-
1
-
-
0004211170
-
-
4 th ed. Georg Thieme: Stuttgart.
-
Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D. Pharmaceutical Substance: Synthesis, Patents, Applications, 4 th ed.; Georg Thieme: Stuttgart, 2001.
-
(2001)
Pharmaceutical Substance: Synthesis, Patents, Applications
-
-
Kleemann, A.1
Engel, J.2
Kutscher, B.3
Reichert, D.4
-
3
-
-
7444242751
-
-
Nakao, Y.; Oda, S.; Hiyama, T. J. Am. Chem. Soc. 2004, 126, 13904
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13904
-
-
Nakao, Y.1
Oda, S.2
Hiyama, T.3
-
5
-
-
68149110231
-
-
Yu, D.-G.; Yu, M.; Guan, B.-T.; Li, B.-J.; Zheng, Y.; Wu, Z.-H.; Shi, Z.-J. Org. Lett. 2009, 11, 3374
-
(2009)
Org. Lett.
, vol.11
, pp. 3374
-
-
Yu, D.-G.1
Yu, M.2
Guan, B.-T.3
Li, B.-J.4
Zheng, Y.5
Wu, Z.-H.6
Shi, Z.-J.7
-
10
-
-
0000095492
-
-
Sakakibara, Y.; Okuda, F.; Shimobayashi, A.; Kirino, K.; Sakai, M.; Uchino, N.; Takagi, K. Bull. Chem. Soc. Jpn. 1988, 61, 1985
-
(1988)
Bull. Chem. Soc. Jpn.
, vol.61
, pp. 1985
-
-
Sakakibara, Y.1
Okuda, F.2
Shimobayashi, A.3
Kirino, K.4
Sakai, M.5
Uchino, N.6
Takagi, K.7
-
12
-
-
0003094578
-
-
For the catalytic cyanation using NaCN, see
-
For the catalytic cyanation using NaCN, see: Okano, T.; Iwahara, M.; Kiji, J. Synlett 1998, 243
-
(1998)
Synlett
, pp. 243
-
-
Okano, T.1
Iwahara, M.2
Kiji, J.3
-
13
-
-
0028343676
-
-
Tschaen, D. M.; Desmond, R.; King, A. O.; Fortin, M. C.; Pipik, B.; King, S.; Verhoeven, T. R. Synth. Commun. 1994, 24, 887
-
(1994)
Synth. Commun.
, vol.24
, pp. 887
-
-
Tschaen, D.M.1
Desmond, R.2
King, A.O.3
Fortin, M.C.4
Pipik, B.5
King, S.6
Verhoeven, T.R.7
-
15
-
-
0000945375
-
-
For the catalytic cyanation using TMSCN, see
-
For the catalytic cyanation using TMSCN, see: Chatani, N.; Hanafusa, T. J. Org. Chem. 1986, 51, 4714
-
(1986)
J. Org. Chem.
, vol.51
, pp. 4714
-
-
Chatani, N.1
Hanafusa, T.2
-
18
-
-
33744786786
-
-
Chen, X.; Hao, X.-S.; Goodhue, C. E.; Yu, J.-Q. J. Am. Chem. Soc. 2006, 128, 6790
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 6790
-
-
Chen, X.1
Hao, X.-S.2
Goodhue, C.E.3
Yu, J.-Q.4
-
19
-
-
70349923078
-
-
Jia, X.; Yang, D.; Zhang, S.; Cheng, J. Org. Lett. 2009, 11, 4716
-
(2009)
Org. Lett.
, vol.11
, pp. 4716
-
-
Jia, X.1
Yang, D.2
Zhang, S.3
Cheng, J.4
-
20
-
-
73149090817
-
-
Jia, X.; Yang, D.; Wang, W.; Luo, F.; Cheng, J. J. Org. Chem. 2009, 74, 9470
-
(2009)
J. Org. Chem.
, vol.74
, pp. 9470
-
-
Jia, X.1
Yang, D.2
Wang, W.3
Luo, F.4
Cheng, J.5
-
21
-
-
0037432906
-
-
Sundermeier, M.; Zapf, A.; Beller, M. Angew. Chem., Int. Ed. 2003, 42, 1661
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 1661
-
-
Sundermeier, M.1
Zapf, A.2
Beller, M.3
-
22
-
-
77951003571
-
-
Park, E. J.; Lee, S.; Chang, S. J. Org. Chem. 2010, 75, 2760
-
(2010)
J. Org. Chem.
, vol.75
, pp. 2760
-
-
Park, E.J.1
Lee, S.2
Chang, S.3
-
24
-
-
78650897165
-
-
Anbarasan, P.; Neumann, H.; Beller, M. Angew. Chem., Int. Ed. 2011, 50, 519
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 519
-
-
Anbarasan, P.1
Neumann, H.2
Beller, M.3
-
26
-
-
79958007738
-
-
Ren, X.; Chen, J.; Chen, F.; Cheng, J. Chem. Commun. 2011, 47, 6725
-
(2011)
Chem. Commun.
, vol.47
, pp. 6725
-
-
Ren, X.1
Chen, J.2
Chen, F.3
Cheng, J.4
-
28
-
-
80054721587
-
-
Zhang, G.; Ren, X.; Chen, J.; Hu, M.; Cheng, J. Org. Lett. 2011, 13, 5004
-
(2011)
Org. Lett.
, vol.13
, pp. 5004
-
-
Zhang, G.1
Ren, X.2
Chen, J.3
Hu, M.4
Cheng, J.5
-
29
-
-
77955786895
-
-
Liskey, C. W.; Liao, X.; Hartwig, J. F. J. Am. Chem. Soc. 2010, 132, 11389
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 11389
-
-
Liskey, C.W.1
Liao, X.2
Hartwig, J.F.3
-
30
-
-
79951846136
-
-
Zhang, G.; Zhang, L.; Hu, M.; Cheng, J. Adv. Synth. Catal. 2011, 353, 291
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 291
-
-
Zhang, G.1
Zhang, L.2
Hu, M.3
Cheng, J.4
-
31
-
-
0037433554
-
-
For a precedent example of Cu-catalyzed domino halide exchange-cyanation of aryl bromides using NaCN, see
-
For a precedent example of Cu-catalyzed domino halide exchange-cyanation of aryl bromides using NaCN, see: Zanon, J.; Klapars, A.; Buchwald, S. L. J. Am. Chem. Soc. 2003, 125, 2890
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 2890
-
-
Zanon, J.1
Klapars, A.2
Buchwald, S.L.3
-
33
-
-
57449108893
-
-
Kim, J.; Lee, S. Y.; Lee, J.; Do, Y.; Chang, S. J. Org. Chem. 2008, 73, 9454
-
(2008)
J. Org. Chem.
, vol.73
, pp. 9454
-
-
Kim, J.1
Lee, S.Y.2
Lee, J.3
Do, Y.4
Chang, S.5
-
34
-
-
33748275848
-
-
It is postulated that the partial olefin isomerization occurs during the Cu-mediated oxidative addition of in situ formed β-iodostyrene
-
It is postulated that the partial olefin isomerization occurs during the Cu-mediated oxidative addition of in situ formed β-iodostyrene: Li, L.-H.; Pan, Z.-L.; Duan, X.-H.; Liang, Y.-M. Synlett 2006, 2094
-
(2006)
Synlett
, pp. 2094
-
-
Li, L.-H.1
Pan, Z.-L.2
Duan, X.-H.3
Liang, Y.-M.4
-
36
-
-
33751155775
-
-
Vedejs, E.; Chapman, R. W.; Fields., S. C.; Lin, S.; Schrimpf, M. R. J. Org. Chem. 1995, 60, 3020
-
(1995)
J. Org. Chem.
, vol.60
, pp. 3020
-
-
Vedejs, E.1
Chapman, R.W.2
Fields, S.3
Lin, S.4
Schrimpf, M.R.5
-
39
-
-
78650886604
-
-
Shirakawa, E.; Uchiyama, N.; Hayashi, T. J. Org. Chem. 2011, 76, 25
-
(2011)
J. Org. Chem.
, vol.76
, pp. 25
-
-
Shirakawa, E.1
Uchiyama, N.2
Hayashi, T.3
-
40
-
-
77952794676
-
-
Chiba, S.; Zhang, L.; Lee, J.-Y. J. Am. Chem. Soc. 2010, 132, 7266
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7266
-
-
Chiba, S.1
Zhang, L.2
Lee, J.-Y.3
-
42
-
-
4644306818
-
-
Mohan, K. V. V. K.; Narender, N.; Kulkarni, S. J. Tetrahedron Lett. 2004, 45, 8015
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8015
-
-
Mohan, K.V.V.K.1
Narender, N.2
Kulkarni, S.J.3
-
43
-
-
0032514998
-
-
Anderson, B. A.; Bell, E. C.; Ginah, F. O.; Harn, N. K.; Pagh, L. M.; Wepsiec, J. P. J. Org. Chem. 1998, 63, 8224
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8224
-
-
Anderson, B.A.1
Bell, E.C.2
Ginah, F.O.3
Harn, N.K.4
Pagh, L.M.5
Wepsiec, J.P.6
-
44
-
-
0142010015
-
-
Arvela, R. K.; Leadbeater, N. E.; Torenius, H. M.; Tye, H. Org. Biomol. Chem. 2003, 1, 1119
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 1119
-
-
Arvela, R.K.1
Leadbeater, N.E.2
Torenius, H.M.3
Tye, H.4
|