FULL PAPERS
Kotov, C. C. Scarborough, S. S. Stahl, Inorg. Chem.
Am. Chem. Soc. 2014, 136, 195–202; e) D. Yadagiri, P.
Anbarasan, Org. Lett. 2014, 16, 2510–2513; f) X. Ma, S.
Pan, H. Wang, W. Chen, Org. Lett. 2014, 16, 4554–4557;
g) D. J. Jung, H. J. Jeon, J. H. Kim, Y. Kim, S.-g. Lee,
Org. Lett. 2014, 16, 2208–2211.
´
2007, 46, 1910–1923; c) A. Minatti, K. Muniz, Chem.
Soc. Rev. 2007, 36, 1142–1152; d) S. S. Stahl, Angew.
Chem. 2004, 116, 3480–3501; Angew. Chem. Int. Ed.
2004, 43, 3400–3420; e) C. Liu, H. Zhang, W. Shi, A.
Lei, Chem. Rev. 2011, 111, 1780–1824; f) E. M. Beccalli,
G. Broggini, M. Martinelli, S. Sottocornola, Chem. Rev.
2007, 107, 5318–5365; g) M. Johannsen, K. A. Jørgen-
sen, Chem. Rev. 1998, 98, 1689–1708.
[13] a) T. Miura, Y. Funakoshi, M. Morimoto, T. Biyajima,
M. Murakami, J. Am. Chem. Soc. 2012, 134, 17440–
17443; b) J. Kim, S. Chang, Angew. Chem. 2014, 126,
2235–2239; Angew. Chem. Int. Ed. 2014, 53, 2203–2207.
[14] N. Panda, A. K. Jena, M. Raghavender, ACS Catal.
2012, 2, 539–545.
[15] J. M. Lee, D.-S. Ahn, D. Y. Jung, J. Lee, Y. Do, S. K.
Kim, S. Chang, J. Am. Chem. Soc. 2006, 128, 12954–
12962.
[16] C. Cox, D. Ferraris, N. N. Murthy, T. Lectka, J. Am.
Chem. Soc. 1996, 118, 5333–5334.
[17] N. Panda, R. Mothkuri, J. Org. Chem. 2012, 77, 9407–
9412.
[4] a) S. S. A. Shah, G. Rivera, M. Ashfaq, Mini Rev. Med.
Chem. 2013, 13, 70–86; b) X. Chen, S. Hussain, S.
Parveen, S. Zhang, Y. Yang, C. Zhu, Curr. Med. Chem.
2012, 19, 3578–3604; c) A. Scozzafava, T. Owa, A. Mas-
trolorenzo, C. T. Supuran, Curr. Med. Chem. 2003, 10,
925–953.
[5] P. G. M. Wuts, T. W. Greene, in: Greeneꢀs Protective
Groups in Organic Synthesis, 4th edn., John Wiley &
Sons Inc, Hoboken, NJ, 2007, Chapter 7.
[6] a) S. Yamasaki, M. Kanai, M. Shibasaki, J. Am. Chem.
Soc. 2001, 123, 1256–1257; b) L. C. Pattenden, H.
Adams, S. A. Smith, J. P. A. Harrity, Tetrahedron 2008,
64, 2951–2961; c) S. Toumieux, P. Compain, O. R.
Martin, J. Org. Chem. 2008, 73, 2155–2162; d) J. B. Fel-
tenberger, R. Hayashi, Y. Tang, E. S. C. Babiash, R. P.
Hsung, Org. Lett. 2009, 11, 3666–3669; e) N. C. Mancey,
N. Sandon, A.-L. Auvinet, R. J. Butlin, W. Czechtizky,
J. P. A. Harrity, Chem. Commun. 2011, 47, 9804–9806;
f) R. W. Bates, K. Sivarajan, B. F. Straub, J. Org. Chem.
2011, 76, 6844–6848; g) D. F. Taber, P. W. DeMatteo, J.
Org. Chem. 2012, 77, 4235–4241; h) N. Gigant, I. Gillai-
zeau, Org. Lett. 2012, 14, 4622–4625; i) M. Yoshida, K.
Kinoshita, K. Namba, Org. Biomol. Chem. 2014, 12,
2394–2403; j) C.-B. Yu, K. Gao, D.-S. Wang, L. Shi, Y.-
G. Zhou, Chem. Commun. 2011, 47, 5052–5054;
k) L. D. Elliott, J. W. Wrigglesworth, B. Cox, G. C.
Lloyd-Jones, K. I. Booker-Milburn, Org. Lett. 2011, 13,
728–731.
[7] a) Sulfur-Containing Reagents, in: Handbook of Re-
agents for Organic Synthesis, (Ed.: L. A. Paquette),
Wiley & Sons Ltd., Chichester, U.K., 2009; b) P. Valen-
ta, P. J. Carroll, P. J. Walsh, J. Am. Chem. Soc. 2010,
132, 14179–14190; c) A. Sato, H. Yorimitsu, K. Oshima,
Bull. Korean Chem. Soc. 2010, 31, 570–576.
[8] L. S. Hegedus, M. S. Holden, J. Org. Chem. 1986, 51,
1171–1174.
[9] J. Xu, Y. Fu, B. Xiao, T. Gong, Q. Guo, Tetrahedron
Lett. 2010, 51, 5476–5479.
[18] Atomic absorption spectroscopy of the yellow precipi-
tate showed it to contain Pd.
[19] C. E. Houlden, C. D. Bailey, J. G. Ford, M. R.; Gagne,
G. C. Lloyd-Jones, K. I. Booker-Milburn, J. Am. Chem.
Soc. 2008, 130, 10066–10067.
[20] M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuse-
ria, M. A. Robb, J. R. Cheeseman, G. Scalmani, V.
Barone, B. Mennucci, G. A. Petersson, H. Nakatsuji,
M. Caricato, X. Li, H. P. Hratchian, A. F. Izmaylov, J.
Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, M.
Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida,
T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven,
J. A. Montgomery Jr, J. E. Peralta, F. Ogliaro, M. Bear-
park, J. J. Heyd, E. Brothers, K. N. Kudin, V. N. Staro-
verov, T. Keith, R. Kobayashi, J. Normand, K. Ragha-
vachari, A. Rendell, J. C. Burant, S. S. Iyengar, J.
Tomasi, M. Cossi, N. Rega, J. M. Millam, M. Klene,
J. E. Knox, J. B. Cross, V. Bakken, C. Adamo, J. Jara-
millo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J.
Austin, R. Cammi, C. Pomelli, J. W. Ochterski, R. L.
Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth,
P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Dan-
iels, O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski,
D. J. Fox, Gaussian 09, Revision D.01; Gaussian, Inc.,
Wallingford CT, 2013.
[21] a) M. B. Hay, J. P. Wolfe, J. Am. Chem. Soc. 2005, 127,
16468–16476; b) C. Amatore, A. Jutand, Acc. Chem.
Res. 2000, 33, 314–321; c) F. Zaera, Catal. Lett. 2003,
91, 1–10.
[10] C. B. Bheeter, R. Jin, J. K. Bera, P. H. Dixneuf, H.
[22] Y. C. Fan, O. Kwon, Molecules 2011, 16, 3802–3825.
[23] Reaction of 4a with acrylophenone produces 3-(N-
methyl-N-tosylamino)-1-phenylpropan-1-one in 71%
yield.
[24] a) N. Ohmura, A. Nakamura, A. Hamasaki, M. Toku-
naga, Eur. J. Org. Chem. 2008, 5042–5045; b) F. Guibꢂ,
Tetrahedron 1998, 54, 2967–3042.
Doucet, Adv. Synth. Catal. 2014, 356, 119–124.
[11] H. Hu, J. Tian, Y. Liu, Y. Liu, F. Shi, X. Wang, Y. Kan,
C. Wang, J. Org. Chem. 2015, 80, 2842–2847.
[12] For representative examples, see: a) N. Sarkar, A.
Banerjee, S. G. Nelson, J. Am. Chem. Soc. 2008, 130,
9222–9223; b) N. Jiang, Z. Ma, Z. Qu, X. Xing, L. Xie,
J. Wang, J. Org. Chem. 2003, 68, 893–900; c) F. Xiao, J.
Wang, J. Org. Chem. 2006, 71, 5789–5791; d) S. Chupra-
kov, B. T. Worrell, N. Selander, R. K. Sit, V. V. Fokin, J.
[25] K. Moriyama, Y. Nakamura, H. Togo, Org. Lett. 2014,
16, 3812–3815.
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