COMMUNICATIONS
One-Pot Assembly of Fused Heterocycles
1995, 60, 4991; d) H. Cano-Yelo, A. Deronzier, J. Pho-
tochem. 1987, 37, 315; Baran has recently reported one
similar work with boronic acids and trifluoroborates as
substrates, see: e) J. W. Lockner, D. D. Dixon, R. Ris-
gaard, P. S. Baran, Org. Lett. 2011, 13, 5628.
d) M. S. Yusubov, D. Y. Svitich, M. S. Larkina, V. V.
Zhdankin, Arkivoc 2013, 364; e) A. Parra, S. Reboredo,
Chem. Eur. J. 2013, 19, 17244; f) M. S. Yusubov, V. V.
Zhdankin, Curr. Org. Synth. 2012, 9, 247; g) H. Liang,
M. A. Ciufolini, Angew. Chem. 2011, 123, 12051;
Angew. Chem. Int. Ed. 2011, 50, 11849; h) N. R.
Deprez, M. S. Sanford, Inorg. Chem. 2007, 46, 1924;
i) R. D. Richardson, T. Wirth, Angew. Chem. 2006, 118,
4510; Angew. Chem. Int. Ed. 2006, 45, 4402.
[4] For recent reviews on this topic, see: a) N. Rodriguez,
L. J. Goossen, Chem. Soc. Rev. 2011, 40, 5030; for
recent reports, see: b) C. Wang, I. Piel, F. Glorius, J.
Am. Chem. Soc. 2009, 131, 4194; c) S. Maetani, T. Fu-
kuyama, I. Ryu, Org. Lett. 2013, 15, 2754.
[5] a) B. Xiao, T.-J. Gong, Z.-J. Liu, J.-H. Liu, D.-F. Luo, J.
Xu, L. Liu, J. Am. Chem. Soc. 2011, 133, 9250; b) Y.
Wei, N. Yoshikai, Org. Lett. 2011, 13, 5504; c) D. M.
Ferguson, S. R. Rudolph, D. Kalyani, ACS Catal. 2014,
4, 2395; d) J. Zhao, Y. Wang, Y. He, L. Liu, Q. Zhu,
Org. Lett. 2012, 14, 1078; e) N.-J. Wang, S.-T. Mei, L.
Shuai, Y. Yuan, Y. Wei, Org. Lett. 2014, 16, 3040; f) H.-
W. Liang, W. Ding, K. Jiang, L. Shuai, Y. Yuan, Y. Wei,
Y.-C. Chen, Org. Lett. 2015, 17, 2764.
[10] For selected reviews on iodonium ylides, see: a) V. V.
Zhdankin, P. J. Stang, Chem. Rev. 2008, 108, 5299; b) P.
Müller, Acc. Chem. Res. 2004, 37, 243; c) E. Malami-
dou-Xenikaki, S. Spyroudis, Synlett 2008, 2725;
d) R. M. Moriarty, J. Org. Chem. 2005, 70, 2893; e) O.
Prakash, Aldrichimica Acta 1995, 28, 63. For examples
on aryliodonium ylides, see: f) N. Panda, I. Mattan,
D. K. Nayak, J. Org. Chem. 2015, 80, 6590; g) T. Kasa-
hara, Y. J. Jang, L. Racicot, D. Panagopoulos, S. H.
Liang, M. A. Ciufolini, Angew. Chem. 2014, 126, 9791;
Angew. Chem. Int. Ed. 2014, 53, 9637; h) R. M. Moriar-
ty, S. Tyagi, D. Ivanov, M. Constantinescu, J. Am.
Chem. Soc. 2008, 130, 7564; i) E. G. Bakalbassis, S.
Spyroudis, E. Tsiotra, J. Org. Chem. 2006, 71, 7060;
j) S. Koulouri, E. Malamidou-Xenikaki, S. Spyroudis,
M. Tsanakopoulou, J. Org. Chem. 2005, 70, 8780; k) Q.
Zhu, J. Wu, R. Fathi, Z. Yang, Org. Lett. 2002, 4, 3333;
l) G. Wells, A. Seaton, M. F. G. Stevens, J. Med. Chem.
2000, 43, 1550; m) P. B. Kokil, P. M. Nair, Tetrahedron
Lett. 1977, 18, 4113.
[11] For selected reviews, see: a) L. Ackermann, Chem.
Rev. 2011, 111, 1315; b) L. McMurray, F. OꢀHara, M. J.
Gaunt, Chem. Soc. Rev. 2011, 40, 1885; c) I. V. Seregin,
V. Gevorgyan, Chem. Soc. Rev. 2007, 36, 1173; d) D.
Alberico, M. E. Scott, M. Lautens, Chem. Rev. 2007,
107, 174.
[12] For the preparation of quinolinone, see: a) M. Ravi, P.
Chauhan, R. Kant, S. K. Shukla, P. P. Yadav, J. Org.
Chem. 2015, 80, 5369; b) J. Pinto, V. L. M. Silva,
A. M. G. Silva, L. M. N. B. F. Santos, A. M. S. Silva, J.
Org. Chem. 2015, 80, 6649; for examples on the syn-
thetic utility of quinolinone, see: c) I. T. Raheem, S. N.
Goodman, E. N. Jacobsen, J. Am. Chem. Soc. 2004,
126, 706; d) J. Huang, Y. Chen, A. O. King, M. Dilme-
ghani, R. D. Larsen, M. M. Faul, Org. Lett. 2008, 10,
2609.
[6] a) D. E. Ames, A. Opalko, Synthesis 1983, 234; b) Z.
Liu, R. C. Larock, Org. Lett. 2004, 6, 3739; c) L.-C.
Campeau, M. Parisien, A. Jean, K. Fagnou, J. Am.
Chem. Soc. 2006, 128, 581; d) J. Liu, A. E. Fitzgerald,
N. S. Mani, J. Org. Chem. 2008, 73, 2951.
[7] For recent reviews on this topic, see: a) C. S. Yeung,
V. M. Dong, Chem. Rev. 2011, 111, 1215; b) D. Zhao, J.
You, C. Hu, Chem. Eur. J. 2011, 17, 5466; c) C.-J. Li,
Acc. Chem. Res. 2009, 42, 335; for recent reports, see:
d) W. Sun, M. Wang, Y. Zhang, L. Wang, Org. Lett.
2015, 17, 426; e) S. Trosien, P. Bçttger, S. R. Waldvogel,
Org. Lett. 2014, 16, 402; f) L. Niu, H. Yang, Y. Jiang,
H. Fu, Adv. Synth. Catal. 2013, 355, 3625; g) B. LiØ-
gault, D. Lee, M. P. Huestis, D. R. Stuart, K. Fagnou, J.
Org. Chem. 2008, 73, 5022; h) J. Zhao, R. C. Larock, J.
Org. Chem. 2006, 71, 5340; i) Q. Huang, M. A. Campo,
T. Yao, Q. Tian, R. C. Larock, J. Org. Chem. 2004, 69,
8251; j) H. Hagelin, J. D. Oslob, B. kermark, Chem.
Eur. J. 1999, 5, 2413.
[8] T. Watanabe, S. Oishi, N. Fujii, H. Ohno, J. Org. Chem.
2009, 74, 4720.
[9] For recent reviews on hypervalent iodine chemistry,
see: a) J. Charpentier, N. Früh, A. Togni, Chem. Rev.
2015, 115, 650; b) D.-Q. Dong, S.-H. Hao, Z.-L. Wang,
C. Chen, Org. Biomol. Chem. 2014, 12, 4278; c) V. V.
Zhdankin, Hypervalent Iodine Chemistry: Preparation,
Structure, and Synthetic Applications of Polyvalent
Iodine Compounds, Wiley-VCH, Weinheim, 2013;
[13] G.-L. Xi, Z.-Q. Liu, J. Agric. Food Chem. 2014, 62,
5636, and references cited therein.
Adv. Synth. Catal. 2016, 358, 353 – 357
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