Organic Letters
Letter
K.; Miura, M. J. Am. Chem. Soc. 2015, 137, 6460−6463. (d) Jia, T.;
Cao, P.; Wang, B.; Lou, Y.; Yin, X.; Wang, M.; Liao, J. J. Am. Chem.
Soc. 2015, 137, 13760−13763. (e) Logan, K. M.; Brown, M. K.
Angew. Chem., Int. Ed. 2017, 56, 851−855. (f) Lee, J.; Radomkit, S.;
Torker, S.; del Pozo, J.; Hoveyda, A. H. Nat. Chem. 2018, 10, 99−108.
(12) For some selected examples with alkynes, see: (a) Alfaro, R.;
Notes
The authors declare no competing financial interest.
ACKNOWLEDGMENTS
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We thank the “1000 Yonth Talents Plan”, Shanghai Pujiang
Program, NFS of China (Grant No. 21801188), and Tongji
University for financial support. Many thanks to Prof. G. Yin
(Wuhan University) and Prof. Q. Cai (Fudan University) for
their helpful discussion. We thank Ms. Alison McGonagle for
polishing the manuscript.
́
Parra, A.; Aleman, J.; García Ruano, J. L.; Tortosa, M. J. Am. Chem.
Soc. 2012, 134, 15165−15168. (b) Zhang, L.; Cheng, J.; Carry, B.;
Hou, Z. J. Am. Chem. Soc. 2012, 134, 14314−14317.
(13) For some selected examples with allenes, see: (a) Zhao, W.;
Montgomery, J. J. Am. Chem. Soc. 2016, 138, 9763−9766. (b) Meng,
F.; McGrath, K. P.; Hoveyda, A. H. Nature 2014, 513, 367−374.
́
(14) (a) Burns, A. R.; Solana Gonzalez, J.; Lam, H. W. Angew. Chem.,
Int. Ed. 2012, 51, 10827−10831. (b) Liu, P.; Fukui, Y.; Tian, P.; He,
Z.-T.; Sun, C.-Y.; Wu, N.-Y.; Lin, G.-Q. J. Am. Chem. Soc. 2013, 135,
11700−11703. Very recently, the Meek group reported a Cu-
catalyzed borylative cyclization of alkynes via vinyl-BPin intermediate,
see: Zanghi, J. M.; Liu, S.; Meek, S. J. Org. Lett. 2019, 21, 5172.
(15) (a) Meng, F.; Jang, H.; Jung, B.; Hoveyda, A. H. Angew. Chem.,
Int. Ed. 2013, 52, 5046−5051. (b) Cheng, F.; Lu, W.; Huang, W.;
Wen, L.; Li, M.; Meng, F. Chemical Science 2018, 9, 4992−4998.
(c) Gan, X.-C.; Zhang, Q.; Jia, X.-S.; Yin, L. Org. Lett. 2018, 20,
1070−1073.
(16) For some selected addition to imines, see: (a) Jang, H.; Romiti,
F.; Torker, S.; Hoveyda, A. H. Nat. Chem. 2017, 9, 1269−1275.
(b) Jiang, L.; Cao, P.; Wang, M.; Chen, B.; Wang, B.; Liao, J. Angew.
Chem., Int. Ed. 2016, 55, 13854−13858. (c) Yeung, K.; Ruscoe, R. E.;
Rae, J.; Pulis, A. P.; Procter, D. J. Angew. Chem., Int. Ed. 2016, 55,
11912−11916. For a selected palladium-catalyzed reaction, see:
(d) Sieber, J. D.; Morken, J. P. J. Am. Chem. Soc. 2006, 128, 74−75.
(17) This method was utilized by several group to study the reaction
scopes, for selected examples, see: (a) Wang, Z.; Bachman, S.;
Dudnik, A. S.; Fu, G. C. Angew. Chem., Int. Ed. 2018, 57, 14529−
14532. (b) Moon, P. J.; Wei, Z.; Lundgren, R. J. J. Am. Chem. Soc.
2018, 140, 17418−17422.
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E
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