FULL PAPERS
D. G. Hall, Chem. Rev. 2009, 109, 4439–4486; d) L.-Q.
Lu, J.-R. Chen, W.-J. Xiao, Acc. Chem. Res. 2012, 45,
1278–1293; e) C. M. R. Volla, I. Atodiresei, M. Ruep-
ing, Chem. Rev. 2014, 114, 2390–2431.
16, 544–547; e) W. Dai, H. Lu, X. Li, F. Shi, S.-J. Tu,
Chem. Eur. J. 2014, 20, 11382–11389; f) Y.-Y. Gui, J.
Yang, L.-W. Qi, X. Wang, F. Tian, X.-N. Li, L. Peng, L.-
X. Wang, Org. Biomol. Chem. 2015, 13, 6371–6379;
g) K. Zhao, Y. Zhi, X. Li, R. Puttreddy, K. Rissanen,
D. Enders, Chem. Commun. 2016, 52, 2249–2252. For
selected examples of diastereoselective construction of
bispirooxindoles, see: h) Q. Xu, D. Wang, Y. Wei, M.
Shi, ChemistryOpen 2014, 3, 93–98; i) S. Wu, X. Zhu,
W. He, R. Wang, X. Xie, D. Qin, L. Jing, Z. Chen, Tet-
rahedron 2013, 69, 11084–11091.
[5] For selected examples, see: a) M. Bella, S. Kobbel-
gaard, K. A. Jørgensen, J. Am. Chem. Soc. 2005, 127,
3670–3671; b) X.-H. Chen, Q. Wei, S.-W. Luo, H. Xiao,
L.-Z. Gong, J. Am. Chem. Soc. 2009, 131, 13819–13825;
c) M.-N. Cheng, H. Wang, L.-Z. Gong, Org. Lett. 2011,
13, 2418–2421; d) L. Wang, X.-M. Shi, W.-P. Dong, L.-P.
Zhu, R. Wang, Chem. Commun. 2013, 49, 3458–3460;
e) T. Arai, H. Ogawa, A. Awata, M. Sato, M. Watabe,
M. Yamanaka, Angew. Chem. 2015, 127, 1615–1617;
Angew. Chem. Int. Ed. 2015, 54, 1595–1599; f) Q.-S.
Sun, H. Zhu, Y.-J. Chen, X.-D. Yang, X.-W. Sun, G.-Q.
Lin, Angew. Chem. 2015, 127, 13451–13455; Angew.
Chem. Int. Ed. 2015, 54, 13253–13257; g) K. S. Halskov,
F. Kniep, V. H. Lauridsen, E. H. Iversen, B. S. Don-
slund, K. A. Jørgensen, J. Am. Chem. Soc. 2015, 137,
1685–1691; h) P.-F. Zheng, Q. Ouyang, S.-L. Niu, L.
Shuai, Y. Yuan, K. Jiang, T.-Y. Liu, Y.-C. Chen, J. Am.
Chem. Soc. 2015, 137, 9390–9399; i) L. Chen, Z.-J. Wu,
M.-L. Zhang, D.-F. Yue, X.-M. Zhang, X.-Y. Xu, W.-C.
Yuan, J. Org. Chem. 2015, 80, 12668–12675.
[8] a) G. Bergonzini, P. Melchiorre, Angew. Chem. 2012,
124, 995–998; Angew. Chem. Int. Ed. 2012, 51, 971–974;
b) M. Retini, G. Bergonzinia, P. Melchiorre, Chem.
Commun. 2012, 48, 3336–3338; c) M. Silvi, I. Chatter-
jee, Y. Liu, P. Melchiorre, Angew. Chem. 2013, 125,
10980–10983; Angew. Chem. Int. Ed. 2013, 52, 10780–
10783.
[9] For selected examples, see: a) J. P. Malerich, K. Hagi-
hara, V. H. Rawal, J. Am. Chem. Soc. 2008, 130, 14416–
14417; b) Y. Zhu, J. P. Malerich, V. H. Rawal, Angew.
Chem. 2010, 122, 157–160; Angew. Chem. Int. Ed. 2010,
49, 153–156; c) K. S. Yang, A. E. Nibbs, Y. E. Tꢄrkmen,
V. H. Rawal, J. Am. Chem. Soc. 2013, 135, 16050–
16053. For reviews, see: d) J. Alemꢂn, A. Parra, H.
Jiang, K. A. Jørgensen, Chem. Eur. J. 2011, 17, 6890–
6899; e) R. I. Storer, C. Aciro, L. H. Jones, Chem. Soc.
Rev. 2011, 40, 2330–2346; f) P. Chauhan, S. Mahajan, U.
Kaya, D. Hack, D. Enders, Adv. Synth. Catal. 2015, 357,
253–281.
[6] B. Tan, N. R. Candeias, C. F. Barbas III, Nat. Chem.
2011, 3, 473–477.
[7] For selected examples of enantioselective construction
of bispirooxindoles, see: a) F. Zhong, X. Han, Y. Wang,
Y. Lu, Angew. Chem. 2011, 123, 7983–7987; Angew.
Chem. Int. Ed. 2011, 50, 7837–7841; b) W. Sun, G. Zhu,
C. Wu, L. Hong, R. Wang, Chem. Eur. J. 2012, 18,
6737–6741; c) Y.-L. Liu, X. Wang, Y.-L. Zhao, F. Zhu,
X.-P. Zeng, L. Chen, C.-H. Wang, X.-L. Zhao, J. Zhou,
Angew. Chem. 2013, 125, 13980–13984; Angew. Chem.
Int. Ed. 2013, 52, 13735–13739; d) W. Sun, L. Hong, G.
Zhu, Z. Wang, X. Wei, J. Ni, R. Wang, Org. Lett. 2014,
[10] CCDC 1483994 (for 3d) contains the supplementary
crystallographic data for this paper. These data can be
obtained free of charge from The Cambridge Crystallo-
Adv. Synth. Catal. 0000, 000, 0 – 0
7
ꢁ 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
ÞÞ
These are not the final page numbers!