-
1
-
-
11844274689
-
-
Shimizu, M.; Hiyama, T. Angew. Chem., Int. Ed. 2005, 44, 214
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 214
-
-
Shimizu, M.1
Hiyama, T.2
-
2
-
-
34848848499
-
-
Muller, K.; Faeh, C.; Diederich, F. Science 2007, 317, 1881
-
(2007)
Science
, vol.317
, pp. 1881
-
-
Muller, K.1
Faeh, C.2
Diederich, F.3
-
3
-
-
38149070200
-
-
Purser, S.; Moore, P. R.; Swallow, S.; Gouverneur, V. Chem. Soc. Rev. 2008, 37, 320
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 320
-
-
Purser, S.1
Moore, P.R.2
Swallow, S.3
Gouverneur, V.4
-
5
-
-
79952189007
-
-
A key review, see
-
A key review, see: Roy, S.; Gregg, B. T.; Gribble, G. W.; Le, V.-D.; Roy, S. Tetrahedron 2011, 67, 2161
-
(2011)
Tetrahedron
, vol.67
, pp. 2161
-
-
Roy, S.1
Gregg, B.T.2
Gribble, G.W.3
Le, V.-D.4
Roy, S.5
-
7
-
-
84855467454
-
-
Litvinas, N. D.; Fier, P. S.; Hartwig, J. F. Angew. Chem., Int. Ed. 2012, 51, 536
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 536
-
-
Litvinas, N.D.1
Fier, P.S.2
Hartwig, J.F.3
-
8
-
-
84862907871
-
-
Zhao, Y.; Hu, J. Angew. Chem., Int. Ed. 2012, 51, 1033
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 1033
-
-
Zhao, Y.1
Hu, J.2
-
9
-
-
79957603696
-
-
Furuya, T.; Kamlet, A. S.; Ritter, T. Nature 2011, 473, 470
-
(2011)
Nature
, vol.473
, pp. 470
-
-
Furuya, T.1
Kamlet, A.S.2
Ritter, T.3
-
10
-
-
84862069135
-
-
Besset, T.; Schneider, C.; Cahard, D. Angew. Chem., Int. Ed. 2012, 51, 5048
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 5048
-
-
Besset, T.1
Schneider, C.2
Cahard, D.3
-
11
-
-
84882268052
-
-
Liang, T.; Neumann, C. N.; Ritter, T. Angew. Chem., Int. Ed. 2012, 52, 8214
-
(2012)
Angew. Chem., Int. Ed.
, vol.52
, pp. 8214
-
-
Liang, T.1
Neumann, C.N.2
Ritter, T.3
-
14
-
-
83055177179
-
-
2Cl, and it was in agreement with our recent observation that the free anilines could form the byproduct sulphonamide (Table 1, entry 4). See
-
2Cl, and it was in agreement with our recent observation that the free anilines could form the byproduct sulphonamide (Table 1, entry 4). See: Nagib, D. A.; MacMillan, D. W. C. Nature 2011, 480, 224
-
(2011)
Nature
, vol.480
, pp. 224
-
-
Nagib, D.A.1
Macmillan, D.W.C.2
-
15
-
-
84874025068
-
-
Zhang, L.-S.; Chen, K.; Chen, G.; Li, B.; Luo, S.; Guo, Q.; Wei, J.; Shi, Z. Org. Lett. 2013, 15, 10
-
(2013)
Org. Lett.
, vol.15
, pp. 10
-
-
Zhang, L.-S.1
Chen, K.2
Chen, G.3
Li, B.4
Luo, S.5
Guo, Q.6
Wei, J.7
Shi, Z.8
-
16
-
-
84876920518
-
-
Cai, S.; Chen, C.; Sun, Z.; Xi, C. Chem. Commun. 2013, 49, 4552
-
(2013)
Chem. Commun.
, vol.49
, pp. 4552
-
-
Cai, S.1
Chen, C.2
Sun, Z.3
Xi, C.4
-
17
-
-
84876723163
-
-
Xie, J.; Xue, Q.; Jin, H.; Li, H.; Cheng, Y.; Zhu, C. Chem. Sci. 2013, 4, 1281
-
(2013)
Chem. Sci.
, vol.4
, pp. 1281
-
-
Xie, J.1
Xue, Q.2
Jin, H.3
Li, H.4
Cheng, Y.5
Zhu, C.6
-
18
-
-
84878668534
-
-
Xie, J.; Xu, P.; Li, H.; Xue, Q.; Jin, H.; Cheng, Y.; Zhu, C. Chem. Commun. 2013, 49, 5672
-
(2013)
Chem. Commun.
, vol.49
, pp. 5672
-
-
Xie, J.1
Xu, P.2
Li, H.3
Xue, Q.4
Jin, H.5
Cheng, Y.6
Zhu, C.7
-
19
-
-
84890224125
-
-
Xie, J.; Jin, H.; Xu, P.; Zhu, C. Tetrahedron Lett. 2014, 55, 36
-
(2014)
Tetrahedron Lett.
, vol.55
, pp. 36
-
-
Xie, J.1
Jin, H.2
Xu, P.3
Zhu, C.4
-
20
-
-
77953990194
-
-
Yoon, T. P.; Ischay, M. A.; Du, J. N. Nat. Chem. 2010, 2, 527
-
(2010)
Nat. Chem.
, vol.2
, pp. 527
-
-
Yoon, T.P.1
Ischay, M.A.2
Du, J.N.3
-
22
-
-
84863643233
-
-
Xuan, J.; Xiao, W.-J. Angew. Chem., Int. Ed. 2012, 51, 6828
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 6828
-
-
Xuan, J.1
Xiao, W.-J.2
-
23
-
-
84880124916
-
-
Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Chem. Rev. 2013, 113, 5322
-
(2013)
Chem. Rev.
, vol.113
, pp. 5322
-
-
Prier, C.K.1
Rankic, D.A.2
Macmillan, D.W.C.3
-
24
-
-
84862777465
-
-
Lqbal, N.; Choi, S.; Ko, E.; Cho, E. J. Tetrahedron Lett. 2012, 53, 2005
-
(2012)
Tetrahedron Lett.
, vol.53
, pp. 2005
-
-
Lqbal, N.1
Choi, S.2
Ko, E.3
Cho, E.J.4
-
25
-
-
77955577649
-
-
The electrophilic trifluoromethylation reaction of anilines with Togni's reagent also occured when it was carried out at high temperature in the presence of Lewis acids. However, the reaction conditions resulted in a limited scope. See
-
The electrophilic trifluoromethylation reaction of anilines with Togni's reagent also occured when it was carried out at high temperature in the presence of Lewis acids. However, the reaction conditions resulted in a limited scope. See: Wiehn, M. S.; Vinogradova, E. V.; Togni, A. J. Fluorine Chem. 2010, 131, 951
-
(2010)
J. Fluorine Chem.
, vol.131
, pp. 951
-
-
Wiehn, M.S.1
Vinogradova, E.V.2
Togni, A.3
-
26
-
-
84866396889
-
-
Yasu, Y.; Koike, T.; Akita, M. Angew. Chem., Int. Ed. 2012, 51, 9567
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 9567
-
-
Yasu, Y.1
Koike, T.2
Akita, M.3
-
27
-
-
84877136034
-
-
Yasu, Y.; Koike, T.; Akita, M. Org. Lett. 2013, 15, 2136
-
(2013)
Org. Lett.
, vol.15
, pp. 2136
-
-
Yasu, Y.1
Koike, T.2
Akita, M.3
-
28
-
-
84874056108
-
-
Mizuta, S.; Verhoog, S.; Engle, K. M.; Khotavivattana, T.; O'Dui00ll, M.; Wheelhouse, K.; Rassias, G.; Médebielle, M.; Gouverneur, V. J. Am. Chem. Soc. 2013, 135, 2505
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 2505
-
-
Mizuta, S.1
Verhoog, S.2
Engle, K.M.3
Khotavivattana, T.4
O'Duill, M.5
Wheelhouse, K.6
Rassias, G.7
Médebielle, M.8
Gouverneur, V.9
-
29
-
-
68249144236
-
-
Nagib, D. A.; Scott, M. E.; MacMillan, D. W. C. J. Am. Chem. Soc. 2009, 131, 10875
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 10875
-
-
Nagib, D.A.1
Scott, M.E.2
Macmillan, D.W.C.3
-
30
-
-
84891810003
-
-
Iqbal, N.; Jung, J.; Park, S.; Cho, E. J. Angew. Chem., Int. Ed. 2014, 53, 539
-
(2014)
Angew. Chem., Int. Ed.
, vol.53
, pp. 539
-
-
Iqbal, N.1
Jung, J.2
Park, S.3
Cho, E.J.4
-
31
-
-
80052298009
-
-
Ji, Y.; Brueckl, T.; Baxter, R. D.; Fujiwara, Y.; Seiple, I. B.; Su, S.; Blackmond, D. G.; Baran, P. S. Proc. Natl. Acad. Sci. U.S.A. 2011, 108, 14411
-
(2011)
Proc. Natl. Acad. Sci. U.S.A.
, vol.108
, pp. 14411
-
-
Ji, Y.1
Brueckl, T.2
Baxter, R.D.3
Fujiwara, Y.4
Seiple, I.B.5
Su, S.6
Blackmond, D.G.7
Baran, P.S.8
-
32
-
-
84880029578
-
-
Wilger, D. J.; Gesmundo, N. J.; Nicewicz, D. A. Chem. Sci. 2013, 4, 3160
-
(2013)
Chem. Sci.
, vol.4
, pp. 3160
-
-
Wilger, D.J.1
Gesmundo, N.J.2
Nicewicz, D.A.3
-
33
-
-
84873892009
-
-
Wu, X.; Chu, L.; Qing, F.-L. Angew. Chem., Int. Ed. 2013, 52, 2198
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 2198
-
-
Wu, X.1
Chu, L.2
Qing, F.-L.3
-
34
-
-
80052851561
-
-
Parsons, A. T.; Buchwald, S. L. Angew. Chem., Int. Ed. 2011, 50, 9120
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 9120
-
-
Parsons, A.T.1
Buchwald, S.L.2
-
35
-
-
84879336685
-
-
Liu, X.; Xiong, F.; Huang, X.; Xu, L.; Li, P.; Wu, X. Angew. Chem., Int. Ed. 2013, 52, 6962
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 6962
-
-
Liu, X.1
Xiong, F.2
Huang, X.3
Xu, L.4
Li, P.5
Wu, X.6
-
36
-
-
84887516902
-
-
Feng, C.; Loh, T.-P. Angew. Chem., Int. Ed. 2013, 52, 12414
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 12414
-
-
Feng, C.1
Loh, T.-P.2
-
37
-
-
84875718798
-
-
Egami, H.; Shimizu, R.; Kawamura, S.; Sodeoka, M. Angew. Chem., Int. Ed. 2013, 52, 4000
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 4000
-
-
Egami, H.1
Shimizu, R.2
Kawamura, S.3
Sodeoka, M.4
-
38
-
-
84883545162
-
-
Chen, Z.; Bai, W.; Wang, S.; Yang, B.; Tu, Y.-Q.; Zhang, F. Angew. Chem., Int. Ed. 2013, 52, 9781
-
(2013)
Angew. Chem., Int. Ed.
, vol.52
, pp. 9781
-
-
Chen, Z.1
Bai, W.2
Wang, S.3
Yang, B.4
Tu, Y.-Q.5
Zhang, F.6
-
39
-
-
77955877752
-
-
Huang, A.; Moretto, A.; Janz, K.; Lowe, M.; Bedard, P. W.; Tam, S.; Di, L.; Clerin, V.; Sushkova, N.; Tchernychev, B.; Tsao, D.; Keith, J.; Shaw, J.; Schaub, R. G.; Wang, Q.; Kaila, N. J. Med. Chem. 2010, 53, 6003
-
(2010)
J. Med. Chem.
, vol.53
, pp. 6003
-
-
Huang, A.1
Moretto, A.2
Janz, K.3
Lowe, M.4
Bedard, P.W.5
Tam, S.6
Di, L.7
Clerin, V.8
Sushkova, N.9
Tchernychev, B.10
Tsao, D.11
Keith, J.12
Shaw, J.13
Schaub, R.G.14
Wang, Q.15
Kaila, N.16
-
40
-
-
84896988599
-
-
Akira, N.; Katsuyata, I.; Kiyoshi, K.; Sho, H.; Akira, N. Nippon Noyaku Gakkaishi 1989, 14, 23
-
(1989)
Nippon Noyaku Gakkaishi
, vol.14
, pp. 23
-
-
Akira, N.1
Katsuyata, I.2
Kiyoshi, K.3
Sho, H.4
Akira, N.5
|