-
1
-
-
38149070200
-
-
S. Purser, P. R. Moore, S. Swallow, V. Gouverneur, Chem. Soc. Rev. 2008, 37, 320–330.
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 320-330
-
-
Purser, S.1
Moore, P.R.2
Swallow, S.3
Gouverneur, V.4
-
2
-
-
84961296061
-
-
Y. Zhou, J. Wang, Z. Gu, S. Wang, W. Zhu, J. L. Aceña, V. A. Soloshonok, K. Izawa, H. Liu, Chem. Rev. 2016, 116, 422–518.
-
(2016)
Chem. Rev.
, vol.116
, pp. 422-518
-
-
Zhou, Y.1
Wang, J.2
Gu, Z.3
Wang, S.4
Zhu, W.5
Aceña, J.L.6
Soloshonok, V.A.7
Izawa, K.8
Liu, H.9
-
4
-
-
84890981047
-
-
Wiley, Weinheim
-
V. A. Petrov, Flourinated Heterocyclic Compounds: Synthesis Chemistry, and Applications, Vol. 1, Wiley, Weinheim, 2009.
-
(2009)
Flourinated Heterocyclic Compounds: Synthesis Chemistry, and Applications, Vol. 1
-
-
Petrov, V.A.1
-
6
-
-
84856342543
-
-
B. A. Khan, A. E. Buba, L. J. Gooßen, Chem. Eur. J. 2012, 18, 1577–1581.
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 1577-1581
-
-
Khan, B.A.1
Buba, A.E.2
Gooßen, L.J.3
-
7
-
-
84874881615
-
-
Y. Li, L. Wu, H. Neumann, M. Beller, Chem. Commun. 2013, 49, 2628–2630.
-
(2013)
Chem. Commun.
, vol.49
, pp. 2628-2630
-
-
Li, Y.1
Wu, L.2
Neumann, H.3
Beller, M.4
-
8
-
-
84855450542
-
-
T. Liu, X. Shao, Y. Wu, Q. Shen, Angew. Chem. Int. Ed. 2012, 51, 540–543;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 540-543
-
-
Liu, T.1
Shao, X.2
Wu, Y.3
Shen, Q.4
-
9
-
-
84857939979
-
-
Angew. Chem. 2012, 124, 555–558.
-
(2012)
Angew. Chem.
, vol.124
, pp. 555-558
-
-
-
10
-
-
79951643235
-
-
T. D. Senecal, A. T. Parsons, S. L. Buchwald, J. Org. Chem. 2011, 76, 1174–1176.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 1174-1176
-
-
Senecal, T.D.1
Parsons, A.T.2
Buchwald, S.L.3
-
11
-
-
79955032814
-
-
J. Xu, D.-F. Luo, B. Xiao, Z.-J. Liu, T.-J. Gong, Y. Fu, L. Liu, Chem. Commun. 2011, 47, 4300–4302.
-
(2011)
Chem. Commun.
, vol.47
, pp. 4300-4302
-
-
Xu, J.1
Luo, D.-F.2
Xiao, B.3
Liu, Z.-J.4
Gong, T.-J.5
Fu, Y.6
Liu, L.7
-
12
-
-
84867340538
-
-
Y. Ye, S. A. Künzi, M. S. Sanford, Org. Lett. 2012, 14, 4979–4981.
-
(2012)
Org. Lett.
, vol.14
, pp. 4979-4981
-
-
Ye, Y.1
Künzi, S.A.2
Sanford, M.S.3
-
14
-
-
0037160365
-
-
T. Ishiyama, J. Takagi, K. Ishida, N. Miyaura, N. R. Anastasi, J. F. Hartwig, J. Am. Chem. Soc. 2002, 124, 390–391.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 390-391
-
-
Ishiyama, T.1
Takagi, J.2
Ishida, K.3
Miyaura, N.4
Anastasi, N.R.5
Hartwig, J.F.6
-
20
-
-
84923072299
-
-
A. A. Toutov, W.-B. Liu, K. N. Betz, A. Fedorov, B. M. Stoltz, R. H. Grubbs, Nature 2015, 518, 80–84.
-
(2015)
Nature
, vol.518
, pp. 80-84
-
-
Toutov, A.A.1
Liu, W.-B.2
Betz, K.N.3
Fedorov, A.4
Stoltz, B.M.5
Grubbs, R.H.6
-
22
-
-
33644919105
-
-
P. Eisenberger, S. Gischig, A. Togni, Chem. Eur. J. 2006, 12, 2579–2586.
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 2579-2586
-
-
Eisenberger, P.1
Gischig, S.2
Togni, A.3
-
24
-
-
0006598557
-
-
I. Ruppert, K. Schlich, W. Volbach, Tetrahedron Lett. 1984, 25, 2195–2198.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 2195-2198
-
-
Ruppert, I.1
Schlich, K.2
Volbach, W.3
-
25
-
-
0026343720
-
-
B. R. Langlois, E. Laurent, N. Roidot, Tetrahedron Lett. 1991, 32, 7525–7528.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 7525-7528
-
-
Langlois, B.R.1
Laurent, E.2
Roidot, N.3
-
27
-
-
79953675070
-
-
H. Morimoto, T. Tsubogo, N. D. Litvinas, J. F. Hartwig, Angew. Chem. Int. Ed. 2011, 50, 3793–3798;
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 3793-3798
-
-
Morimoto, H.1
Tsubogo, T.2
Litvinas, N.D.3
Hartwig, J.F.4
-
28
-
-
79960643289
-
-
Angew. Chem. 2011, 123, 3877–3882.
-
(2011)
Angew. Chem.
, vol.123
, pp. 3877-3882
-
-
-
29
-
-
84855467454
-
-
N. D. Litvinas, P. S. Fier, J. F. Hartwig, Angew. Chem. Int. Ed. 2012, 51, 536–539;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 536-539
-
-
Litvinas, N.D.1
Fier, P.S.2
Hartwig, J.F.3
-
30
-
-
84857968575
-
-
Angew. Chem. 2012, 124, 551–554.
-
(2012)
Angew. Chem.
, vol.124
, pp. 551-554
-
-
-
31
-
-
84896920241
-
-
M. G. Mormino, P. S. Fier, J. F. Hartwig, Org. Lett. 2014, 16, 1744–1747.
-
(2014)
Org. Lett.
, vol.16
, pp. 1744-1747
-
-
Mormino, M.G.1
Fier, P.S.2
Hartwig, J.F.3
-
32
-
-
85043196173
-
-
Although some reactions without added benzoquinone form the trifluoromethylarene in good yield, most reactions of arenes which are not sensitive to oxidation occurred in about 20 % higher yield in the presence of benzoquinone than in the absence of this oxidant. See the Supporting Information for a series of comparisons in the presence and absence of benzoquinone
-
Although some reactions without added benzoquinone form the trifluoromethylarene in good yield, most reactions of arenes which are not sensitive to oxidation occurred in about 20 % higher yield in the presence of benzoquinone than in the absence of this oxidant. See the Supporting Information for a series of comparisons in the presence and absence of benzoquinone.
-
-
-
-
33
-
-
85099671947
-
-
This assertion is supported by the observation of additional Aryl−CF, compounds by, F NMR spectroscopy.
-
19F NMR spectroscopy.
-
-
-
-
34
-
-
84907027312
-
-
S. A. Sadler, H. Tajuddin, I. A. I. Mkhalid, A. S. Batsanov, D. Albesa-Jove, M. S. Cheung, A. C. Maxwell, L. Shukla, B. Roberts, D. C. Blakemore, Z. Lin, T. B. Marder, P. G. Steel, Org. Biomol. Chem. 2014, 12, 7318–7327.
-
(2014)
Org. Biomol. Chem.
, vol.12
, pp. 7318-7327
-
-
Sadler, S.A.1
Tajuddin, H.2
Mkhalid, I.A.I.3
Batsanov, A.S.4
Albesa-Jove, D.5
Cheung, M.S.6
Maxwell, A.C.7
Shukla, L.8
Roberts, B.9
Blakemore, D.C.10
Lin, Z.11
Marder, T.B.12
Steel, P.G.13
-
35
-
-
77955577649
-
-
M. S. Wiehn, E. V. Vinogradova, A. Togni, J. Fluorine Chem. 2010, 131, 951–957.
-
(2010)
J. Fluorine Chem.
, vol.131
, pp. 951-957
-
-
Wiehn, M.S.1
Vinogradova, E.V.2
Togni, A.3
-
36
-
-
71249126515
-
-
T. Kino, Y. Nagase, Y. Ohtsuka, K. Yamamoto, D. Uraguchi, K. Tokuhisa, T. Yamakawa, J. Fluorine Chem. 2010, 131, 98–105.
-
(2010)
J. Fluorine Chem.
, vol.131
, pp. 98-105
-
-
Kino, T.1
Nagase, Y.2
Ohtsuka, Y.3
Yamamoto, K.4
Uraguchi, D.5
Tokuhisa, K.6
Yamakawa, T.7
-
37
-
-
0000540418
-
-
J.-J. Yang, R. L. Kirchmeier, J. M. Shreeve, J. Org. Chem. 1998, 63, 2656–2660.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 2656-2660
-
-
Yang, J.-J.1
Kirchmeier, R.L.2
Shreeve, J.M.3
-
38
-
-
85043201402
-
-
Reaxys Search
-
Reaxys Search.
-
-
-
|