{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,22]],"date-time":"2026-09-22T08:22:36Z","timestamp":1790065356678,"version":"4.0.1"},"reference-count":65,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2017,6,12]],"date-time":"2017-06-12T00:00:00Z","timestamp":1497225600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Top Curr Chem (Z)"],"published-print":{"date-parts":[[2017,8]]},"DOI":"10.1007\/s41061-017-0153-4","type":"journal-article","created":{"date-parts":[[2017,6,12]],"date-time":"2017-06-12T06:59:17Z","timestamp":1497250757000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":64,"title":["An Update on Isocyanide-Based Multicomponent Reactions in Polymer Science"],"prefix":"10.1007","volume":"375","author":[{"given":"Audrey","family":"Llevot","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andreas C.","family":"Boukis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stefan","family":"Oelmann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katharina","family":"Wetzel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4448-5279","authenticated-orcid":false,"given":"Michael A. R.","family":"Meier","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2017,6,12]]},"reference":[{"key":"153_CR1","volume-title":"Multicomponent reactions","author":"J Zhu","year":"2006","unstructured":"Zhu J, Bienaym\u00e9 H (2006) Multicomponent reactions. John Wiley, New Jersey"},{"key":"153_CR2","doi-asserted-by":"crossref","DOI":"10.1002\/9783527678174","volume-title":"Multicomponent reactions in organic synthesis","author":"J Zhu","year":"2014","unstructured":"Zhu J, Wang Q, Wang M (2014) Multicomponent reactions in organic synthesis. John Wiley, New Jersey"},{"key":"153_CR3","first-page":"25","volume":"75","author":"A Strecker","year":"1850","unstructured":"Strecker A (1850) Liebigs Ann Chem 75:25","journal-title":"Liebigs Ann Chem"},{"key":"153_CR4","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1002\/jlac.18540910309","volume":"91","author":"A Strecker","year":"1854","unstructured":"Strecker A (1854) Ueber einen neuen aus Aldehyd-Ammoniak und Blaus\u00e4ure entstehenden K\u00f6rper. Justus Liebigs Annalen der Chemie 91:349","journal-title":"Justus Liebigs Annalen der Chemie"},{"key":"153_CR5","first-page":"181","volume":"51","author":"M Passerini","year":"1921","unstructured":"Passerini M (1921) Isonitriles. II. Compounds with aldehydes or with ketones and monobasic organic acids. Gazz Chim Ital 51:181","journal-title":"Gazz Chim Ital"},{"key":"153_CR6","first-page":"386","volume":"71","author":"I Ugi","year":"1959","unstructured":"Ugi I (1959) Versuche mit Isonitrilen. Angew Chem Int Ed 71:386","journal-title":"Angew Chem Int Ed"},{"key":"153_CR7","first-page":"126","volume":"51","author":"M Passerini","year":"1921","unstructured":"Passerini M, Simone L (1921) Sopra gli isonitrili (I). Composto del p-isonitril-azobenzolo con acetone ed acido acetico. Gazz Chim 51:126","journal-title":"Gazz Chim"},{"key":"153_CR8","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1002\/ange.19600720709","volume":"72","author":"I Ugi","year":"1960","unstructured":"Ugi I, Steinbr\u00fcckner C (1960) \u00dcber ein neues Kondensations-Prinzip. Angew Chem 72:267","journal-title":"Angew Chem"},{"key":"153_CR9","doi-asserted-by":"crossref","first-page":"886","DOI":"10.1002\/cber.191004301151","volume":"43","author":"O Mumm","year":"1910","unstructured":"Mumm O (1910) Umsetzung von S\u00e4ureimidchloriden mit Salzen organischer S\u00e4uren und mit Cyankalium. Ber Dtsch Chem Ges 43:886","journal-title":"Ber Dtsch Chem Ges"},{"key":"153_CR10","doi-asserted-by":"crossref","first-page":"1790","DOI":"10.1021\/ja1113003","volume":"133","author":"O Kreye","year":"2011","unstructured":"Kreye O, T\u00f3th T, Meier MAR (2011) Introducing multicomponent reactions to polymer science: Passerini reactions of renewable monomers. J Am Chem Soc 133:1790","journal-title":"J Am Chem Soc"},{"key":"153_CR11","doi-asserted-by":"crossref","first-page":"1695","DOI":"10.1007\/s11426-015-5447-1","volume":"58","author":"X Jiang","year":"2015","unstructured":"Jiang X, Feng C, Lu G, Huang X (2015) Application of named reactions in polymer synthesis. Sci China Chem 58:1695","journal-title":"Sci China Chem"},{"key":"153_CR12","doi-asserted-by":"crossref","first-page":"8233","DOI":"10.1039\/C5PY01398D","volume":"6","author":"B Yang","year":"2015","unstructured":"Yang B, Zhao Y, Wei Y, Fu C, Tao L (2015) The Ugi reaction in polymer chemistry: syntheses, applications and perspectives. Polym Chem 6:8233","journal-title":"Polym Chem"},{"key":"153_CR13","first-page":"61","volume-title":"Multi-component and sequential reactions in polymer synthesis","author":"A Sehlinger","year":"2015","unstructured":"Sehlinger A, Meier MAR (2015) In: Theato P (ed) Multi-component and sequential reactions in polymer synthesis. Springer International, Cham, p 61"},{"key":"153_CR14","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1002\/anie.201305538","volume":"53","author":"R Kakuchi","year":"2014","unstructured":"Kakuchi R (2014) Multicomponent reactions in polymer synthesis. Angew Chem Int Ed 53:46","journal-title":"Angew Chem Int Ed"},{"key":"153_CR15","doi-asserted-by":"crossref","first-page":"3560","DOI":"10.1021\/ol101433v","volume":"12","author":"M Rubinshtein","year":"2010","unstructured":"Rubinshtein M, James CR, Young JL, Ma YJ, Kobayashi Y, Gianneschi NC, Yang J (2010) Facile procedure for generating side chain functionalized poly(\u03b1-hydroxy acid) copolymers from aldehydes via a versatile Passerini-type condensation. Org Lett 12:3560","journal-title":"Org Lett"},{"key":"153_CR16","doi-asserted-by":"crossref","first-page":"2207","DOI":"10.1002\/macp.201400187","volume":"215","author":"O Kreye","year":"2014","unstructured":"Kreye O, Trefzger C, Sehlinger A, Meier MAR (2014) Multicomponent reactions with a convertible isocyanide: efficient and versatile grafting of ADMET-derived polymers. Macromol Chem Phys 215:2207","journal-title":"Macromol Chem Phys"},{"key":"153_CR17","doi-asserted-by":"crossref","first-page":"2821","DOI":"10.1002\/macp.201300517","volume":"214","author":"A Sehlinger","year":"2013","unstructured":"Sehlinger A, de Espinosa LM, Meier MAR (2013) Synthesis of diverse asymmetric \u03b1,\u03c9-dienes via the Passerini three-component reaction for head-to-tail ADMET polymerization. Macromol Chem Phys 214:2821","journal-title":"Macromol Chem Phys"},{"key":"153_CR18","doi-asserted-by":"crossref","first-page":"6031","DOI":"10.1021\/ma401125j","volume":"46","author":"A Sehlinger","year":"2013","unstructured":"Sehlinger A, Kreye O, Meier MAR (2013) Tunable polymers obtained from Passerini multicomponent reaction derived acrylate monomers. Macromolecules 46:6031","journal-title":"Macromolecules"},{"key":"153_CR19","doi-asserted-by":"crossref","first-page":"44","DOI":"10.1039\/C4PY01147C","volume":"6","author":"S Schmidt","year":"2015","unstructured":"Schmidt S, Koldevitz M, Noy J-M, Roth PJ (2015) Multicomponent isocyanide-based synthesis of reactive styrenic and (meth)acrylic monomers and their RAFT (co)polymerization. Polym Chem 6:44","journal-title":"Polym Chem"},{"key":"153_CR20","doi-asserted-by":"crossref","first-page":"436","DOI":"10.1039\/C4PY01238K","volume":"6","author":"J-M Noy","year":"2015","unstructured":"Noy J-M, Koldevitz M, Roth PJ (2015) Thiol-reactive functional poly(meth)acrylates: multicomponent monomer synthesis, RAFT (co)polymerization and highly efficient thiol-para-fluoro postpolymerization modification. Polym Chem 6:436","journal-title":"Polym Chem"},{"key":"153_CR21","doi-asserted-by":"crossref","first-page":"1928","DOI":"10.1039\/C4PY01558D","volume":"6","author":"Y Pei","year":"2015","unstructured":"Pei Y, Noy J-M, Roth PJ, Lowe AB (2015) Thiol-reactive Passerini-methacrylates and polymorphic surface functional soft matter nanoparticles via ethanolic RAFT dispersion polymerization and post-synthesis modification. Polym Chem 6:1928","journal-title":"Polym Chem"},{"key":"153_CR22","doi-asserted-by":"crossref","first-page":"5787","DOI":"10.1039\/C4SM00729H","volume":"10","author":"Y Pei","year":"2014","unstructured":"Pei Y, Dharsana NC, van Hensbergen JA, Burford RP, Roth PJ, Lowe AB (2014) RAFT dispersion polymerization of 3-phenylpropyl methacrylate with poly[2-(dimethylamino)ethyl methacrylate] macro-CTAs in ethanol and associated thermoreversible polymorphism. Soft Matter 10:5787","journal-title":"Soft Matter"},{"key":"153_CR23","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1002\/ejlt.201200196","volume":"115","author":"M Czapiewski von","year":"2013","unstructured":"von Czapiewski M, Kreye O, Mutlu H, Meier MAR (2013) Cross-metathesis versus palladium-catalyzed C-H activation: Acetoxy ester functionalization of unsaturated fatty acid methyl esters. Eur J Lipid Sci Technol 115:76","journal-title":"Eur J Lipid Sci Technol"},{"key":"153_CR24","doi-asserted-by":"crossref","first-page":"359","DOI":"10.1016\/j.eurpolymj.2016.08.034","volume":"83","author":"M Czapiewski von","year":"2016","unstructured":"von Czapiewski M, Gugau K, Todorovic L, Meier MAR (2016) Synthesis of polyacrylates from limonene by catalytic oxidation and multi-component reaction. Eur Polym J 83:359","journal-title":"Eur Polym J"},{"key":"153_CR25","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1021\/ol102658d","volume":"13","author":"G Sabitha","year":"2011","unstructured":"Sabitha G, Nayak S, Bhikshapathi M, Yadav JS (2011) Palladium hydroxide catalyzed isomerization of primary allylic alcohols to aldehydes: application to the formal synthesis of (\u2212)-Brevisamide. Org Lett 13:382","journal-title":"Org Lett"},{"key":"153_CR26","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1016\/j.eurpolymj.2015.01.032","volume":"65","author":"A Sehlinger","year":"2015","unstructured":"Sehlinger A, Ochsenreither K, Bartnick N, Meier MAR (2015) Potentially biocompatible polyacrylamides derived by the Ugi four-component reaction. Eur Polym J 65:313","journal-title":"Eur Polym J"},{"key":"153_CR27","doi-asserted-by":"crossref","first-page":"2583","DOI":"10.1021\/bm100521x","volume":"11","author":"A Galperin","year":"2010","unstructured":"Galperin A, Long TJ, Ratner BD (2010) Degradable, thermo-sensitive poly(N-isopropyl acrylamide)-based scaffolds with controlled porosity for tissue engineering applications. Biomacromolecules 11:2583","journal-title":"Biomacromolecules"},{"key":"153_CR28","doi-asserted-by":"crossref","first-page":"925","DOI":"10.1002\/pi.4675","volume":"63","author":"H Kawaguchi","year":"2014","unstructured":"Kawaguchi H (2014) Thermoresponsive microhydrogels: preparation, properties and applications. Polym Int 63:925","journal-title":"Polym Int"},{"key":"153_CR29","doi-asserted-by":"crossref","first-page":"93","DOI":"10.1016\/B978-0-12-417136-7.00006-9","volume":"120","author":"T Vignaud","year":"2014","unstructured":"Vignaud T, Ennomani H, Th\u00e9ry M (2014) Polyacrylamide hydrogel micropatterning. Methods Cell Biol 120:93","journal-title":"Methods Cell Biol"},{"key":"153_CR30","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/j.eurpolymj.2014.07.022","volume":"59","author":"MP Algi","year":"2014","unstructured":"Algi MP, Okay O (2014) Highly stretchable self-healing poly(N,N-dimethylacrylamide) hydrogels. Eur Polym J 59:113","journal-title":"Eur Polym J"},{"key":"153_CR31","doi-asserted-by":"crossref","first-page":"98","DOI":"10.1002\/masy.201000098","volume":"311","author":"J Kienberger","year":"2012","unstructured":"Kienberger J, Kreutzwiesner E, Noormofidi N, Klarholz I, Harms C, Slugovc C (2012) Towards the antimicrobial finishing of poly(isoprene). Macromol Symposia 311:98","journal-title":"Macromol Symposia"},{"key":"153_CR32","doi-asserted-by":"crossref","first-page":"2236","DOI":"10.1002\/pola.26001","volume":"50","author":"J Kienberger","year":"2012","unstructured":"Kienberger J, Noormofidi N, M\u00fchlbacher I, Klarholz I, Harms C, Slugovc C (2012) Antimicrobial equipment of poly(isoprene) applying thiol-ene chemistry. J Polym Sci 50:2236","journal-title":"J Polym Sci"},{"key":"153_CR33","doi-asserted-by":"crossref","first-page":"1300","DOI":"10.1021\/mz300456p","volume":"1","author":"X-X Deng","year":"2012","unstructured":"Deng X-X, Li L, Li Z-L, Lv A, Du F-S, Li Z-C (2012) Sequence regulated poly(ester-amide)s based on Passerini reaction. ACS Macro Lett 1:1300","journal-title":"ACS Macro Lett"},{"key":"153_CR34","doi-asserted-by":"crossref","first-page":"444","DOI":"10.1039\/C2PY20927F","volume":"4","author":"Y-Z Wang","year":"2013","unstructured":"Wang Y-Z, Deng X-X, Li L, Li Z-L, Du F-S, Li Z-C (2013) One-pot synthesis of polyamides with various functional side groups via Passerini reaction. Polym Chem 4:444","journal-title":"Polym Chem"},{"key":"153_CR35","doi-asserted-by":"crossref","first-page":"9554","DOI":"10.1021\/ma402191r","volume":"46","author":"L-J Zhang","year":"2013","unstructured":"Zhang L-J, Deng X-X, Du F-S, Li Z-C (2013) Chemical synthesis of functional poly(4-hydroxybutyrate) with controlled degradation via intramolecular cyclization. Macromolecules 46:9554","journal-title":"Macromolecules"},{"key":"153_CR36","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1016\/j.eurpolymj.2013.10.019","volume":"50","author":"A Sehlinger","year":"2014","unstructured":"Sehlinger A, Schneider R, Meier MAR (2014) Passerini addition polymerization of an AB-type monomer\u2014a convenient route to versatile polyesters. Eur Polym J 50:150","journal-title":"Eur Polym J"},{"key":"153_CR37","doi-asserted-by":"crossref","first-page":"2592","DOI":"10.1021\/acs.macromol.6b00096","volume":"49","author":"J Zhang","year":"2016","unstructured":"Zhang J, Zhang M, Du F-S, Li Z-C (2016) Synthesis of functional polycaprolactones via Passerini multicomponent polymerization of 6-oxohexanoic acid and isocyanides. Macromolecules 49:2592","journal-title":"Macromolecules"},{"key":"153_CR38","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1016\/j.colsurfb.2014.12.030","volume":"126","author":"W Lin","year":"2015","unstructured":"Lin W, Guan X, Sun T, Huang Y, Jing X, Xie Z (2015) Reduction-sensitive amphiphilic copolymers made via multi-component Passerini reaction for drug delivery. Colloids Surf 126:217","journal-title":"Colloids Surf"},{"key":"153_CR39","doi-asserted-by":"crossref","first-page":"2774","DOI":"10.1021\/ma500504w","volume":"47","author":"A Sehlinger","year":"2014","unstructured":"Sehlinger A, Dannecker P-K, Kreye O, Meier MAR (2014) Diversely substituted polyamides: macromolecular design using the Ugi four-component reaction. Macromolecules 47:2774","journal-title":"Macromolecules"},{"key":"153_CR40","doi-asserted-by":"crossref","first-page":"1866","DOI":"10.1002\/marc.201400385","volume":"35","author":"A Sehlinger","year":"2014","unstructured":"Sehlinger A, Schneider R, Meier MA (2014) Ugi reactions with CO2: access to functionalized polyurethanes, polycarbonates, polyamides, and polyhydantoins. Macromol Rapid Commun 35:1866","journal-title":"Macromol Rapid Commun"},{"key":"153_CR41","doi-asserted-by":"crossref","first-page":"1680","DOI":"10.1002\/pola.27610","volume":"53","author":"N Gangloff","year":"2015","unstructured":"Gangloff N, Nahm D, D\u00f6ring L, Kuckling D, Luxenhofer R (2015) Polymerization via the Ugi-reaction using aromatic monomers. J Polym Sci 53:1680","journal-title":"J Polym Sci"},{"key":"153_CR42","doi-asserted-by":"crossref","first-page":"3272","DOI":"10.1039\/C6GC00372A","volume":"18","author":"M Hartweg","year":"2016","unstructured":"Hartweg M, Becer CR (2016) Direct polymerization of levulinic acid via Ugi multicomponent reaction. Green Chem 18:3272","journal-title":"Green Chem"},{"key":"153_CR43","doi-asserted-by":"crossref","first-page":"1049","DOI":"10.1021\/acsmacrolett.6b00530","volume":"5","author":"X Zhang","year":"2016","unstructured":"Zhang X, Wang S, Liu J, Xie Z, Luan S, Xiao C, Tao Y, Wang X (2016) Ugi reaction of natural amino acids: a general route toward facile synthesis of polypeptoids for bioapplications. ACS Macro Lett 5:1049","journal-title":"ACS Macro Lett"},{"key":"153_CR44","doi-asserted-by":"crossref","first-page":"317","DOI":"10.1002\/marc.201300779","volume":"35","author":"O Kreye","year":"2014","unstructured":"Kreye O, Kugele D, Faust L, Meier MAR (2014) Divergent dendrimer synthesis via the Passerini three-component reaction and olefin cross-metathesis. Macromol Rapid Commun 35:317","journal-title":"Macromol Rapid Commun"},{"key":"153_CR45","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1021\/mz500207z","volume":"3","author":"X-X Deng","year":"2014","unstructured":"Deng X-X, Du F-S, Li Z-C (2014) Combination of orthogonal ABB and ABC multicomponent reactions toward efficient divergent synthesis of dendrimers with structural diversity. ACS Macro Lett 3:667","journal-title":"ACS Macro Lett"},{"key":"153_CR46","unstructured":"Wessjohann L, Henze M, Kreye O, Rivera D (2013) WO Patent 134,607, 2011. European Patent 2563847"},{"key":"153_CR47","doi-asserted-by":"crossref","first-page":"3292","DOI":"10.1021\/ol301263v","volume":"14","author":"J-A Jee","year":"2012","unstructured":"Jee J-A, Spagnuolo LA, Rudick JG (2012) Convergent synthesis of dendrimers via the Passerini three-component reaction. Org Lett 14:3292","journal-title":"Org Lett"},{"key":"153_CR48","doi-asserted-by":"crossref","first-page":"5456","DOI":"10.1039\/C4CC10091C","volume":"51","author":"J-A Jee","year":"2015","unstructured":"Jee J-A, Song S, Rudick JG (2015) Enhanced reactivity of dendrons in the Passerini three-component reaction. Chem Commun 51:5456","journal-title":"Chem Commun"},{"key":"153_CR49","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1071\/CH13450","volume":"67","author":"X-X Deng","year":"2014","unstructured":"Deng X-X, Cui Y, Wang Y-Z, Du F-S, Li Z-C (2014) Graft copolymers with polyamide backbones via combination of Passerini multicomponent polymerization and controlled chain-growth polymerization. Aust J Chem 67:555","journal-title":"Aust J Chem"},{"key":"153_CR50","doi-asserted-by":"crossref","first-page":"865","DOI":"10.1002\/pola.26443","volume":"51","author":"L Li","year":"2013","unstructured":"Li L, Kan X-W, Deng X-X, Song C-C, Du F-S, Li Z-C (2013) Simultaneous dual end-functionalization of PEG via the Passerini three-component reaction for the synthesis of ABC miktoarm terpolymers. J Polym Sci 51:865","journal-title":"J Polym Sci"},{"key":"153_CR51","doi-asserted-by":"crossref","first-page":"1857","DOI":"10.1039\/C5PY02030A","volume":"7","author":"S Oelmann","year":"2016","unstructured":"Oelmann S, Solleder SC, Meier MAR (2016) Controlling molecular weight and polymer architecture during the Passerini three component step-growth polymerization. Polym Chem 7:1857","journal-title":"Polym Chem"},{"key":"153_CR52","doi-asserted-by":"crossref","first-page":"13010","DOI":"10.1002\/anie.201406766","volume":"53","author":"H Mutlu","year":"2014","unstructured":"Mutlu H, Lutz J-F (2014) Reading polymers: sequencing of natural and synthetic macromolecules. Angew Chem Int Ed 53:13010","journal-title":"Angew Chem Int Ed"},{"key":"153_CR53","doi-asserted-by":"crossref","first-page":"3383","DOI":"10.1039\/b806413j","volume":"38","author":"N Badi","year":"2009","unstructured":"Badi N, Lutz J-F (2009) Sequence control in polymer synthesis. Chem Soc Rev 38:3383","journal-title":"Chem Soc Rev"},{"key":"153_CR54","doi-asserted-by":"crossref","first-page":"1651","DOI":"10.1007\/s11426-015-5476-9","volume":"58","author":"C Qu","year":"2015","unstructured":"Qu C, He J (2015) Recent developments in the synthesis of sequence controlled polymers. Sci China Chem 58:1651","journal-title":"Sci China Chem"},{"key":"153_CR55","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1038\/nchem.1958","volume":"6","author":"H Colquhoun","year":"2014","unstructured":"Colquhoun H, Lutz J-F (2014) Information-containing macromolecules. Nat Chem 6:455","journal-title":"Nat Chem"},{"key":"153_CR56","doi-asserted-by":"crossref","first-page":"2025","DOI":"10.1002\/chem.200701223","volume":"14","author":"L Hartmann","year":"2008","unstructured":"Hartmann L, H\u00e4fele S, Peschka-S\u00fcss R, Antonietti M, B\u00f6rner HG (2008) Tailor-made poly(amidoamine)s for controlled complexation and condensation of DNA. Chemistry 14:2025","journal-title":"Chemistry"},{"key":"153_CR57","doi-asserted-by":"crossref","first-page":"4742","DOI":"10.1021\/ja2004494","volume":"133","author":"T Terashima","year":"2011","unstructured":"Terashima T, Mes T, De Greef TFA, Gillissen MAJ, Besenius P, Palmans ARA, Meijer EW (2011) Single-chain folding of polymers for catalytic systems in water. J Am Chem Soc 133:4742","journal-title":"J Am Chem Soc"},{"key":"153_CR58","doi-asserted-by":"crossref","first-page":"1734","DOI":"10.1007\/s11426-015-5448-0","volume":"58","author":"L Yang","year":"2015","unstructured":"Yang L, Zhang Z, Cheng B, You Y, Wu D, Hong C (2015) Two tandem multicomponent reactions for the synthesis of sequence-defined polymers. Sci China Chem 58:1734","journal-title":"Sci China Chem"},{"key":"153_CR59","doi-asserted-by":"crossref","first-page":"711","DOI":"10.1002\/anie.201308960","volume":"53","author":"SC Solleder","year":"2014","unstructured":"Solleder SC, Meier MAR (2014) Sequence control in polymer chemistry through the Passerini three-component reaction. Angew Chem Int Ed 53:711","journal-title":"Angew Chem Int Ed"},{"key":"153_CR60","doi-asserted-by":"crossref","first-page":"3201","DOI":"10.1039\/C5PY00424A","volume":"6","author":"SC Solleder","year":"2015","unstructured":"Solleder SC, Wetzel KS, Meier MAR (2015) Dual side chain control in the synthesis of novel sequence-defined oligomers through the Ugi four-component reaction. Polym Chem 6:3201","journal-title":"Polym Chem"},{"key":"153_CR61","doi-asserted-by":"crossref","first-page":"1204","DOI":"10.1002\/anie.201509398","volume":"55","author":"SC Solleder","year":"2016","unstructured":"Solleder SC, Zengel D, Wetzel KS, Meier MAR (2016) A scalable and high-yield strategy for the synthesis of sequence-defined macromolecules. Angew Chem Int Ed 55:1204","journal-title":"Angew Chem Int Ed"},{"key":"153_CR62","doi-asserted-by":"crossref","first-page":"3828","DOI":"10.1039\/C5PY00392J","volume":"6","author":"A Sehlinger","year":"2015","unstructured":"Sehlinger A, Verbraeken B, Meier MAR, Hoogenboom R (2015) Versatile side chain modification via isocyanide-based multicomponent reactions: tuning the LCST of poly(2-oxazoline)s. Polym Chem 6:3828","journal-title":"Polym Chem"},{"key":"153_CR63","doi-asserted-by":"crossref","first-page":"4263","DOI":"10.1039\/C6PY00734A","volume":"7","author":"L Xue","year":"2016","unstructured":"Xue L, Xiong X, Chen K, Luan Y, Chen G, Chen H (2016) Modular synthesis of glycopolymers with well-defined sugar units in the side chain via Ugi reaction and click chemistry: hetero vs. homo. Polym Chem 7:4263","journal-title":"Polym Chem"},{"key":"153_CR64","doi-asserted-by":"crossref","first-page":"2704","DOI":"10.1039\/C4PY00001C","volume":"5","author":"B Yang","year":"2014","unstructured":"Yang B, Zhao Y, Fu C, Zhu C, Zhang Y, Wang S, Wei Y, Tao L (2014) Introducing the Ugi reaction into polymer chemistry as a green click reaction to prepare middle-functional block copolymers. Polym Chem 5:2704","journal-title":"Polym Chem"},{"key":"153_CR65","doi-asserted-by":"crossref","first-page":"4867","DOI":"10.1039\/C6PY00781C","volume":"7","author":"H Wu","year":"2016","unstructured":"Wu H, Yang B, Zhao Y, Wei Y, Wang Z, Wang X, Tao L (2016) Fluorescent protein-reactive polymers via one-pot combination of the Ugi reaction and RAFT polymerization. Polym Chem 7:4867","journal-title":"Polym Chem"}],"container-title":["Topics in Current Chemistry"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s41061-017-0153-4\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s41061-017-0153-4.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s41061-017-0153-4.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,6,24]],"date-time":"2024-06-24T18:29:55Z","timestamp":1719253795000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s41061-017-0153-4"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,6,12]]},"references-count":65,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2017,8]]}},"alternative-id":["153"],"URL":"https:\/\/doi.org\/10.1007\/s41061-017-0153-4","relation":{},"ISSN":["2365-0869","2364-8961"],"issn-type":[{"value":"2365-0869","type":"print"},{"value":"2364-8961","type":"electronic"}],"subject":[],"published":{"date-parts":[[2017,6,12]]},"article-number":"66"}}