrylamide) via a thiol-ene click reaction
    • J.W. Chan, B. Yu, C.E. Hoyle, and A.B. Lowe Convergent synthesis of 3-arm star polymers from RAFT-prepared poly(N,N-diethylacrylamide) via a thiol-ene click reaction Chem Commun 40 2008 4959 4961
    • (2008) Chem Commun , vol.40 , pp. 4959-4961
    • Chan, J.W.1    Yu, B.2    Hoyle, C.E.3    Lowe, A.B.4
  • 146
    • 67650915504 scopus 로고    scopus 로고
    • Modification of RAFT-polymers via thiol-ene reactions: A general route to functional polymers and new architectures
    • C. Boyer, A. Granville, T.P. Davis, and V. Bulmus Modification of RAFT-polymers via thiol-ene reactions: a general route to functional polymers and new architectures J Polym Sci, Part A: Polym Chem 47 15 2009 3773 3794
    • (2009) J Polym Sci, Part A: Polym Chem , vol.47 , Issue.15 , pp. 3773-3794
    • Boyer, C.1    Granville, A.2    Davis, T.P.3    Bulmus, V.4
  • 148
    • 72449121868 scopus 로고    scopus 로고
    • Hyperbranched polymers by thiol-yne chemistry: From small molecules to functional polymers
    • D. Konkolewicz, A. Gray-Weale, and S. Perrier Hyperbranched polymers by thiol-yne chemistry: from small molecules to functional polymers J Am Chem Soc 131 50 2009 18075 18077
    • (2009) J Am Chem Soc , vol.131 , Issue.50 , pp. 18075-18077
    • Konkolewicz, D.1    Gray-Weale, A.2    Perrier, S.3
  • 149
    • 78649836287 scopus 로고    scopus 로고
    • Hyperbranched alternating block copolymers using thiol-yne chemistry: Materials with tuneable properties
    • D. Konkolewicz, C.K. Poon, A. Gray-Weale, and S. Perrier Hyperbranched alternating block copolymers using thiol-yne chemistry: materials with tuneable properties Chem Commun 47 1 2011 239 241
    • (2011) Chem Commun , vol.47 , Issue.1 , pp. 239-241
    • Konkolewicz, D.1    Poon, C.K.2    Gray-Weale, A.3    Perrier, S.4
  • 150
    • 6144270853 scopus 로고
    • Preparation of polymeric condensation products containing functional thiol side chains - Polyurethans
    • C.G. Overberger, and H. Aschkenasy Preparation of polymeric condensation products containing functional thiol side chains - polyurethans J Am Chem Soc 82 16 1960 4357 4360
    • (1960) J Am Chem Soc , vol.82 , Issue.16 , pp. 4357-4360
    • Overberger, C.G.1    Aschkenasy, H.2
  • 151
    • 0000135067 scopus 로고
    • Protection and polymerization of functional monomers. 9. Synthesis of poly[1-(4-mercaptomethylphenyl)ethylene] by hydrolysis of poly(1-[4-(tert-butyldimethylsilylthiomethyl)-phenyl]ethylene) produced with a radical initiator
    • K. Yamaguchi, T. Kato, A. Hirao, and S. Nakahama Protection and polymerization of functional monomers. 9. Synthesis of poly[1-(4-mercaptomethylphenyl)ethylene] by hydrolysis of poly(1-[4-(tert-butyldimethylsilylthiomethyl)-phenyl]ethylene) produced with a radical initiator Makromol Chem, Rapid Commun 8 4 1987 203 207
    • (1987) Makromol Chem, Rapid Commun , vol.8 , Issue.4 , pp. 203-207
    • Yamaguchi, K.1    Kato, T.2    Hirao, A.3    Nakahama, S.4
  • 152
    • 0001443121 scopus 로고
    • Synthesis of biodegradable polyesteramides with pendant functional-groups
    • P. Veld, P.J. Dijkstra, and J. Feijen Synthesis of biodegradable polyesteramides with pendant functional-groups Macromol Chem Phys 193 11 1992 2713 2730
    • (1992) Macromol Chem Phys , vol.193 , Issue.11 , pp. 2713-2730
    • Veld, P.1    Dijkstra, P.J.2    Feijen, J.3
  • 153
    • 0031163398 scopus 로고    scopus 로고
    • Synthesis and properties of microgel bearing a mercapto group
    • N. Kihara, C. Kanno, and T. Fukutomi Synthesis and properties of microgel bearing a mercapto group J Polym Sci, Part A: Polym Chem 35 8 1997 1443 1451
    • (1997) J Polym Sci, Part A: Polym Chem , vol.35 , Issue.8 , pp. 1443-1451
    • Kihara, N.1    Kanno, C.2    Fukutomi, T.3
  • 154
    • 0001210221 scopus 로고    scopus 로고
    • Synthesis and radical polymerization of an optically active monomer derived from cysteine
    • H. Kudo, F. Sanda, and T. Endo Synthesis and radical polymerization of an optically active monomer derived from cysteine Macromol Chem Phys 200 5 1999 1232 1239
    • (1999) Macromol Chem Phys , vol.200 , Issue.5 , pp. 1232-1239
    • Kudo, H.1    Sanda, F.2    Endo, T.3
  • 155
    • 0034443303 scopus 로고    scopus 로고
    • Synthesis of a block copolymer of l-lactide and depsipeptide with pendant thiol groups
    • T. Ouchi, H. Seike, H. Miyazaki, F. Tasaka, and Y. Ohya Synthesis of a block copolymer of l-lactide and depsipeptide with pendant thiol groups Des Monomers Polym 3 3 2000 279 287
    • (2000) Des Monomers Polym , vol.3 , Issue.3 , pp. 279-287
    • Ouchi, T.1    Seike, H.2    Miyazaki, H.3    Tasaka, F.4    Ohya, Y.5
  • 157
    • 40549136872 scopus 로고    scopus 로고
    • Facile, efficient routes to diverse protected thiols and to their deprotection and addition to create functional polymers by thiol-ene coupling
    • R.L.A. David, and J.A. Kornfield Facile, efficient routes to diverse protected thiols and to their deprotection and addition to create functional polymers by thiol-ene coupling Macromolecules 41 4 2008 1151 1161
    • (2008) Macromolecules , vol.41 , Issue.4 , pp. 1151-1161
    • David, R.L.A.1    Kornfield, J.A.2
  • 158
    • 45849097267 scopus 로고    scopus 로고
    • Synthesis of sulfur-containing polyacetylenes and fabrication of their hybrids with ZnO nanoparticles
    • H. Xu, J.K. Jin, Y. Mao, J.Z. Sun, F. Yang, and W. Zhang Yuan Synthesis of sulfur-containing polyacetylenes and fabrication of their hybrids with ZnO nanoparticles Macromolecules 41 11 2008 3874 3883
    • (2008) Macromolecules , vol.41 , Issue.11 , pp. 3874-3883
    • Xu, H.1    Jin, J.K.2    Mao, Y.3    Sun, J.Z.4    Yang, F.5    Zhang Yuan, W.6
  • 159
    • 84857515108 scopus 로고    scopus 로고
    • Acrylamide-based copolymers bearing photoreleasable thiols for subsequent thiol-ene functionalization
    • G. Delaittre, T. Pauloehrl, M. Bastmeyer, and C. Barner-Kowollik Acrylamide-based copolymers bearing photoreleasable thiols for subsequent thiol-ene functionalization Macromolecules 45 4 2012 1792 1802
    • (2012) Macromolecules , vol.45 , Issue.4 , pp. 1792-1802
    • Delaittre, G.1    Pauloehrl, T.2    Bastmeyer, M.3    Barner-Kowollik, C.4
  • 160
    • 84858438642 scopus 로고    scopus 로고
    • Synthesis of thiol functionalized poly(meth)acrylates through enzymatic catalysis and a subsequent one pot reaction process
    • E. Hrsic, H. Keul, and M. Möller Synthesis of thiol functionalized poly(meth)acrylates through enzymatic catalysis and a subsequent one pot reaction process Eur Polym J 48 4 2012 761 768
    • (2012) Eur Polym J , vol.48 , Issue.4 , pp. 761-768
    • Hrsic, E.1    Keul, H.2    Möller, M.3
  • 161
    • 84856184932 scopus 로고    scopus 로고
    • Synthesis of well-defined polythiol copolymers by RAFT polymerization
    • R. Nicolaÿ Synthesis of well-defined polythiol copolymers by RAFT polymerization Macromolecules 45 2 2012 821 827
    • (2012) Macromolecules , vol.45 , Issue.2 , pp. 821-827
    • Nicolaÿ, R.1
  • 162
    • 84855465378 scopus 로고    scopus 로고
    • Synthetic pathways enables the design of functionalized poly(lactic acid) with pendant mercapto groups
    • D. Pappalardo, S. Målberg, A. Finne-Winstrad, and A.-C. Albertsson Synthetic pathways enables the design of functionalized poly(lactic acid) with pendant mercapto groups J Polym Sci, Part A: Polym Chem 50 4 2012 792 800
    • (2012) J Polym Sci, Part A: Polym Chem , vol.50 , Issue.4 , pp. 792-800
    • Pappalardo, D.1    Målberg, S.2    Finne-Winstrad, A.3    Albertsson, A.-C.4
  • 163
    • 84858438598 scopus 로고    scopus 로고
    • Ambient temperature polymer modification by in situ phototriggered deprotection and thiol-ene chemistry
    • T. Pauloehrl, G. Delaittre, M. Bastmeyer, and C. Barner-Kowollik Ambient temperature polymer modification by in situ phototriggered deprotection and thiol-ene chemistry Polym Chem 3 7 2012 1740 1749
    • (2012) Polym Chem , vol.3 , Issue.7 , pp. 1740-1749
    • Pauloehrl, T.1    Delaittre, G.2    Bastmeyer, M.3    Barner-Kowollik, C.4
  • 164
    • 84886905014 scopus 로고    scopus 로고
    • Evaluation of thiocarbonyl and thioester moieties as thiol protecting groups for controlled radical polymerization
    • M. Le Neindre, B. Magny, and R. Nicolay Evaluation of thiocarbonyl and thioester moieties as thiol protecting groups for controlled radical polymerization Polym Chem 4 22 2013 5577 5584
    • (2013) Polym Chem , vol.4 , Issue.22 , pp. 5577-5584
    • Le Neindre, M.1    Magny, B.2    Nicolay, R.3
  • 165
    • 84897970553 scopus 로고    scopus 로고
    • One-pot deprotection and functionalization of polythiol copolymers via six different thiol-X reactions
    • M. Le Neindre, and R. Nicolay One-pot deprotection and functionalization of polythiol copolymers via six different thiol-X reactions Polym Int 63 5 2014 887 893
    • (2014) Polym Int , vol.63 , Issue.5 , pp. 887-893
    • Le Neindre, M.1    Nicolay, R.2
  • 166
    • 84890493182 scopus 로고    scopus 로고
    • Acetyl protected thiol methacrylic polymers as effective ligands to keep quantum dots in luminescent standby mode
    • M. Liras, I. Quijada-Garrido, M. Palacios-Cuesta, S. Munoz-Durieux, and O. Garcia Acetyl protected thiol methacrylic polymers as effective ligands to keep quantum dots in luminescent standby mode Polym Chem 5 2 2014 433 442
    • (2014) Polym Chem , vol.5 , Issue.2 , pp. 433-442
    • Liras, M.1    Quijada-Garrido, I.2    Palacios-Cuesta, M.3    Munoz-Durieux, S.4    Garcia, O.5
  • 167
    • 84904437693 scopus 로고    scopus 로고
    • Polythiol copolymers with precise architectures: A platform for functional materials
    • M. Le Neindre, and R. Nicolay Polythiol copolymers with precise architectures: a platform for functional materials Polym Chem 2014
    • (2014) Polym Chem
    • Le Neindre, M.1    Nicolay, R.2
  • 168
    • 64149107876 scopus 로고    scopus 로고
    • Direct enzymatic synthesis of a polyester with free pendant mercapto groups
    • M. Kato, K. Toshima, and S. Matsumura Direct enzymatic synthesis of a polyester with free pendant mercapto groups Biomacromolecules 10 2 2009 366 373
    • (2009) Biomacromolecules , vol.10 , Issue.2 , pp. 366-373
    • Kato, M.1    Toshima, K.2    Matsumura, S.3
  • 169
    • 77958169120 scopus 로고    scopus 로고
    • Preparation of gelatinous reversible addition-fragmentation chain transfer agents "rAFT Gel" via chemoselective polycondensations of a dicarboxylic acid containing a mercapto group and diols
    • K. Yamamoto, and A. Takasu Preparation of gelatinous reversible addition-fragmentation chain transfer agents "RAFT Gel" via chemoselective polycondensations of a dicarboxylic acid containing a mercapto group and diols Macromolecules 43 20 2010 8519 8523
    • (2010) Macromolecules , vol.43 , Issue.20 , pp. 8519-8523
    • Yamamoto, K.1    Takasu, A.2
  • 170
    • 0032211994 scopus 로고    scopus 로고
    • Delivery of antisense oligonucleotides using HPMA polymer: Synthesis of a thiol polymer and its conjugation to water-soluble molecules
    • L.X. Wang, J. Kristensen, and D.E. Ruffner Delivery of antisense oligonucleotides using HPMA polymer: synthesis of a thiol polymer and its conjugation to water-soluble molecules Bioconjugate Chem 9 6 1998 749 757
    • (1998) Bioconjugate Chem , vol.9 , Issue.6 , pp. 749-757
    • Wang, L.X.1    Kristensen, J.2    Ruffner, D.E.3
  • 171
    • 0242662545 scopus 로고    scopus 로고
    • A new pH-responsive and glutathione-reactive, endosomal membrane-disruptive polymeric carrier for intracellular delivery of biomolecular drugs
    • V. Bulmus, M. Woodward, L. Lin, N. Murthy, P. Stayton, and A. Hoffman A new pH-responsive and glutathione-reactive, endosomal membrane-disruptive polymeric carrier for intracellular delivery of biomolecular drugs J Controlled Release 93 2 2003 105 120
    • (2003) J Controlled Release , vol.93 , Issue.2 , pp. 105-120
    • Bulmus, V.1    Woodward, M.2    Lin, L.3    Murthy, N.4    Stayton, P.5    Hoffman, A.6
  • 172
    • 17444413755 scopus 로고    scopus 로고
    • Combining atom transfer radical polymerization and disulfide/thiol redox chemistry: A route to well-defined (bio)degradable polymeric materials
    • N.V. Tsarevsky, and K. Matyjaszewski Combining atom transfer radical polymerization and disulfide/thiol redox chemistry: a route to well-defined (bio)degradable polymeric materials Macromolecules 38 8 2005 3087 3092
    • (2005) Macromolecules , vol.38 , Issue.8 , pp. 3087-3092
    • Tsarevsky, N.V.1    Matyjaszewski, K.2
  • 173
    • 48449102772 scopus 로고    scopus 로고
    • Synthesis of versatile thiol-reactive polymer scaffolds via RAFT polymerization
    • L.J. Wong, C. Boyer, Z.F. Jia, H.M. Zareie, T.P. Davis, and V. Bulmus Synthesis of versatile thiol-reactive polymer scaffolds via RAFT polymerization Biomacromolecules 9 7 2008 1934 1944
    • (2008) Biomacromolecules , vol.9 , Issue.7 , pp. 1934-1944
    • Wong, L.J.1    Boyer, C.2    Jia, Z.F.3    Zareie, H.M.4    Davis, T.P.5    Bulmus, V.6
  • 174
    • 70349466216 scopus 로고    scopus 로고
    • Biocompatible and degradable nanogels via oxidation reactions of synthetic thiomers in inverse miniemulsion
    • J. Groll, S. Singh, K. Albrecht, and M. Moeller Biocompatible and degradable nanogels via oxidation reactions of synthetic thiomers in inverse miniemulsion J Polym Sci, Part A: Polym Chem 47 20 2009 5543 5549
    • (2009) J Polym Sci, Part A: Polym Chem , vol.47 , Issue.20 , pp. 5543-5549
    • Groll, J.1    Singh, S.2    Albrecht, K.3    Moeller, M.4
  • 175
    • 70350244445 scopus 로고    scopus 로고
    • Synthesis and characterization of thermoresponsive polymers containing reduction-sensitive disulfide linkage
    • L. Li, X. Jiang, and R. Zhuo Synthesis and characterization of thermoresponsive polymers containing reduction-sensitive disulfide linkage J Polym Sci, Part A: Polym Chem 47 22 2009 5989 5997
    • (2009) J Polym Sci, Part A: Polym Chem , vol.47 , Issue.22 , pp. 5989-5997
    • Li, L.1    Jiang, X.2    Zhuo, R.3
  • 176
    • 78650843996 scopus 로고    scopus 로고
    • Kinetic analyses of disulfide formation between thiol groups attached to linear poly(acrylamide)
    • N. Hisano, H. Iwata, Y. Teramura, H. Chen, and Y. Ikada Kinetic analyses of disulfide formation between thiol groups attached to linear poly(acrylamide) J Polym Sci, Part A: Polym Chem 49 3 2011 671 679
    • (2011) J Polym Sci, Part A: Polym Chem , vol.49 , Issue.3 , pp. 671-679
    • Hisano, N.1    Iwata, H.2    Teramura, Y.3    Chen, H.4    Ikada, Y.5
  • 177
    • 80455147519 scopus 로고    scopus 로고
    • PH-responsive polymer-antigen vaccine bioconjugates
    • E.F. Crownover, A.J. Convertine, and P.S. Stayton PH-responsive polymer-antigen vaccine bioconjugates Polym Chem 2 7 2012 1499 1504
    • (2012) Polym Chem , vol.2 , Issue.7 , pp. 1499-1504
    • Crownover, E.F.1    Convertine, A.J.2    Stayton, P.S.3
  • 179
    • 84858013351 scopus 로고    scopus 로고
    • Double modular modification of thiolactone-containing polymers: Towards polythiols and derived structures
    • P. Espeel, F. Goethals, M.M. Stamenovic, L. Petton, and F.E. Du Prez Double modular modification of thiolactone-containing polymers: towards polythiols and derived structures Polym Chem 3 4 2012 1007 1015
    • (2012) Polym Chem , vol.3 , Issue.4 , pp. 1007-1015
    • Espeel, P.1    Goethals, F.2    Stamenovic, M.M.3    Petton, L.4    Du Prez, F.E.5
  • 180
    • 84879379043 scopus 로고    scopus 로고
    • One-pot double modification of p(NIPAAm): A tool for designing tailor-made multiresponsive polymers
    • S. Reinicke, P. Espeel, M.M. Stamenovic, and F.E. Du Prez One-pot double modification of p(NIPAAm): a tool for designing tailor-made multiresponsive polymers ACS Macro Lett 2 6 2013 539 543
    • (2013) ACS Macro Lett , vol.2 , Issue.6 , pp. 539-543
    • Reinicke, S.1    Espeel, P.2    Stamenovic, M.M.3    Du Prez, F.E.4
  • 181
    • 0032135925 scopus 로고    scopus 로고
    • Living free-radical polymerization by reversible addition-fragmentation chain transfer: The RAFT process
    • J. Chiefari, Y.K. Chong, F. Ercole, J. Krstina, J. Jeffery, and T.P.T. Le Living free-radical polymerization by reversible addition-fragmentation chain transfer: the RAFT process Macromolecules 31 16 1998 5559 5562
    • (1998) Macromolecules , vol.31 , Issue.16 , pp. 5559-5562
    • Chiefari, J.1    Chong, Y.K.2    Ercole, F.3    Krstina, J.4    Jeffery, J.5    Le, T.P.T.6
  • 182
    • 33750518377 scopus 로고    scopus 로고
    • Living radical polymerization by the RAFT process - A first update
    • G. Moad, E. Rizzardo, and S.H. Thang Living radical polymerization by the RAFT process - a first update Aust J Chem 59 10 2006 669 692
    • (2006) Aust J Chem , vol.59 , Issue.10 , pp. 669-692
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 183
    • 70749084818 scopus 로고    scopus 로고
    • Living radical polymerization by the RAFT process - A second update
    • G. Moad, E. Rizzardo, and S.H. Thang Living radical polymerization by the RAFT process - a second update Aust J Chem 62 11 2009 1402 1472
    • (2009) Aust J Chem , vol.62 , Issue.11 , pp. 1402-1472
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 184
    • 84866101193 scopus 로고    scopus 로고
    • Living radical polymerization by the RAFT process - A third update
    • G. Moad, E. Rizzardo, and S.H. Thang Living radical polymerization by the RAFT process - a third update Aust J Chem 65 8 2012 985 1076
    • (2012) Aust J Chem , vol.65 , Issue.8 , pp. 985-1076
    • Moad, G.1    Rizzardo, E.2    Thang, S.H.3
  • 185
    • 0035781106 scopus 로고    scopus 로고
    • New polymer synthesis by nitroxide mediated living radical polymerizations
    • C.J. Hawker, A.W. Bosman, and E. Harth New polymer synthesis by nitroxide mediated living radical polymerizations Chem Rev 101 12 2001 3661 3688
    • (2001) Chem Rev , vol.101 , Issue.12 , pp. 3661-3688
    • Hawker, C.J.1    Bosman, A.W.2    Harth, E.3
  • 186
    • 4544224356 scopus 로고    scopus 로고
    • Atom transfer radical polymerization of 1-ethoxyethyl (meth)acrylate: Facile route toward near-monodisperse poly((meth)acrylic acid)
    • W. Van Camp, F.E. Du Prez, and S.A.F. Bon Atom transfer radical polymerization of 1-ethoxyethyl (meth)acrylate: facile route toward near-monodisperse poly((meth)acrylic acid) Macromolecules 37 18 2004 6673 6675
    • (2004) Macromolecules , vol.37 , Issue.18 , pp. 6673-6675
    • Van Camp, W.1    Du Prez, F.E.2    Bon, S.A.F.3
  • 187
    • 25144520186 scopus 로고    scopus 로고
    • RAFT polymerization of 1-ethoxyethyl acrylate: A novel route toward near-monodisperse poly(acrylic acid) and derived block copolymer structures
    • R. Hoogenboom, U.S. Schubert, W. Van Camp, and F.E. Du Prez RAFT polymerization of 1-ethoxyethyl acrylate: a novel route toward near-monodisperse poly(acrylic acid) and derived block copolymer structures Macromolecules 38 18 2005 7653 7659
    • (2005) Macromolecules , vol.38 , Issue.18 , pp. 7653-7659
    • Hoogenboom, R.1    Schubert, U.S.2    Van Camp, W.3    Du Prez, F.E.4
  • 188
    • 34547179800 scopus 로고    scopus 로고
    • Graft copolymers by a combination of ATRP and two different consecutive click reactions
    • N.V. Tsarevsky, S.A. Bencherif, and K. Matyjaszewski Graft copolymers by a combination of ATRP and two different consecutive click reactions Macromolecules 40 13 2007 4439 4445
    • (2007) Macromolecules , vol.40 , Issue.13 , pp. 4439-4445
    • Tsarevsky, N.V.1    Bencherif, S.A.2    Matyjaszewski, K.3
  • 189
    • 71949089490 scopus 로고    scopus 로고
    • Fabrication of porous "clickable" polymer beads and rods through generation of high internal phase emulsion (HIPE) droplets in a simple microfluidic device
    • M.T. Gokmen, W. Van Camp, P.J. Colver, S.A.F. Bon, and F.E. Du Prez Fabrication of porous "clickable" polymer beads and rods through generation of high internal phase emulsion (HIPE) droplets in a simple microfluidic device Macromolecules 42 23 2009 9289 9294
    • (2009) Macromolecules , vol.42 , Issue.23 , pp. 9289-9294
    • Gokmen, M.T.1    Van Camp, W.2    Colver, P.J.3    Bon, S.A.F.4    Du Prez, F.E.5
  • 190
    • 84899515192 scopus 로고    scopus 로고
    • Multifunctional nanoworms and nanorods through a one-step aqueous dispersion polymerization
    • Z. Jia, V.A. Bobrin, N.P. Truong, M. Gillard, and M.J. Monteiro Multifunctional nanoworms and nanorods through a one-step aqueous dispersion polymerization J Am Chem Soc 136 16 2014 5824 5827
    • (2014) J Am Chem Soc , vol.136 , Issue.16 , pp. 5824-5827
    • Jia, Z.1    Bobrin, V.A.2    Truong, N.P.3    Gillard, M.4    Monteiro, M.J.5
  • 191
    • 11944250862 scopus 로고
    • Polymers containing disulfide, tetrasulfide, diselenide and ditelluride linkages in the main-chain
    • K. Kishore, and K. Ganesh Polymers containing disulfide, tetrasulfide, diselenide and ditelluride linkages in the main-chain Polym Synth/Polym Eng 121 1995 81 121
    • (1995) Polym Synth/Polym Eng , vol.121 , pp. 81-121
    • Kishore, K.1    Ganesh, K.2
  • 192
    • 0030443727 scopus 로고    scopus 로고
    • Design, synthesis, and analysis of disulfide cross-linked DNA duplexes
    • S.E. Osborne, J. Volker, S.Y. Stevens, K.J. Breslauer, and G.D. Glick Design, synthesis, and analysis of disulfide cross-linked DNA duplexes J Am Chem Soc 118 48 1996 11993 12003
    • (1996) J Am Chem Soc , vol.118 , Issue.48 , pp. 11993-12003
    • Osborne, S.E.1    Volker, J.2    Stevens, S.Y.3    Breslauer, K.J.4    Glick, G.D.5
  • 193
    • 0030765627 scopus 로고    scopus 로고
    • Making and breaking disulfide bonds
    • S. Raina, and D. Missiakas Making and breaking disulfide bonds Annu Rev Microbiol 51 1997 179 202
    • (1997) Annu Rev Microbiol , vol.51 , pp. 179-202
    • Raina, S.1    Missiakas, D.2
  • 194
    • 50849108562 scopus 로고    scopus 로고
    • Recent developments in disulfide bond formation
    • D. Witt Recent developments in disulfide bond formation Synth-Stuttgart 16 2008 2491 2509
    • (2008) Synth-Stuttgart , vol.16 , pp. 2491-2509
    • Witt, D.1
  • 195
    • 80052372197 scopus 로고    scopus 로고
    • Multiple ways to make disulfides
    • N.J. Bulleid, and L. Ellgaard Multiple ways to make disulfides Trends Biochem Sci 36 9 2011 485 492
    • (2011) Trends Biochem Sci , vol.36 , Issue.9 , pp. 485-492
    • Bulleid, N.J.1    Ellgaard, L.2
  • 196
    • 84880091003 scopus 로고    scopus 로고
    • Disulfide-cleavage-triggered chemosensors and their biological applications
    • M.H. Lee, Z. Yang, C.W. Lim, Y.H. Lee, S. Dongbang, and C. Kang Disulfide-cleavage-triggered chemosensors and their biological applications Chem Rev 113 7 2013 5071 5109
    • (2013) Chem Rev , vol.113 , Issue.7 , pp. 5071-5109
    • Lee, M.H.1    Yang, Z.2    Lim, C.W.3    Lee, Y.H.4    Dongbang, S.5    Kang, C.6
  • 197
    • 84893119472 scopus 로고    scopus 로고
    • Multifaceted roles of disulfide bonds. Peptides as therapeutics
    • M. Gongora-Benitez, J. Tulla-Puche, and F. Albericio Multifaceted roles of disulfide bonds. Peptides as therapeutics Chem Rev 114 2 2014 901 926
    • (2014) Chem Rev , vol.114 , Issue.2 , pp. 901-926
    • Gongora-Benitez, M.1    Tulla-Puche, J.2    Albericio, F.3
  • 200
    • 65449156761 scopus 로고    scopus 로고
    • Dynamic covalent polymers: Reorganizable polymers with dynamic covalent bonds
    • T. Maeda, H. Otsuka, and A. Takahara Dynamic covalent polymers: reorganizable polymers with dynamic covalent bonds Prog Polym Sci 34 7 2009 581 604
    • (2009) Prog Polym Sci , vol.34 , Issue.7 , pp. 581-604
    • Maeda, T.1    Otsuka, H.2    Takahara, A.3
  • 201
    • 84897625761 scopus 로고    scopus 로고
    • Disulfide exchange: Exposing supramolecular reactivity through dynamic covalent chemistry
    • S.P. Black, J.K.M. Sanders, and A.R. Stefankiewicz Disulfide exchange: exposing supramolecular reactivity through dynamic covalent chemistry Chem Soc Rev 43 6 2014 1861 1872
    • (2014) Chem Soc Rev , vol.43 , Issue.6 , pp. 1861-1872
    • Black, S.P.1    Sanders, J.K.M.2    Stefankiewicz, A.R.3
  • 202
    • 84897584703 scopus 로고    scopus 로고
    • Functional systems with orthogonal dynamic covalent bonds
    • A. Wilson, G. Gasparini, and S. Matile Functional systems with orthogonal dynamic covalent bonds Chem Soc Rev 43 6 2014 1948 1962
    • (2014) Chem Soc Rev , vol.43 , Issue.6 , pp. 1948-1962
    • Wilson, A.1    Gasparini, G.2    Matile, S.3
  • 203
    • 77951915791 scopus 로고    scopus 로고
    • Covalent adaptable networks (CANS): A unique paradigm in cross-linked polymers
    • C.J. Kloxin, T.F. Scott, B.J. Adzima, and C.N. Bowman Covalent adaptable networks (CANS): a unique paradigm in cross-linked polymers Macromolecules 43 6 2010 2643 2653
    • (2010) Macromolecules , vol.43 , Issue.6 , pp. 2643-2653
    • Kloxin, C.J.1    Scott, T.F.2    Adzima, B.J.3    Bowman, C.N.4
  • 204
    • 84860173900 scopus 로고    scopus 로고
    • Covalent adaptable networks: Reversible bond structures incorporated in polymer networks
    • C.N. Bowman, and C.J. Kloxin Covalent adaptable networks: reversible bond structures incorporated in polymer networks Angew Chem Int Ed 51 18 2012 4272 4274
    • (2012) Angew Chem Int Ed , vol.51 , Issue.18 , pp. 4272-4274
    • Bowman, C.N.1    Kloxin, C.J.2
  • 205
    • 84881398586 scopus 로고    scopus 로고
    • Covalent adaptable networks: Smart, reconfigurable and responsive network systems
    • C.J. Kloxin, and C.N. Bowman Covalent adaptable networks: smart, reconfigurable and responsive network systems Chem Soc Rev 42 17 2013 7161 7173
    • (2013) Chem Soc Rev , vol.42 , Issue.17 , pp. 7161-7173
    • Kloxin, C.J.1    Bowman, C.N.2
  • 206
    • 79955010736 scopus 로고    scopus 로고
    • Self-healing materials based on disulfide links
    • J. Canadell, H. Goossens, and B. Klumperman Self-healing materials based on disulfide links Macromolecules 44 8 2011 2536 2541
    • (2011) Macromolecules , vol.44 , Issue.8 , pp. 2536-2541
    • Canadell, J.1    Goossens, H.2    Klumperman, B.3
  • 207
    • 78650278337 scopus 로고    scopus 로고
    • Using the dynamic bond to access macroscopically responsive structurally dynamic polymers
    • R.J. Wojtecki, M.A. Meador, and S.J. Rowan Using the dynamic bond to access macroscopically responsive structurally dynamic polymers Nat Mater 10 1 2011 14 27
    • (2011) Nat Mater , vol.10 , Issue.1 , pp. 14-27
    • Wojtecki, R.J.1    Meador, M.A.2    Rowan, S.J.3
  • 208
    • 84862908363 scopus 로고    scopus 로고
    • Self-healing polymer films based on thiol-disulfide exchange reactions and self-healing kinetics measured using atomic force microscopy
    • J.A. Yoon, J. Kamada, K. Koynov, J. Mohin, R. Nicolay, and Y. Zhang Self-healing polymer films based on thiol-disulfide exchange reactions and self-healing kinetics measured using atomic force microscopy Macromolecules 45 1 2012 142 149
    • (2012) Macromolecules , vol.45 , Issue.1 , pp. 142-149
    • Yoon, J.A.1    Kamada, J.2    Koynov, K.3    Mohin, J.4    Nicolay, R.5    Zhang, Y.6
  • 209
    • 84882356943 scopus 로고    scopus 로고
    • Self-healing systems based on disulfide-thiol exchange reactions
    • M. Pepels, I. Filot, B. Klumperman, and H. Goossens Self-healing systems based on disulfide-thiol exchange reactions Polym Chem 4 18 2013 4955 4965
    • (2013) Polym Chem , vol.4 , Issue.18 , pp. 4955-4965
    • Pepels, M.1    Filot, I.2    Klumperman, B.3    Goossens, H.4
  • 210
    • 69249085260 scopus 로고    scopus 로고
    • Synthetic approaches for the preparation of cyclic polymers
    • B.A. Laurent, and S.M. Grayson Synthetic approaches for the preparation of cyclic polymers Chem Soc Rev 38 8 2009 2202 2213
    • (2009) Chem Soc Rev , vol.38 , Issue.8 , pp. 2202-2213
    • Laurent, B.A.1    Grayson, S.M.2
  • 211
    • 72949117217 scopus 로고    scopus 로고
    • Cyclic polymers: Synthetic strategies and physical properties
    • H.R. Kricheldorf Cyclic polymers: synthetic strategies and physical properties J Polym Sci, Part A: Polym Chem 48 2 2010 251 284
    • (2010) J Polym Sci, Part A: Polym Chem , vol.48 , Issue.2 , pp. 251-284
    • Kricheldorf, H.R.1
  • 212
    • 80051652326 scopus 로고    scopus 로고
    • Topological polymer chemistry: A cyclic approach toward novel polymer properties and functions
    • T. Yamamoto, and Y. Tezuka Topological polymer chemistry: a cyclic approach toward novel polymer properties and functions Polym Chem 2 9 2011 1930 1941
    • (2011) Polym Chem , vol.2 , Issue.9 , pp. 1930-1941
    • Yamamoto, T.1    Tezuka, Y.2
  • 214
    • 33846206371 scopus 로고    scopus 로고
    • Synthesis of monocyclic and linear polystyrene using the reversible coupling/cleavage of thiol/disulfide groups
    • M.R. Whittaker, Y.-K. Goh, H. Gemici, T.M. Legge, S. Perrier, and M.J. Monteiro Synthesis of monocyclic and linear polystyrene using the reversible coupling/cleavage of thiol/disulfide groups Macromolecules 39 26 2006 9028 9034
    • (2006) Macromolecules , vol.39 , Issue.26 , pp. 9028-9034
    • Whittaker, M.R.1    Goh, Y.-K.2    Gemici, H.3    Legge, T.M.4    Perrier, S.5    Monteiro, M.J.6
  • 216
    • 80052327714 scopus 로고    scopus 로고
    • Additive-free clicking for polymer functionalization and coupling by tetrazine-norbornene chemistry
    • C.F. Hansell, P. Espeel, M.M. Stamenovic, I.A. Barker, A.P. Dove, and F.E. Du Prez Additive-free clicking for polymer functionalization and coupling by tetrazine-norbornene chemistry J Am Chem Soc 133 35 2011 13828 13831
    • (2011) J Am Chem Soc , vol.133 , Issue.35 , pp. 13828-13831
    • Hansell, C.F.1    Espeel, P.2    Stamenovic, M.M.3    Barker, I.A.4    Dove, A.P.5    Du Prez, F.E.6
  • 217
    • 79960529843 scopus 로고    scopus 로고
    • Norbornenyl-based RAFT agents for the preparation of functional polymers via thiol-ene chemistry
    • M.M. Stamenovic, P. Espeel, W. Van Camp, and F.E. Du Prez Norbornenyl-based RAFT agents for the preparation of functional polymers via thiol-ene chemistry Macromolecules 44 14 2011 5619 5630
    • (2011) Macromolecules , vol.44 , Issue.14 , pp. 5619-5630
    • Stamenovic, M.M.1    Espeel, P.2    Van Camp, W.3    Du Prez, F.E.4
  • 218
    • 84875770048 scopus 로고    scopus 로고
    • Straightforward synthesis of functionalized cyclic polymers in high yield via RAFT and thiolactone-disulfide chemistry
    • M.M. Stamenovic, P. Espeel, E. Baba, T. Yamamoto, Y. Tezuka, and F.E. Du Prez Straightforward synthesis of functionalized cyclic polymers in high yield via RAFT and thiolactone-disulfide chemistry Polym Chem 4 1 2013 184 193
    • (2013) Polym Chem , vol.4 , Issue.1 , pp. 184-193
    • Stamenovic, M.M.1    Espeel, P.2    Baba, E.3    Yamamoto, T.4    Tezuka, Y.5    Du Prez, F.E.6
  • 219
    • 70450186565 scopus 로고    scopus 로고
    • Sequence control in polymer synthesis
    • N. Badi, and J.-F. Lutz Sequence control in polymer synthesis Chem Soc Rev 38 12 2009 3383 3390
    • (2009) Chem Soc Rev , vol.38 , Issue.12 , pp. 3383-3390
    • Badi, N.1    Lutz, J.-F.2
  • 220
    • 69249207273 scopus 로고    scopus 로고
    • Precision polymers: Monodisperse, monomer-sequence-defined segments to target future demands of polymers in medicine
    • L. Hartmann, and H.G. Borner Precision polymers: monodisperse, monomer-sequence-defined segments to target future demands of polymers in medicine Adv Mater 21 32-33 2009 3425 3431
    • (2009) Adv Mater , vol.21 , Issue.3233 , pp. 3425-3431
    • Hartmann, L.1    Borner, H.G.2
  • 221
    • 77950796120 scopus 로고    scopus 로고
    • Sequence-controlled polymerizations: The next holy grail in polymer science?
    • J.F. Lutz Sequence-controlled polymerizations: the next holy grail in polymer science? Polym Chem 1 1 2010 55 62
    • (2010) Polym Chem , vol.1 , Issue.1 , pp. 55-62
    • Lutz, J.F.1
  • 222
    • 78651431186 scopus 로고    scopus 로고
    • Precision polymers - Modern tools to understand and program macromolecular interactions
    • H.G. Borner Precision polymers - modern tools to understand and program macromolecular interactions Macromol Rapid Commun 32 2 2011 115 126
    • (2011) Macromol Rapid Commun , vol.32 , Issue.2 , pp. 115-126
    • Borner, H.G.1
  • 223
    • 84872543571 scopus 로고    scopus 로고
    • Microstructure control: An underestimated parameter in recent polymer design
    • N. Badi, D. Chan-Seng, and J.-F. Lutz Microstructure control: an underestimated parameter in recent polymer design Macromol Chem Phys 214 2 2013 135 142
    • (2013) Macromol Chem Phys , vol.214 , Issue.2 , pp. 135-142
    • Badi, N.1    Chan-Seng, D.2    Lutz, J.-F.3
  • 224
    • 84888626615 scopus 로고    scopus 로고
    • Writing on polymer chains
    • J.-F. Lutz Writing on polymer chains Acc Chem Res 46 11 2013 2696 2705
    • (2013) Acc Chem Res , vol.46 , Issue.11 , pp. 2696-2705
    • Lutz, J.-F.1
  • 226
    • 34547770971 scopus 로고    scopus 로고
    • A facile procedure for controlling monomer sequence distribution in radical chain polymerizations
    • S. Pfeifer, and J.-F. Lutz A facile procedure for controlling monomer sequence distribution in radical chain polymerizations J Am Chem Soc 129 31 2007 9542 9543
    • (2007) J Am Chem Soc , vol.129 , Issue.31 , pp. 9542-9543
    • Pfeifer, S.1    Lutz, J.-F.2
  • 227
    • 57149131991 scopus 로고    scopus 로고
    • Development of a library of N-substituted maleimides for the local functionalization of linear polymer chains
    • S. Pfeifer, and J.-F. Lutz Development of a library of N-substituted maleimides for the local functionalization of linear polymer chains Chem Eur J 14 35 2008 10949 10957
    • (2008) Chem Eur J , vol.14 , Issue.35 , pp. 10949-10957
    • Pfeifer, S.1    Lutz, J.-F.2
  • 228
    • 84900314248 scopus 로고    scopus 로고
    • Precision polymers: A kinetic approach for functional poly(norbornenes)
    • D. Moatsou, C.F. Hansell, and R.K. O'Reilly Precision polymers: a kinetic approach for functional poly(norbornenes) Chem Sci 5 6 2014 2246 2250
    • (2014) Chem Sci , vol.5 , Issue.6 , pp. 2246-2250
    • Moatsou, D.1    Hansell, C.F.2    O'Reilly, R.K.3
  • 229
    • 78349270178 scopus 로고    scopus 로고
    • Multistep DNA-templated reactions for the synthesis of functional sequence controlled oligomers
    • M.L. McKee, P.J. Milnes, J. Bath, E. Stulz, A.J. Turberfield, and R.K. O'Reilly Multistep DNA-templated reactions for the synthesis of functional sequence controlled oligomers Angew Chem Int Ed 49 43 2010 7948 7951
    • (2010) Angew Chem Int Ed , vol.49 , Issue.43 , pp. 7948-7951
    • McKee, M.L.1    Milnes, P.J.2    Bath, J.3    Stulz, E.4    Turberfield, A.J.5    O'Reilly, R.K.6
  • 230
    • 77958491280 scopus 로고    scopus 로고
    • Template-assisted selective radical addition toward sequence-regulated polymerization: Lariat capture of target monomer by template initiator
    • S. Ida, M. Ouchi, and M. Sawamoto Template-assisted selective radical addition toward sequence-regulated polymerization: lariat capture of target monomer by template initiator J Am Chem Soc 132 42 2010 14748 14750
    • (2010) J Am Chem Soc , vol.132 , Issue.42 , pp. 14748-14750
    • Ida, S.1    Ouchi, M.2    Sawamoto, M.3
  • 231
    • 79960927307 scopus 로고    scopus 로고
    • Sequence-regulated radical polymerization with a metal-templated monomer: Repetitive ABA sequence by double cyclopolymerization
    • Y. Hibi, M. Ouchi, and M. Sawamoto Sequence-regulated radical polymerization with a metal-templated monomer: repetitive ABA sequence by double cyclopolymerization Angew Chem Int Ed 50 32 2011 7434 7437
    • (2011) Angew Chem Int Ed , vol.50 , Issue.32 , pp. 7434-7437
    • Hibi, Y.1    Ouchi, M.2    Sawamoto, M.3
  • 232
    • 78651436778 scopus 로고    scopus 로고
    • Designer template initiator for sequence regulated polymerization: Systems design for substrate-selective metal-catalyzed radical addition and living radical polymerization
    • S. Ida, M. Ouchi, and M. Sawamoto Designer template initiator for sequence regulated polymerization: systems design for substrate-selective metal-catalyzed radical addition and living radical polymerization Macromol Rapid Commun 32 2 2011 209 214
    • (2011) Macromol Rapid Commun , vol.32 , Issue.2 , pp. 209-214
    • Ida, S.1    Ouchi, M.2    Sawamoto, M.3
  • 234
    • 84875420027 scopus 로고    scopus 로고
    • Enzyme-free translation of DNA into sequence-defined synthetic polymers structurally unrelated to nucleic acids
    • J. Niu, R. Hili, and D.R. Liu Enzyme-free translation of DNA into sequence-defined synthetic polymers structurally unrelated to nucleic acids Nat Chem 5 4 2013 282 292
    • (2013) Nat Chem , vol.5 , Issue.4 , pp. 282-292
    • Niu, J.1    Hili, R.2    Liu, D.R.3
  • 235
    • 84872137433 scopus 로고    scopus 로고
    • Sequence-specific peptide synthesis by an artificial small-molecule machine
    • B. Lewandowski, G. De Bo, J.W. Ward, M. Papmeyer, S. Kuschel, and M.J. Aldegunde Sequence-specific peptide synthesis by an artificial small-molecule machine Science 339 6116 2013 189 193
    • (2013) Science , vol.339 , Issue.6116 , pp. 189-193
    • Lewandowski, B.1    De Bo, G.2    Ward, J.W.3    Papmeyer, M.4    Kuschel, S.5    Aldegunde, M.J.6
  • 236
    • 84885123533 scopus 로고    scopus 로고
    • Rapid and quantitative one-pot synthesis of sequence-controlled polymers by radical polymerization
    • G. Gody, T. Maschmeyer, P.B. Zetterlund, and S. Perrier Rapid and quantitative one-pot synthesis of sequence-controlled polymers by radical polymerization Nat Commun 2013 4
    • (2013) Nat Commun , pp. 4
    • Gody, G.1    Maschmeyer, T.2    Zetterlund, P.B.3    Perrier, S.4
  • 237
    • 84876893933 scopus 로고    scopus 로고
    • Precision synthesis of acrylate multiblock copolymers from consecutive microreactor RAFT polymerizations
    • J. Vandenbergh, Tdm Ogawa, and T. Junkers Precision synthesis of acrylate multiblock copolymers from consecutive microreactor RAFT polymerizations J Polym Sci, Part A: Polym Chem 51 11 2013 2366 2374
    • (2013) J Polym Sci, Part A: Polym Chem , vol.51 , Issue.11 , pp. 2366-2374
    • Vandenbergh, J.1    Ogawa, T.2    Junkers, T.3
  • 238
    • 78650770524 scopus 로고    scopus 로고
    • Polymers for control freaks: Sequence-defined poly(amidoamine)s and their biomedical applications
    • L. Hartmann Polymers for control freaks: sequence-defined poly(amidoamine)s and their biomedical applications Macromol Chem Phys 212 1 2011 8 13
    • (2011) Macromol Chem Phys , vol.212 , Issue.1 , pp. 8-13
    • Hartmann, L.1
  • 239
    • 78651446668 scopus 로고    scopus 로고
    • Precise positioning of chiral building blocks in monodisperse. Sequence-defined polyamides
    • S. Mosca, F. Wojcik, and L. Hartmann Precise positioning of chiral building blocks in monodisperse. Sequence-defined polyamides Macromol Rapid Commun 32 2 2011 197 202
    • (2011) Macromol Rapid Commun , vol.32 , Issue.2 , pp. 197-202
    • Mosca, S.1    Wojcik, F.2    Hartmann, L.3
  • 240
    • 67649989355 scopus 로고    scopus 로고
    • Liquid-phase synthesis of block copolymers containing sequence-ordered segments
    • S. Pfeifer, Z. Zarafshani, N. Badi, and J.-F. Lutz Liquid-phase synthesis of block copolymers containing sequence-ordered segments J Am Chem Soc 131 26 2009 9195 9197
    • (2009) J Am Chem Soc , vol.131 , Issue.26 , pp. 9195-9197
    • Pfeifer, S.1    Zarafshani, Z.2    Badi, N.3    Lutz, J.-F.4
  • 241
    • 77951575017 scopus 로고    scopus 로고
    • Tailor-made soluble polymer supports: Synthesis of a series of ATRP initiators containing labile wang linkers
    • S. Pfeifer, and J.-F. Lutz Tailor-made soluble polymer supports: synthesis of a series of ATRP initiators containing labile wang linkers Macromol Chem Phys 211 8 2010 940 947
    • (2010) Macromol Chem Phys , vol.211 , Issue.8 , pp. 940-947
    • Pfeifer, S.1    Lutz, J.-F.2
  • 242
    • 84859018497 scopus 로고    scopus 로고
    • "inverse" synthesis of polymer bioconjugates using soluble supports
    • A. Meszynska, N. Badi, H.G. Boerner, and J.-F. Lutz "Inverse" synthesis of polymer bioconjugates using soluble supports Chem Commun 48 32 2012 3887 3889
    • (2012) Chem Commun , vol.48 , Issue.32 , pp. 3887-3889
    • Meszynska, A.1    Badi, N.2    Boerner, H.G.3    Lutz, J.-F.4
  • 243
    • 20744456789 scopus 로고
    • Solid phase peptide synthesis. I. The synthesis of a tetrapeptide
    • R.B. Merrifield Solid phase peptide synthesis. I. The synthesis of a tetrapeptide J Am Chem Soc 85 14 1963 2149 2154
    • (1963) J Am Chem Soc , vol.85 , Issue.14 , pp. 2149-2154
    • Merrifield, R.B.1
  • 244
    • 0025232814 scopus 로고
    • Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids
    • G.B. Fields, and R.L. Noble Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids Int J Pept Protein Res 35 3 1990 161 214
    • (1990) Int J Pept Protein Res , vol.35 , Issue.3 , pp. 161-214
    • Fields, G.B.1    Noble, R.L.2
  • 245
    • 0026606239 scopus 로고
    • Advances in the synthesis of oligonucleotides by the phosphoramidite approach
    • S.L. Beaucage, and R.P. Iyer Advances in the synthesis of oligonucleotides by the phosphoramidite approach Tetrahedron 48 12 1992 2223 2311
    • (1992) Tetrahedron , vol.48 , Issue.12 , pp. 2223-2311
    • Beaucage, S.L.1    Iyer, R.P.2
  • 246
    • 0000908874 scopus 로고
    • Efficient method for the preparation of peptoids oligo(N-substituted glycines) by submonomer solid-phase synthesis
    • R.N. Zuckermann, J.M. Kerr, S.B.H. Kent, and W.H. Moos Efficient method for the preparation of peptoids oligo(N-substituted glycines) by submonomer solid-phase synthesis J Am Chem Soc 114 26 1992 10646 10647
    • (1992) J Am Chem Soc , vol.114 , Issue.26 , pp. 10646-10647
    • Zuckermann, R.N.1    Kerr, J.M.2    Kent, S.B.H.3    Moos, W.H.4
  • 248
    • 0025767755 scopus 로고
    • 2-Chlorotrityl chloride resin - Studies on anchoring of FMOC-amino acids and peptide cleavage
    • K. Barlos, O. Chatzi, D. Gatos, and G. Stavropoulos 2-Chlorotrityl chloride resin - studies on anchoring of FMOC-amino acids and peptide cleavage Int J Pept Protein Res 37 6 1991 513 520
    • (1991) Int J Pept Protein Res , vol.37 , Issue.6 , pp. 513-520
    • Barlos, K.1    Chatzi, O.2    Gatos, D.3    Stavropoulos, G.4
  • 249
    • 47349086967 scopus 로고    scopus 로고
    • Development of a tandem base-catalyzed, triphenylphosphine-mediated disulfide reduction-Michael addition
    • A. Bartolozzi, H.M. Foudoulakis, and B.M. Cole Development of a tandem base-catalyzed, triphenylphosphine-mediated disulfide reduction-Michael addition Synth-Stuttgart 13 2008 2023 2032
    • (2008) Synth-Stuttgart , vol.13 , pp. 2023-2032
    • Bartolozzi, A.1    Foudoulakis, H.M.2    Cole, B.M.3
  • 250
    • 79951530579 scopus 로고    scopus 로고
    • Introducing multicomponent reactions to polymer science: Passerini reactions of renewable monomers
    • O. Kreye, T. Toth, and M.A.R. Meier Introducing multicomponent reactions to polymer science: Passerini reactions of renewable monomers J Am Chem Soc 133 6 2011 1790 1792
    • (2011) J Am Chem Soc , vol.133 , Issue.6 , pp. 1790-1792
    • Kreye, O.1    Toth, T.2    Meier, M.A.R.3
  • 251
    • 84890560091 scopus 로고    scopus 로고
    • Synthesis of diverse asymmetric alpha, omega-dienes via the Passerini three-component reaction for head-to-tail ADMET polymerization
    • A. Sehlinger, L.M. de Espinosa, and M.A.R. Meier Synthesis of diverse asymmetric alpha, omega-dienes via the Passerini three-component reaction for head-to-tail ADMET polymerization Macromol Chem Phys 214 24 2013 2821 2828
    • (2013) Macromol Chem Phys , vol.214 , Issue.24 , pp. 2821-2828
    • Sehlinger, A.1    De Espinosa, L.M.2    Meier, M.A.R.3
  • 252
    • 84881581426 scopus 로고    scopus 로고
    • Tunable polymers obtained from Passerini multicomponent reaction derived acrylate monomers
    • A. Sehlinger, O. Kreye, and M.A.R. Meier Tunable polymers obtained from Passerini multicomponent reaction derived acrylate monomers Macromolecules 46 15 2013 6031 6037
    • (2013) Macromolecules , vol.46 , Issue.15 , pp. 6031-6037
    • Sehlinger, A.1    Kreye, O.2    Meier, M.A.R.3
  • 253
    • 84895057493 scopus 로고    scopus 로고
    • Divergent dendrimer synthesis via the Passerini three-component reaction and Olefin cross-metathesis
    • O. Kreye, D. Kugele, L. Faust, and M.A.R. Meier Divergent dendrimer synthesis via the Passerini three-component reaction and Olefin cross-metathesis Macromol Rapid Commun 35 3 2014 317 322
    • (2014) Macromol Rapid Commun , vol.35 , Issue.3 , pp. 317-322
    • Kreye, O.1    Kugele, D.2    Faust, L.3    Meier, M.A.R.4
  • 254
    • 84891631743 scopus 로고    scopus 로고
    • Passerini addition polymerization of an AB-type monomer - A convenient route to versatile polyesters
    • A. Sehlinger, R. Schneider, and M.A.R. Meier Passerini addition polymerization of an AB-type monomer - a convenient route to versatile polyesters Eur Polym J 50 2014 150 157
    • (2014) Eur Polym J , vol.50 , pp. 150-157
    • Sehlinger, A.1    Schneider, R.2    Meier, M.A.R.3
  • 255
    • 84891862569 scopus 로고    scopus 로고
    • Sequence control in polymer chemistry through the Passerini three-component reaction
    • S.C. Solleder, and M.A.R. Meier Sequence control in polymer chemistry through the Passerini three-component reaction Angew Chem Int Ed 53 3 2014 711 714
    • (2014) Angew Chem Int Ed , vol.53 , Issue.3 , pp. 711-714
    • Solleder, S.C.1    Meier, M.A.R.2
  • 256
    • 84879034376 scopus 로고    scopus 로고
    • Synthesis of sequence-ordered polymers via sequential addition of monomers in one pot
    • J.-J. Yan, D. Wang, D.-C. Wu, and Y.-Z. You Synthesis of sequence-ordered polymers via sequential addition of monomers in one pot Chem Commun 49 54 2013 6057 6059
    • (2013) Chem Commun , vol.49 , Issue.54 , pp. 6057-6059
    • Yan, J.-J.1    Wang, D.2    Wu, D.-C.3    You, Y.-Z.4
  • 257
    • 84876554327 scopus 로고    scopus 로고
    • A novel multifunctional coupler; Concept of coupling and proof of principle
    • S. Mommer, K. Lamberts, H. Keul, and M. Möller A novel multifunctional coupler; Concept of coupling and proof of principle Chem Comm 49 2013 3288 3290
    • (2013) Chem Comm , vol.49 , pp. 3288-3290
    • Mommer, S.1    Lamberts, K.2    Keul, H.3    Möller, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.