A Combined Photochemical and Multicomponent Reaction Approach to Precision Oligomers

We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component reaction (P‐3CR) and a Diels–Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit ca...

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Published inChemistry : a European journal Vol. 24; no. 14; pp. 3413 - 3419
Main Authors Konrad, Waldemar, Bloesser, Fabian R., Wetzel, Katharina S., Boukis, Andreas C., Meier, Michael A. R., Barner‐Kowollik, Christopher
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 07.03.2018
Wiley Subscription Services, Inc
Subjects
Chains
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Conjugation
convergent
Dienes
Ionization
Ions
Magnetic resonance spectroscopy
Mass spectrometry
Mass spectroscopy
multicomponent reactions
NMR spectroscopy
Oligomers
Photochemical reactions
Photochemicals
photochemistry
Physical Sciences
Science & Technology
Sebacic acid
sequence control
sequence-defined macromolecules
Switching
sequence control
multicomponent reactions
ACRYLATE OLIGOMERS
ITERATIVE EXPONENTIAL-GROWTH
SOLID-PHASE SYNTHESIS
convergent
STRATEGY
sequence-defined macromolecules
COPOLYMERS
DENDRIMERS
SCALABLE SYNTHESIS
OLIGONUCLEOTIDES
photochemistry
POLYMER CHEMISTRY
Online AccessGet full text

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Abstract We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component reaction (P‐3CR) and a Diels–Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit carrying an isocyano group for chain extension by P‐3CR and a maleimide moiety for photoenol conjugation enabling a modular approach for chain growth. Monodisperse oligomers are accessible in a stepwise fashion by switching between both reaction types. Employing sebacic acid as a core unit allows the synthesis of a library of symmetric sequence‐defined oligomers. The oligomers consist of alternating P‐3CR and photoblocks with molecular weights up to 3532.16 g mol−1, demonstrating the successful switching from P‐3CR to photoenol conjugation. In‐depth characterization was carried out including size‐exclusion chromatography (SEC), high‐resolution electrospray ionization mass spectrometry (ESI‐MS) and NMR spectroscopy, evidencing the monodisperse nature of the precision oligomers. Sequence control: The synthesis of multifunctional precision sequence‐defined linear macromolecules becomes possible by fusing a highly efficient photochemical and multicomponent reaction approach entailing alternating Passerini and photoblocks. The growth of the oligomers is based on a convergent chain extension concept of sebacic acid with building blocks on demand in an orthogonal fashion (see figure).
AbstractList We introduce the convergent synthesis of linear monodisperse sequence-defined oligomers through a unique approach, combining the Passerini three-component reaction (P-3CR) and a Diels-Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit carrying an isocyano group for chain extension by P-3CR and a maleimide moiety for photoenol conjugation enabling a modular approach for chain growth. Monodisperse oligomers are accessible in a stepwise fashion by switching between both reaction types. Employing sebacic acid as a core unit allows the synthesis of a library of symmetric sequence-defined oligomers. The oligomers consist of alternating P-3CR and photoblocks with molecular weights up to 3532.16 g mol-1 , demonstrating the successful switching from P-3CR to photoenol conjugation. In-depth characterization was carried out including size-exclusion chromatography (SEC), high-resolution electrospray ionization mass spectrometry (ESI-MS) and NMR spectroscopy, evidencing the monodisperse nature of the precision oligomers.
Abstract We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component reaction (P‐3CR) and a Diels–Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit carrying an isocyano group for chain extension by P‐3CR and a maleimide moiety for photoenol conjugation enabling a modular approach for chain growth. Monodisperse oligomers are accessible in a stepwise fashion by switching between both reaction types. Employing sebacic acid as a core unit allows the synthesis of a library of symmetric sequence‐defined oligomers. The oligomers consist of alternating P‐3CR and photoblocks with molecular weights up to 3532.16 g mol −1 , demonstrating the successful switching from P‐3CR to photoenol conjugation. In‐depth characterization was carried out including size‐exclusion chromatography (SEC), high‐resolution electrospray ionization mass spectrometry (ESI‐MS) and NMR spectroscopy, evidencing the monodisperse nature of the precision oligomers.
We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component reaction (P‐3CR) and a Diels–Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit carrying an isocyano group for chain extension by P‐3CR and a maleimide moiety for photoenol conjugation enabling a modular approach for chain growth. Monodisperse oligomers are accessible in a stepwise fashion by switching between both reaction types. Employing sebacic acid as a core unit allows the synthesis of a library of symmetric sequence‐defined oligomers. The oligomers consist of alternating P‐3CR and photoblocks with molecular weights up to 3532.16 g mol−1, demonstrating the successful switching from P‐3CR to photoenol conjugation. In‐depth characterization was carried out including size‐exclusion chromatography (SEC), high‐resolution electrospray ionization mass spectrometry (ESI‐MS) and NMR spectroscopy, evidencing the monodisperse nature of the precision oligomers.
We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component reaction (P‐3CR) and a Diels–Alder (DA) reaction based on photocaged dienes. A set of oligomers is prepared resting on a Passerini linker unit carrying an isocyano group for chain extension by P‐3CR and a maleimide moiety for photoenol conjugation enabling a modular approach for chain growth. Monodisperse oligomers are accessible in a stepwise fashion by switching between both reaction types. Employing sebacic acid as a core unit allows the synthesis of a library of symmetric sequence‐defined oligomers. The oligomers consist of alternating P‐3CR and photoblocks with molecular weights up to 3532.16 g mol−1, demonstrating the successful switching from P‐3CR to photoenol conjugation. In‐depth characterization was carried out including size‐exclusion chromatography (SEC), high‐resolution electrospray ionization mass spectrometry (ESI‐MS) and NMR spectroscopy, evidencing the monodisperse nature of the precision oligomers. Sequence control: The synthesis of multifunctional precision sequence‐defined linear macromolecules becomes possible by fusing a highly efficient photochemical and multicomponent reaction approach entailing alternating Passerini and photoblocks. The growth of the oligomers is based on a convergent chain extension concept of sebacic acid with building blocks on demand in an orthogonal fashion (see figure).
Author Wetzel, Katharina S.
Boukis, Andreas C.
Konrad, Waldemar
Bloesser, Fabian R.
Barner‐Kowollik, Christopher
Meier, Michael A. R.
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  organization: Queensland University of Technology (QUT)
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Cites_doi 10.1002/anie.201509398
10.1039/c3cc45994b
10.1038/ncomms13672
10.1038/natrevmats.2016.24
10.1073/pnas.1508599112
10.1002/marc.201600711
10.1021/jacs.6b07120
10.1039/c7py00713b
10.1021/cr990308c
10.1038/NCHEM.2346
10.1039/c4cc08756a
10.1021/acsnano.6b01333
10.1002/anie.201702512
10.1038/nbt1171
10.1002/chem.201703877
10.1021/Jacs.6b04964
10.1126/science.1238149
10.1038/nchem.1806
10.1007/s10989-006-9053-0
10.1021/acsnano.7b02820
10.1002/adfm.201604595
10.1021/acsmacrolett.7b00024
10.1002/marc.201700469
10.1038/nchem.530
10.1021/acs.macromol.7b01737
10.1021/cr000045i
10.1038/NCHEM.2508
10.1038/ncomms11064
10.1002/anie.201702384
10.1039/c5sc02035b
10.1002/anie.201509864
10.1002/anie.201307439
10.1039/C5SC02035B
10.1002/ange.201509864
10.1021/jacs.6b04964
10.1002/ange.19850971004
10.1039/C7PY00713B
10.1002/ange.201702512
10.1002/anie.198507993
10.1002/(SICI)1521-3757(19981016)110:20<2954::AID-ANGE2954>3.0.CO;2-G
10.1002/ange.201307439
10.1002/anie.201701659
10.1002/ange.201702384
10.1039/C4CC08756A
10.1126/science.8134834
10.1016/S0040-4020(01)88752-4
10.1002/(SICI)1521-3773(19981102)37:20<2796::AID-ANIE2796>3.0.CO;2-K
10.1002/ange.201701659
10.1002/(SICI)1521-3757(19990401)111:7<934::AID-ANGE934>3.0.CO;2-4
10.1038/nchem.2508
10.1038/nchem.2346
10.1039/C3CC45994B
10.1002/ange.201509398
10.1073/pnas.89.20.9367
10.1002/(SICI)1521-3773(19990401)38:7<884::AID-ANIE884>3.0.CO;2-K
10.1021/ja00897a025
10.1021/ja00102a082
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Issue 14
Keywords sequence control
multicomponent reactions
ACRYLATE OLIGOMERS
ITERATIVE EXPONENTIAL-GROWTH
SOLID-PHASE SYNTHESIS
convergent
STRATEGY
sequence-defined macromolecules
COPOLYMERS
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References 2017; 6
2017; 8
2001; 101
1994; 116
2015; 6
2013; 49
2015; 51
2017; 27
1963; 85
1999 1999; 38 111
1985 1985; 24 97
2017; 23
2016; 10
2013; 341
2017 2017; 56 129
2013; 5
2015; 7
2007; 13
2005; 23
2013 2013; 52 125
1998 1998; 37 110
2017; 50
2016; 7
2016; 1
2016 2016; 55 128
2017; 38
2017; 11
1994; 263
2015; 112
2016; 138
2000; 100
1992; 48
2010; 2
1992; 89
2016; 8
FRECHET, JMJ (WOS:A1994NC04000024) 1994; 263
Solleder, SC (WOS:000412595600013) 2017; 23
Merrifield, R. B. (000426764400008.34) 1985; 97
IUPAC (000426764400008.1) 1997
Porel, M (WOS:000376529000016) 2016; 8
Jiang, Y (WOS:000381062600009) 2016; 138
Mueller, P (WOS:000404808000124) 2017; 11
Konig, N. F. (000426764400008.23) 2017; 129
MERRIFIELD, RB (WOS:A19633101B00025) 1963; 85
Xu, J. (000426764400008.47) 2017; 56
Schmidt, BVKJ (WOS:000327450500005) 2013; 5
Fischer, M (WOS:000079641000002) 1999; 38
Fischer, M. (000426764400008.11) 1999; 111
Barnes, JC (WOS:000361753200010) 2015; 7
Vandenbergh, J (WOS:000361212000050) 2015; 6
Espeel, P. (000426764400008.8) 2013; 125
Lutz, JF (WOS:000322884800029) 2013; 341
Chen, CL (WOS:000376825100045) 2016; 10
Grate, JW (WOS:000372660400009) 2016; 55
Lutz, JF (WOS:000273820700009) 2010; 2
Xu, J. (000426764400008.48) 2017; 129
Konig, NF (WOS:000402857800055) 2017; 56
Karamessini, D (WOS:000391926700015) 2017; 27
Hibi, Y (WOS:000372500000001) 2016; 7
SIMON, RJ (WOS:A1992JT97700001) 1992; 89
Lee, CC (WOS:000233866300028) 2005; 23
Lutz, JF (WOS:000377671300004) 2016; 1
Estupinan, D (WOS:000397478700009) 2017; 6
Huang, YH (WOS:000401791900032) 2017; 56
Zydziak, N (WOS:000348213200004) 2015; 51
Martens, S (WOS:000387095000005) 2016; 138
Grate, JW (000426764400008.15) 2016; 128
Fu, CK (WOS:000407639500002) 2017; 8
YOUNG, JK (WOS:A1994PT13000082) 1994; 116
Vandenbergh, J (WOS:000325723900005) 2013; 49
Eritja, R (WOS:000247236500008) 2007; 13
Solleder, SC (WOS:000368070000069) 2016; 55
Zydziak, N (WOS:000388873200001) 2016; 7
BEAUCAGE, SL (WOS:A1992HJ78500001) 1992; 48
Burel, A (WOS:000413885100050) 2017; 50
MERRIFIELD, RB (WOS:A1985AVC9200001) 1985; 24
Espeel, P (WOS:000327802100020) 2013; 52
Sol-leder, S. C. (000426764400008.40) 2016; 128
Cheng, RP (WOS:000171545400011) 2001; 101
Martens, S (WOS:000418413800002) 2017; 38
Huang, Z. (000426764400008.19) 2017; 129
Uhlmann, E (WOS:000076892300002) 1998; 37
Herzner, H (WOS:000165902600010) 2000; 100
Solleder, SC (WOS:000400651500002) 2017; 38
Uhlmann, E. (000426764400008.43) 1998; 110
Leibfarth, FA (WOS:000360005600039) 2015; 112
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References_xml – volume: 5
  start-page: 990
  year: 2013
  end-page: 992
  publication-title: Nat. Chem.
– volume: 8
  start-page: 4637
  year: 2017
  end-page: 4643
  publication-title: Polym. Chem.
– volume: 7
  start-page: 810
  year: 2015
  end-page: 815
  publication-title: Nat. Chem.
– volume: 51
  start-page: 1799
  year: 2015
  end-page: 1802
  publication-title: Chem. Commun.
– volume: 55 128
  start-page: 1204 1222
  year: 2016 2016
  end-page: 1207 1225
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 8
  start-page: 590
  year: 2016
  end-page: 596
  publication-title: Nat. Chem.
– volume: 56 129
  start-page: 5877 5971
  year: 2017 2017
  end-page: 5881 5975
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 38
  start-page: 1600711
  year: 2017
  publication-title: Macromol. Rapid Commun.
– volume: 49
  start-page: 10358
  year: 2013
  end-page: 10360
  publication-title: Chem. Commun.
– volume: 48
  start-page: 2223
  year: 1992
  end-page: 2311
  publication-title: Tetrahedron
– volume: 100
  start-page: 4495
  year: 2000
  end-page: 4538
  publication-title: Chem. Rev.
– volume: 138
  start-page: 9369
  year: 2016
  end-page: 9372
  publication-title: J. Am. Chem. Soc.
– volume: 101
  start-page: 3219
  year: 2001
  end-page: 3232
  publication-title: Chem. Rev.
– volume: 52 125
  start-page: 13261 13503
  year: 2013 2013
  end-page: 13264 13506
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 10
  start-page: 5314
  year: 2016
  end-page: 5320
  publication-title: ACS Nano
– volume: 56 129
  start-page: 7297 7403
  year: 2017 2017
  end-page: 7301 7407
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 24 97
  start-page: 799 801
  year: 1985 1985
  end-page: 810 812
  publication-title: Angew. Chem. Int. Ed. Engl. Angew. Chem.
– volume: 23
  start-page: 1517
  year: 2005
  publication-title: Nat. Biotechnol.
– volume: 89
  start-page: 9367
  year: 1992
  end-page: 9371
  publication-title: Proc. Natl. Acad. Sci. USA
– volume: 7
  start-page: 11064
  year: 2016
  publication-title: Nat. Commun.
– volume: 38
  start-page: 1700469
  year: 2017
  publication-title: Macromol. Rapid Commun.
– volume: 50
  start-page: 8290
  year: 2017
  end-page: 8296
  publication-title: Macromolecules
– volume: 23
  start-page: 13906
  year: 2017
  end-page: 13909
  publication-title: Chem. Eur. J.
– volume: 37 110
  start-page: 2796 2954
  year: 1998 1998
  end-page: 2823 2983
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 116
  start-page: 10841
  year: 1994
  end-page: 10842
  publication-title: J. Am. Chem. Soc.
– volume: 6
  start-page: 5753
  year: 2015
  end-page: 5761
  publication-title: Chem. Sci.
– volume: 112
  start-page: 10617
  year: 2015
  end-page: 10622
  publication-title: Proc. Natl. Acad. Sci. USA
– volume: 138
  start-page: 14182
  year: 2016
  end-page: 14185
  publication-title: J. Am. Chem. Soc.
– volume: 2
  start-page: 84
  year: 2010
  end-page: 85
  publication-title: Nat. Chem.
– volume: 7
  start-page: 13672
  year: 2016
  publication-title: Nat. Commun.
– volume: 27
  start-page: 1604595
  year: 2017
  publication-title: Adv. Funct. Mater.
– volume: 55 128
  start-page: 3925 3993
  year: 2016 2016
  end-page: 3930 3998
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 6
  start-page: 229
  year: 2017
  end-page: 234
  publication-title: ACS Macro Lett.
– volume: 13
  start-page: 53
  year: 2007
  end-page: 68
  publication-title: Int. J. Pept. Res. Ther.
– volume: 263
  start-page: 1710
  year: 1994
  end-page: 1715
  publication-title: Science
– volume: 56 129
  start-page: 6544 6644
  year: 2017 2017
  end-page: 6547 6647
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 11
  start-page: 6396
  year: 2017
  end-page: 6403
  publication-title: ACS Nano
– volume: 1
  start-page: 16024
  year: 2016
  publication-title: Nat. Rev. Mater.
– volume: 85
  start-page: 2149
  year: 1963
  end-page: 2154
  publication-title: J. Am. Chem. Soc.
– volume: 38 111
  start-page: 884 934
  year: 1999 1999
  end-page: 905 955
  publication-title: Angew. Chem. Int. Ed. Angew. Chem.
– volume: 341
  start-page: 1238149
  year: 2013
  publication-title: Science
– year: 1997
  ident: 000426764400008.1
  publication-title: Compendium of Chemical Terminology
  contributor:
    fullname: IUPAC
– volume: 55
  start-page: 1204
  year: 2016
  ident: WOS:000368070000069
  article-title: A Scalable and High-Yield Strategy for the Synthesis of Sequence-Defined Macromolecules
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201509398
  contributor:
    fullname: Solleder, SC
– volume: 263
  start-page: 1710
  year: 1994
  ident: WOS:A1994NC04000024
  article-title: FUNCTIONAL POLYMERS AND DENDRIMERS - REACTIVITY, MOLECULAR ARCHITECTURE, AND INTERFACIAL ENERGY
  publication-title: SCIENCE
  contributor:
    fullname: FRECHET, JMJ
– volume: 49
  start-page: 10358
  year: 2013
  ident: WOS:000325723900005
  article-title: Synthesis of sequence controlled acrylate oligomers via consecutive RAFT monomer additions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c3cc45994b
  contributor:
    fullname: Vandenbergh, J
– volume: 7
  start-page: ARTN 13672
  year: 2016
  ident: WOS:000388873200001
  article-title: Coding and decoding libraries of sequence-defined functional copolymers synthesized via photoligation
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/ncomms13672
  contributor:
    fullname: Zydziak, N
– volume: 1
  start-page: ARTN 16024
  year: 2016
  ident: WOS:000377671300004
  article-title: From precision polymers to complex materials and systems
  publication-title: NATURE REVIEWS MATERIALS
  doi: 10.1038/natrevmats.2016.24
  contributor:
    fullname: Lutz, JF
– volume: 112
  start-page: 10617
  year: 2015
  ident: WOS:000360005600039
  article-title: Scalable synthesis of sequence-defined, unimolecular macromolecules by Flow-IEG
  publication-title: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
  doi: 10.1073/pnas.1508599112
  contributor:
    fullname: Leibfarth, FA
– volume: 38
  start-page: ARTN 1600711
  year: 2017
  ident: WOS:000400651500002
  article-title: Recent Progress in the Design of Monodisperse, Sequence-Defined Macromolecules
  publication-title: MACROMOLECULAR RAPID COMMUNICATIONS
  doi: 10.1002/marc.201600711
  contributor:
    fullname: Solleder, SC
– volume: 89
  start-page: 9367
  year: 1992
  ident: WOS:A1992JT97700001
  article-title: PEPTOIDS - A MODULAR APPROACH TO DRUG DISCOVERY
  publication-title: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
  contributor:
    fullname: SIMON, RJ
– volume: 138
  start-page: 14182
  year: 2016
  ident: WOS:000387095000005
  article-title: Automated Synthesis of Monodisperse Oligomers, Featuring Sequence Control and Tailored Functionalization
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b07120
  contributor:
    fullname: Martens, S
– volume: 8
  start-page: 4637
  year: 2017
  ident: WOS:000407639500002
  article-title: RAFT-mediated, visible light-initiated single unit monomer insertion and its application in the synthesis of sequence-defined polymers
  publication-title: POLYMER CHEMISTRY
  doi: 10.1039/c7py00713b
  contributor:
    fullname: Fu, CK
– volume: 100
  start-page: 4495
  year: 2000
  ident: WOS:000165902600010
  article-title: Synthesis of glycopeptides containing carbohydrate and peptide recognition motifs
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr990308c
  contributor:
    fullname: Herzner, H
– volume: 128
  start-page: 1222
  year: 2016
  ident: 000426764400008.40
  publication-title: Angew. Chem.
  contributor:
    fullname: Sol-leder, S. C.
– volume: 7
  start-page: 810
  year: 2015
  ident: WOS:000361753200010
  article-title: Iterative exponential growth of stereo- and sequence-controlled polymers
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/NCHEM.2346
  contributor:
    fullname: Barnes, JC
– volume: 51
  start-page: 1799
  year: 2015
  ident: WOS:000348213200004
  article-title: Photo-induced sequence defined macromolecules via hetero bifunctional synthons
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c4cc08756a
  contributor:
    fullname: Zydziak, N
– volume: 10
  start-page: 5314
  year: 2016
  ident: WOS:000376825100045
  article-title: Surface-Directed Assembly of Sequence Defined Synthetic Polymers into Networks of Hexagonally Patterned Nanoribbons with Controlled Functionalities
  publication-title: ACS NANO
  doi: 10.1021/acsnano.6b01333
  contributor:
    fullname: Chen, CL
– volume: 56
  start-page: 6544
  year: 2017
  ident: WOS:000401791900032
  article-title: Amide-Directed C-H Sodiation by a Sodium Hydride/Iodide Composite
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201702512
  contributor:
    fullname: Huang, YH
– volume: 110
  start-page: 2954
  year: 1998
  ident: 000426764400008.43
  publication-title: Angew. Chem.
  contributor:
    fullname: Uhlmann, E.
– volume: 111
  start-page: 934
  year: 1999
  ident: 000426764400008.11
  publication-title: Angew. Chem.
  contributor:
    fullname: Fischer, M.
– volume: 23
  start-page: 1517
  year: 2005
  ident: WOS:000233866300028
  article-title: Designing dendrimers for biological applications
  publication-title: NATURE BIOTECHNOLOGY
  doi: 10.1038/nbt1171
  contributor:
    fullname: Lee, CC
– volume: 97
  start-page: 801
  year: 1985
  ident: 000426764400008.34
  publication-title: Angew. Chem.
  contributor:
    fullname: Merrifield, R. B.
– volume: 23
  start-page: 13906
  year: 2017
  ident: WOS:000412595600013
  article-title: Combining Two Methods of Sequence Definition in a Convergent Approach: Scalable Synthesis of Highly Defined and Multifunctionalized Macromolecules
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201703877
  contributor:
    fullname: Solleder, SC
– volume: 138
  start-page: 9369
  year: 2016
  ident: WOS:000381062600009
  article-title: Iterative Exponential Growth Synthesis and Assembly of Uniform Diblock Copolymers
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/Jacs.6b04964
  contributor:
    fullname: Jiang, Y
– volume: 341
  start-page: 628
  year: 2013
  ident: WOS:000322884800029
  article-title: Sequence-Controlled Polymers
  publication-title: SCIENCE
  doi: 10.1126/science.1238149
  contributor:
    fullname: Lutz, JF
– volume: 5
  start-page: 990
  year: 2013
  ident: WOS:000327450500005
  article-title: POLYMER CHEMISTRY Macromolecules made to order
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/nchem.1806
  contributor:
    fullname: Schmidt, BVKJ
– volume: 116
  start-page: 10841
  year: 1994
  ident: WOS:A1994PT13000082
  article-title: SYNTHESIS OF SEQUENCE-SPECIFIC PHENYLACETYLENE OLIGOMERS ON AN INSOLUBLE SOLID SUPPORT
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: YOUNG, JK
– volume: 13
  start-page: 53
  year: 2007
  ident: WOS:000247236500008
  article-title: Solid-phase synthesis of modified oligonucleotides
  publication-title: INTERNATIONAL JOURNAL OF PEPTIDE RESEARCH AND THERAPEUTICS
  doi: 10.1007/s10989-006-9053-0
  contributor:
    fullname: Eritja, R
– volume: 129
  start-page: 6644
  year: 2017
  ident: 000426764400008.19
  publication-title: Angew. Chem.
  contributor:
    fullname: Huang, Z.
– volume: 11
  start-page: 6396
  year: 2017
  ident: WOS:000404808000124
  article-title: Molecular Switch for Sub-Diffraction Laser Lithography by Photoenol Intermediate-State Cis-Trans Isomerization
  publication-title: ACS NANO
  doi: 10.1021/acsnano.7b02820
  contributor:
    fullname: Mueller, P
– volume: 56
  start-page: 5877
  year: 2017
  ident: 000426764400008.47
  publication-title: Angew. Chem. Int. Ed.
  contributor:
    fullname: Xu, J.
– volume: 37
  start-page: 2797
  year: 1998
  ident: WOS:000076892300002
  article-title: PNA: Synthetic polyamide nucleic acids with unusual binding properties
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  contributor:
    fullname: Uhlmann, E
– volume: 85
  start-page: 2149
  year: 1963
  ident: WOS:A19633101B00025
  article-title: SOLID PHASE PEPTIDE SYNTHESIS .1. SYNTHESIS OF A TETRAPEPTIDE
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  contributor:
    fullname: MERRIFIELD, RB
– volume: 27
  start-page: ARTN 1604595
  year: 2017
  ident: WOS:000391926700015
  article-title: Identification-Tagging of Methacrylate-Based Intraocular Implants Using Sequence Defined Polyurethane Barcodes
  publication-title: ADVANCED FUNCTIONAL MATERIALS
  doi: 10.1002/adfm.201604595
  contributor:
    fullname: Karamessini, D
– volume: 129
  start-page: 5971
  year: 2017
  ident: 000426764400008.48
  publication-title: Angew. Chem.
  contributor:
    fullname: Xu, J.
– volume: 128
  start-page: 3993
  year: 2016
  ident: 000426764400008.15
  article-title: Triazine-based sequence- de- fined polymers with side- chain diversity and backbone- backbone interaction motifs
  publication-title: Angew Chem
  contributor:
    fullname: Grate, JW
– volume: 38
  start-page: 885
  year: 1999
  ident: WOS:000079641000002
  article-title: Dendrimers: From design to application - A progress report
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  contributor:
    fullname: Fischer, M
– volume: 6
  start-page: 229
  year: 2017
  ident: WOS:000397478700009
  article-title: Self-Reporting Fluorescent Step-Growth RAFT Polymers Based on Nitrile Imine-Mediated Tetrazole-ene Cycloaddition Chemistry
  publication-title: ACS MACRO LETTERS
  doi: 10.1021/acsmacrolett.7b00024
  contributor:
    fullname: Estupinan, D
– volume: 38
  start-page: ARTN 1700469
  year: 2017
  ident: WOS:000418413800002
  article-title: Click and Click-Inspired Chemistry for the Design of Sequence-Controlled Polymers
  publication-title: MACROMOLECULAR RAPID COMMUNICATIONS
  doi: 10.1002/marc.201700469
  contributor:
    fullname: Martens, S
– volume: 2
  start-page: 84
  year: 2010
  ident: WOS:000273820700009
  article-title: POLYMER CHEMISTRY A controlled sequence of events
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/nchem.530
  contributor:
    fullname: Lutz, JF
– volume: 24
  start-page: 799
  year: 1985
  ident: WOS:A1985AVC9200001
  article-title: SOLID-PHASE SYNTHESIS (NOBEL LECTURE)
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH
  contributor:
    fullname: MERRIFIELD, RB
– volume: 50
  start-page: 8290
  year: 2017
  ident: WOS:000413885100050
  article-title: MS-DECODER: Milliseconds Sequencing of Coded Polymers
  publication-title: MACROMOLECULES
  doi: 10.1021/acs.macromol.7b01737
  contributor:
    fullname: Burel, A
– volume: 129
  start-page: 7403
  year: 2017
  ident: 000426764400008.23
  publication-title: Angew. Chem.
  contributor:
    fullname: Konig, N. F.
– volume: 101
  start-page: 3219
  year: 2001
  ident: WOS:000171545400011
  article-title: beta-peptides: From structure to function
  publication-title: CHEMICAL REVIEWS
  doi: 10.1021/cr000045i
  contributor:
    fullname: Cheng, RP
– volume: 8
  start-page: 591
  year: 2016
  ident: WOS:000376529000016
  article-title: Sequence-defined bioactive macrocycles via an acid-catalysed cascade reaction
  publication-title: NATURE CHEMISTRY
  doi: 10.1038/NCHEM.2508
  contributor:
    fullname: Porel, M
– volume: 7
  start-page: ARTN 11064
  year: 2016
  ident: WOS:000372500000001
  article-title: A strategy for sequence control in vinyl polymers via iterative controlled radical cyclization
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/ncomms11064
  contributor:
    fullname: Hibi, Y
– volume: 56
  start-page: 7297
  year: 2017
  ident: WOS:000402857800055
  article-title: A Simple Post-Polymerization Modification Method for Controlling Side-Chain Information in Digital Polymers
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201702384
  contributor:
    fullname: Konig, NF
– volume: 125
  start-page: 13503
  year: 2013
  ident: 000426764400008.8
  publication-title: Angew. Chem.
  contributor:
    fullname: Espeel, P.
– volume: 6
  start-page: 5753
  year: 2015
  ident: WOS:000361212000050
  article-title: Synthesis of sequence-defined acrylate oligomers via photo-induced copper-mediated radical monomer insertions
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c5sc02035b
  contributor:
    fullname: Vandenbergh, J
– volume: 55
  start-page: 3925
  year: 2016
  ident: WOS:000372660400009
  article-title: Triazine-Based Sequence-Defined Polymers with Side-Chain Diversity and Backbone-Backbone Interaction Motifs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201509864
  contributor:
    fullname: Grate, JW
– volume: 48
  start-page: 2223
  year: 1992
  ident: WOS:A1992HJ78500001
  article-title: ADVANCES IN THE SYNTHESIS OF OLIGONUCLEOTIDES BY THE PHOSPHORAMIDITE APPROACH
  publication-title: TETRAHEDRON
  contributor:
    fullname: BEAUCAGE, SL
– volume: 52
  start-page: 13261
  year: 2013
  ident: WOS:000327802100020
  article-title: Multifunctionalized Sequence-Defined Oligomers from a Single Building Block
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201307439
  contributor:
    fullname: Espeel, P
– ident: e_1_2_2_40_2
  doi: 10.1039/C5SC02035B
– ident: e_1_2_2_20_3
  doi: 10.1002/ange.201509864
– ident: e_1_2_2_32_1
– ident: e_1_2_2_3_2
  doi: 10.1038/nchem.530
– ident: e_1_2_2_38_2
  doi: 10.1021/jacs.6b04964
– ident: e_1_2_2_22_2
  doi: 10.1002/ange.19850971004
– ident: e_1_2_2_23_1
– ident: e_1_2_2_19_2
  doi: 10.1039/C7PY00713B
– ident: e_1_2_2_51_2
  doi: 10.1021/acsnano.7b02820
– ident: e_1_2_2_18_3
  doi: 10.1002/ange.201702512
– ident: e_1_2_2_14_2
  doi: 10.1038/ncomms13672
– ident: e_1_2_2_45_2
  doi: 10.1002/anie.201307439
– ident: e_1_2_2_22_1
  doi: 10.1002/anie.198507993
– ident: e_1_2_2_47_2
  doi: 10.1021/acsnano.6b01333
– ident: e_1_2_2_11_2
  doi: 10.1002/marc.201700469
– ident: e_1_2_2_20_2
  doi: 10.1002/anie.201509864
– ident: e_1_2_2_36_1
– ident: e_1_2_2_26_1
  doi: 10.1021/cr990308c
– ident: e_1_2_2_24_2
  doi: 10.1021/cr000045i
– ident: e_1_2_2_25_3
  doi: 10.1002/(SICI)1521-3757(19981016)110:20<2954::AID-ANGE2954>3.0.CO;2-G
– ident: e_1_2_2_16_2
  doi: 10.1021/jacs.6b07120
– ident: e_1_2_2_44_1
– ident: e_1_2_2_45_3
  doi: 10.1002/ange.201307439
– ident: e_1_2_2_39_1
– ident: e_1_2_2_42_2
  doi: 10.1002/anie.201701659
– ident: e_1_2_2_46_3
  doi: 10.1002/ange.201702384
– ident: e_1_2_2_50_2
  doi: 10.1021/acsmacrolett.7b00024
– ident: e_1_2_2_7_2
  doi: 10.1002/anie.201509398
– ident: e_1_2_2_49_1
– ident: e_1_2_2_1_1
– ident: e_1_2_2_17_2
  doi: 10.1039/C4CC08756A
– ident: e_1_2_2_15_2
  doi: 10.1002/chem.201703877
– ident: e_1_2_2_27_1
– ident: e_1_2_2_2_2
  doi: 10.1038/natrevmats.2016.24
– ident: e_1_2_2_10_2
  doi: 10.1002/adfm.201604595
– ident: e_1_2_2_29_2
  doi: 10.1007/s10989-006-9053-0
– ident: e_1_2_2_34_2
  doi: 10.1126/science.8134834
– ident: e_1_2_2_28_2
  doi: 10.1016/S0040-4020(01)88752-4
– ident: e_1_2_2_25_2
  doi: 10.1002/(SICI)1521-3773(19981102)37:20<2796::AID-ANIE2796>3.0.CO;2-K
– ident: e_1_2_2_35_2
  doi: 10.1038/nbt1171
– ident: e_1_2_2_43_1
  doi: 10.1073/pnas.1508599112
– ident: e_1_2_2_48_1
– ident: e_1_2_2_46_2
  doi: 10.1002/anie.201702384
– ident: e_1_2_2_42_3
  doi: 10.1002/ange.201701659
– ident: e_1_2_2_5_2
  doi: 10.1038/ncomms11064
– ident: e_1_2_2_6_2
  doi: 10.1038/nchem.1806
– ident: e_1_2_2_33_3
  doi: 10.1002/(SICI)1521-3757(19990401)111:7<934::AID-ANGE934>3.0.CO;2-4
– ident: e_1_2_2_8_2
  doi: 10.1038/nchem.2508
– ident: e_1_2_2_12_2
  doi: 10.1002/marc.201600711
– ident: e_1_2_2_9_2
  doi: 10.1021/acs.macromol.7b01737
– ident: e_1_2_2_37_2
  doi: 10.1038/nchem.2346
– ident: e_1_2_2_41_2
  doi: 10.1039/C3CC45994B
– ident: e_1_2_2_4_2
  doi: 10.1126/science.1238149
– ident: e_1_2_2_7_3
  doi: 10.1002/ange.201509398
– ident: e_1_2_2_30_1
  doi: 10.1073/pnas.89.20.9367
– ident: e_1_2_2_13_1
– ident: e_1_2_2_33_2
  doi: 10.1002/(SICI)1521-3773(19990401)38:7<884::AID-ANIE884>3.0.CO;2-K
– ident: e_1_2_2_18_2
  doi: 10.1002/anie.201702512
– ident: e_1_2_2_21_1
  doi: 10.1021/ja00897a025
– ident: e_1_2_2_31_1
  doi: 10.1021/ja00102a082
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Snippet We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini three‐component...
We introduce the convergent synthesis of linear monodisperse sequence-defined oligomers through a unique approach, combining the Passerini three-component...
Abstract We introduce the convergent synthesis of linear monodisperse sequence‐defined oligomers through a unique approach, combining the Passerini...
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SubjectTerms Chains
Chemical synthesis
Chemistry
Chemistry, Multidisciplinary
Conjugation
convergent
Dienes
Ionization
Ions
Magnetic resonance spectroscopy
Mass spectrometry
Mass spectroscopy
multicomponent reactions
NMR spectroscopy
Oligomers
Photochemical reactions
Photochemicals
photochemistry
Physical Sciences
Science & Technology
Sebacic acid
sequence control
sequence-defined macromolecules
Switching
Title A Combined Photochemical and Multicomponent Reaction Approach to Precision Oligomers
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchem.201705939
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