Subscribe to RSS
DOI: 10.1055/s-0041-1737882
Biaryl Coupling of Aryldiazonium Salts and Arylboronic Acids Catalysed by Gold
This work was supported by the Consejo Nacional de Ciencia y Tecnología (CONACyT) (A1-S-7805), and Dirección General de Asuntos del Personal Académico (DGAPA), Universidad Nacional Autónoma de México (IN208120). I.M.-M. thanks CONACyT for a scholarship (701363).
Abstract
A gold-catalysed coupling of aryldiazonium salts with arylboronic acids is described. The reactions proceed in satisfactory yields under irradiation with blue LEDs in the presence of KF and a catalytic amount of ascorbic acid. Notably, 4-nitrobenzendiazonium tetrafluoroborate is sufficiently reactive to undergo the coupling with a variety of arylboronic acids in the absence of aryl radical initiators. The coupling is applicable for electron-donating and electron-withdrawing groups present at the para, ortho, and meta positions of both substrates.
Supporting Information
- Supporting information for this article is available online at https://doi.org/ 10.1055/s-0041-1737882.
- Supporting Information
Publication History
Received: 14 December 2021
Accepted after revision: 13 January 2022
Article published online:
24 February 2022
© 2022. Thieme. All rights reserved
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1a Dagne E, Steglich W. Phytochemistry 1984; 23: 1729
- 1b Hubbard BK, Walsh CT. Angew. Chem. Int. Ed. 2003; 42: 730 ; Angew. Chem. 2003, 115, 752
- 1c Bringmann G, Mortimer AJ. P, Keller PA, Gresser MJ, Garner J, Breuning M. Angew. Chem. Int. Ed. 2005; 44: 5384
- 1d Kozlowski MC, Morgan BJ, Linton EC. Chem. Soc. Rev. 2009; 38: 3193
-
1e
Fleming FF,
Yao L,
Ravikumar PC,
Funk L,
Shook BC.
J. Med. Chem. 2010; 53: 7902
- 1f Farmer LJ, Ledeboer MW, Hoock T, Arnost MJ, Bethiel RS. J. Med. Chem. 2015; 58: 7195
- 1g Jamali H, Khan HA, Tjin CC, Ellman JA. ACS Med. Chem. Lett. 2016; 7: 847
- 1h Witten MR, Wissler L, Snow M, Geschiwindner S, Read JA, Brandon NJ, Nairn AC, Lombroso PJ, Käck H, Ellman JA. J. Med. Chem. 2017; 60: 9299
- 2 Hassan J, Sévignon M, Goozi C, Schulz E, Lemaire M. Chem. Rev. 2002; 102: 1359
- 3a Miyaura N, Suzuki A. Chem. Rev. 1995; 95: 2457
- 3b Martin R, Buchwald SL. Acc. Chem. Res. 2008; 41: 1461
- 3c Paul S, Islam MdM, Islam SkM. RSC Adv. 2015; 5: 42193
- 3d Hussain I, Capricho J, Yawer MA. Adv. Synth. Catal. 2016; 358: 3320
- 3e Lamblin M, Nassar-Hardy L, Hierso J.-C, Fouquet E, Felpin FX. Adv. Synth. Catal. 2010; 352: 33
- 3f Ayogu JI, Onobedje EA. Catal. Sci. Technol. 2019; 9: 5233
- 3g Jose DE, Kanchana US, Mathew TV, Anilkumar G. J. Organomet. Chem. 2020; 927: 121538
- 3h Kadu BS. Catal. Sci. Technol. 2021; 11: 1186
- 4a Molander GA, Ellis N. Acc. Chem. Res. 2007; 40: 275
- 4b Doucet H. Eur. J. Org. Chem. 2008; 2013
- 4c Lennox AJ. J, Lloyd-Jones GC. Chem. Soc. Rev. 2014; 43: 412
- 4d de Jesus Hiller N, do Ama al e Silva NA, Tavares TA, Faria RX, Eberlin MN, de Luna Martins D. Eur. J. Org. Chem. 2020; 4841
- 5 Littke AF, Dai C, Fu GC. J. Am. Chem. Soc. 2000; 122: 4020
- 6a Darses S, Jeffery T, Genêt J.-P, Brayer J.-L, Demoute JP. Tetrahedron Lett. 1996; 37: 3857
- 6b Darses S, Genêt J.-P. Tetrahedron Lett. 1997; 38: 4393
- 6c Sengupta S, Bhattacharyya S. J. Org. Chem. 1997; 62: 3405
- 7a Roglans A, Pla-Quintana A, Moreno-Mañas M. Chem. Rev. 2006; 106: 4622
- 7b Bonin H, Fouquet E, Felpin F.-X. Adv. Synth. Catal. 2011; 353: 3063
- 8a Gauchot V, Lee A.-L. Chem. Commun. 2016; 52: 10163
- 8b Cornilleau T, Hermange P, Fouquet E. Chem. Commun. 2016; 52: 10040
- 8c Witzel S, Xie J, Rudolph M, Hashmi AS. K. Adv. Synth. Catal. 2017; 359: 1522
- 8d Sauer C, Liu Y, De Nisi A, Protti S, Fagnoni M, Bandini M. ChemCatChem 2017; 9: 4456
- 8e Tabey A, Berlande M, Hermange P, Fouquet E. Chem. Commun. 2018; 54: 12867
- 8f Witzel S, Sekine K, Rudolph M, Hashmi AS. K. Chem. Commun. 2018; 54: 13802
- 8g Barbero M, Dughera S. Tetrahedron 2018; 74: 5758
- 9a Kim S, Rojas-Martin J, Toste FD. Chem. Sci. 2016; 7: 85
- 9b Alcaide B, Almendros P, Busto E, Lázaro-Milla C. J. Org. Chem. 2017; 82: 2177
- 9c Alcaide B, Almendros P, Bustos E, Herrera F, Lázaro-Milla C, Luna A. Adv. Synth. Catal. 2017; 359: 2640
- 9d Akram MO, Mali PS, Patil NT. Org. Lett. 2017; 19: 3075
- 9e Chakrabarty I, Akram MO, Biswas S, Patil NT. Chem. Commun. 2018; 54: 7223
- 9f Xie J, Sekine K, Witzel S, Krämer P, Rudolph M, Rominger F, Hashmi AS. K. Angew. Chem. Int. Ed. 2018; 57: 16648 ; Angew. Chem. 2018, 130, 16890
- 9g Arylgermanes: Sherborne GJ, Gevondian AG, Funez-Ardoiz I, Dahiya A, Fricke C, Schoenebeck F. Angew. Chem. Int. Ed. 2020; 59: 15543
- 9h Stannanes: Akram MO, Shinde PS, Chintawar CC, Patil NT. Org. Biomol. Chem. 2018; 16: 2865
- 10a Joost M, Amgoune A, Bourissou D. Angew. Chem. Int. Ed. 2015; 54: 15022
- 10b Miró J, del Pozo C. Chem. Rev. 2016; 116: 11924
- 10c Zeineddine A, Estévez L, Mallet-Ladeira S, Miqueu K, Amgoune A, Bourissou D. Nat. Commun. 2017; 8: 565
- 10d Akram MO, Das A, Chakrabarty I, Patil NT. Org. Lett. 2019; 21: 8101
- 10e Rodriguez J, Zeineddine A, Sosa-Carrizo ED, Miqueu K, Saffon-Merceron N, Amgoune A, Bourissou D. Chem. Sci. 2019; 10: 7183
- 10f Bhoyare VW, Tathe AG, Das A, Chintawar CC, Patil NT. Chem. Soc. Rev. 2021; 50: 10422
- 10g Banerjee S, Bhoyare VW, Patil NT. Chem. Commun. 2020; 56: 2677
- 10h Rodríguez J, Adet N, Saffon-Merceron N, Bourissou D. Chem. Commun. 2020; 56: 94
- 11a Hopkinson MN, Sahoo B, Li J.-L, Glorius F. Chem. Eur. J. 2014; 20: 3874
- 11b Zhang M, Zhu C, Ye L.-W. Synthesis 2017; 49: 1150
- 11c Xie J, Jin H, Hashmi AS. K. Chem. Soc. Rev. 2017; 46: 5193
- 11d Akram MO, Banerjee S, Saswade SS, Bedi V, Patil NT. Chem. Commun. 2018; 54: 11069
- 11e Zidan M, Rohe S, McCallum T, Barriault L. Catal. Sci. Technol. 2018; 8: 6019
- 11f Nijamudheen A, Datta A. Chem. Eur. J. 2020; 26: 1442
- 11g Medina-Mercado I, Porcel P. Chem. Eur. J. 2020; 26: 16206
- 11h Rocchigiani L, Bochmann M. Chem. Rev. 2021; 121: 8364
- 11i Witzel S, Hashmi AS. K, Xie J. Chem. Rev. 2021; 121: 8868
- 11j Font P, Ribas X. Eur. J. Inorg. Chem. 2021; 26: 2556
- 12a Cai R, Lu M, Aguilera EY, Xi Y, Akhmedov NG, Petersen JL, Chen H, Shi X. Angew. Chem. Int. Ed. 2015; 54: 8772 ; Angew. Chem. 2015, 127, 8896
- 12b Peng H, Cai R, Xu C, Chen H, Shi X. Chem. Sci. 2016; 7: 6190
- 12c Dong B, Peng H, Motika SE, Shi X. Chem. Eur. J. 2017; 23: 11093
- 12d Jimoh AA, Hosseyni S, Ye X, Wotjas L, Hu Y, Shi X. Chem. Commun. 2019; 55: 8150
- 12e Yuan T, Tang Q, Shan C, Ye X, Wang J, Zhao P, Wotjas L, Hadler N, Chen H, Shi X. J. Am. Chem. Soc. 2021; 143: 4074
- 13a Asomoza-Solís EO, Rojas-Ocampo J, Toscano RA, Porcel S. Chem. Commun. 2016; 52: 7295
- 13b Carrillo-Arcos UA, Porcel S. Org. Biomol. Chem. 2018; 11: 1837
- 14a Medina-Mercado I, Asomoza-Solís EO, Martínez-González E, Ugalde-Saldívar VM, Ledesma-Olvera LG, Barquera-Lozada JE, Gómez-Vidales V, Barroso-Flores J, Frontana-Uribe BA, Porcel S. Chem. Eur. J. 2020; 26: 634
- 14b Medina-Mercado I, Colin-Molina A, Barquera-Lozada JE, Rodríguez-Molina B, Porcel S. ACS. Catal. 2021; 11: 8968
- 15 Winston MS, Wolf WJ, Toste FD. J. Am. Chem. Soc. 2015; 137: 7921
- 16 Kumar R, Linden A, Nevado C. J. Am. Chem. Soc. 2016; 138: 13790
- 17a Zhang Q, Zhang Z.-Q, Fu Y, Yu H.-Z. ACS Catal. 2016; 6: 798
- 17b Bhattacharjee R, Datta A. Chem. Eur. J. 2018; 24: 13636
- 17c Liu Y, Yang Y, Zhu R, Liu C, Zhang D. Chem. Eur. J. 2018; 24: 14119
- 17d Taschinski S, Döpp R, Ackermann M, Rominger F, de Vries F, Menger MF. S. J, Rudolph M, Hashmi AS. K, Klein JE. M. N. Angew. Chem. Int. Ed. 2019; 58: 16988 ; Angew. Chem. 2019, 131, 17144
- 17e Liu Y, Zhu R, Liu C, Zhang D. Org. Chem. Front. 2021; 9: 147
- 17f Witzel S, Hoffmann M, Rudolph M, Rominger F, Dreuw A, Hashmi AS. K. Adv. Synth. Catal. 2021; 364: 581
- 17g Alcaide B, Almendros P, Aparicio B, Lázaro-Milla C, Luna A, Nieto Faza O. Adv. Synth. Catal. 2017; 359: 2789
- 17h Lázaro-Milla C, Busto E, Burgos I, Nieto Faza O, Almendros P. J. Catal. 2020; 391: 48
- 18 Armarego WL. F, Chai CL. L. Purification of Laboratory Chemicals . Elsevier Science & Technology; Amsterdam: 2003
- 19 Doyle MP, Bryker WJ. J. Org. Chem. 1979; 44: 1572
- 20 Cho S.-D, Kim H.-K, Yim H.-S, Kim M.-R, Lee J.-K, Kim J.-J, Yoon Y.-J. Tetrahedron 2007; 63: 1345
- 21 Grossman O, Gelman D. Org. Lett. 2006; 8: 1189
- 22 Zhang G. Synthesis 2005; 537
- 23 Zhou W.-J, Wang K.-H, Wang J.-X, Huang D.-F. Eur. J. Org. Chem. 2010; 416
- 24 Qin C, Lu W. J. Org. Chem. 2008; 73: 7424
- 25 Zhang G. J. Chem. Res. 2004; 9: 593
- 26 Song C, Ma Y, Chai Q, Ma C, Jiang W, Andrus MB. Tetrahedron 2005; 61: 7438
- 27 Sherborne GJ, Gevondian AG, Funes-Ardoiz J, Dahiya A, Fricke C, Schoenebeck F. Angew. Chem. Int. Ed. 2020; 59: 15543
- 28 Schiek M, Al-Shamery K, Lützen A. Synthesis 2007; 613
- 29 Kumar NS. C. R, Raj IV. P, Sudalai A. J. Mol. Catal. A: Chem. 2007; 269: 218
- 30 Ahmed J, Chakraborty S, Jose A, Sreejyothi P, Mandal SK. J. Am. Chem. Soc. 2018; 140: 8330
- 31 Standaert RF, Park SB. J. Org. Chem. 2006; 71: 7952
- 32 Shi S, Zhang Y. J. Org. Chem. 2007; 72: 5927
- 33 Bernhardt S, Manolikakes G, Kunz T, Knochel P. Angew. Chem. Int. Ed. 2011; 39: 9205
- 34 Yu D.-G, Yu M, Guan B.-T, Li B.-J, Zheng Y, Wu Z.-H, Shi Z.-J. Org. Lett. 2009; 11: 3374
- 35 Qiu J, Wang L, Liu M, Shen Q, Tang J. Tetrahedron Lett. 2011; 52: 6489
- 36 Papoian V, Minehan T. J. Org. Chem. 2008; 73: 7376
- 37 Desmarets C, Omar-Amrani R, Walcarius A, Lambert J, Champagne B, Fort Y, Schneider R. Tetrahedron 2008; 64: 372
- 38 Nagaki A, Ashikari Y, Kawaguchi T, Mandai K, Aizawa Y. J. Am. Chem. Soc. 2020; 142: 17039
- 39 Schiek M, Al-Shamery K, Lützen A. Synthesis 2007; 4: 613
- 40 Sinha N, Champagne PA, Rodríguez MJ, Lu Y, Kopach ME, Mitchell D, Organ MG. Chem. Eur. J. 2009; 25: 6508
- 41 Rao S, Mague JT, Balakrishna MS. Dalton Trans. 2013; 42: 11695
- 42 Lipshutz BH, Frieman BA, Lee C.-T, Lower A, Nihan DM, Taft BR. Chem. Asian J. 2006; 1: 417
- 43 Ackermann L, Gschrei CJ, Althammer A, Riederer M. Chem. Commun. 2006; 13: 1419
- 44 Sapountzis I, Lin W, Kofink CC, Despotopoulou C, Knochel P. Angew. Chem. Int. Ed. 2005; 44: 1654
- 45 Bai L, Wang J.-X. Adv. Synth. Catal. 2008; 350: 315
- 46 Felpin F.-X, Fouquet E. Adv. Synth. Catal. 2008; 350: 863
- 47 Watson DA, Su M, Teverovsky G, Zhang Y, García-Fortanet J, Kinzel T, Buchwald SL. Science 2009; 325: 1661
- 48 Dektar JL, Hacker NP. J. Org. Chem. 1990; 55: 639
- 49 Moreno-Mañas M, Pleixats R, Serra-Muns A. Synthesis 2006; 3001
- 50 Lourdusamy E, Arumugam S. ARKIVOC 2007; (xiv): 126
- 51 Caron L, Campeau L.-C, Fagnou K. Org. Lett. 2008; 10: 4533
For selected reviews on the Suzuki–Miyaura reaction, see:
Examples of couplings of other aryl nucleophiles catalysed by gold. Arylsilanes:
For reviews and selected examples on Au(I)/Au(III) catalytic couplings, see:
For reviews on gold-catalysed reactions with aryldiazonium salts, see:
For other base-promoted reactions with gold, see:
For related DFT studies on Au(I)/Au(III) couplings, see: