UPDATES
Matteo Bergami et al.
McCluskey, C. P. Gordon, Org. Biomol. Chem. 2014,
12, 9562–9571.
[21] N. J. W. Straathof, H. P. L. Gemoets, X. Wang, J. C.
Schouten, V. Hessel, T. Nol, ChemSusChem 2014, 7,
1612–1617.
[22] M. Baghbanzadeh, T. N. Glasnov, C. O. Kappe, J. Flow
Chem. 2013, 3, 109–113.
[23] Z. He, M. Bae, J. Wu, T. F. Jamison, Angew. Chem.
2014, 126, 14679–14683; Angew. Chem. Int. Ed. 2014,
53, 14451–14455.
[24] K. Ueno, F. Kitagawa, N. Kitamura, Lab Chip 2002, 2,
231–234.
[25] D. Cantillo, C. Mateos, J. A. Rincon, O. de Frutos, C. O.
Kappe, Chem. Eur. J. 2015, 21, 12894–12898.
[26] a) H. Qrareya, C. Raviola, S. Protti, M. Fagnoni, A.
Albini, J. Org. Chem. 2013, 78, 6016–6024; b) H. Qrar-
eya, S. Protti, M. Fagnoni, J. Org. Chem. 2014, 79,
11527–11533.
[10] W. Shu, S. L. Buchwald, Angew. Chem. 2012, 124,
5451–5454; Angew. Chem. Int. Ed. 2012, 51, 5355–5358.
[11] a) E. R. Murphy, J. R. Martinelli, N. Zaborenko, S. L.
Buchwald, K. F. Jensen, Angew. Chem. 2007, 119, 1764–
1767; Angew. Chem. Int. Ed. 2007, 46, 1734–1737; b) Q.
Deng, R. Shen, Z. Zhao, M. Yan, L. Zhang, Chem.
Eng. J. 2015, 262, 1168–1174.
[12] a) Z. He, T. F. Jamison, Angew. Chem. 2014, 126, 3421–
3425; Angew. Chem. Int. Ed. 2014, 53, 3353–3357;
b) B. K. Singh, C. V. Stevens, D. R. J. Acke, V. S.
Parmar, E. V. Van der Eycken, Tetrahedron Lett. 2009,
50, 15–18; c) F. Ullah, T. Samarakoon, A. Rolfe, R. D.
Kurtz, P. R. Hanson, M. G. Organ, Chem. Eur. J. 2010,
16, 10959–10962.
[13] X. Wang, G. D. Cuny, T. Nol, Angew. Chem. 2013,
125, 8014–8018; Angew. Chem. Int. Ed. 2013, 52, 7860–
7864.
[14] a) R. L. Hartman, J. R. Naber, N. Zaborenko, S. L.
Buchwald, K. F. Jensen, Org. Process Res. Dev. 2010,
14, 1347–1357; b) A. Caron, A. C. Hernandez-Perez,
S. K. Collins, Org. Process Res. Dev. 2014, 18, 1571–
1574; c) T. Nçel, J. R. Naber, R. L. Hartman, J. P.
McMullen, K. F. Jensen, S. L. Buchwald, Chem. Sci.
2011, 2, 287–290.
[27] C. Raviola, D. Ravelli, S. Protti, A. Albini, M. Fagnoni,
Synlett 2015, 26, 471–478.
[28] a) S. Protti, M. Fagnoni, A. Albini, Org. Biomol. Chem.
2005, 3, 2868–2871; b) A. Fraboni, M. Fagnoni, A.
Albini, J. Org. Chem. 2003, 68, 4886–4893; c) S. Protti,
M. Fagnoni, A. Albini, J. Org. Chem. 2012, 77, 6473–
6479.
[29] V. Dichiarante, M. Fagnoni, A. Albini, J. Org. Chem.
2010, 75, 1271–1274.
[30] F. Bonassi, D. Ravelli, S. Protti, M. Fagnoni, Adv.
[15] A. Albini, L. Germani in Handbook of Synthetic Pho-
tochemistry, (Eds.: A. Albini, M. Fagnoni), Wiley-VCH
Verlag, Weinheim, 2010, pp 1–24.
Synth. Catal. 2015, 357, 3687–3695.
[31] C. Jimenez-Gonzalez, C. S. Ponder, Q. B. Broxterman,
J. B. Manley, Org. Process Res. Dev. 2011, 15, 912–917.
[32] D. Ravelli, S. Protti, M. Fagnoni, A. Albini, Curr. Org.
Chem. 2013, 17, 2366–2373.
[16] Y. Su, N. J. W. Straathof, V. Hessel, T. Nol, Chem. Eur.
J. 2014, 20, 10562–10589.
[17] a) M. Oelgemçller, O. Shvydkiv, Molecules 2011, 16,
7522–7550; b) O. Shvydkiv, M. Oelgemçller, in: CRC
Handbook of Organic Photochemistry and Photobiolo-
gy, (Eds.: A. Griesbeck, M. Oelgemoeller, F. Ghetti),
3rd edn., CRC Press, 2012, pp 49–72; c) M. Oelgemçl-
ler, Chem. Eng. Technol. 2012, 35, 1144–1152; d) M.
Neumann, K. Zeitler, Org. Lett. 2012, 14, 2658–2661.
[18] a) J. P. Knowles, L. D. Elliott, K. I. Booker-Milburn,
Beilstein J. Org. Chem. 2012, 8, 2025–2052; b) Z. J. Gar-
lets, J. D. Nguyen, C. R. J. Stephenson, Isr. J. Chem.
2014, 54, 351–360.
[19] J. W. Tucker, Y. Zhang, T. F. Jamison, C. R. J. Stephen-
son, Angew. Chem. 2012, 124, 4220–4223; Angew.
Chem. Int. Ed. 2012, 51, 4144–4147.
[20] J. W. Beatty, J. J. Douglas, K. P. Cole, C. R. J. Stephen-
son, Nat. Commun. 2015, 6, DOI: 10.1038/
ncomms8919.
[33] L. D. Elliott, J. P. Knowles, P. J. Koovits, K. G. Maskill,
M. J. Ralph, G. Lejeune, L. J. Edwards, R. I. Robinson,
I. R. Clemens, B. Cox, D. D. Pascoe, G. Koch, M.
Eberle, M. B. Berry, K. I. Booker-Milburn, Chem. Eur.
J. 2014, 20, 15226–15232.
[34] a) B. P. Mason, K. E. Price, J. L. Steinbacher, A. R.
Bogdan, D. T. McQuade, Chem. Rev. 2007, 107, 2300–
2318; b) L. Vaccaro, D. Lanari, A. Marrocchi, G. Strap-
paveccia, Green Chem. 2014, 16, 3680–3704; c) L.
Malet-Sanz, S. L. Flavien, J. Med. Chem. 2012, 55,
4062–4098; d) B. Gutmann, D. Cantillo, C. O. Kappe,
Angew. Chem. 2015, 127, 6788–6832; Angew Chem. Int.
Ed. 2015, 54, 6688–6728.
[35] C. Pavia, E. Ballerini, L. A. Bivona, F. Giacalone, C.
Aprile, L. Vaccaro, M. Gruttadauria, Adv. Synth. Catal.
2013, 355, 2007–2018.
[36] E. M. Schuster, P. Wipf, Isr. J. Chem. 2014, 54, 361–370.
1172
ꢀ 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Adv. Synth. Catal. 2016, 358, 1164 – 1172