Rutjes, F. P. J. T. : 2022 Science of Synthesis, 2021/4: Click Chemistry DOI: 10.1055/sos-SD-235-00003
Click Chemistry

2.1 Introduction to CuAAC

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Book

Editor: Rutjes, F. P. J. T.

Authors: Agrahari, A. K.; Alabugin, I. V. ; Beke-Somfai, T. ; Blanco-Ania, D. ; Bratlie, K. M. ; Carlson, J. C. T. ; Friscourt, F. ; Giel, M.-C. ; Harris, T. ; Houk, K. N. ; Janssen, L. J. N.; Kacprzak, K. M.; Kann, N. ; Kovalová, A.; Kuba, W. ; La Venia, A.; Liskamp, R. M. J. ; Meuleman, T. J.; Mikula, H. ; Mishra, A.; Moses, J. E. ; Ort, F. F.; Page, K. M.; Paterson, A. J. ; Rutkowski, J.; Singh, R.; Sinha, A. K.; Skiera, I.; Smedley, C. J. ; Svatunek, D. ; Tiwari, V. K. ; van Hest, J. C. M. ; Vrabel, M. ; Wilkovitsch, M. ; Xu, Z.; Zhang, C.

Title: Click Chemistry

Print ISBN: 9783132435568; Online ISBN: 9783132435575; Book DOI: 10.1055/b000000077

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Reference Libraries



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Type: Multivolume Edition

 


F. F. Ort; F. P. J. T. Rutjes

Abstract

The basic principles of the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), widely considered to be the first click reaction, are described. This involves amongst others the concept of click reactions, the mechanism of CuAAC, the synthesis and reactivity of organic azides and acetylenes, an overview of most commonly used copper(I) catalysts and ligands, the properties of 1,2,3-triazoles and their resemblance to amides, and a general overview of the scope and limitations of this reaction.

 
  • 3 Himo F, Lovell T, Hilgraf R, Rostovtsev VV, Noodleman L, Sharpless KB, Fokin VV. J. Am. Chem. Soc.. 2005; 127: 210
  • 4 Huisgen R. Angew. Chem. Int. Ed. Engl.. 1963; 2: 633
  • 10 Breugst M, Reissig H.-U. Angew. Chem. Int. Ed.. 2020; 59: 12293
  • 11 Danese M, Bon M, Piccini G, Passerone D. Phys. Chem. Chem. Phys.. 2019; 21: 19281
  • 12 Padwa A, Comprehensive Organic Synthesis. Trost BM, Fleming I. Pergamon; Oxford 1991. Vol. 4, pp 1069–1109.
  • 13 Tornøe CW, Christensen C, Meldal M. J. Org. Chem.. 2002; 67: 3057
  • 14 Rostovtsev VV, Green LG, Fokin VV, Sharpless KB. Angew. Chem. Int. Ed.. 2002; 41: 2596
  • 15 Johansson JR, Beke-Somfai T, Said Stålsmeden A, Kann N. Chem. Rev.. 2016; 116: 14726
  • 16 Zhang L, Chen X, Xue P, Sun HHY, Williams ID, Sharpless KB, Fokin VV, Jia G. J. Am. Chem. Soc.. 2005; 127: 15998
  • 17 Meng X, Xu X, Gao T, Chen B. Eur. J. Org. Chem.. 2010; 5409
  • 18 Luo Q, Jia G, Sun J, Lin Z. J. Org. Chem.. 2014; 79: 11970
  • 19 Hong L, Lin W, Zhang F, Liu R, Zhou X. Chem. Commun. (Cambridge). 2013; 49: 5589
  • 20 Banerji B, Chandrasekhar K, Killi SK, Pramanik SK, Uttam P, Sen S, Maiti NC. R. Soc. Open Sci.. 2016; 3: 160090
  • 22 Díaz Arado O, Mönig H, Wagner H, Franke J.-H, Langewisch G, Held PA, Studer A, Fuchs H. ACS Nano. 2013; 7: 8509
  • 23 Gomes RS, Jardim GAM, de Carvalho RL, Araujo MH, da Silva Júnior EN. Tetrahedron. 2019; 75: 3697
  • 24 Worrell BT, Malik JA, Fokin VV. Science (Washington, D. C.). 2013; 340: 457
  • 25 Jin L, Tolentino DR, Melaimi M, Bertrand G. Sci. Adv.. 2015; 1: e1 500 304
  • 26 Iacobucci C, Reale S, Gal J.-F, De Angelis F. Angew. Chem. Int. Ed.. 2015; 54: 3065
  • 27 Nolte C, Mayer P, Straub BF. Angew. Chem. Int. Ed.. 2007; 46: 2101
  • 28 El Ayouchia HB, Bahsis L, Anane H, Domingo LR, Stiriba S.-E. RSC Adv.. 2018; 8: 7670
  • 31 Garratt PJ, Comprehensive Heterocyclic Chemistry II. Katritzky AR, Rees CW, Scriven EFV. Pergamon; Oxford 1996. pp 127–163.
  • 32 Albert A, Taylor PJ. J. Chem. Soc., Perkin Trans. 2. 1989; 1903
  • 33 Rachwal S, Katritzky AR, Comprehensive Heterocyclic Chemistry III. Katritzky AR, Ramsden CA, Scriven EFV, Taylor RJK. Elsevier; Oxford 2008. pp 1–158.
  • 34 Curtis ADM, Jennings N, Comprehensive Heterocyclic Chemistry III. Katritzky AR, Ramsden CA, Scriven EFV, Taylor RJK. Elsevier; Oxford 2008. 159–209.
  • 35 Kashyap A, Silakari O, Key Heterocycle Cores for Designing Multitargeting Molecules. Silakari O. Elsevier; 2018. 323–342.
  • 36 Ram VJ, Sethi A, Nath M, Pratap R, The Chemistry of Heterocycles. Ram VJ, Sethi A, Nath M, Pratap R. Elsevier; 2019. 149–478.
  • 37 Schulze B, Schubert US. Chem. Soc. Rev.. 2014; 43: 2522
  • 38 Cyrański MK, Schleyer PvR, Krygowski TM, Jiao H, Hohlneicher G. Tetrahedron. 2003; 59: 1657
  • 39 Vianello R, Maksić ZB. Mol. Phys.. 2005; 103: 209
  • 40 Palmer MH, Findlay RH, Gaskell AJ. J. Chem. Soc., Perkin Trans. 2. 1974; 420
  • 41 Jug K, Chiodo S, Calaminici P, Avramopoulos A, Papadopoulos MG. J. Phys. Chem. A. 2003; 107: 4172
  • 42 Begtrup M, Nielsen C, Nygaard L, Samdal S, Sjøgren C, Sørensen G, Khan S, Vilkov L, Rypdal K. Acta Chem. Scand.. 1988; 42: 500
  • 43 Kolb HC, Sharpless KB. Drug Discovery Today. 2003; 8: 1128
  • 44 Catalán J, Sánchez-Cabezudo M, De Paz JLG, Elguero J, Taft RW, Anvia F. J. Comput. Chem.. 1989; 10: 426
  • 45 Tomás F, Abboud J.-LM, Laynez J, Notario R, Santos L, Nilsson SO, Catalán J, Claramunt RM, Elguero J. J. Am. Chem. Soc.. 1989; 111: 7348
  • 46 Matulis VE, Halauko YS, Ivashkevich OA, Gaponik PN. THEOCHEM. 2009; 909: 19
  • 47 Shen K, Fu Y, Li J.-N, Liu L, Guo Q.-X. Tetrahedron. 2007; 63: 1568
  • 48 Fombona S, Pérez J, Díaz J, Riera L. Chem.–Eur. J.. 2017; 23: 17870
  • 49 Massarotti A, Aprile S, Mercalli V, Del Grosso E, Grosa G, Sorba G, Tron GC. ChemMedChem. 2014; 9: 2497
  • 50 Dheer D, Singh V, Shankar R. Bioorg. Chem.. 2017; 71: 30
  • 51 Cappel NO, Fernelius WC. J. Org. Chem.. 1940; 5: 40
  • 53 Burton DE, Lambie AJ, Lane DWJ, Newbold GT, Percival A. J. Chem. Soc. C. 1968; 1268
  • 54 Bozorov K, Zhao J, Aisa HA. Bioorg. Med. Chem.. 2019; 27: 3511
  • 55 Agalave SG, Maujan SR, Pore VS. Chem.–Asian J.. 2011; 6: 2696
  • 56 Kharb R, Sharma PC, Yar MS. J. Enzyme Inhib. Med. Chem.. 2011; 26: 1
  • 57 Jain A, Piplani P. Mini-Rev. Med. Chem.. 2019; 19: 1298
  • 58 Rani A, Singh G, Singh A, Maqbool U, Kaur G, Singh J. RSC Adv.. 2020; 10: 5610
  • 60 Mohammed I, Kummetha IR, Singh G, Sharova N, Lichinchi G, Dang J, Stevenson M, Rana TM. J. Med. Chem.. 2016; 59: 7677
  • 61 Bi F, Ji S, Venter H, Liu J, Semple SJ, Ma S. Bioorg. Med. Chem. Lett.. 2018; 28: 884
  • 62 Bonandi E, Christodoulou MS, Fumagalli G, Perdicchia D, Rastelli G, Passarella D. Drug Discovery Today. 2017; 22: 1572
  • 63 Doiron JE, Le CA, Bacsa J, Breton GW, Martin KL, Aller SG, Turlington M. ChemMedChem. 2020; 15: 1720
  • 64 Bräse S, Lesch B, Zimmermann V. Science of Synthesis. 2010; 41: 543
  • 65 Bräse S, Keck D. Science of Synthesis. 2007; 31: 1827
  • 67 Ghosh AK, Sarkar A, Brindisi M. Org. Biomol. Chem.. 2018; 16: 2006
  • 68 Fringuelli F, Piermatti O, Pizzo F, Vaccaro L. J. Org. Chem.. 1999; 64: 6094
  • 69 Guerin DJ, Horstmann TE, Miller SJ. Org. Lett.. 1999; 1: 1107
  • 70 Barral K, Moorhouse AD, Moses JE. Org. Lett.. 2007; 9: 1809
  • 71 Goddard-Borger ED, Stick RV. Org. Lett.. 2007; 9: 3797
  • 72 Smith MB. Organic Synthesis. Academic; Boston 2017. 309–418.
  • 73 Name Reactions for Functional Group Transformations. Li JJ, Corey EJ. Wiley; Hoboken, NJ 2007. 85–158.
  • 74 Conrow RE, Dean WD. Org. Process Res. Dev.. 2008; 12: 1285
  • 75 Kolb HC, Finn MG, Sharpless KB. Angew. Chem. Int. Ed.. 2001; 40: 2004
  • 76 Bräse S, Gil C, Knepper K, Zimmermann V. Angew. Chem. Int. Ed.. 2005; 44: 5188
  • 77 Synthesizing, Purifying, and Handling Organic Azides, University of California, Santa Barbara; available online at www.ehs.ucsb.edu/files/docs/ls/factsheets/Azides_FS26.pdf (accessed July 2021).
  • 78 Azide Compounds, Forida State University; available online at safety.fsu.edu/safety_manual/Azide%20Compounds.pdf (accessed July 2021).
  • 79 Information on Azide Compounds, Stanford University; available online at ehs.stanford.edu/reference/information-azide-compounds (accessed July 2021).
  • 80 Keicher T, Löbbecke S, Organic Azides: Syntheses and Applications. Bräse S, Banert K. Wiley; Chichester, UK 2010. pp  1–27.
  • 81 Safe Handling of Sodium Azide, Environment, Health and Safety Department, University of Wisconsin-Madison; available online at ehs.wisc.edu/wp-content/uploads/sites/25/2017/01/SafeHandlingOfSodiumAzide.pdf (accessed July 2021).
  • 82 Shaw R, Elagamy A, Althagafi I, Pratap R. Org. Biomol. Chem.. 2020; 18: 3797
  • 84 Bruice PY. Organic Chemistry. Pearson; Boston 2014
  • 85 Crabtree RH. The Organometallic Chemistry of the Transition Metals. Wiley; Hoboken, NJ 2014. 134–139, 405.
  • 86 Rolla G, De Biasio V, Giovenzana GB, Botta M, Tei L. Dalton Trans.. 2018; 47: 10660
  • 87 Shenawi-Khalil S, Sonavane SU, Sasson Y. Tetrahedron Lett.. 2012; 53: 2295
  • 89 Rej S, Pramanik S, Tsurugi H, Mashima K. Chem. Commun. (Cambridge). 2017; 53: 13157
  • 91 Desai NB, McKelvie N, Ramirez F. J. Am. Chem. Soc.. 1962; 84: 1745
  • 92 Offenbacher AR, Zhu H, Klinman JP. Tetrahedron Lett.. 2016; 57: 4537
  • 93 Huh DH, Jeong JS, Lee HB, Ryu H, Kim YG. Tetrahedron. 2002; 58: 9925
  • 94 Van Hijfte L, Kolb M, Witz P. Tetrahedron Lett.. 1989; 30: 3655
  • 95 Beshai M, Dhudshia B, Mills R, Thadani AN. Tetrahedron Lett.. 2008; 49: 6794
  • 96 Colvin EW, Hamill BJ. J. Chem. Soc., Chem. Commun.. 1973; 151
  • 97 Colvin EW, Hamill BJ. J. Chem. Soc., Perkin Trans. 1. 1977; 869
  • 98 Habrant D, Rauhala V, Koskinen AMP. Chem. Soc. Rev.. 2010; 39: 2007
  • 99 Roth GJ, Liepold B, Muller SG, Bestmann HJ. Synthesis. 2004; 59
  • 100 Baldwin JE, Bonacorsi SJ, Burrell RC. J. Org. Chem.. 1998; 63: 4721
  • 101 Libman NM, Kuznetsov SG, Gorchakov VS, Golikov SN, Lebedeva BP. Pharm. Chem. J.. 1986; 20: 759
  • 102 Kim SH, Park SH, Choi JH, Chang S. Chem.–Asian J.. 2011; 6: 2618
  • 103 Hein JE, Tripp JC, Krasnova LB, Sharpless KB, Fokin VV. Angew. Chem. Int. Ed.. 2009; 48: 8018
  • 104 Meldal M, Tornøe CW. Chem. Rev.. 2008; 108: 2952
  • 105 Chassaing S, Bénéteau V, Pale P. Catal. Sci. Technol.. 2016; 6: 923
  • 106 Alonso F, Moglie Y, Radivoy G. Acc. Chem. Res.. 2015; 48: 2516
  • 107 Diez-Gonzalez S. Curr. Org. Chem.. 2011; 15: 2830
  • 108 Hein JE, Fokin VV. Chem. Soc. Rev.. 2010; 39: 1302
  • 110 Caprioglio D, Torretta S, Ferrari M, Travelli C, Grolla AA, Condorelli F, Genazzani AA, Minassi A. Bioorg. Med. Chem.. 2016; 24: 140
  • 111 Alho DPS, Salvador JAR, Cascante M, Marin S. Molecules. 2019; 24: 766
  • 112 Huo J, Lin C, Liang J. React. Funct. Polym.. 2020; 152: 104531
  • 113 Eissa AM, Khosravi E. Eur. Polym. J.. 2011; 47: 61
  • 114 Yoo EJ, Ahlquist M, Bae I, Sharpless KB, Fokin VV, Chang S. J. Org. Chem.. 2008; 73: 5520
  • 115 Yoo EJ, Ahlquist M, Kim SH, Bae I, Fokin VV, Sharpless KB, Chang S. Angew. Chem. Int. Ed.. 2007; 46: 1730
  • 117 Cassidy MP, Raushel J, Fokin VV. Angew. Chem. Int. Ed.. 2006; 45: 3154
  • 118 Yoo EJ, Park SH, Lee SH, Chang S. Org. Lett.. 2009; 11: 1155
  • 119 Xu X, Cheng D, Li J, Guo H, Yan J. Org. Lett.. 2007; 9: 1585
  • 120 Kislukhin AA, Hong VP, Breitenkamp KE, Finn MG. Bioconjugate Chem.. 2013; 24: 684
  • 121 Bertrand P, Gesson JP. J. Org. Chem.. 2007; 72: 3596
  • 122 Wang D, Chen S, Chen B. Tetrahedron Lett.. 2014; 55: 7026
  • 124 Morris JC, Chiche J, Grellier C, Lopez M, Bornaghi LF, Maresca A, Supuran CT, Pouysségur J, Poulsen S.-A. J. Med. Chem.. 2011; 54: 6905
  • 125 Worrell BT, Hein JE, Fokin VV. Angew. Chem. Int. Ed.. 2012; 51: 11791
  • 126 Witulski B, Alayrac C. Science of Synthesis. 2006; 24: 905
  • 127 Rao DS, Reddy TR, Kashyap S. Org. Biomol. Chem.. 2018; 16: 1508
  • 128 Meng L.-G, Cai P.-J, Guo Q.-X, Xue S. Synth. Commun.. 2008; 38: 225
  • 129 Yao M, Zhang J, Yang S, Liu E, Xiong H. Synlett. 2020; 31: 1102
  • 130 Sun J, Kozmin SA. J. Am. Chem. Soc.. 2005; 127: 13512
  • 131 Shi W, Guan Z, Cai P, Chen H. J. Catal.. 2017; 353: 199
  • 132 Yao M, Zhang J, Yang S, Xiong H, Li L, Liu E, Shi H. RSC Adv.. 2020; 10: 3946
  • 133 Chan TR, Hilgraf R, Sharpless KB, Fokin VV. Org. Lett.. 2004; 6: 2853
  • 134 Berg R, Straub BF. Beilstein J. Org. Chem.. 2013; 9: 2715
  • 135 Sindhu J, Singh H, Khurana JM, Bhardwaj JK, Saraf P, Sharma C. Med. Chem. Res.. 2016; 25: 1813
  • 136 Nagesh HN, Suresh A, Reddy MN, Suresh N, Subbalakshmi J, Chandra Sekhar KVG. RSC Adv.. 2016; 6: 15884
  • 137 Shin J.-A, Oh S.-J, Lee H.-Y, Lim Y.-G. Catal. Sci. Technol.. 2017; 7: 2450
  • 138 Díaz Velázquez H, Ruiz García Y, Vandichel M, Madder A, Verpoort F. Org. Biomol. Chem.. 2014; 12: 9350
  • 140 Liu P.-Y, Jiang N, Zhang J, Wei X, Lin H.-H, Yu X.-Q. Chem. Biodiversity. 2006; 3: 958
  • 141 Hong V, Presolski SI, Ma C, Finn MG. Angew. Chem. Int. Ed.. 2009; 48: 9879
  • 143 Li S, Cai H, He J, Chen H, Lam S, Cai T, Zhu Z, Bark SJ, Cai C. Bioconjugate Chem.. 2016; 27: 2315
  • 144 Dirks AJ, Cornelissen JJLM, Nolte RJM. Bioconjugate Chem.. 2009; 20: 1129
  • 145 El-Sagheer AH, Brown T. J. Am. Chem. Soc.. 2009; 131: 3958
  • 146 Kočalka P, El-Sagheer AH, Brown T. ChemBioChem. 2008; 9: 1280
  • 147 Kumar R, El-Sagheer A, Tumpane J, Lincoln P, Wilhelmsson LM, Brown T. J. Am. Chem. Soc.. 2007; 129: 6859
  • 148 Reddy KR, Rajgopal K, Kantam ML. Synlett. 2006; 957
  • 149 Brotherton WS, Michaels HA, Simmons JT, Clark RJ, Dalal NS, Zhu L. Org. Lett.. 2009; 11: 4954
  • 150 Gonzalez-Silva K, Rendon-Nava D, Alvarez-Hernández A, Mendoza-Espinosa D. New J. Chem.. 2019; 43: 16538
  • 151 Kuijpers BHM, Groothuys S, Keereweer AR, Quaedflieg PJLM, Blaauw RH, van Delft FL, Rutjes FPJT. Org. Lett.. 2004; 6: 3123
  • 152 Adzima BJ, Tao Y, Kloxin CJ, DeForest CA, Anseth KS, Bowman CN. Nature Chem.. 2011; 3: 256
  • 153 Arslan M, Yilmaz G, Yagci Y. Polym. Chem.. 2015; 6: 8168
  • 154 Dadashi-Silab S, Yagci Y. Tetrahedron Lett.. 2015; 56: 6440
  • 155 Sandmann B, Happ B, Vitz J, Hager MD, Burtscher P, Moszner N, Schubert US. Polym. Chem.. 2013; 4: 3938
  • 156 Arslan M, Bicak TC, Pulido BA, Nunes SP, Yagci Y. Eur. Polym. J.. 2018; 100: 298
  • 157 Yilmaz G, Iskin B, Yagci Y. Macromol. Chem. Phys.. 2014; 215: 662
  • 158 Tasdelen MA, Yagci Y. Angew. Chem. Int. Ed.. 2013; 52: 5930
  • 160 Taskin OS, Yilmaz G, Yagci Y. ACS Macro Lett.. 2016; 5: 103
  • 161 Chen RT, Marchesan S, Evans RA, Styan KE, Such GK, Postma A, McLean KM, Muir BW, Caruso F. Biomacromolecules. 2012; 13: 889
  • 162 Devaraj NK, Dinolfo PH, Chidsey CED, Collman JP. J. Am. Chem. Soc.. 2006; 128: 1794
  • 163 Ku S.-Y, Wong K.-T, Bard AJ. J. Am. Chem. Soc.. 2008; 130: 2392
  • 164 Lhenry S, Leroux YR, Orain C, Conan F, Cosquer N, Le Poul N, Reinaud O, Le Mest Y, Hapiot P. Langmuir. 2014; 30: 4501
  • 165 Shida N, Ishiguro Y, Atobe M, Fuchigami T, Inagi S. ACS Macro Lett.. 2012; 1: 656
  • 166 Rydzek G, Thomann J.-S, Ben Ameur N, Jierry L, Mésini P, Ponche A, Contal C, El Haitami AE, Voegel J.-C, Senger B, Schaaf P, Frisch B, Boulmedais F. Langmuir. 2010; 26: 2816
  • 167 Tasdelen MA, Kiskan B, Yagci Y. Prog. Polym. Sci.. 2016; 52: 19
  • 168 Brotherton WS.
  • 169 Shao C, Wang X, Zhang Q, Luo S, Zhao J, Hu Y. J. Org. Chem.. 2011; 76: 6832
  • 170 Eppel S, Portnoy M. Tetrahedron Lett.. 2013; 54: 5056
  • 171 Leophairatana P, Samanta S, De Silva CC, Koberstein JT. J. Am. Chem. Soc.. 2017; 139: 3756
  • 172 Angell Y, Burgess K. Angew. Chem. Int. Ed.. 2007; 46: 3649
  • 173 Tanaka K, Kageyama C, Fukase K. Tetrahedron Lett.. 2007; 48: 6475
  • 174 Smith NW, Polenz BP, Johnson SB, Dzyuba SV. Tetrahedron Lett.. 2010; 51: 550
  • 175 Moorman RM, Collier MB, Frohock BH, Womble MD, Chalker JM. Org. Biomol. Chem.. 2015; 13: 1974
  • 176 Sreedhar B, Surendra Reddy P. Synth. Commun.. 2007; 37: 805
  • 177 Li X, Chen X, Jiang Y, Chen S, Qu L, Qu Z, Yuan J, Shi H. J. Heterocycl. Chem.. 2016; 53: 1402
  • 178 Jølck RI, Berg RH, Andresen TL. Bioconjugate Chem.. 2010; 21: 807
  • 179 Lal S, Díez-González S. J. Org. Chem.. 2011; 76: 2367
  • 180 Pérez-Balderas F, Ortega-Muñoz M, Morales-Sanfrutos J, Hernández-Mateo F, Calvo-Flores FG, Calvo-Asín JA, Isac-García J, Santoyo-González F. Org. Lett.. 2003; 5: 1951
  • 181 Wang D, Zhao M, Liu X, Chen Y, Li N, Chen B. Org. Biomol. Chem.. 2012; 10: 229
  • 182 Haldón E, Nicasio MC, Pérez PJ. Org. Biomol. Chem.. 2015; 13: 9528
  • 183 Wang C, Yang F, Cao Y, He X, Tang Y, Li Y. RSC Adv.. 2017; 7: 9567
  • 184 Kupracz L, Hartwig J, Wegner J, Ceylan S, Kirschning A. Beilstein J. Org. Chem.. 2011; 7: 1441
  • 185 Ötvös SB, Georgiádes , Mándity IM, Kiss L, Fülöp F. Beilstein J. Org. Chem.. 2013; 9: 1508
  • 186 Appukkuttan P, Dehaen W, Fokin VV, Van der Eycken E. Org. Lett.. 2004; 6: 4223
  • 187 Lee CY, Held R, Sharma A, Baral R, Nanah C, Dumas D, Jenkins S, Upadhaya S, Du W. J. Org. Chem.. 2013; 78: 11221
  • 188 Cravotto G, Fokin VV, Garella D, Binello A, Boffa L, Barge A. J. Comb. Chem.. 2010; 12: 13
  • 189 Kappe CO, Van der Eycken E. Chem. Soc. Rev.. 2010; 39: 1280
  • 190 Jiang Y, He X, Zhang W, Li X, Guo N, Zhao Y, Xu G, Li W. RSC Adv.. 2015; 5: 73340
  • 191 Hatit MZC, Reichenbach LF, Tobin JM, Vilela F, Burley GA, Watson AJB. Nature Commun.. 2018; 9: 4021
  • 192 Bogdan AR, Sach NW. Adv. Synth. Catal.. 2009; 351: 849
  • 193 Lipshutz BH, Taft BR. Angew. Chem. Int. Ed.. 2006; 45: 8235
  • 194 Sharghi H, Beyzavi MH, Safavi A, Doroodmand MM, Khalifeh R. Adv. Synth. Catal.. 2009; 351: 2391
  • 195 Sharghi H, Ebrahimpourmoghaddam S, Doroodmand MM, Purkhosrow A. Asian J. Org. Chem.. 2012; 1: 377
  • 196 Xiong X, Chen H, Tang Z, Jiang Y. RSC Adv.. 2014; 4: 9830
  • 197 Mukherjee N, Ahammed S, Bhadra S, Ranu BC. Green Chem.. 2013; 15: 389
  • 198 Chtchigrovsky M, Primo A, Gonzalez P, Molvinger K, Robitzer M, Quignard F, Taran F. Angew. Chem. Int. Ed.. 2009; 48: 5916
  • 200 Chavan PV, Pandit KS, Desai UV, Kulkarni MA, Wadgaonkar PP. RSC Adv.. 2014; 4: 42137
  • 201 Rajender Reddy K, Rajgopal K, Lakshmi Kantam M. Catal. Lett.. 2007; 114: 36
  • 202 Girard C, Önen E, Aufort M, Beauvière S, Samson E, Herscovici J. Org. Lett.. 2006; 8: 1689
  • 203 Deraedt C, Pinaud N, Astruc D. J. Am. Chem. Soc.. 2014; 136: 12092
  • 204 Moore E, McInnes SJ, Vogt A, Voelcker NH. Tetrahedron Lett.. 2011; 52: 2327
  • 205 Chassaing S, Sani Souna Sido A, Alix A, Kumarraja M, Pale P, Sommer J. Chem.–Eur. J.. 2008; 14: 6713
  • 206 Neumann S, Biewend M, Rana S, Binder WH. Macromol. Rapid Commun.. 2020; 41: 1900 359
  • 207 Golas PL, Tsarevsky NV, Sumerlin BS, Matyjaszewski K. Macromolecules. 2006; 39: 6451
  • 208 Presolski SI, Hong V, Cho S.-H, Finn MG. J. Am. Chem. Soc.. 2010; 132: 14570
  • 210 Campbell-Verduyn LS, Mirfeizi L, Dierckx RA, Elsinga PH, Feringa BL. Chem. Commun. (Cambridge). 2009; 2139
  • 211 Wang F, Fu H, Jiang Y, Zhao Y. Green Chem.. 2008; 10: 452
  • 212 Fabbrizzi P, Cicchi S, Brandi A, Sperotto E, van Koten G. Eur. J. Org. Chem.. 2009; 5423