Chemistry - A European Journal
10.1002/chem.201605772
COMMUNICATION
J. Waser, Chem. Commun. 2011, 47, 102-115; g) L. F. Silva, B.
Olofsson, Nat. Prod. Rep. 2011, 28, 1722-1754; h) E. A. Merritt, B.
Olofsson, Angew. Chem. Int. Ed. 2009, 48, 9052-9070; i) T. Wirth,
Angew. Chem. Int. Ed. 2005, 44, 3656-3665.
[
2]
a) J. P. Brand, J. Waser, Chem. Soc. Rev. 2012, 41, 4165-4179; b) V.
V. Zhdankin, P. J. Stang, Tetrahedron 1998, 54, 10927-10966.
J. Kaschel, D. B. Werz, Angew. Chem. Int. Ed. 2015, 54, 8876-8878.
a) J. P. Brand, J. Charpentier, J. Waser, Angew. Chem. Int. Ed. 2009,
[
[
3]
4]
4
4
8, 9346-9349; b) J. P. Brand, J. Waser, Angew. Chem. Int. Ed. 2010,
9, 7304-7307; c) G. L. Tolnai, S. Ganss, J. P. Brand, J. Waser, Org.
Lett. 2013, 15, 112-115; d) K. D. Collins, F. Lied, F. Glorius, Chem.
Commun. 2014, 50, 4459-4461; e) C. Feng, T.-P. Loh, Angew. Chem.
Int. Ed. 2014, 53, 2722-2726; f) C. Feng, D. Feng, T.-P. Loh, Chem.
Commun. 2014, 50, 9865-9868; g) C. Feng, D. Feng, Y. Luo, T.-P. Loh,
Org. Lett. 2014, 16, 5956-5959; h) F. Xie, Z. Qi, S. Yu, X. Li, J. Am.
Chem. Soc. 2014, 136, 4780-4787; i) X. Zhang, Z. Qi, J. Gao, X. Li, Org.
Biomol. Chem. 2014, 12, 9329-9332; j) P. Finkbeiner, U. Kloeckner, B.
J. Nachtsheim, Angew. Chem. Int. Ed. 2015, 54, 4949-4952; k) H.
Wang, F. Xie, Z. S. Qi, X. Li, Org. Lett. 2015, 17, 920-923; l) Z.-Z.
Zhang, B. Liu, C.-Y. Wang, B.-F. Shi, Org. Lett. 2015, 17, 4094-4097.
a) X. Liu, Z. Wang, X. Cheng, C. Li, J. Am. Chem. Soc. 2012, 134,
[
5]
1
4330-14333; b) H. Huang, G. Zhang, L. Gong, S. Zhang, Y. Chen, J.
Am. Chem. Soc. 2014, 136, 2280-2283; c) H. Huang, G. Zhang, Y.
Chen, Angew. Chem. Int. Ed. 2015, 54, 7872-7876; d) F. Le Vaillant, T.
Courant, J. Waser, Angew. Chem. Int. Ed. 2015, 54, 11200-11204; e) H.
Wang, L.-N. Guo, S. Wang, X.-H. Duan, Org. Lett. 2015, 17, 3054-
3
057; f) Q.-Q. Zhou, W. Guo, W. Ding, X. Wu, X. Chen, L.-Q. Lu, W.-J.
Xiao, Angew. Chem. Int. Ed. 2015, 54, 11196-11199.
[
6]
a) S. Nicolai, S. Erard, D. F. Gonzalez, J. Waser, Org. Lett. 2010, 12,
3
1
84-387; b) Z. Wang, L. Li, Y. Huang, J. Am. Chem. Soc. 2014, 136,
2233-12236; c) D. F. Gonzalez, J. P. Brand, R. Mondiere, J. Waser,
Adv. Synth. Catal. 2013, 355, 1631-1639; d) X. Wu, S. Shirakawa, K.
Maruoka, Org. Biomol. Chem. 2014, 12, 5388-5392; e) R. Frei, M. D.
Wodrich, D. P. Hari, P. A. Bonin, C. Chauvier, J. Waser, J. Am. Chem.
Soc. 2014, 136, 16563-16573; f) M. D. Wodrich, P. Caramenti, J.
Waser, Org. Lett. 2016, 18, 60-63; g) Y. Li, J. Waser, Angew. Chem. Int.
Ed. 2015, 54, 5438-5442.
[
7]
a) B. Lu, J. Wu, N. Yoshikai, J. Am. Chem. Soc. 2014, 136, 11598-
1
1
2
1601; b) J. Wu, N. Yoshikai, Angew. Chem. Int. Ed. 2015, 54, 11107-
1111; c) J. Wu, X. Deng, H. Hirao, N. Yoshikai, J. Am. Chem. Soc.
016, 138, 9105-9108.
[
[
8]
9]
D. P. Hari, J. Waser, J. Am. Chem. Soc. 2016, 138, 2190-2193.
Z. Wang, X. Li, Y. Huang, Angew. Chem. Int. Ed. 2013, 52, 14219-
1
4223.
[
10] For a recent report on the synthesis of related alkenylbenziodoxolones,
see: Stridfeldt, E.; Seemann, A.; Bouma, M. J.; Dey, C.; Ertan, A.;
Olofsson, B. Chem. Eur. J. 2016, 22, 16066-16070.
[
[
[
11] A. Ariafard, Organometallics 2014, 33, 7318-7324.
12] T. Miura, N. Iwasawa, J. Am. Chem. Soc. 2002, 124, 518-519.
13] CCDC 1057849 (4a) and 1521973 (10) contain the supplementary
crystallographic data for this paper. These data can be obtained free of
charge from the Cambridge Crystallographic Data Centre via
http://www.ccdc.cam.ac.uk/data_request/cif.
[
[
[
14] A. Ariafard, ACS Catal. 2014, 4, 2896-2907.
15] N. R. Deprez, M. S. Sanford, Inorg. Chem. 2007, 46, 1924-1935.
16] V. Mamane, P. Hannen, A. Fürstner, Chem. Eur. J. 2004, 10, 4556-
4
575.
This article is protected by copyright. All rights reserved.