-
4
-
-
74849140182
-
-
Johansson, C. C. C.; Colacot, T. J. Angew. Chem., Int. Ed. 2010, 49, 676 10.1002/anie.200903424
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 676
-
-
Johansson, C.C.C.1
Colacot, T.J.2
-
5
-
-
84919667761
-
-
Sivanandan, S. T.; Shaji, A.; Ibnusaud, I.; Seechurn, C. C. C. J.; Colacot, T. J. Eur. J. Org. Chem. 2015, 2015, 38 10.1002/ejoc.201403301
-
(2015)
Eur. J. Org. Chem.
, vol.2015
, pp. 38
-
-
Sivanandan, S.T.1
Shaji, A.2
Ibnusaud, I.3
Seechurn, C.C.C.J.4
Colacot, T.J.5
-
6
-
-
0030776292
-
-
Satoh, T.; Kawamura, Y.; Miura, M.; Nomura, M. Angew. Chem., Int. Ed. Engl. 1997, 36, 1740 10.1002/anie.199717401
-
(1997)
Angew. Chem., Int. Ed. Engl.
, vol.36
, pp. 1740
-
-
Satoh, T.1
Kawamura, Y.2
Miura, M.3
Nomura, M.4
-
13
-
-
33645893476
-
-
Singh, F. V.; Vatsyayan, R.; Roy, U.; Goel, A. Bioorg. Med. Chem. Lett. 2006, 16, 2734 10.1016/j.bmcl.2006.02.012
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2734
-
-
Singh, F.V.1
Vatsyayan, R.2
Roy, U.3
Goel, A.4
-
14
-
-
63149146752
-
-
Singh, F. V.; Parihar, A.; Chaurasia, S.; Singh, A. B.; Singh, S. P.; Tamrakar, A. K.; Srivastava, A. K.; Goel, A. Bioorg. Med. Chem. Lett. 2009, 19, 2158 10.1016/j.bmcl.2009.02.118
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2158
-
-
Singh, F.V.1
Parihar, A.2
Chaurasia, S.3
Singh, A.B.4
Singh, S.P.5
Tamrakar, A.K.6
Srivastava, A.K.7
Goel, A.8
-
15
-
-
84879062991
-
-
Vitale, P.; Tacconelli, S.; Perrone, M. G.; Malerba, P.; Simone, L.; Scilimati, A.; Lavecchia, A.; Dovizio, M.; Marcantoni, E.; Bruno, A.; Patrignani, P. J. Med. Chem. 2013, 56, 4277 10.1021/jm301905a
-
(2013)
J. Med. Chem.
, vol.56
, pp. 4277
-
-
Vitale, P.1
Tacconelli, S.2
Perrone, M.G.3
Malerba, P.4
Simone, L.5
Scilimati, A.6
Lavecchia, A.7
Dovizio, M.8
Marcantoni, E.9
Bruno, A.10
Patrignani, P.11
-
16
-
-
84941919616
-
-
Wolfe, J. P. Georg Thieme Verlag: Stuttgart
-
Marsden, S. P. In Cross Coupling and Heck-Type Reactions 2, Carbon-Heteroatom Cross-Coupling and C-C Cross Coupling of Acidic C-H Nucleophiles, Science of Synthesis; Wolfe, J. P., Ed.; Georg Thieme Verlag: Stuttgart, 2013; pp 565-620.
-
(2013)
Cross Coupling and Heck-Type Reactions 2, Carbon-Heteroatom Cross-Coupling and C-C Cross Coupling of Acidic C-H Nucleophiles, Science of Synthesis
, pp. 565-620
-
-
Marsden, S.P.1
-
18
-
-
79960903755
-
-
Liu, C.; Deng, Y.; Wang, J.; Yang, Y.; Tang, S.; Lei, A. Angew. Chem., Int. Ed. 2011, 50, 7337 10.1002/anie.201101638
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 7337
-
-
Liu, C.1
Deng, Y.2
Wang, J.3
Yang, Y.4
Tang, S.5
Lei, A.6
-
21
-
-
79953694204
-
-
Hesp, K. D.; Lundgren, R. J.; Stradiotto, M. J. Am. Chem. Soc. 2011, 133, 5194 10.1021/ja200009c
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 5194
-
-
Hesp, K.D.1
Lundgren, R.J.2
Stradiotto, M.3
-
22
-
-
84920744230
-
-
Rotta-Loria, N. L.; Borzenko, A.; Alsabeh, P. G.; Lavery, C. B.; Stradiotto, M. Adv. Synth. Catal. 2015, 357, 100 10.1002/adsc.201400903
-
(2015)
Adv. Synth. Catal.
, vol.357
, pp. 100
-
-
Rotta-Loria, N.L.1
Borzenko, A.2
Alsabeh, P.G.3
Lavery, C.B.4
Stradiotto, M.5
-
23
-
-
84877711237
-
-
Li, P.; Lü, B.; Fu, C.; Ma, S. Adv. Synth. Catal. 2013, 355, 1255 10.1002/adsc.201300207
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 1255
-
-
Li, P.1
Lü, B.2
Fu, C.3
Ma, S.4
-
24
-
-
84941907228
-
-
Gäbler, C.; Korb, M.; Schaarschmidt, D.; Hildebrandt, A.; Lang, H. Adv. Synth. Catal. 2014, 356, 2979 10.1002/adsc.201400235
-
(2014)
Adv. Synth. Catal.
, vol.356
, pp. 2979
-
-
Gäbler, C.1
Korb, M.2
Schaarschmidt, D.3
Hildebrandt, A.4
Lang, H.5
-
25
-
-
84864607963
-
-
Apart from aryl halides, aryl imidazolylsuflonates were found to be applicable substrates; see: Ackermann, L.; Mehta, V. P. Chem.-Eur. J. 2012, 18, 10230 10.1002/chem.201201394
-
(2012)
Chem. - Eur. J.
, vol.18
, pp. 10230
-
-
Ackermann, L.1
Mehta, V.P.2
-
26
-
-
84941884445
-
-
CyPF-tBu = (R)-1-[(SP)-2-(dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine. During the completion of our experimental works, a related paper appeared; see: MacQueen, P. M.; Chisholm, A. J.; Hargreaves, B. K. V.; Stradiotto, M. Chem.-Eur. J. 2015, 21, 11006 10.1002/chem.201500834
-
(2015)
Chem. - Eur. J.
, vol.21
, pp. 11006
-
-
MacQueen, P.M.1
Chisholm, A.J.2
Hargreaves, B.K.V.3
Stradiotto, M.4
-
28
-
-
0033997284
-
-
Fox, J. M.; Huang, X. H.; Chieffi, A.; Buchwald, S. L. J. Am. Chem. Soc. 2000, 122, 1360 10.1021/ja993912d
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 1360
-
-
Fox, J.M.1
Huang, X.H.2
Chieffi, A.3
Buchwald, S.L.4
-
29
-
-
0000096644
-
-
Ehrentraut, A.; Zapf, A.; Beller, M. Adv. Synth. Catal. 2002, 344, 209 10.1002/1615-4169(200202)344:2<209::AID-ADSC209>3.0.CO;2-5
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 209
-
-
Ehrentraut, A.1
Zapf, A.2
Beller, M.3
-
31
-
-
38349078282
-
-
Liao, X.; Weng, Z.; Hartwig, J. F. J. Am. Chem. Soc. 2008, 130, 195 10.1021/ja074453g
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 195
-
-
Liao, X.1
Weng, Z.2
Hartwig, J.F.3
-
32
-
-
84874951682
-
-
Jia, T.; Bellomo, A.; Baina, K. E. L.; Dreher, S. D.; Walsh, P. J. J. Am. Chem. Soc. 2013, 135, 3740 10.1021/ja4009776
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 3740
-
-
Jia, T.1
Bellomo, A.2
Baina, K.E.L.3
Dreher, S.D.4
Walsh, P.J.5
-
33
-
-
84875964658
-
-
Zheng, B.; Jia, T.; Walsh, P. Org. Lett. 2013, 15, 1690 10.1021/ol400472v
-
(2013)
Org. Lett.
, vol.15
, pp. 1690
-
-
Zheng, B.1
Jia, T.2
Walsh, P.3
-
34
-
-
84882790079
-
-
Zheng, B.; Jia, T.; Walsh, P. Org. Lett. 2013, 15, 4190 10.1021/ol4019002
-
(2013)
Org. Lett.
, vol.15
, pp. 4190
-
-
Zheng, B.1
Jia, T.2
Walsh, P.3
-
36
-
-
84940005196
-
-
Wong, S. M.; Yuen, O. Y.; Choy, P. Y.; Kwong, F. Y. Coord. Chem. Rev. 2015, 293-294, 158 10.1016/j.ccr.2015.01.017
-
(2015)
Coord. Chem. Rev.
, vol.293-294
, pp. 158
-
-
Wong, S.M.1
Yuen, O.Y.2
Choy, P.Y.3
Kwong, F.Y.4
-
37
-
-
84880531972
-
-
Chow, W. K.; Yuen, O. Y.; Choy, P. Y.; So, C. M.; Lau, C. P.; Wong, W. T.; Kwong, F. Y. RSC Adv. 2013, 3, 12518 10.1039/c3ra22905j
-
(2013)
RSC Adv.
, vol.3
, pp. 12518
-
-
Chow, W.K.1
Yuen, O.Y.2
Choy, P.Y.3
So, C.M.4
Lau, C.P.5
Wong, W.T.6
Kwong, F.Y.7
-
38
-
-
79957843865
-
-
Yeung, P. Y.; Chung, C. H.; Kwong, F. Y. Org. Lett. 2011, 13, 2912 10.1021/ol2009522
-
(2011)
Org. Lett.
, vol.13
, pp. 2912
-
-
Yeung, P.Y.1
Chung, C.H.2
Kwong, F.Y.3
-
39
-
-
78651446257
-
-
So, C. M.; Lau, C. P.; Kwong, F. Y. Chem.-Eur. J. 2011, 17, 761 10.1002/chem.201002354
-
(2011)
Chem. - Eur. J.
, vol.17
, pp. 761
-
-
So, C.M.1
Lau, C.P.2
Kwong, F.Y.3
-
40
-
-
34548190562
-
-
Yip, S. F.; Cheung, H. Y.; Zhou, Z.; Kwong, F. Y. Org. Lett. 2007, 9, 3469 10.1021/ol701473p
-
(2007)
Org. Lett.
, vol.9
, pp. 3469
-
-
Yip, S.F.1
Cheung, H.Y.2
Zhou, Z.3
Kwong, F.Y.4
-
41
-
-
84922689433
-
-
Choy, P. Y.; Luk, K. C.; Wu, Y.; So, C. M.; Wang, L.-L.; Kwong, F. Y. J. Org. Chem. 2015, 80, 1457 10.1021/jo502386w
-
(2015)
J. Org. Chem.
, vol.80
, pp. 1457
-
-
Choy, P.Y.1
Luk, K.C.2
Wu, Y.3
So, C.M.4
Wang, L.-L.5
Kwong, F.Y.6
-
42
-
-
84925384804
-
-
Yuen, O. Y.; Charoensak, M.; So, C. M.; Kuhakarn, C.; Kwong, F. Y. Chem.-Asian J. 2015, 10, 857 10.1002/asia.201500048
-
(2015)
Chem. - Asian J.
, vol.10
, pp. 857
-
-
Yuen, O.Y.1
Charoensak, M.2
So, C.M.3
Kuhakarn, C.4
Kwong, F.Y.5
-
43
-
-
84941925610
-
-
Wolfe, J. P. Georg Thieme Verlag: Stuttgart
-
Wu, Y.; Wang, J.; Kwong, F. Y. In Cross Coupling and Heck-Type Reactions 2, Carbon-Heteroatom Cross-Coupling and C-C Cross Coupling of Acidic C-H Nucleophiles, Science of Synthesis; Wolfe, J. P., Ed.; Georg Thieme Verlag: Stuttgart, 2013; pp 621-646.
-
(2013)
Cross Coupling and Heck-Type Reactions 2, Carbon-Heteroatom Cross-Coupling and C-C Cross Coupling of Acidic C-H Nucleophiles, Science of Synthesis
, pp. 621-646
-
-
Wu, Y.1
Wang, J.2
Kwong, F.Y.3
-
44
-
-
0037112673
-
-
Littke, A. F.; Fu, G. C. Angew. Chem., Int. Ed. 2002, 41, 4176 10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 4176
-
-
Littke, A.F.1
Fu, G.C.2
-
46
-
-
51149214207
-
-
The indicated C-3 position of indole is estimated to be 1013 times more reactive than benzene for electrophilic attack; see: Laws, A. P.; Taylor, R. J. Chem. Soc., Perkin Trans. 2 1987, 591 10.1039/p29870000591
-
(1987)
J. Chem. Soc., Perkin Trans. 2
, pp. 591
-
-
Laws, A.P.1
Taylor, R.2
-
47
-
-
63849273180
-
-
Zhang, H.; Luo, X.; Wongkhan, K.; Duan, H.; Li, Q.; Xhu, L.; Wang, J.; Batsanov, A. S.; Howard, J. A. K.; Marder, T. B.; Lei, A. Chem.-Eur. J. 2009, 15, 3823 10.1002/chem.200802209
-
(2009)
Chem. - Eur. J.
, vol.15
, pp. 3823
-
-
Zhang, H.1
Luo, X.2
Wongkhan, K.3
Duan, H.4
Li, Q.5
Xhu, L.6
Wang, J.7
Batsanov, A.S.8
Howard, J.A.K.9
Marder, T.B.10
Lei, A.11
-
49
-
-
84924414753
-
-
For a recent reference describing the specially designed biaryl-type phosphine ligand for a difficult RE process, see: Li, C.; Chen, T.; Li, B.; Xiao, G.; Tang, W. Angew. Chem., Int. Ed. 2015, 54, 3792 10.1002/anie.201411518
-
(2015)
Angew. Chem., Int. Ed.
, vol.54
, pp. 3792
-
-
Li, C.1
Chen, T.2
Li, B.3
Xiao, G.4
Tang, W.5
-
51
-
-
12344337315
-
-
Ligand cost and catalyst loading become two of the most important factors in production-scale catalysis; see: Schlummer, B.; Scholz, U. Adv. Synth. Catal. 2004, 346, 1599 10.1002/adsc.200404216
-
(2004)
Adv. Synth. Catal.
, vol.346
, pp. 1599
-
-
Schlummer, B.1
Scholz, U.2
|