Organic Letters
Letter
Research Trust Bank of America, N.A., Trustee, and NIH (No.
R01HL139793) is acknowledged.
REFERENCES
■
(1) For reviews, see: (a) Lawrence, S. A. Amines: Synthesis, Properties
and Applications; Cambridge University Press: Cambridge, 2004.
(b) Froidevaux, V.; Negrell, C.; Caillol, S.; Pascault, J.-P.; Boutevin, B.
Chem. Rev. 2016, 116, 14181−14224. (c) Ricci, A., Ed. Amino Group
Chemistry: From Synthesis to the Life Sciences; Wiley−VCH: Weinheim,
Germany, 2008.
(2) For reviews, see: (a) Marvin, C. C. In Comprehensive Organic
Synthesis, 2nd Edition, Vol. 6; Knochel, P., Molander, G. A., Eds.;
Elsevier: New York, 2014; pp 34−99. (b) Rappoport, Z. The
Chemistry of Anilines, Parts 1 and 2; Wiley: New York, 2007. (c) Singh,
G. S. Mini-Rev. Med. Chem. 2016, 16, 892−904. (d) Yudin, A. K., Ed.
Catalyzed Carbon-Heteroatom Bond Formation; Wiley−VCH: Wein-
heim, Germany, 2011. (e) Baehn, S.; Imm, S.; Neubert, L.; Zhang, M.;
Neumann, H.; Beller, M. ChemCatChem 2011, 3, 1853−1864.
(3) For select examples, see: (a) Dong, X.; Liu, Q.; Dong, Y.; Liu, H.
Chem. - Eur. J. 2017, 23, 2481−2511. (b) Gao, H.; Zhou, Z.; Kwon,
D.-H.; Coombs, J.; Jones, S.; Behnke, N. E.; Ess, D. H.; Kurti, L. Nat.
̈
Chem. 2016, 9, 681−688. (c) Kattamuri, P. V.; Yin, J.; Siriwongsup,
S.; Kwon, D.-H.; Ess, D. H.; Li, Q.; Li, G.; Yousufuddin, M.;
Richardson, P. F.; Sutton, S. C.; Kurti, L. J. Am. Chem. Soc. 2017, 139,
̈
11184−11196. (d) Starkov, P.; Jamison, T. F.; Marek, I. Chem. - Eur.
J. 2015, 21, 5278−5300. (e) Miki, Y.; Hirano, K.; Satoh, T.; Miura,
M. Org. Lett. 2013, 15, 172−175.
(4) For reviews, see: (a) Heravi, M. M.; Kheilkordi, Z.; Zadsirjan, V.;
Heydari, M.; Malmir, M. J. Organomet. Chem. 2018, 861, 17−104.
(b) Kunz, K.; Scholz, U.; Ganzer, D. Synlett 2003, 2428−2439.
(c) Hartwig, J. F. Acc. Chem. Res. 2008, 41, 1534−1544. (d) Ruiz-
Castillo, P.; Buchwald, S. L. Chem. Rev. 2016, 116, 12564−12649.
(5) For select examples, see: (a) Du Bois, J. Org. Process Res. Dev.
2011, 15, 758−762. (b) Collet, F.; Lescot, C.; Dauban, P. Chem. Soc.
Rev. 2011, 40, 1926−1936. (c) Chang, J. W. W.; Ton, T. M. U.; Chan,
P. W. H. Chem. Record 2011, 11, 331−357. (d) Davies, H. M. L.;
Manning, J. R. Nature 2008, 451, 417−424.
(6) For notable recent examples, see: (a) Kim, H.; Heo, J.; Kim, J.;
Baik, M.-H.; Chang, S. J. Am. Chem. Soc. 2018, 140, 14350−14356.
(b) Timsina, Y. N.; Gupton, B. F.; Ellis, K. C. ACS Catal. 2018, 8,
5732−5776. (c) Liu, J.; Wu, K.; Shen, T.; Liang, Y.; Zou, M.; Zhu, Y.;
Li, X.; Li, X.; Jiao, N. Chem. - Eur. J. 2017, 23, 563−567.
(d) Hendrick, C. E.; Bitting, K. J.; Cho, S.; Wang, Q. J. Am. Chem.
Soc. 2017, 139, 11622−11628. (e) Legnani, L.; Cerai, G. P.; Morandi,
B. ACS Catal. 2016, 6, 8162−8165. (f) Li, Q.; Zhang, S.-Y.; He, G.;
Ai, Z.; Nack, W. A.; Chen, G. Org. Lett. 2014, 16, 1764−1767.
(7) (a) Jat, J. L.; Paudyal, M. P.; Gao, H.; Xu, Q.-L.; Yousufuddin,
M.; Devarajan, D.; Ess, D. H.; Kurti, L.; Falck, J. R. Science 2014, 343,
̈
61−65. (b) Sabir, S.; Pandey, C. B.; Yadav, A. K.; Tiwari, B.; Jat, J. L.
J. Org. Chem. 2018, 83, 12255−12260.
(8) Paudyal, M. P.; Adebesin, A. M.; Burt, S. R.; Ess, D. H.; Ma, Z.;
Ku
(9) Ma, Z.; Zhou, Z.; Ku
9886−9890.
(10) Jones, W. D. Acc. Chem. Res. 2003, 36, 140−146.
̈
rti, L.; Falck, J. R. Science 2016, 353, 1144−1147.
̈
rti, L. Angew. Chem., Int. Ed. 2017, 56,
D
Org. Lett. XXXX, XXX, XXX−XXX