Campagne, J.-M.  et al.: 2024 Science of Synthesis, 2024/3: Knowledge Updates 2024/3 DOI: 10.1055/sos-SD-109-00715
Knowledge Updates 2024/3

9.9.6 Furans (Update 2024)

More Information

Book

Editors: Campagne, J.-M. ; Donohoe, T. J.; Drabowicz, J. ; Fuerstner, A. ; Jiang, X. ; Wang, M. ; Wirth, T.

Authors: Durandetti, M. ; Fan, Q. ; Favre-Réguillon, A. ; Franck, X. ; Gulder, T. ; Kiełbasiński, P. ; Kretzschmar, M. ; Kwiatkowska, M. ; Kwiecień, H. U.; Leclerc, E. ; Marciniszyn, J. P.; Mita, T. ; Rawat, V. K. ; Walker, J. C. L. ; Zhu, H.

Title: Knowledge Updates 2024/3

Online ISBN: 9783132457089; Book DOI: 10.1055/b000000969

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

Science of Synthesis Knowledge Updates



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

 


Abstract

This review is an update to the earlier Science of Synthesis contributions presenting methods for the synthesis of furans. It focuses on the literature published between 2011 and 2022. In the last decade, a number of new methods for the synthesis of furans from acyclic functionalized molecules have been developed. Many of the methods are based on (mixed) transition-metal catalysis, which induces several combinations of isomerizations, rearrangements, and cyclizations, leading to reactions that are termed cycloisomerizations. Multicomponent reactions for the synthesis of furans are also included.

 
  • 1 König B. Science of Synthesis 2001; 9: 183
  • 2 Hou X.-L, Peng X.-S, Yeung K.-S, Wong HNC. Science of Synthesis Knowledge Updates 2011; 2: 261
  • 3 Donnelly DMX, Meegan MJ, In: Comprehensive Heterocyclic Chemistry Katritzky AR, Rees CW. Pergamon Oxford 1984; 4. 657
  • 4 Senning A, In: Comprehensive Heterocyclic Chemistry III Katritzky AR, Rees CW, Scriven EFV, Taylor RJK. Elsevier Oxford 2008; 3. 389
  • 5 Wong HNC, Yeung K.-S, Yang Z, In: Comprehensive Heterocyclic Chemistry III Katritzky AR, Rees CW, Scriven EFV, Taylor RJK. Elsevier Oxford 2008; 3. 407
  • 6 Graening T, Thrun F, In: Comprehensive Heterocyclic Chemistry III Katritzky AR, Rees CW, Scriven EFV, Taylor RJK. Elsevier Oxford 2008; 3. 497
  • 7 Yeung K.-S, Yang Z, Peng X.-S, Hou X.-L, In: Progress in Heterocyclic Chemistry Gribble GW, Joule JA. Elsevier Oxford 2011; 22. 181
  • 8 Ke Z, Tsui GC, Peng X.-S, Yeung Y.-Y, In: Progress in Heterocyclic Chemistry Gribble GW, Joule JA. Elsevier Oxford 2018; 30. 169
  • 9 Kwiecień H, In: Progress in Heterocyclic Chemistry Gribble GW, Joule JA. Elsevier Oxford 2020; 32. 241
  • 10 Line NJ, Burns AC, Butler SC, Casbohm J, Forsyth CJ. Chem.–Eur. J. 2016; 22: 17 983
  • 11 Roach J, Shenvi RA. Bioorg. Med. Chem. Lett. 2018; 28: 1436
  • 12 Aoyagi Y, Yamazaki A, Nakatsugawa C, Fukaya H, Takeya K, Kawauchi S, Izumi H. Org. Lett. 2008; 10: 4429
  • 13 Levin S, Nani RR, Reisman SE. Org. Lett. 2010; 12: 780
  • 14 Levin S, Nani RR, Reisman SE. J. Am. Chem. Soc. 2011; 133: 774
  • 15 Zhang J, Tang X, Li J, Li P, de Voogd NJ, Ni X, Jin X, Yao X, Li P, Li G. J. Nat. Prod. 2013; 76: 600
  • 16 Chianese G, Yu H.-B, Yang F, Sirignano C, Luciano P, Han B.-N, Khan S, Lin H.-W, Taglialatela-Scafati O. J. Org. Chem. 2016; 81: 5135
  • 17 Kuniyoshi M, Wahome PG, Miono T, Hashimoto T, Yokoyama M, Shrestha KL, Higa T. J. Nat. Prod. 2005; 68: 1314
  • 18 Fürstner A. Angew. Chem. Int. Ed. 2003; 42: 3582
  • 19 Hu DX, Withall DM, Challis GL, Thomson RJ. Chem. Rev. 2016; 116: 7818
  • 20 Mawlong I, Kumar MSS, Singh D. Phytochem. Rev. 2016; 15: 121
  • 21 Chen VY, Kwon O. Angew. Chem. Int. Ed. 2021; 60: 8874
  • 22 Schoenauer S, Schieberle P. J. Agric. Food Chem. 2018; 66: 4189
  • 23 Mesías M, Morales FJ. Foods 2017; 6: 14
  • 24 Vranová J, Ciesarová Z. Czech J. Food Sci. 2009; 27: 1
  • 25 Istasse T, Richel A. RSC Adv. 2020; 10: 23 720
  • 26 Gogar R, Viamajala S, Relue PA, Varanasi S. ACS Sustainable Chem. Eng. 2021; 9: 3428
  • 27 Tong X, Ma Y, Li Y. Appl. Catal., A 2010; 385: 1
  • 28 Karlinskii BY, Romashov LV, Galkin KI, Kislitsyn PG, Ananikov VP. Synthesis 2019; 51: 1235
  • 29 Hughes JME, Gleason JL. Angew. Chem. Int. Ed. 2017; 56: 10 830
  • 30 Li Z, Zhang L, Qiu FG. Asian J. Org. Chem. 2014; 3: 52
  • 31 Kalaitzakis D, Montagnon T, Antonatou E, Vassilikogiannakis G. Org. Lett. 2013; 15: 3715
  • 32 Nilson MG, Funk RL. J. Am. Chem. Soc. 2011; 133: 12 451
  • 33 Sunnam SK, Prasad KR. Synthesis 2013; 45: 1991
  • 34 Prasad KR, Revu O. J. Org. Chem. 2014; 79: 1461
  • 35 Harrar K, Reiser O. Chem. Commun. (Cambridge) 2012; 48: 3457
  • 36 Taylor RD, MacCoss M, Lawson ADG. J. Med. Chem. 2014; 57: 5845
  • 37 Banerjee R, Kumar HKS, Banerjee M. Int. J. Rev. Life Sci. 2012; 2: 7
  • 38 Dishi O, Malakar P, Shimon LJW, Ruhman S, Gidron O. Chem.–Eur. J. 2021; 27: 17 794
  • 39 Bai H.-T, Lin H.-C, Luh T.-Y. J. Org. Chem. 2010; 75: 4591
  • 40 Criado A, Vilas-Varela M, Cobas A, Pérez D, Peña D, Guitián E. J. Org. Chem. 2013; 78: 12 637
  • 41 Kotha S, Todeti S, Gopal MB, Datta A. ACS Omega 2017; 2: 6291
  • 42 Huang P, Du J, Biewer MC, Stefan MC. J. Mater. Chem. A 2015; 3: 6244
  • 43 Gandini A, Lacerda TM. Macromol. Mater. Eng. 2022; 307: 2 100 902
  • 44 Horner KE, Karadakov PB. J. Org. Chem. 2013; 78: 8037
  • 45 Chen Y, Li G, Liu Y. Adv. Synth. Catal. 2011; 353: 392
  • 46 Yeung K.-S. Top. Heterocycl. Chem. 2012; 29: 47
  • 47 Chen Y, Chen M, Liu Y. Angew. Chem. Int. Ed. 2012; 51: 6181
  • 48 Cardoza S, Shrivash MK, Das P, Tandon V. J. Org. Chem. 2021; 86: 1330
  • 49 Bheeter CB, Chen L, Soulé J.-F, Doucet H. Catal. Sci. Technol. 2016; 6: 2005
  • 50 Chen H, Farizyan M, van Gemmeren M. Eur. J. Org. Chem. 2020; 6318
  • 51 Guo Y, Quan T, Lu Y, Luo T. J. Am. Chem. Soc. 2017; 139: 6815
  • 52 Zhu L, Luo J, Hong R. Org. Lett. 2014; 16: 2162
  • 53 Lehner V, Davies HML, Reiser O. Org. Lett. 2017; 19: 4722
  • 54 Dong Z, Liu C.-H, Wang Y, Lin M, Yu Z.-X. Angew. Chem. Int. Ed. 2013; 52: 14 157
  • 55 Alves AJS, Lopes SMM, Henriques MSC, Paixão JA, Pinho e Melo TMVD. Eur. J. Org. Chem. 2017; 4011
  • 56 Shukla P, Asati A, Bhardiya SR, Singh M, Rai VK, Rai A. J. Org. Chem. 2020; 85: 7772
  • 57 Lei L, Yao Y.-Y, Jiang L.-J, Lu X, Liang C, Mo D.-L. J. Org. Chem. 2020; 85: 3059
  • 58 Parr BT, Green SA, Davies HML. J. Am. Chem. Soc. 2013; 135: 4716
  • 59 Huang X, Thor W, Feng X, Kang L, Yang M, Lee C.-S, Cheng Y.-K, He S. Org. Chem. Front. 2020; 7: 255
  • 60 Villar L, Uria U, Martínez JI, Prieto L, Reyes E, Carrillo L, Vicario JL. Angew. Chem. Int. Ed. 2017; 56: 10 535
  • 61 Krenske EH, Houk KN, Harmata M. Org. Lett. 2010; 12: 444
  • 62 Montaña AM, Grima PM, Castellví M, Batalla C, Font-Bardia M. Tetrahedron 2012; 68: 9982
  • 63 Dota K, Shimizu T, Hasegawa S, Miyashita M, Tanino K. Tetrahedron Lett. 2011; 52: 910
  • 64 Kucherov FA, Romashov LV, Averochkin GM, Ananikov VP. ACS Sustainable Chem. Eng. 2021; 9: 3011
  • 65 Yu F, Li G, Gao P, Gong H, Liu Y, Wu Y, Cheng B, Zhai H. Org. Lett. 2010; 12: 5135
  • 66 Padwa A, Flick AC. Adv. Heterocycl. Chem. 2013; 110: 1
  • 67 Hu J, Wang Z, Gong Y. Eur. J. Org. Chem. 2016; 3603
  • 68 Liu Z.-Y, Zhang M, Wang X.-C. J. Am. Chem. Soc. 2020; 142: 581
  • 69 Sun N, Xie X, Chen H, Liu Y. Chem.–Eur. J. 2016; 22: 14 175
  • 70 Lofstrand VA, McIntosh KC, Almehmadi YA, West FG. Org. Lett. 2019; 21: 6231
  • 71 Chen Y, Wang L, Sun N, Xie X, Zhou X, Chen H, Li Y, Liu Y. Chem.–Eur. J. 2014; 20: 12 015
  • 72 Nejrotti S, Marra F, Priola E, Maranzana A, Prandi C. J. Org. Chem. 2021; 86: 8295
  • 73 Ahmadi S, Ghanbar M. Synthesis 2021; 53: 775
  • 74 Yang J.-M, Tang X.-Y, Shi M. Chem.–Eur. J. 2015; 21: 4534
  • 75 Kalaitzakis D, Triantafyllakis M, Alexopoulou I, Sofiadis M, Vassilikogiannakis G. Angew. Chem. Int. Ed. 2014; 53: 13 201
  • 76 Yang L, Wang J, Wang Y, Li X, Liu W, Zhang Z, Xie X. J. Org. Chem. 2021; 86: 14 311
  • 77 Oswald JP, Woerpel KA. J. Org. Chem. 2018; 83: 9067
  • 78 Gryparis C, Lykakis IN, Efe C, Zaravinos I.-P, Vidali T, Kladou E, Stratakis M. Org. Biomol. Chem. 2011; 9: 5655
  • 79 Kalaitzakis D, Kouridaki A, Noutsias D, Montagnon T, Vassilikogiannakis G. Angew. Chem. Int. Ed. 2015; 54: 6283
  • 80 Montagnon T, Kalaitzakis D, Sofiadis M, Vassilikogiannakis G. Org. Biomol. Chem. 2016; 14: 8636
  • 81 Wysocki J, Ortega N, Glorius F. Angew. Chem. Int. Ed. 2014; 53: 8751
  • 82 Pauli L, Tannert R, Scheil R, Pfaltz A. Chem.–Eur. J. 2015; 21: 1482
  • 83 Blanc A, Bénéteau V, Weibel J.-M, Pale P. Org. Biomol. Chem. 2016; 14: 9184
  • 84 Kaur N. Synth. Commun. 2019; 49: 743
  • 85 Nejrotti S, Prandi C. Synthesis 2021; 53: 1046
  • 86 Pal T, Lahiri GK, Maiti D. Eur. J. Org. Chem. 2020; 6859
  • 87 Serdyuk O, Butin A, Abaev V. J. Fluorine Chem. 2010; 131: 296
  • 88 Deepthi A, Babu BP, Balachandran AL. Org. Prep. Proced. Int. 2019; 51: 409
  • 89 Peterson LA. Chem. Res. Toxicol. 2013; 26: 6
  • 90 Ventura SPM, Morais P, Coelho JAS, Sintra T, Coutinho JAP, Afonso CAP. Green Chem. 2016; 18: 4733
  • 91 Wang M, Xiang J.-C, Cheng Y, Wu Y.-D, Wu A.-X. Org. Lett. 2016; 18: 524
  • 92 Liu Y, Hu Y, Cao Z, Zhan X, Luo W, Liu Q, Guo C. Adv. Synth. Catal. 2019; 361: 1084
  • 93 Wen Y, Zhu S, Jiang H, Wang A, Chen Z. Synlett 2011; 1023
  • 94 Wang L, Li J, Lv Y, Zhao G, Gao S. Synlett 2012; 23: 1074 corrigendum: Synlett 2012; 23: 1558
  • 95 Jin H, Rudolph M, Rominger F, Hashmi ASK. ACS Catal. 2019; 9: 11 663
  • 96 Yamashita K, Yamamoto Y, Nishiyama H. J. Am. Chem. Soc. 2012; 134: 7660
  • 97 Yamamoto Y. Synlett 2017; 28: 1250
  • 98 Jiang H, Zeng W, Li Y, Wu W, Huang L, Fu W. J. Org. Chem. 2012; 77: 5179
  • 99 Irudayanathan FM, Raja GCE, Lee S. Tetrahedron 2015; 71: 4418
  • 100 Tateishi K, Matsumoto Y, Saito A. Eur. J. Org. Chem. 2019; 5603
  • 101 Wu J, Yoshikai N. Angew. Chem. Int. Ed. 2015; 54: 11 107
  • 102 Lu B, Wu J, Yoshikai N. J. Am. Chem. Soc. 2014; 136: 11 598
  • 103 Liang Y.-X, Yang M, He B.-W, Zhao Y.-L. Org. Lett. 2020; 22: 7640
  • 104 Nun P, Dupuy S, Gaillard S, Poater A, Cavallo L, Nolan SP. Catal. Sci. Technol. 2011; 1: 58
  • 105 Kramer S, Madsen JLH, Rottländer M, Skrydstrup T. Org. Lett. 2010; 12: 2758
  • 106 Dateer RB, Pati K, Liu R.-S. Chem. Commun. (Cambridge) 2012; 48: 7200
  • 107 Shen W.-B, Tang X.-T, Zhang T.-T, Liu S.-Y, He J.-M, Su T.-F. Org. Lett. 2020; 22: 6799
  • 108 Hossain ML, Ye F, Zhang Y, Wang J. Tetrahedron 2014; 70: 6957
  • 109 Swenson AK, Higgins KE, Brewer MG, Brennessel WW, Coleman MG. Org. Biomol. Chem. 2012; 10: 7483
  • 110 Guo H, Zhang S, Yu X, Feng X, Yamamoto Y, Bao M. ACS Catal. 2021; 11: 10 789
  • 111 Xia L, Lee YR. Eur. J. Org. Chem. 2014; 3430
  • 112 Ji D, Liu K, Sun J. Org. Lett. 2018; 20: 7708
  • 113 Zheng Y, Perfetto A, Luise D, Ciofini I, Miesch L. Org. Lett. 2021; 23: 5528
  • 114 Cui X, Xu X, Wojtas L, Kim MM, Zhang XP. J. Am. Chem. Soc. 2012; 134: 19 981
  • 115 Zhu S, Li F, Empel C, Jana S, Pei C, Koenigs RM. Adv. Synth. Catal. 2022; 364: 3149
  • 116 Kuruba BK, Vasanthkumar S, Emmanuvel L. Tetrahedron 2017; 73: 3093
  • 117 Hong C, Yu S, Liu Z, Xu Z, Zhang Y. J. Org. Chem. 2022; 87: 11 979
  • 118 Tan WW, Yoshikai N. J. Org. Chem. 2016; 81: 5566
  • 119 Jiang Y, Khong VZY, Lourdusamy E, Park C.-M. Chem. Commun. (Cambridge) 2012; 48: 3133
  • 120 Cai H, Thombal RS, Li X, Lee YR. Adv. Synth. Catal. 2019; 361: 1
  • 121 Liang H, He X, Zhang Y, Chen B, Ouyang J.-s, Li Y, Pan B, Reddy CVS, Chan WTK, Qiu L. Chem. Commun. (Cambridge) 2020; 56: 11 429
  • 122 Peng Y, Luo J, Feng Q, Tang Q. Eur. J. Org. Chem. 2016; 5169
  • 123 Ghazvini M, Shahvelayati AS, Sabri A, Nasrabadi FZ. Khim. Geterotsikl. Soedin. 2016; 52: 161 Chem. Heterocycl. Compd. (Engl. Transl.) 2016; 52: 161
  • 124 Aoyama T, Nagaoka T, Takido T, Kodomari M. Synthesis 2011; 619
  • 125 Ren L, Luo J, Tan L, Tang Q. J. Org. Chem. 2022; 87: 3167
  • 126 York M. Tetrahedron Lett. 2011; 52: 6267
  • 127 Wang J, Chen S, Wu W, Wen S, Weng Z. J. Org. Chem. 2019; 84: 15 685
  • 128 Chang S, Desai S, Leznoff DB, Merbouh N, Britton R. Eur. J. Org. Chem. 2013; 3219
  • 129 Wang S, Jia W.-L, Wang L, Liu Q, Wu L.-Z. Chem.–Eur. J. 2016; 22: 13 794
  • 130 Han Y.-Y, Jiao Y.-Y, Ren D, Hu Z, Shen S, Yu S. Asian J. Org. Chem. 2017; 6: 414
  • 131 Jiang H, Cheng Y, Zhang Y, Yu S. Org. Lett. 2013; 15: 4884
  • 132 Quintavalla A, Veronesi R, Speziali L, Martinelli A, Zaccheroni N, Mummolo L, Lombardo M. Adv. Synth. Catal. 2022; 364: 362
  • 133 Lin M.-H, Kuo C.-K, Huang Y.-C, Tsai Y.-T, Tsai C.-H, Liang K.-Y, Li Y.-S, Chuang T.-H. Tetrahedron 2014; 70: 5513
  • 134 Wang Q, Yang L, Fan X. Synlett 2014; 25: 687
  • 135 Wang L.-C, Geng H.-Q, Peng J.-B, Wu X.-F. Eur. J. Org. Chem. 2020; 2605
  • 136 Kale A, Medishetti N, Nanubolu JB, Atmakur K. Tetrahedron Lett. 2018; 59: 4168
  • 137 Cao H, Zhan H, Wu J, Zhong H, Lin Y, Zhang H. Eur. J. Org. Chem. 2012; 2318
  • 138 Chen P, Cao W, Li X, Shi D. Adv. Synth. Catal. 2021; 363: 4789
  • 139 Li J, Liu L, Ding D, Sun J, Ji Y, Dong J. Org. Lett. 2013; 15: 2884
  • 140 Guguloth V, Balaboina R, Thirukovela NS, Vadde R. Org. Biomol. Chem. 2021; 19: 7438
  • 141 Ronaghi N, Fialho DM, Jones CW, France S. J. Org. Chem. 2020; 85: 15 337
  • 142 Ronaghi N, Shade D, Moon HJ, Najmi S, Cleveland JW, Walton KS, France S, Jones CW. ACS Sustainable Chem. Eng. 2021; 9: 11 581
  • 143 Huang W, Liu C, Gu Y. Adv. Synth. Catal. 2017; 359: 1811
  • 144 Schickmous B, Christoffers J. Eur. J. Org. Chem. 2014; 4410
  • 145 Yue Y, Zhang Y, Song W, Zhang X, Liu J, Zhuo K. Adv. Synth. Catal. 2014; 356: 2459
  • 146 Payra S, Saha A, Guchhait S, Banerjee S. RSC Adv. 2016; 6: 33 462
  • 147 Lou J, Wang Q, Wu K, Wu P, Yu Z. Org. Lett. 2017; 19: 3287
  • 148 Lad BS, Katukojvala S. ACS Catal. 2018; 8: 11 807
  • 149 Huang Y, Li X, Yu Y, Zhu C, Wu W, Jiang H. J. Org. Chem. 2016; 81: 5014
  • 150 You C, Zhang Z, Tu Y, Tang H, Wang Y, Long D, Zhao J. J. Org. Chem. 2020; 85: 3902
  • 151 Zhang X, Dai W, Wu W, Cao S. Org. Lett. 2015; 17: 2708
  • 152 Zhang W, Xu W. Chem. Heterocycl. Compd. (Engl. Transl.) 2017; 53: 615
  • 153 Schmidt D, Malakar CC, Beifuss U. Org. Lett. 2014; 16: 4862
  • 154 Ballini R, Gabrielli S, Palmieri A. Synlett 2010; 2468
  • 155 Li L, Zhao M.-N, Ren Z.-H, Li J, Guan Z.-H. Synthesis 2012; 44: 532
  • 156 Nair DK, Mobin SM, Namboothiri INN. Tetrahedron Lett. 2012; 53: 3349
  • 157 Mane V, Kumar T, Pradhan S, Katiyar S, Namboothiri INN. RSC Adv. 2015; 5: 69 990
  • 158 Huang W.-Y, Chen Y.-C, Chen K. Chem.–Asian J. 2012; 7: 688
  • 159 Li H.-L, Wang Y, Sun P.-P, Luo X, Shen Z, Deng W.-P. Chem.–Eur. J. 2016; 22: 9348
  • 160 He M.-X, Yao Y, Ai C.-Z, Mo Z.-Y, Wu Y.-Z, Zhou Q, Pan Y.-M, Tang H.-T. Org. Chem. Front. 2022; 9: 781
  • 161 He C, Guo S, Ke J, Hao J, Xu H, Chen H, Lei A. J. Am. Chem. Soc. 2012; 134: 5766
  • 162 Singh A, Bimal D, Kumar R, Maikhuri VK, Thirumal M, Senapati NN, Prasad AK. Synth. Commun. 2018; 48: 2339
  • 163 Mohanty A, Roy S. Eur. J. Org. Chem. 2019; 6702
  • 164 Ma Y, Zhang S, Yang S, Song F, You J. Angew. Chem. Int. Ed. 2014; 53: 7870
  • 165 Han C, Tian X, Song L, Liu Y, Hashmi ASK. Org. Chem. Front. 2021; 8: 6546
  • 166 Liu W.-B, Chen C, Zhang Q. Synth. Commun. 2013; 43: 951
  • 167 Yan R, Huang J, Luo J, Wen P, Huang G, Liang Y. Synlett 2010; 1071
  • 168 Wang S, Liu C, Jia J, Zha C, Xie M, Zhang N. Tetrahedron 2016; 72: 6684
  • 169 Guo P, Yuan G.-C, Xu L.-H, Ye K.-Y. Org. Chem. Front. 2022; 9: 1628
  • 170 Wang S, Song M, Li X, Huang Y, Zhao T, Wei Z, Lan Y, Tan H. Org. Lett. 2020; 22: 8752
  • 171 Yu J.-T, Shi B, Peng H, Sun S, Chu H, Jiang Y, Cheng J. Org. Lett. 2015; 17: 3643
  • 172 Zeng W, Wu W, Jiang H, Sun Y, Chen Z. Tetrahedron Lett. 2013; 54: 4605
  • 173 Reddy CR, Reddy MD. J. Org. Chem. 2014; 79: 106
  • 174 Li Q, He X, Tao J, Xie M, Wang H, Li R, Shang Y. Adv. Synth. Catal. 2019; 361: 1874
  • 175 Deng B, Rao CB, Zhang R, Li J, Liang Y, Zhao Y, Gao M, Dong D. Adv. Synth. Catal. 2019; 361: 4549
  • 176 Gujarathi S, Zheng G. Tetrahedron 2015; 71: 6183
  • 177 Yaragorla S, Dada R, Pareek A, Singh G. RSC Adv. 2016; 6: 28 865
  • 178 Zhang L, Mou N.-J, Xiao D.-R, Zhuang X, Lin X.-L, Cai T, Luo Q.-L. Org. Chem. Front. 2021; 8: 1155
  • 179 Reddy CR, Mohammed SZ, Kumaraswamy P. Org. Biomol. Chem. 2015; 13: 8310
  • 180 Wang Y, Pritchard GJ, Kimber MC. Eur. J. Org. Chem. 2020; 2914
  • 181 Cao H, Jiang H.-F, Huang H.-W, Zhao J.-W. Org. Biomol. Chem. 2011; 9: 7313
  • 182 Hu J, Wei Y, Tong X. Org. Lett. 2011; 13: 3068
  • 183 Sydnes LK, Isanov R, Sengee M, Livi F. Synth. Commun. 2013; 43: 2898
  • 184 Cao H, Zhan H, Cen J, Lin J, Lin Y, Zhu Q, Fu M, Jiang H. Org. Lett. 2013; 15: 1080
  • 185 Guo P, Wang C, Chen Y, Ou C, Jiang H, Chen W, Chen W, Cao H. RSC Adv. 2016; 6: 39 563
  • 186 Ghosh M, Mishra S, Hajra A. J. Org. Chem. 2015; 80: 5364
  • 187 Raimondi W, Dauzonne D, Constantieux T, Bonne D, Rodriguez J. Eur. J. Org. Chem. 2012; 6119
  • 188 Ghosh M, Mishra S, Monir K, Hajra A. Org. Biomol. Chem. 2015; 13: 309
  • 189 Yang Y, Yao J, Zhang Y. Org. Lett. 2013; 15: 3206
  • 190 Agasti S, Pal T, Achar TK, Maiti S, Pal D, Mandal S, Daud K, Lahiri GK, Maiti D. Angew. Chem. Int. Ed. 2019; 58: 11 039
  • 191 Verma F, Singh PK, Bhardiya SR, Singh M, Rai A, Rai VK. New J. Chem. 2017; 41: 4937
  • 192 Fernandes R, Mhaske K, Narayan R. Tetrahedron 2022; 103: 132 553
  • 193 Wu Y, Huang Z, Luo Y, Liu D, Deng Y, Yi H, Lee J.-F, Pao C.-W, Chen J.-L, Lei A. Org. Lett. 2017; 19: 2330
  • 194 Naveen T, Deb A, Maiti D. Angew. Chem. Int. Ed. 2017; 56: 1111
  • 195 Manna S, Antonchick AP. Org. Lett. 2015; 17: 4300
  • 196 Luo Z, Fang Y, Zhao Y, Liu P, Xu X, Feng C, Li Z, He J. RSC Adv. 2016; 6: 5436
  • 197 Cao H, Jiang H, Mai R, Zhu S, Qi C. Adv. Synth. Catal. 2010; 352: 143
  • 198 Cao H, Jiang H, Huang H. Synthesis 2011; 1019
  • 199 Huang H, Jiang H, Cao H, Zhao J, Shi D. Tetrahedron 2012; 68: 3135
  • 200 Cao H, Jiang H, Yuan G, Chen Z, Qi C, Huang H. Chem.–Eur. J. 2010; 16: 10 553
  • 201 Chong Q, Xin X, Wang C, Wu F, Wang H, Shi J, Wan B. J. Org. Chem. 2014; 79: 2105
  • 202 Hosseyni S, Su Y, Shi X. Org. Lett. 2015; 17: 6010
  • 203 Meng S, Wang Y, Liu J, Zheng J, Qian X, Wang Q. Org. Lett. 2022; 24: 757
  • 204 Ge G.-C, Mo D.-L, Ding C.-H, Dai L.-X, Hou X.-L. Org. Lett. 2012; 14: 5756
  • 205 Nitsch D, Bach T. J. Org. Chem. 2014; 79: 6372
  • 206 Lian Y, Huber T, Hesp KD, Bergman RG, Ellman JA. Angew. Chem. Int. Ed. 2013; 52: 629
  • 207 Hummel JR, Ellman JA. J. Am. Chem. Soc. 2015; 137: 490
  • 208 Zhang T, Xie C, Sakata H, Nakajima K, Shimoyama T, Watanabe T, Maekawa H. Eur. J. Org. Chem. 2020; 2237
  • 209 Lai J, Liang Y, Liu T, Tang S. Org. Lett. 2016; 18: 2066
  • 210 Liu J, Ye W, Qing X, Wang C. J. Org. Chem. 2016; 81: 7970
  • 211 Kondoh A, Aita K, Ishikawa S, Terada M. Org. Lett. 2020; 22: 2105
  • 212 Silwal S, Rahaim SR. Tetrahedron Lett. 2015; 56: 5738
  • 213 Ghandi M, Zarezadeh N. Tetrahedron 2013; 69: 8668
  • 214 Zhang T, Maekawa H. Org. Lett. 2017; 19: 6602
  • 215 Jin H, Fürstner A. Angew. Chem. Int. Ed. 2020; 59: 13 618
  • 216 Sherikar MS, Bettadapur KR, Lanke V, Prabhu KR. Org. Biomol. Chem. 2021; 19: 7470
  • 217 Trofimov BA, Bidusenko IA, Schmidt EY, Ushakov IA, Vashchenko AV. Asian J. Org. Chem. 2017; 6: 707
  • 218 Kong L, Shao Y, Li Y, Liu Y, Li Y. J. Org. Chem. 2015; 80: 12 641
  • 219 Wang Q, Liu Z, Lou J, Yu Z. Org. Lett. 2018; 20: 6007
  • 220 Li M, Zhou W. Synlett 2020; 31: 2035
  • 221 Chen K.-W, Syu S, Jang Y.-J, Lin W. Org. Biomol. Chem. 2011; 9: 2098
  • 222 Lee Y.-T, Lee Y.-T, Lee C.-J, Sheu C.-N, Lin B.-Y, Wang J.-H, Lin W. Org. Biomol. Chem. 2013; 11: 5156
  • 223 Wang D.-L, Dong Z, Xu J, Li D. Chin. Chem. Lett. 2013; 24: 622
  • 224 Lee C.-J, Chang T.-H, Yu J.-K, Reddy GM, Hsiao M.-Y, Lin W. Org. Lett. 2016; 18: 3758
  • 225 Hu J, Fei Y, Zhao H, Wang Z, Li C, Li J. Chem. Commun. (Cambridge) 2019; 55: 8394
  • 226 Mahida AK, Kale SB, Das U. Eur. J. Org. Chem. 2017; 6427
  • 227 Beerappa M, Shivashankar K. J. Heterocycl. Chem. 2017; 54: 2197
  • 228 Damavandi S, Sandaroos R, Pashirzad M. Res. Chem. Intermed. 2012; 38: 1969
  • 229 He Y, Lou J, Yu Z, Zhou Y.-G. Chem.–Eur. J. 2020; 26: 4941
  • 230 Zhang Z, Huang A, Ma L, Xu J.-H, Zhang M. RSC Adv. 2022; 12: 15 190
  • 231 Erguven H, Zhou C, Arndtsen BA. Chem. Sci. 2021; 12: 15 077
  • 232 Dong J, Du H, Xu J. RSC Adv. 2019; 9: 25 034
  • 233 Yuan Y, Tan H, Kong L, Zheng Z, Xu M, Huang J, Li Y. Org. Biomol. Chem. 2019; 17: 2725
  • 234 El Arba M, Dibrell SE, Meece F, Frantz DE. Org. Lett. 2018; 20: 5886
  • 235 Chen L, Fang Y, Zhao Q, Shi M, Li C. Tetrahedron Lett. 2010; 51: 3678
  • 236 Chen P, Meng Y, Yang Q, Wu J, Xiao Y, Gorja DR, Song C, Chang J. RSC Adv. 2015; 5: 79 906
  • 237 Luo J, Lu D, Peng Y, Tang Q. Asian J. Org. Chem. 2017; 6: 1546
  • 238 Liu H, Ji F, Chen Y, Gao Y, Wang J, Zhang M, Liu F, Sha Q. Chem.–Eur. J. 2021; 27: 5225
  • 239 Mao S, Gao Y.-R, Zhang S.-L, Guo D.-D, Wang Y.-Q. Eur. J. Org. Chem. 2015; 876
  • 240 Wang G, Guan Z, Tang R, He Y. Synth. Commun. 2010; 40: 370
  • 241 Verma RS, Mishra M, Pandey CB, Kumar S, Tiwari B. J. Org. Chem. 2020; 85: 8166
  • 242 Guo S.-T, Xu J, Zhang X.-L, Xiong X.-S, Zhang L, Wang D.-L, Zhang S.-Q. Heterocycles 2021; 102: 105
  • 243 Mao S, Zhu X.-Q, Gao Y.-R, Guo D.-D, Wang Y.-Q. Chem.–Eur. J. 2015; 21: 11 335
  • 244 Shou J.-Y, Qing F.-L. Angew. Chem. Int. Ed. 2022; 61: e202208860
  • 245 Chan C.-K, Chan Y.-L, Tsai Y.-L, Chang M.-Y. J. Org. Chem. 2016; 81: 8112
  • 246 Chobanov NM, Shaibakova MG, Popod'ko NR, Khafizova LO, Dzhemilev UM. Tetrahedron 2017; 73: 5639
  • 247 Chen L, Du Y, Zeng X.-P, Shi T.-D, Zhou F, Zhou J. Org. Lett. 2015; 17: 1557
  • 248 Yang Y, Ni F, Shu W.-M, Wu A.-X. Tetrahedron 2014; 70: 6733
  • 249 Rajeshkumar V, Neelamegam C, Anandan S. Org. Biomol. Chem. 2019; 17: 982
  • 250 Vijayaprasad P, Venkanna A, Shanker M, Kishan E, Rao PV. RSC Adv. 2017; 7: 10 524
  • 251 Iwamoto A, Katori A, Sashihara Y, Kojima S. Chem. Lett. 2012; 41: 1586
  • 252 Placais C, Donnard M, Panossian A, Vors J.-P, Bernier D, Pazenok S, Leroux FR. Org. Lett. 2021; 23: 4915
  • 253 Walker JCL, Werrel S, Donohoe TJ. Chem.–Eur. J. 2019; 25: 13 114
  • 254 Lenden P, Entwistle DA, Willis MC. Angew. Chem. Int. Ed. 2011; 50: 10 657
  • 255 Mondal K, Pan SC. J. Org. Chem. 2017; 82: 4415
  • 256 Haut F.-L, Habiger C, Wein LA, Wurst K, Podewitz M, Magauer T. J. Am. Chem. Soc. 2021; 143: 1216
  • 257 Bernhard Y, Gilbert J, Bousquet T, Favrelle-Huret A, Zinck P, Pellegrini S, Pelinski L. Eur. J. Org. Chem. 2019; 7870
  • 258 Erdenebileg U, Høstmark I, Polden K, Sydnes LK. J. Org. Chem. 2014; 79: 1213
  • 259 Pennell MN, Foster RW, Turner PG, Hailes HC, Tame CJ, Sheppard TD. Chem. Commun. (Cambridge) 2014; 50: 1302
  • 260 Hoffmann M, Miaskiewicz S, Weibel J.-M, Pale P, Blanc A. Beilstein J. Org. Chem. 2013; 9: 1774
  • 261 Li B, Shen N, Yang Y, Zhang X, Fan X. Org. Lett. 2021; 23: 388
  • 262 Yadav NN, Jeong H, Ha H.-J. ACS Omega 2017; 2: 7525
  • 263 Schneider CC, Caldeira H, Gay BM, Back DF, Zeni G. Org. Lett. 2010; 12: 936
  • 264 Riedel S, Maichle-Mössmer C, Maier ME. J. Org. Chem. 2017; 82: 12 798
  • 265 Horký F, Císařová I, Štěpnička P. Organometallics 2021; 40: 427
  • 266 Hrizi A, Thiery E, Romdhani-Younes M, Jacquemin J, Thibonnet J. Eur. J. Org. Chem. 2021; 3798
  • 267 Du X, Chen H, Chen Y, Chen J, Liu Y. Synlett 2011; 1010
  • 268 Vicente R, González J, Riesgo L, González J, López LA. Angew. Chem. Int. Ed. 2012; 51: 8063
  • 269 González J, González J, Peréz-Calleja C, López LA, Vicente R. Angew. Chem. Int. Ed. 2013; 52: 5853
  • 270 González MJ, López LA, Vicente R. Org. Lett. 2014; 16: 5780
  • 271 Chen T, Wu W, Weng Z. Tetrahedron 2019; 75: 130 751
  • 272 Ma J, Jiang H, Zhu S. Org. Lett. 2014; 16: 4472
  • 273 Xia Y, Chen L, Qu P, Ji G, Feng S, Xiao Q, Zhang Y, Wang J. J. Org. Chem. 2016; 81: 10 484
  • 274 Peil S, Fürstner A. Angew. Chem. Int. Ed. 2019; 58: 18 476
  • 275 Chen Z.-W, Luo M.-T, Ye D.-N, Zhou Z.-G, Ye M, Liu L.-X. Synth. Commun. 2014; 44: 1825
  • 276 Wan Y, Zhu Y, Peng H, Deng G. J. Org. Chem. 2022; 87: 281
  • 277 Hong K, Shu J, Dong S, Zhang Z, He Y, Liu M, Huang J, Hu W, Xu X. ACS Catal. 2022; 12: 14 185
  • 278 Zhan H, Lin X, Qiu Y, Du Z, Li P, Li Y, Cao H. Eur. J. Org. Chem. 2013; 2284
  • 279 Pei C, Rong G.-W, Yu Z.-X, Xu X.-F. J. Org. Chem. 2018; 83: 13 243
  • 280 Mao S, Tang L, Wu C, Tu X, Gao Q, Deng G. Org. Lett. 2019; 21: 2416
  • 281 Xia Y, Qu S, Xiao Q, Wang Z.-X, Qu P, Chen L, Liu Z, Tian L, Huang Z, Zhang Y, Wang J. J. Am. Chem. Soc. 2013; 135: 13 502
  • 282 Xia Y, Ge R, Chen L, Liu Z, Xiao Q, Zhang Y, Wang J. J. Org. Chem. 2015; 80: 7856
  • 283 Wang T, Zhang J. Dalton Trans. 2010; 39: 4270
  • 284 González J, López LA, Vicente R. Chem. Commun. (Cambridge) 2014; 50: 8536
  • 285 Liu P, Sun J. Org. Lett. 2017; 19: 3482
  • 286 Tang L, Zhang Y, Deng G. J. Org. Chem. 2021; 86: 13 245
  • 287 Peng H, Wan Y, Zhang Y, Deng G. Chem. Commun. (Cambridge) 2020; 56: 1417
  • 288 Hu F, Xia Y, Ma C, Zhang Y, Wang J. J. Org. Chem. 2016; 81: 3275
  • 289 Hamal KB, Chalifoux WA. J. Org. Chem. 2017; 82: 12 920
  • 290 Clark JS, Romiti F, Hogg KF, Hamid MHSA, Richter SC, Boyer A, Redman JC, Farrugia LJ. Angew. Chem. Int. Ed. 2015; 54: 5744
  • 291 Ren Y, Meng L.-G, Peng T, Wang L. Org. Lett. 2018; 20: 4430
  • 292 Jiang Q, Li A, Liu X, Yu Y, Zhu B, Cao H. J. Org. Chem. 2022; 87: 7056
  • 293 Wu W, Chen Y, Li M, Hu W, Lin X. J. Org. Chem. 2019; 84: 14 529
  • 294 Clark JS, Boyer A, Aimon A, García PE, Lindsay DM, Symington ADF, Danoy Y. Angew. Chem. Int. Ed. 2012; 51: 12 128
  • 295 McAulay K, Clark JS. Chem.–Eur. J. 2017; 23: 9761
  • 296 Li M, Yang F, Yuan T, Li H, Li J, Chen Z.-S, Ji K. J. Org. Chem. 2019; 84: 12 617
  • 297 Xu C, Wittmann S, Gemander M, Ruohonen V, Clark JS. Org. Lett. 2017; 19: 3556
  • 298 Rodríguez A, Moran WJ. Tetrahedron Lett. 2011; 52: 2605
  • 299 Tu X, Peng H, Deng G. Tetrahedron 2020; 76: 131 421
  • 300 Tsuji H, Yamagata K.-I, Ueda Y, Nakamura E. Synlett 2011; 1015
  • 301 Golonka AN, Schindler CS. Tetrahedron 2017; 73: 4109
  • 302 Chang M.-Y, Cheng Y.-C, Lu Y.-J. Org. Lett. 2015; 17: 1264
  • 303 Chang M.-Y, Lai K.-X. Synthesis 2019; 51: 3410
  • 304 Morcillo SP, Leboeuf D, Bour C, Gandon V. Chem.–Eur. J. 2016; 22: 16 974
  • 305 Nandi GC, Soumini K. J. Org. Chem. 2016; 81: 11 909
  • 306 Pace DP, Robidas R, Tran UPN, Legault CY, Nguyen TV. J. Org. Chem. 2021; 86: 8154
  • 307 Sklar DE, Helbling AV, Liu Y, Downey CW. Tetrahedron Lett. 2021; 87: 153 424
  • 308 Rao HSP, Satish V, Kanniyappan S, Kumari P. Tetrahedron 2018; 74: 6047
  • 309 Lozovskiy SV, Vasilyev AV. Adv. Synth. Catal. 2020; 362: 3121
  • 310 Schitter T, Roy NJ, Jones PG, Werz DB. Org. Lett. 2019; 21: 640
  • 311 Maiti D, Halder A, Pillai AS, Sarkar SD. J. Org. Chem. 2021; 86: 16 084
  • 312 Li J, Rudolph M, Rominger F, Xie J, Hashmi ASK. Adv. Synth. Catal. 2016; 358: 207
  • 313 Li E, Yao W, Xie X, Wang C, Shao Y, Li Y. Org. Biomol. Chem. 2012; 10: 2960
  • 314 Li E, Cheng X, Wang C, Shao Y, Li Y. J. Org. Chem. 2012; 77: 7744
  • 315 Shiroodi RK, Rivera Vera CI, Dudnik AS, Gevorgyan V. Tetrahedron Lett. 2015; 56: 3251
  • 316 Li Y, Wheeler KA, Dembinski R. Org. Biomol. Chem. 2012; 10: 2395
  • 317 Ryu T, Eom D, Shin S, Son J.-Y, Lee PH. Org. Lett. 2017; 19: 452
  • 318 Lan S, Liu R, Kong X, Liu J, Luo B, Yang S, Fang X. Org. Lett. 2021; 23: 1504
  • 319 Chen W.-L, Li J, Zhu Y.-H, Ye L.-T, Hu W, Mo W.-M. ARKIVOC 2011; ix 381 ;available online at www.arkat-usa.org/
  • 320 Qian L.-L, Yi R, Min X.-T, Hu Y.-C, Wan B, Chen Q.-A. Tetrahedron 2020; 76: 131 327
  • 321 Li W, Zhang J. Chem. Commun. (Cambridge) 2010; 46: 8839
  • 322 Xu Y, Sun J. Org. Lett. 2021; 23: 853
  • 323 Rauniyar V, Wang ZJ, Burks HE, Toste FD. J. Am. Chem. Soc. 2011; 133: 8486
  • 324 Gao H, Wu X, Zhang J. Chem.–Eur. J. 2011; 17: 2838
  • 325 Wang Y, Zhang Z.-M, Liu F, He Y, Zhang J. Org. Lett. 2018; 20: 6403
  • 326 He T, Gao P, Qiu Y.-F, Yan X.-B, Liu X.-Y, Liang Y.-M. RSC Adv. 2013; 3: 19 913
  • 327 Zhou L, Zhang M, Li W, Zhang J. Angew. Chem. Int. Ed. 2014; 53: 6542
  • 328 Tanpure SD, Kuo T.-C, Cheng M.-J, Liu R.-S. ACS Catal. 2022; 12: 536
  • 329 Zheng Y, Chi Y, Bao M, Qiu L, Xu X. J. Org. Chem. 2017; 82: 2129
  • 330 Qi J, Teng Q, Thirupathi N, Tung C.-H, Xu Z. Org. Lett. 2019; 21: 692
  • 331 Kardile RD, Liu R.-S. Org. Lett. 2020; 22: 8229
  • 332 Li L, Kail S, Weber SM, Hilt G. Angew. Chem. Int. Ed. 2021; 60: 23 661
  • 333 Yu Y, Chen Y, Wu W, Jiang H. Chem. Commun. (Cambridge) 2017; 53: 640
  • 334 Cho C.-H, Shi F, Jung D.-I, Neuenswander B, Lushington GH, Larock RC. ACS Comb. Sci. 2012; 14: 403
  • 335 Gabriele B, Plastina P, Vetere MV, Veltri L, Mancuso R, Salerno G. Tetrahedron Lett. 2010; 51: 3565
  • 336 Gabriele B, Mancuso R, Maltese V, Veltri L, Salerno G. J. Org. Chem. 2012; 77: 8657
  • 337 Gabriele B, Veltri L, Plastina P, Mancuso R, Vetere MV, Maltese V. J. Org. Chem. 2013; 78: 4919
  • 338 Ballmann M, Ruer PC, Hofnagel O, Hiller W, Krause N. ACS Sustainable Chem. Eng. 2022; 10: 7288
  • 339 Liu W.-T, Xu Z.-L, Mou X.-Q, Zhang B.-H, Bao W, Wang S.-H, Lee D, Lei L.-S, Zhang K. Org. Biomol. Chem. 2017; 15: 6333
  • 340 Rajesh M, Puri S, Kant R, Reddy MS. Org. Lett. 2016; 18: 4332
  • 341 Barboza AA, Neto AC, Rosset IG, Jardim GAM, Ferreira MAB. J. Org. Chem. 2021; 86: 3923
  • 342 Wang C, Li Z, Ju Y, Koo S. Eur. J. Org. Chem. 2012; 6976
  • 343 Undeela S, Ramchandra JP, Menon RS. Tetrahedron Lett. 2014; 55: 5667
  • 344 Liu J, Liu Q.-Y, Fang X.-X, Liu G.-Q, Ling Y. Org. Biomol. Chem. 2018; 16: 7454
  • 345 Masal DP, Choudhury R, Singh A, Reddy DS. J. Org. Chem. 2022; 87: 556
  • 346 Li M.-B, Posevins D, Geoffroy A, Zhu C, Bäckvall J.-E. Angew. Chem. Int. Ed. 2020; 59: 1992
  • 347 Palisse A, Kirsch SF. Eur. J. Org. Chem. 2014; 7095
  • 348 Zorba L, Kidonakis M, Saridakis I, Stratakis M. Org. Lett. 2019; 21: 5552
  • 349 Li Y, Brand JP, Waser J. Angew. Chem. Int. Ed. 2013; 52: 6743
  • 350 Xia Y, Xia Y, Ge R, Liu Z, Xiao Q, Zhang Y, Wang J. Angew. Chem. Int. Ed. 2014; 53: 3917
  • 351 Zhang J, Yang Q, Zhu Y, Wang J, Deng G. J. Org. Chem. 2020; 85: 2395
  • 352 Miao M, Xu X, Xu L, Ren H. Eur. J. Org. Chem. 2014; 5896
  • 353 Yan J, Jiang M, Song L.-P, Liu J.-T. Adv. Synth. Catal. 2020; 362: 2882
  • 354 Yasukawa N, Yamada Y, Furugen C, Miki Y, Sajiki H, Sawama Y. Org. Lett. 2021; 23: 5891
  • 355 Cheng C, Liu S, Zhu G. J. Org. Chem. 2015; 80: 7604
  • 356 Miyairi A, Oonishi Y, Sato Y. Org. Biomol. Chem. 2021; 19: 9396
  • 357 Wang T, Shi S, Hansmann MH, Rettenmeier E, Rudolph M, Hashmi ASK. Angew. Chem. Int. Ed. 2014; 53: 3715
  • 358 Wang T, Shi S, Rudolph M, Hashmi ASK. Adv. Synth. Catal. 2014; 356: 2337
  • 359 Wang T, Huang L, Shi S, Rudolph M, Hashmi ASK. Chem.–Eur. J. 2014; 20: 14 868
  • 360 Kang JY, Connell BT. J. Org. Chem. 2011; 76: 2379
  • 361 Arroniz C, Chaubet G, Anderson EA. ACS Catal. 2018; 8: 8290
  • 362 Shiroodi RK, Koleda O, Gevorgyan V. J. Am. Chem. Soc. 2014; 136: 13 146
  • 363 Yang Y, Li J, Zhu R, Liu C, Zhang D. ACS Catal. 2018; 8: 9252
  • 364 Wang J, Shen C, Wang T, Mo S, Li X, Zhang Z. Adv. Synth. Catal. 2016; 358: 3943
  • 365 Yu S, Dai L, Shao Y, Li R, Chen Z, Lv N, Chen J. Org. Chem. Front. 2020; 7: 3439
  • 366 Zhu M, Fu W.-J, Xu C, Zou G.-L, Wang Z.-Q, Ji BM. Eur. J. Org. Chem. 2012; 4609
  • 367 Zhang Y, Liu F, Zhang J. Chem.–Eur. J. 2010; 16: 6146
  • 368 Marichev KO, Wang Y, Carranco AM, Garcia EC, Yu Z.-X, Doyle MP. Chem. Commun. (Cambridge) 2018; 54: 9513
  • 369 Zang W, Wei Y, Shi M. Chem. Commun. (Cambridge) 2019; 55: 8126
  • 370 Hu X, Zhou B, Jin H, Liu Y, Zhang L. Chem. Commun. (Cambridge) 2020; 56: 7297
  • 371 Yoshida M, Ohno S, Shishido K. Chem.–Eur. J. 2012; 18: 1604
  • 372 Yu B, Mohamed S, Ardisson J, Lannou M.-I, Sorin G. Chem. Commun. (Cambridge) 2022; 58: 1374
  • 373 Wang A, Lu M, Liu Y. Org. Lett. 2021; 23: 6813
  • 374 Kim HY, Li J.-Y, Oh K. J. Org. Chem. 2012; 77: 11 132
  • 375 Kim HY, Oh K. Org. Lett. 2019; 21: 696
  • 376 Bhatt D, Kim HY, Oh K. Adv. Synth. Catal. 2022; 364: 3617
  • 377 Gharpure SJ, Prasath PV, Shelke YG. Org. Lett. 2019; 21: 223
  • 378 Li X, Jandl C, Bach T. Synthesis 2021; 53: 723
  • 379 Schmidt B, Krehl S, Jablowski E. Org. Biomol. Chem. 2012; 10: 5119
  • 380 Risi C, Zhao F, Castagnolo D. ACS Catal. 2019; 9: 7264
  • 381 Chang C.-A, Gürtzgen S, Johnson EP, Vollhardt KPC. Synthesis 2020; 52: 399
  • 382 Wong JJ, Chen X, Houk KN, Vollhardt KPC. Synthesis 2021; 53: 4279
  • 383 Feng L, Yan H, Yang C, Chen D, Xia W. J. Org. Chem. 2016; 81: 7008
  • 384 Su Z, Xie Z, Wang S, Luo N, Wang C. Org. Biomol. Chem. 2019; 17: 7342
  • 385 Sugiishi T, Matsumura C, Amii H. Org. Biomol. Chem. 2020; 18: 3459
  • 386 He X, Tang Y, Wang Y, Chen J.-B, Xu S, Dou J, Li Y. Angew. Chem. Int. Ed. 2019; 58: 10 698
  • 387 Babu KR, He X, Xu S. Synlett 2020; 31: 117
  • 388 Xie R, Zhao Z, Zhao Y, Li R, Yao J, Miao M. Org. Lett. 2022; 24: 2220
  • 389 Chen J, Ni S, Ma S. Synlett 2011; 931
  • 390 Song C, Dong S, Feng L, Peng X, Wang M, Wang J, Xu Z. Org. Biomol. Chem. 2013; 11: 6258
  • 391 Ni C, Zhao Y, Yang J. ACS Sustainable Chem. Eng. 2020; 8: 12 741
  • 392 Tokareva MA, Pernik I, Lewis W, Messerle BA, Glukhareva TV, Keaveney ST. ACS Catal. 2022; 12: 5574
  • 393 Yang W, Chen Y, Yao Y, Lin Q, Yang D. Adv. Synth. Catal. 2019; 361: 5634
  • 394 Yang Y, Zuo L, Wei K, Guo W. Org. Lett. 2021; 23: 3195
  • 395 Dobesch M, Greiner J, Maas G. Synthesis 2020; 52: 2987
  • 396 Gil de Montes E, Martínez-Bailén M, Carmona AT, Robina I, Moreno-Vargas AJ. J. Org. Chem. 2020; 85: 8923
  • 397 Tuteja J, Nishimura S, Ebitani K. Bull. Chem. Soc. Jpn. 2012; 85: 275
  • 398 Cao Z, Zhu C, Wu W, Zhu D, Qian D, Zhu J, Chang T, Sheng M, Yang X, Liu W. J. Carbohydr. Chem. 2020; 39: 472
  • 399 Schmidt B, Geißler D. Eur. J. Org. Chem. 2011; 7140
  • 400 Raut VS, Jean M, Vanthuyne N, Roussel C, Constantieux T, Bressy C, Bugaut X, Bonne D, Rodriguez J. J. Am. Chem. Soc. 2017; 139: 2140
  • 401 Liu C, Zhou L, Huang W, Wang M, Gu Y. Adv. Synth. Catal. 2016; 358: 900
  • 402 Shigeno M, Hanasaka K, Sasaki K, Nozawa-Kumada K, Kondo Y. Chem.–Eur. J. 2019; 25: 3235
  • 403 Mita T, Masutani H, Ishii S, Sato Y. Synlett 2019; 30: 841
  • 404 Luo W, Jiang K, Li Y, Jiang H, Yin B. Org. Lett. 2020; 22: 2093
  • 405 Shcherbinin VA, Shpuntov PM, Konshin VV, Butin AV. Tetrahedron Lett. 2016; 57: 1473
  • 406 Sanz-Vidal AS, Miró J, Sánchez-Roselló M, del Pozo C, Fustero S. J. Org. Chem. 2016; 81: 6515
  • 407 Belhomme MC, Poisson T, Pannecoucke X. J. Org. Chem. 2014; 79: 7205
  • 408 Baguia H, Evano G. Chem.–Eur. J. 2022; 28: e202103599
  • 409 Su Y.-M, Hou Y, Yin F, Xu Y.-M, Li Y, Zheng X, Wang X.-S. Org. Lett. 2014; 16: 2958
  • 410 Topinka M, Tata RR, Harmata M. Org. Lett. 2014; 16: 4476 corrigendum: Org. Lett. 2014; 16: 5508
  • 411 Chen Y, Liu Y. J. Org. Chem. 2011; 76: 5274
  • 412 Luque-Agudo V, Gil MV, Román E, Serrano JA. Green Chem. 2016; 18: 3844
  • 413 Park SH, Kim JY, Chang S. Org. Lett. 2011; 13: 2372
  • 414 Sevov CS, Hartwig JF. J. Am. Chem. Soc. 2014; 136: 10 625
  • 415 Gorsline BJ, Wang L, Ren P, Carrow BP. J. Am. Chem. Soc. 2017; 139: 9605
  • 416 Zhang Y, Li Z, Liu Z.-Q. Org. Lett. 2012; 14: 226
  • 417 Jiang Z, Zhang L, Dong C, Cai Z, Tang W, Li H, Xu L, Xiao J. Adv. Synth. Catal. 2012; 354: 3225
  • 418 Ncube G, Huestis MP. Organometallics 2019; 38: 76
  • 419 Padala K, Pimparkar S, Madasamy P, Jeganmohan M. Chem. Commun. (Cambridge) 2012; 48: 7140
  • 420 Chen H, Farizyan M, Ghiringhelli F, van Gemmeren M. Angew. Chem. Int. Ed. 2020; 59: 12 213
  • 421 Sala R, Kiala G, Veiros LF, Broggini G, Poli G, Oble J. J. Org. Chem. 2022; 87: 4640
  • 422 Pham MV, Cramer N. Angew. Chem. Int. Ed. 2014; 53: 14 575
  • 423 Schneider T, Heinrich G, Koch R, Maas G. Eur. J. Org. Chem. 2021; 1011
  • 424 Wang Y, Pritchard GJ, Kimber MC. Org. Lett. 2019; 21: 4892
  • 425 Hashmi ASK, Häffner T, Yang W, Pankajakshan S, Schäfer S, Schultes L, Rominger F, Frey W. Chem.–Eur. J. 2012; 18: 10 480
  • 426 Liu C.-H, Yu Z.-X. Org. Chem. Front. 2014; 1: 1205
  • 427 Wang Q, Zhang W.-W, Song H, Wang J, Zheng C, Gu Q, You S.-L. J. Am. Chem. Soc. 2020; 142: 15 678
  • 428 Fernandes R, Mhaske K, Balhara R, Jindal G, Narayan R. Chem.–Asian J. 2022; 17: e202101369
  • 429 Dai C, Huang Z.-H, Liu L, Han Y, Shi D.-Q, Zhao Y. Eur. J. Org. Chem. 2020; 826
  • 430 Shinde VN, Bhuvanesh N, Kumar A, Joshi H. Organometallics 2020; 39: 324
  • 431 Shin T, Kim M, Jung Y, Cho SJ, Kim H, Song H. Chem. Commun. (Cambridge) 2020; 56: 14 404
  • 432 Matsidik R, Martin J, Schmidt S, Obermayer J, Lombeck F, Nübling F, Komber H, Fazzi D, Sommer M. J. Org. Chem. 2015; 80: 980
  • 433 Abdellaoui F, Youssef C, Ammar HB, Soulé J.-F, Doucet H. Synthesis 2014; 46: 3341
  • 434 Ohno A, Sato T, Mase T, Uozumi Y, Yamada YMA. Adv. Synth. Catal. 2020; 362: 4687
  • 435 Zhang X, Liu J, Yang Y, Wang F, Jiang H, Yin B. Org. Chem. Front. 2016; 3: 1105
  • 436 Beladhria A, Yuan K, Ammar HB, Soulé J.-F, Salem RB, Doucet H. Synthesis 2014; 46: 2515
  • 437 Natarajan P, Bala A, Mehta SK, Bhasin KK. Tetrahedron 2016; 72: 2521
  • 438 Sasmal A, Roisnel T, Bera JK, Doucet H, Soulé J.-F. Synthesis 2019; 51: 3241
  • 439 Ambika , Singh PP. Catal. Lett. 2022; 152: 2288
  • 440 Hari DP, Schroll P, König B. J. Am. Chem. Soc. 2012; 134: 2958
  • 441 Rajmohan R, Nisha P, Vairaprakash P. ACS Omega 2019; 4: 14 458
  • 442 Zhou Y, Deng S, Mai S, Song Q. Org. Lett. 2018; 20: 6161
  • 443 Schramm Y, Takeuchi M, Semba K, Nakao Y, Hartwig JF. J. Am. Chem. Soc. 2015; 137: 12 215
  • 444 Sevov CS, Hartwig JF. J. Am. Chem. Soc. 2013; 135: 2116
  • 445 Stoermer MJ, Richter H.-M, Kaufmann DE. Tetrahedron Lett. 2013; 54: 6776
  • 446 Zhang H, Toy PH. Adv. Synth. Catal. 2021; 363: 215
  • 447 Li J.-L, Yue C.-Z, Chen P.-Q, Xiao Y.-C, Chen Y.-C. Angew. Chem. Int. Ed. 2014; 53: 5449
  • 448 Fadeev AA, Makarov AS, Uchuskin MG. J. Org. Chem. 2021; 86: 17 362
  • 449 Zhang X.-R, Zhou S.-L, Yuan Y, Du W, Chen Y.-C. Synlett 2017; 28: 1771
  • 450 Cho YS, Kim ST, Ryu DH. Org. Lett. 2022; 24: 1732
  • 451 Luo W, Yang Y, Liu B, Yin B. J. Org. Chem. 2020; 85: 9396
  • 452 Yuan J, Zhang X, Yang C. RSC Adv. 2021; 11: 13 832
  • 453 Wang S, Ni Z, Huang X, Wang J, Pan Y. Org. Lett. 2014; 16: 5648
  • 454 Zhang L.-Y, Wu Y.-H, Wang N.-X, Gao X.-W, Yan Z, Xu B.-C, Liu N, Wang B.-Z, Xing Y. Eur. J. Org. Chem. 2021; 1446
  • 455 Ernst JB, Rakers L, Glorius F. Synthesis 2017; 49: 260
  • 456 Chen S, Zhu J, Ke J, Li Y, He C. Angew. Chem. Int. Ed. 2022; 61: e202117820
  • 457 Britton L, Skrodzki M, Nichol GS, Dominey AP, Pawluć P, Docherty JH, Thomas SP. ACS Catal. 2021; 11: 6857
  • 458 Donnelly LJ, Faber T, Morrison CA, Nichol GS, Thomas SP, Love JB. ACS Catal. 2021; 11: 7394
  • 459 Britton L, Docherty JH, Dominey AP, Thomas SP. Molecules 2020; 25: 905
  • 460 Hatanaka T, Ohki Y, Tatsumi K. Chem.–Asian J. 2010; 5: 1657
  • 461 Wang Y, Noble A, Sandford C, Aggarwal VK. Angew. Chem. Int. Ed. 2017; 56: 1810
  • 462 Silvi M, Schrof R, Noble A, Aggarwal VK. Chem.–Eur. J. 2018; 24: 4279
  • 463 Kotzabasaki V, Vassilikogiannakis G, Stratakis M. J. Org. Chem. 2016; 81: 4406
  • 464 Montaña AM, Grima PM, Batalla C, Kociok-Köhn G. Tetrahedron: Asymmetry 2014; 25: 677
  • 465 Miygawa N, Murase Y, Okano K, Mori A. Synlett 2017; 28: 1106
  • 466 Mari D, Miyagawa N, Okano K, Mori A. J. Org. Chem. 2018; 83: 14 126
  • 467 Piller FM, Knochel P. Synthesis 2011; 1751
  • 468 Ghosh AK, Born JR, Veitschegger AM, Jurica MS. J. Org. Chem. 2020; 85: 8111
  • 469 Huang G, Yin B. Adv. Synth. Catal. 2019; 361: 5576
  • 470 Chacón-Huete DF, Lasso JD, Szavay P, Covone J, Forgione P. J. Org. Chem. 2021; 86: 515
  • 471 Ishikawa S, Noda Y, Wada M, Nishikata T. J. Org. Chem. 2015; 80: 7555
  • 472 Riley AP, Groer CE, Young D, Ewald AW, Kivell BM, Prisinzano TE. J. Med. Chem. 2014; 57: 10 464
  • 473 Herrera-Luna JC, Díaz DD, Abramov A, Encinas S, Jiménez MC, Pérez-Ruiz R. Org. Lett. 2021; 23: 2320
  • 474 Haner J, Jack K, Nagireddy J, Raheem MA, Durham R, Tam W. Synthesis 2011; 731
  • 475 Zhang X, Tong Y, Li G, Zhao H, Chen G, Yao H, Tong R. Angew. Chem. Int. Ed. 2022; 61: e202205919
  • 476 Skrzyńska A, Przydacz A, Albrecht Ł. Org. Lett. 2015; 17: 5682
  • 477 Su Y.-L, Han Z.-Y, Li Y.-H, Gong L.-Z. ACS Catal. 2017; 7: 7917
  • 478 Przydacz A, Dyguda M, Topolska A, Skrzyńska A, Xu C.-J, Chen Y.-C, Albrecht Ł. Org. Biomol. Chem. 2020; 18: 5816
  • 479 Ren D, Xu L, Wang L, Li S.-S. Org. Lett. 2019; 21: 627
  • 480 Bisht N, Babu SA, Tomar R. Asian J. Org. Chem. 2020; 9: 1225
  • 481 Fournier J, Arseniyadis S, Cossy J. Angew. Chem. Int. Ed. 2012; 51: 7562