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Volumn 52, Issue 65, 2016, Pages 10040-10043

Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: Probing the usefulness of photoredox conditions

(3) Cornilleau, Thomas a Hermange, Philippe a Fouquet, Eric a

a UNIVERSITÉ DE BORDEAUX (France)

Author keywords

[No Author keywords available]

Indexed keywords

2 IODOBENZYL ALCOHOL; ACETONITRILE; ALCOHOL; ALCOHOL DERIVATIVE; ALDEHYDE; BORONIC ACID DERIVATIVE; DIAZONIUM COMPOUND; GOLD; PALLADIUM; PHOTOSENSITIZING AGENT; UNCLASSIFIED DRUG;

ARTICLE; CARBONYLATION; CATALYSIS; CATALYST; CROSS COUPLING REACTION; IRRADIATION; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; SYNTHESIS;

EID: 84981169912 PISSN: 13597345 EISSN: 1364548X Source Type: Journal
DOI: 10.1039/c6cc04239b Document Type: Article

Times cited : (72)

References (57)

1
- 84891577048
- Wiley-VCH, Weinheim, Germany
- Modern Gold Catalyzed Synthesis, ed., A. S. K. Hashmi, and, F. D. Toste, Wiley-VCH, Weinheim, Germany, 2012
- (2012) Modern Gold Catalyzed Synthesis
- Hashmi, A.S.K.¹ Toste, F.D.²

2
- 77749327971
- N. D. Shapiro F. D. Toste Synlett 2010 675
- (2010) Synlett , pp. 675
- Shapiro, N.D.¹ Toste, F.D.²

3
- 84857594600
- M. Rudolph A. S. K. Hashmi Chem. Soc. Rev. 2012 41 2448
- (2012) Chem. Soc. Rev. , vol.41 , pp. 2448
- Rudolph, M.¹ Hashmi, A.S.K.²

4
- 84888628604
- C. Obradors A. M. Echavarren Chem. Commun. 2014 50 16
- (2014) Chem. Commun. , vol.50 , pp. 16
- Obradors, C.¹ Echavarren, A.M.²

5
- 84896514515
- A. Fürstner Acc. Chem. Res. 2014 47 925
- (2014) Acc. Chem. Res. , vol.47 , pp. 925
- Fürstner, A.¹

6
- 84935009621
- R. Dorel A. M Echavarren Chem. Rev. 2015 115 9028
- (2015) Chem. Rev. , vol.115 , pp. 9028
- Dorel, R.¹ Echavarren A, M.²

7
- 84954448762
- M. Joost A. Amgoune D. Bourissou Angew. Chem., Int. Ed. 2015 54 15022
- (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 15022
- Joost, M.¹ Amgoune, A.² Bourissou, D.³

8
- 79960298576
- M. N. Hopkinson A. D. Gee V. Gouverneur Chem.-Eur. J. 2011 17 8248
- (2011) Chem.-Eur. J. , vol.17 , pp. 8248
- Hopkinson, M.N.¹ Gee, A.D.² Gouverneur, V.³

9
- 79851471855
- K. M. Engle T.-S. Mei X. Wang J.-Q. Yu Angew. Chem., Int. Ed. 2011 50 1478
- (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 1478
- Engle, K.M.¹ Mei, T.-S.² Wang, X.³ Yu, J.-Q.⁴

10
- 84866762042
- L. T. Ball G. C. Lloyd-Jones C. A. Russel Science 2012 337 1644
- (2012) Science , vol.337 , pp. 1644
- Ball, L.T.¹ Lloyd-Jones, G.C.² Russel, C.A.³

11
- 33646392116
- D. F. DeTar T. Kosuge J. Am. Chem. Soc. 1958 80 6072
- (1958) J. Am. Chem. Soc. , vol.80 , pp. 6072
- DeTar, D.F.¹ Kosuge, T.²

12
- 33845282410
- M. P. Doyle J. K. Guy K. C. Brown S. N. Mahapatro C. M. VanZyl J. R. Pladziewicz J. Am. Chem. Soc. 1987 109 1536
- (1987) J. Am. Chem. Soc. , vol.109 , pp. 1536
- Doyle, M.P.¹ Guy, J.K.² Brown, K.C.³ Mahapatro, S.N.⁴ VanZyl, C.M.⁵ Pladziewicz, J.R.⁶

13
- 0035936805
- M. N. Weaver S. Z. Janicki P. A. Petillo J. Org. Chem. 2001 66 1138
- (2001) J. Org. Chem. , vol.66 , pp. 1138
- Weaver, M.N.¹ Janicki, S.Z.² Petillo, P.A.³

14
- 60749130242
- G. Schmidt S. Gallon S. Esnouf J.-P. Bourguoin P. Chenevier Chem.-Eur. J. 2009 15 2101
- (2009) Chem.-Eur. J. , vol.15 , pp. 2101
- Schmidt, G.¹ Gallon, S.² Esnouf, S.³ Bourguoin, J.-P.⁴ Chenevier, P.⁵

15
- 84988555163
- M. D. Levin S. Kim F. D. Toste ACS Cent. Sci. 2016 2 293
- (2016) ACS Cent. Sci. , vol.2 , pp. 293
- Levin, M.D.¹ Kim, S.² Toste, F.D.³

16
- 84880124916
- C. K. Prier D. A. Rankic D. W. C. MacMillan Chem. Rev. 2013 113 5322
- (2013) Chem. Rev. , vol.113 , pp. 5322
- Prier, C.K.¹ Rankic, D.A.² MacMillan, D.W.C.³

17
- 84897915531
- M. N. Hopkinson B. Sahoo J.-L. Li F. Glorius Chem.-Eur. J. 2014 20 3874
- (2014) Chem.-Eur. J. , vol.20 , pp. 3874
- Hopkinson, M.N.¹ Sahoo, B.² Li, J.-L.³ Glorius, F.⁴

18
- 84940398603
- R. A. Angnes Z. Li C. R. Correia G. B. Hammond Org. Biomol. Chem. 2015 13 9152
- (2015) Org. Biomol. Chem. , vol.13 , pp. 9152
- Angnes, R.A.¹ Li, Z.² Correia, C.R.³ Hammond, G.B.⁴

19
- 84904740263
- S. Fukuzumi K. Ohkubo Org. Biomol. Chem. 2014 12 6059
- (2014) Org. Biomol. Chem. , vol.12 , pp. 6059
- Fukuzumi, S.¹ Ohkubo, K.²

20
- 84891792138
- D. A. Nicewicz T. M. Nguyen ACS Catal. 2014 4 355
- (2014) ACS Catal. , vol.4 , pp. 355
- Nicewicz, D.A.¹ Nguyen, T.M.²

21
- 84885361505
- T. Koike M. Akita Synlett 2013 2492
- (2013) Synlett , pp. 2492
- Koike, T.¹ Akita, M.²

22
- 84876487932
- B. Sahoo M. N. Hopkinson F. Glorius J. Am. Chem. Soc. 2013 135 5505
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 5505
- Sahoo, B.¹ Hopkinson, M.N.² Glorius, F.³

23
- 84941055830
- M. N. Hopkinson B. Sahoo F. Glorius Adv. Synth. Catal. 2014 356 2794
- (2014) Adv. Synth. Catal. , vol.356 , pp. 2794
- Hopkinson, M.N.¹ Sahoo, B.² Glorius, F.³

24
- 84899500083
- X.-Z. Shu M. Zhang Y. He H. Frei F. D. Toste J. Am. Chem. Soc. 2014 136 5844
- (2014) J. Am. Chem. Soc. , vol.136 , pp. 5844
- Shu, X.-Z.¹ Zhang, M.² He, Y.³ Frei, H.⁴ Toste, F.D.⁵

25
- 84939832830
- D. V. Patil H. Yun S. Shin Adv. Synth. Catal. 2015 357 2622
- (2015) Adv. Synth. Catal. , vol.357 , pp. 2622
- Patil, D.V.¹ Yun, H.² Shin, S.³

26
- 84921341133
- Y. He H. Wu F. D. Toste Chem. Sci. 2015 6 1194
- (2015) Chem. Sci. , vol.6 , pp. 1194
- He, Y.¹ Wu, H.² Toste, F.D.³

27
- 84951197056
- A. Tlahuext-Aca M. N. Hopkinson B. Sahoo F. Glorius Chem. Sci. 2016 7 89
- (2016) Chem. Sci. , vol.7 , pp. 89
- Tlahuext-Aca, A.¹ Hopkinson, M.N.² Sahoo, B.³ Glorius, F.⁴

28
- 84951194469
- S. Kim J. Rojas-Martin F. D. Toste Chem. Sci. 2016 7 85
- (2016) Chem. Sci. , vol.7 , pp. 85
- Kim, S.¹ Rojas-Martin, J.² Toste, F.D.³

29
- 84957577878
- J. Um H. Yun S. Shin Org. Lett. 2016 18 484
- (2016) Org. Lett. , vol.18 , pp. 484
- Um, J.¹ Yun, H.² Shin, S.³

30
- 84960145256
- A. Tlahuext-Aca M. N. Hopkinson R. A. Garza-Sancheza F. Glorius Chem.-Eur. J. 2016 22 5909
- (2016) Chem.-Eur. J. , vol.22 , pp. 5909
- Tlahuext-Aca, A.¹ Hopkinson, M.N.² Garza-Sancheza, R.A.³ Glorius, F.⁴

31
- 84965082718
- B. Alcaide O. Almendros E. Busto A. Luna Adv. Synth. Catal. 2016 358 1526
- (2016) Adv. Synth. Catal. , vol.358 , pp. 1526
- Alcaide, B.¹ Almendros, O.² Busto, E.³ Luna, A.⁴

32
- 84957544359
- Q. Zhang Z.-Q. Zhang Y. Fu H.-Z. Yu ACS Catal. 2016 6 798
- (2016) ACS Catal. , vol.6 , pp. 798
- Zhang, Q.¹ Zhang, Z.-Q.² Fu, Y.³ Yu, H.-Z.⁴

33
- 77956646271
- N. P. Mankad F. D. Toste J. Am. Chem. Soc. 2010 132 12859
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 12859
- Mankad, N.P.¹ Toste, F.D.²

34
- 84897011653
- M. Hofer E. Gomez-Bengoa C. Nevado Organometallics 2014 33 1328
- (2014) Organometallics , vol.33 , pp. 1328
- Hofer, M.¹ Gomez-Bengoa, E.² Nevado, C.³

35
- 84918816343
- Q. Wu C. Du Y. Huang X. Liu Z. Long F. Song J. You Chem. Sci. 2015 6 288
- (2015) Chem. Sci. , vol.6 , pp. 288
- Wu, Q.¹ Du, C.² Huang, Y.³ Liu, X.⁴ Long, Z.⁵ Song, F.⁶ You, J.⁷

36
- 84899868476
- M. Majek F. Filace A. Jacobi von Wangelin Beilstein J. Org. Chem. 2014 10 981
- (2014) Beilstein J. Org. Chem. , vol.10 , pp. 981
- Majek, M.¹ Filace, F.² Jacobi Von Wangelin, A.³

37
- 84941652119
- M. A. Cismesia T. Yoon Chem. Sci. 2015 6 5426
- (2015) Chem. Sci. , vol.6 , pp. 5426
- Cismesia, M.A.¹ Yoon, T.²

38
- 84955172566
- A. Studer A. S. Curran Angew. Chem., Int. Ed. 2016 55 58
- (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 58
- Studer, A.¹ Curran, A.S.²

39
- 84947866890
- R. Cai M. Lu E. Y. Aguilera Y. Xi N. G. Akhmedov J. L. Petersen H. Chen X. Shi Angew. Chem., Int. Ed. 2015 54 8772
- (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 8772
- Cai, R.¹ Lu, M.² Aguilera, E.Y.³ Xi, Y.⁴ Akhmedov, N.G.⁵ Petersen, J.L.⁶ Chen, H.⁷ Shi, X.⁸

40
- 84981207213
- The yields for iodoaryl substrates were described as "low" in note (19) of ref. 11. In our hands, and 3o were isolated, respectively; in 14% yield and 10% yield with Shi's conditions. See the ESI for details
- The yields for iodoaryl substrates were described as "low" in note (19) of ref. 11. In our hands, 3n and 3o were isolated, respectively; in 14% yield and 10% yield with Shi's conditions. See the ESI for details
- , vol.3

41
- 0032509945
- S. Sengupta S. K. Sadhukhan Tetrahedron Lett. 1998 39 715
- (1998) Tetrahedron Lett. , vol.39 , pp. 715
- Sengupta, S.¹ Sadhukhan, S.K.²

42
- 53849101411
- F.-X. Felpin E. Fouquet Adv. Synth. Catal. 2008 350 863
- (2008) Adv. Synth. Catal. , vol.350 , pp. 863
- Felpin, F.-X.¹ Fouquet, E.²

43
- 82055197438
- H. Bonin E. Fouquet F.-X. Felpin Adv. Synth. Catal. 2011 353 3063
- (2011) Adv. Synth. Catal. , vol.353 , pp. 3063
- Bonin, H.¹ Fouquet, E.² Felpin, F.-X.³

44
- 84865796866
- S. Dupuy L. Crawford M. Bühl A. M. Z. Slawin S. P. Nolan Adv. Synth. Catal. 2012 354 2380
- (2012) Adv. Synth. Catal. , vol.354 , pp. 2380
- Dupuy, S.¹ Crawford, L.² Bühl, M.³ Slawin, A.M.Z.⁴ Nolan, S.P.⁵

45
- 84981225080
- For the transmetalation of boronic acids with gold fluoride complexes, see ref. 9
- For the transmetalation of boronic acids with gold fluoride complexes, see ref. 9 a

46
- 84960510911
- L. Huang F. Rominger M. Rudolph A. S. K. Hashmi Angew. Chem., Int. Ed. 2015 55 4808
- (2015) Angew. Chem., Int. Ed. , vol.55 , pp. 4808
- Huang, L.¹ Rominger, F.² Rudolph, M.³ Hashmi, A.S.K.⁴

47
- 84921333570
- T. Cornilleau H. Audrain A. Guillemet P. Hermange E. Fouquet Org. Lett. 2015 17 354
- (2015) Org. Lett. , vol.17 , pp. 354
- Cornilleau, T.¹ Audrain, H.² Guillemet, A.³ Hermange, P.⁴ Fouquet, E.⁵

48
- 79954532428
- P. Hermange A. T. Lindhardt R. H. Taaning K. Bjerglung D. Lupp T. Skrydstrup J. Am. Chem. Soc. 2011 133 6061
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 6061
- Hermange, P.¹ Lindhardt, A.T.² Taaning, R.H.³ Bjerglung, K.⁴ Lupp, D.⁵ Skrydstrup, T.⁶

49
- 80755123259
- S. D. Friis R. H. Taaning A. T. Lindhardt T. Skrydstrup J. Am. Chem. Soc. 2011 133 18114
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 18114
- Friis, S.D.¹ Taaning, R.H.² Lindhardt, A.T.³ Skrydstrup, T.⁴

50
- 84966267415
- S. D. Friis A. T. Lindhardt T. Skrydstrup Acc. Chem. Res. 2016 49 594
- (2016) Acc. Chem. Res. , vol.49 , pp. 594
- Friis, S.D.¹ Lindhardt, A.T.² Skrydstrup, T.³

51
- 84899053260
- S. Kealey A. Gee P. W. Miller J. Labelled Compd. Radiopharm. 2014 57 195
- (2014) J. Labelled Compd. Radiopharm. , vol.57 , pp. 195
- Kealey, S.¹ Gee, A.² Miller, P.W.³

52
- 84925659211
- O. Rahman J. Labelled Compd. Radiopharm. 2015 58 86
- (2015) J. Labelled Compd. Radiopharm. , vol.58 , pp. 86
- Rahman, O.¹

53
- 84970956304
- L. Huang F. Rominger M. Rudolph A. S. K. Hashmi Chem. Commun. 2016 52 6435
- (2016) Chem. Commun. , vol.52 , pp. 6435
- Huang, L.¹ Rominger, F.² Rudolph, M.³ Hashmi, A.S.K.⁴

54
- 84971422033
- E. O. Asomoza-Solis J. Rojas-Ocampo R. A. Toscano S. Porcel Chem. Commun. 2016 52 7295
- (2016) Chem. Commun. , vol.52 , pp. 7295
- Asomoza-Solis, E.O.¹ Rojas-Ocampo, J.² Toscano, R.A.³ Porcel, S.⁴

55
- 51149221039
- J. Vicente M. D. Bermùdez J. Escribano M. P. Carrillo P. G. Jones J. Chem. Soc., Dalton Trans. 1990 3083
- (1990) J. Chem. Soc., Dalton Trans. , pp. 3083
- Vicente, J.¹ Bermùdez, M.D.² Escribano, J.³ Carrillo, M.P.⁴ Jones, P.G.⁵

56
- 0348020031
- J. Vicente M. D. Bermùdez J. Escribano Organometallics 1991 10 3380
- (1991) Organometallics , vol.10 , pp. 3380
- Vicente, J.¹ Bermùdez, M.D.² Escribano, J.³

57
- 84893011475
- W. J. Wolfe M. S. Winston F. D. Toste Nat. Chem. 2014 6 159
- (2014) Nat. Chem. , vol.6 , pp. 159
- Wolfe, W.J.¹ Winston, M.S.² Toste, F.D.³

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