Communication
Organic & Biomolecular Chemistry
A. Trifilieff, K. L. Turner and E. Wissler, Bioorg. Med. Chem.
Lett., 2012, 22, 6280–6285; (b) G. E. Konecny, B. Winterhoff,
83831–83837; (f) J.-B. Peng, X. Qi and X.-F. Wu,
ChemSusChem, 2016, 9, 2279–2283.
E. Y. Guorong, J. Qi, J. Le, M. Shi, M. Dugan, R. Linnartz, 7 (a) S. Cacchi, G. Fabrizi and A. Goggiamani, Org. Lett., 2003,
R. S. Finn and D. J. Slamon, Cancer Res., 2011, 71, 3589;
(c) J. Weiss, D. Theile, Z. Dvorak and W. E. Haefeli,
Pharmaceutics, 2014, 6, 632–650.
5, 4269–4272; (b) S. Korsager, R. H. Taaning and
T. Skrydstrup, J. Am. Chem. Soc., 2013, 135, 2891–2894;
(c) T. Morimoto and K. Kakiuchi, Angew. Chem., Int. Ed.,
2004, 43, 5580–5588; (d) L. Wu, Q. Liu, R. Jackstell and
M. Beller, Angew. Chem., Int. Ed., 2014, 53, 6310–6320;
(e) P. Gautam and B. M. Bhanage, Catal. Sci. Technol., 2015,
5, 4663–4702; (f) X. Qi, L.-B. Jiang, C.-L. Li, R. Li and X.-F. Wu,
Chem. – Asian J., 2015, 10, 1870–1873; (g) X. Qi, R. C.-L. Li,
L.-B. Jiang, W.-Q. Zhang and X.-F. Wu, Catal. Sci. Technol.,
2016, 6, 3099–3107; (h) J.-B. Peng, F.-P. Wu, C.-L. Li, X. Qi
and X.-F. Wu, Eur. J. Org. Chem., 2017, 1434–1437;
(i) F.-P. Wu, J.-B. Peng, L.-S. Meng, X. Qi and X.-F. Wu,
ChemCatChem, 2017, 7, 3121–3124; ( j) Y.-S. Seo, D.-S. Kim
and C.-H. Jun, Chem. – Asian J., 2016, 11, 3508–3512.
2 For selected examples, see: (a) R. Manikandan and
M. Jeganmohan, Org. Lett., 2014, 16, 3568–3571;
(b) C.-C. Huang and N.-C. Chang, Org. Lett., 2008, 10, 673–
676; (c) T. N. Glasnov, W. Stadlbauer and C. O. Kappe, J. Org.
Chem., 2005, 70, 3864–3870; (d) P. R. Angibaud, M. G. Venet,
W. Filliers, R. Broeckx, Y. A. Ligny, P. Muller, V. S. Poncelet
and D. W. End, Eur. J. Org. Chem., 2004, 479–486;
(e) C. Zaugg, G. Schmidt and S. Abele, Org. Process Res. Dev.,
2017, 21, 1003–1011; (f) X. Gao, A. Liang, J. Li, D. Zou,
Y. Wu and Y. Wu, Tetrahedron Lett., 2017, 58, 1917–1920.
3 (a) M. Ikbal, R. Banerjee, S. Atta, A. Jana, D. Dhara, A. Anoop
and N. D. P. Singh, Chem. – Eur. J., 2012, 18, 11968–11975; 8 W.-Y. Yu, W. N. Sit, K.-M. Lai, Z. Zhou and A. S. C. Chan,
(b) H. Asahara, A. Kataoka, S. Hirao and N. Nishiwaki, J. Am. Chem. Soc., 2008, 130, 3304–3306.
Eur. J. Org. Chem., 2015, 3994–3999; (c) B. Ying, J. Xu, 9 (a) H. T. Cao and R. Grée, Tetrahedron Lett., 2009, 50, 1493–
X. Zhu, C. Shen and P. Zhang, ChemCatChem, 2016, 8, 2604–
2608.
4 D. Wang, J. Zhao, Y. Wang, J. Hu, L. Li, L. Miao, H. Feng,
L. Désaubry and P. Yu, Asian J. Org. Chem., 2016, 5, 1442–
1446.
5 L.-Y. Xie, Y. Duan, L.-H. Lu, Y.-J. Li, S. Peng, C. Wu, K.-J. Liu,
Z. Wang and W.-M. He, ACS Sustainable Chem. Eng., 2017, 5,
10407–10412.
6 (a) M. Beller, Applied Homogeneous Catalysis with
Organometallic Compounds, Wiley-VCH, Weinheim, 2nd edn,
2002, vol. 1, pp. 145–156; (b) A. Brennführer, H. Neumann
and M. Beller, Angew. Chem., Int. Ed., 2009, 48, 4114–4133;
(c) B. Gabriele, R. Mancuso and G. Salerno, Eur. J. Org.
Chem., 2012, 6825–6839; (d) J.-B. Peng, X. Qi and X.-F. Wu,
Synlett, 2017, 175–194; (e) X.-F. Wu, RSC Adv., 2016, 6,
1494; (b) S. Ramesh, P. N. Arunachalam and A. Lalith, RSC
Adv., 2013, 3, 8666–8669; (c) Y. Huang, G. Li, J. Huang and
J. You, Org. Chem. Front., 2014, 1, 347–350; (d) B. Khan,
A. A. Khan, R. Kant and D. Koley, Adv. Synth. Catal., 2016,
358, 3753–3758; (e) F. Ling, C. Ai, Y. Lv and W. Zhong, Adv.
Synth. Catal., 2017, 359, 3707–3712; (f) T. T. Nguyen,
L. Grigorjeva and O. Daugulis, Chem. Commun., 2017, 53,
5136–5138; (g) J. Ni, J. Li, Z. Fan and A. Zhang, Org. Lett.,
2016, 18, 5960–5963; (h) R. Sang, Y. Zheng, H. Zhang, X. Wu,
Q. Wang, L. Hai and Y. Wu, Org. Chem. Front., 2018, 5, 648–
652; (i) M. Usman, Z. H. Ren, Y. Y. Wang and Z. H. Guan,
Org. Biomol. Chem., 2017, 15, 1091–1095; ( j) M. Usman,
Z.-H. Ren, Y.-Y. Wang and Z.-H. Guan, RSC Adv., 2016, 6,
107542–107546; (k) N. Xu, D. Li, Y. Zhang and L. Wang, Org.
Biomol. Chem., 2015, 13, 9083–9092.
Org. Biomol. Chem.
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