Please do not adjust margins
ChemComm
Page 4 of 4
COMMUNICATION
Journal Name
Am. Chem. Soc., 2008, 130, 7190-7191. (e) G. Li, L. Wan, G. Zhang, D.
Lewo, J. Spangler, J.-Q. Yu, J. Am. Chem. Soc., 2015, 137, 4391-4397.
2018, 149, 225-237.
DOI: 10.1039/C9CC08879B
5
For transition-metal-catalyzed C-H functionalization of phosphorus- 13 For selected examples of C-H hydroxylation, see: (a) T. Jintoku, K.
containing molecules, see: (a) Z. Zhang, P. H. Dixneuf, J.-F. Soulé,
Chem. Commun., 2018, 54, 7265-7280. (b) Y.-N. Ma, S.-X. Li, S.-D.
Yang, Acc. Chem. Res. 2017, 50, 1480−1492.
Nishimura, K. Takaki, Y. Fujiwara, Chem. Lett., 1990, 1687-1688. (b)
Y.-H. Zhang, J.-Q. Yu, J. Am. Chem. Soc., 2009, 131, 14654-14655. (c)
Y. Yan, P. Feng, Q.-Z. Zheng, Y.-F. Liang, J.-F. Lu, Y. Cui, N. Jiao,
Angew. Chem., Int. Ed., 2013, 52, 5827-5831. (d) Y. Yang, Y. Lin, Y.
Rao, Org. Lett., 2012, 14, 2874-2877. (e) V. S. Thirunavukkarasu, J.
Jonathan Hubrich, L. Ackermann, Org. Lett., 2012, 14, 4210-4213. (f)
X. Yang, G. Shan, Y. Rao, Org. Lett., 2013, 15, 2334-2337. (g) W. Liu,
L. Ackermann, Org. Lett., 2013, 15, 3484-2386. (h) F. Yang, K. Rauch,
K. Kettelhoit, L. Ackermann, Angew. Chem., Int. Ed., 2014, 53, 11285-
11288. (i) X. Chen, X.-S. Hao, C. E. Goodhue, J.-Q. Yu, J. Am. Chem.
Soc., 2006, 128, 6790-6791. (j) X. Li, Y.-H. Liu, W.-J. Gu, Li, B. F.-J.
Chen, B.-F. Shi, Org. Lett., 2014, 16, 3904-3907. (k) X.-Y. Chen, S.
Ozturk, E. J. Sorensen, Org. Lett., 2017, 19, 6280-6283.
6
7
(a) L. Y. Chan, S. Kim, T. Ryu, P. H. Lee, Chem. Commun., 2013, 49,
4682-4684. (b) X. Meng, S. Kim, Org. Lett., 2013, 15, 1910-1913.
(a) H.-L. Wang, R.-B. Hu, H. Zhang, A.-X. Zhou, S.-D. Yang, Org. Lett.,
2013, 15, 5302-5305. (b) H.-Y. Zhang, H.-M. Yi, G.-W. Wang, B. Yang,
S.-D. Yang, Org. Lett., 2013, 15, 6186-6189. (c) Y. Unoh, Y.
Hashimoto, D. Takeda, K. Hirano, T. Satoh, M. Miura, Org. Lett.,
2013, 15, 3258-3261. (d) D. Zhao, C. Nimphius, M. Lindale, F. Glorius,
Org. Lett., 2013, 15, 4504-4507. (e) S. Park, B. Seo, S. Shin, J.-Y. Son,
P. H. Lee, Chem. Commun., 2013, 49, 8671-8673. (f) M. Itoh, Y.
Hashimoto, K. Hirano, T. Satoh, M. Miura, J. Org. Chem., 2013, 78,
8098-8104. (g) D. Gwon, D. Lee, J. Kim, S. Park, S. Chang, Chem. Eur.
J., 2014, 20, 12421-12425. (h) Y.-N. Ma, H.-Y. Zhang, S.-D. Yang, Org.
Lett., 2015, 17, 2034-2037. (i) Z.-J. Du, J. Guan, G.-J. Wu, P. Xu, L.-X.
Gao, F.-S. Han, J. Am. Chem. Soc., 2015, 137, 632-635. (j) S.-X. Li, Y.-
N. Ma, S.-D. Yang, Org. Lett., 2017, 19, 1842-1845. (k) Y. Sun, N.
Cramer, Angew. Chem. Int. Ed., 2017, 56, 364-367. (l) Y.-S. Jang, M.
Dieckmann, N. Cramer, Angew. Chem. Int. Ed., 2017, 56, 15088-
15092. (m) Y. Sun, N. Cramer, Chem. Sci., 2018, 9, 2981-2985.
For reviews on inexpensive metals catalyzed C-H activation reactions,
see : (a) B. Su, Z.-C. Cao, Z.-J. Shi, Acc. Chem. Res., 2015, 48, 886. (b)
B. Zhan, B. Liu, B.-F. Shi, Chin. Sci. Bull., 2015, 60, 2907-2917. (c) M.
Moselage, J. Li, L. Ackermann, ACS. Catal., 2016, 6, 498-525. (d) G.
Cera, L. Ackermann, Top. Curr. Chem., 2016, 374, 191-224. (e) J. Liu,
G. Chen, Z. Tan, Adv. Synth. Catal., 2016, 358, 1174-1194. (f) W.-H.
Rao, B.-F. Shi, Org. Chem. Front., 2016, 3, 1028-1047. (g) M. Shang,
S.-Z. Sun, H.-L. Wang, M.-M. Wang, H.-X. Dai, Synthesis, 2016, 48,
4381-4399. (h) A. Dey, N. Thrimurtulu, C. M. R. Volla, Org. Lett. 2019,
21, 3871- 3875.
8
9
(a) T. T. Nguyen, L. Grigorjeva, Daugulis, O. ACS Catal., 2016, 6, 551-
554. (b) X. Yao, L. Jin, Y. Rao, Asian J. Org. Chem. 2017, 6, 825-830.
10 (a) M. Shang, S.-Z. Sun, H.-X. Dai, J.-Q. Yu, J. Am. Chem. Soc., 2014,
136, 3354-3357. (b) M. Shang, S.-Z. Sun, H.-L. Wang, B. N. Laforteza,
H.-X. Dai, J.-Q. Yu, Angew. Chem. Int. Ed., 2014, 53, 10439-10442. (c)
M. Shang, H.-L. Wang, S.-Z. Sun, H.-X. Dai, J.-Q. Yu, J. Am. Chem. Soc.,
2014, 136, 11590-11593. (d) M. Shang, S.-Z. Sun, H.-X. Dai, J.-Q. Yu,
Org. Lett., 2014, 16, 5666-5669. (e) H.-L. Wang, M. Shang, S.-Z. Sun,
Z.-L. Zhou, B. N. Laforteza, H.-X. Dai, J.-Q. Yu, Org. Lett., 2015, 17,
1228-1231. (f) S.-Z. Sun, M. Shang, H.-L. Wang, H.-X. Lin, H.-X. Dai, J.-
Q. Yu, J. Org. Chem., 2015, 80, 8843-8848. (g) M. Shang, M.-M.
Wang, T. G. Saint-Denis, M.-H. Li, H.-X. Dai, Yu, J.-Q. Angew. Chem.
Int. Ed., 2017, 56, 5317-5321. (h) L.-L. Xu, X. Wang, B. Ma, M.-X. Yin,
H.-X. Lin, H.-X. Dai, J.-Q. Yu, Chem. Sci. 2018, 9, 5160-5164. (i) X.
Wang, X. Yi, H. Xu, H.-X. Dai, Org. Lett. 2019, 21, 5981-5985.
11 (a) T. Hayashi, M. Fukushima, M. Konishi, M. Kumada, Tetrahedron
Lett. 1980, 21, 79-82. b) T. Hayashi, M. Konishi, M. Fukushima, K.
Kanehira, T. Hioki, M. Kumada, J. Org. Chem. 1983, 48, 2195-2202. (c)
Y. Wang, D. Liu, Q. Meng, W. Zhang, Tetrahedron: Asymmetry 2009,
20, 2510-2512. (d) A. Lumbroso, N.R. Vautravers, B. Breit, Org. Lett.
2010, 12, 5498-5501. (e) P. J. Guiry, C. P. Saunders, Adv. Synth. Catal.
2004, 346, 497- 537.
12 (a) W.-S. Huang, S. Liu, D. Zou, M. Thomas, Y. Wang, T. Zhou, J.
Romero, A. Kohlmann, F. Li, J. Qi, L. Cai, T. A. Dwight, Y. Xu, R. Xu, R.
Dodd, A. Toms, L. Parillon, X. Lu, R. Anjum, S. Zhang, F. Wang, J.
Keats, S. D. Wardwell, Y. Ning, Q. Xu, L. E. Moran, Q. K. Mohemmad,
H. G. Jang, T. Clackson, N. I. Narasimhan, V. M. Rivera, X. Zhu, D.
Dalgarno, W. C. Shakespeare, J. Med. Chem. 2016, 59, 4948−4964. (b)
Y. Chen, J. Wu, A. Wang, Z. Qi, T. Jiang, C. Chen, F. Zou, C. Hu, W.
Wang, H. Wu, Z. Hu, W. Wang, B. Wang, L. Wang, T. Ren, S. Zhang,
Q. Liu, J. Liu, Eur. J. Med. Chem. 2017, 139, 674-697. (c) J. Jang, J. B.
Son, C. To, M. Bahcall, S. Y. Kim, S. Y. Kang, M. Mushajiang, Y. Lee, P.
A. Jänne, H. G. Choi, N. S. Gray Eur. J. Med. Chem. 2017, 136, 497-
510. (d) C. Alonso, M. Fuertes, E. Martín-Encinas, A. Selas, G.
4 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins