-
2
-
-
0027913099
-
-
Murai, S.; Kakiuchi, F.; Sekine, S.; Tanaka, Y.; Kamatani, A.; Sonoda, M.; Chatani, N. Nature 1993, 366, 529.
-
(1993)
Nature
, vol.366
, pp. 529
-
-
Murai, S.1
Kakiuchi, F.2
Sekine, S.3
Tanaka, Y.4
Kamatani, A.5
Sonoda, M.6
Chatani, N.7
-
3
-
-
0036589261
-
-
For reviews on the reactions of C-H bonds, see: a
-
For reviews on the reactions of C-H bonds, see: (a) Ritleng, V.; Sirlin, C.; Pfeffer, M. Chem. Rev. 2002, 102, 1731.
-
(2002)
Chem. Rev
, vol.102
, pp. 1731
-
-
Ritleng, V.1
Sirlin, C.2
Pfeffer, M.3
-
4
-
-
0033553817
-
-
Int. Ed
-
(b) Dyker, G. Anvew Chem.. Int. Ed. 1999, 38, 1698.
-
(1698)
Anvew Chem
, vol.38
-
-
Dyker, G.1
-
5
-
-
4244076867
-
-
(c) Naota, T.; Takaya, H.; Murahashi, S. I. Chem. Rev. 1998, 98, 2599.
-
(1998)
Chem. Rev
, vol.98
, pp. 2599
-
-
Naota, T.1
Takaya, H.2
Murahashi, S.I.3
-
6
-
-
33846918696
-
-
(d) Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174.
-
(2007)
Chem. Rev
, vol.107
, pp. 174
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
7
-
-
34248361209
-
-
(e) Campeau, L. C.; Stuart, D. R.; Fagnou, K. Aldrichimica Acta 2007, 40, 35.
-
(2007)
Aldrichimica Acta
, vol.40
, pp. 35
-
-
Campeau, L.C.1
Stuart, D.R.2
Fagnou, K.3
-
9
-
-
33746307336
-
-
For selected recent examples, see: a
-
For selected recent examples, see: (a) Ackermann, L.; Althammer, A.; Born, R. Angew. Chem., Int. Ed. 2006, 45, 2619.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 2619
-
-
Ackermann, L.1
Althammer, A.2
Born, R.3
-
11
-
-
0037442914
-
-
(c) Kakiuchi, R.; Kan, S.; Igi, K.; Chatani, N.; Murai, S. J. Am. Chem. Soc. 2003, 125, 1698.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 1698
-
-
Kakiuchi, R.1
Kan, S.2
Igi, K.3
Chatani, N.4
Murai, S.5
-
12
-
-
11444263216
-
-
(d) Lim, Y. G.; Ahn, J. A.; Jun, C. H. Org. Lett. 2004, 6, 4687.
-
(2004)
Org. Lett
, vol.6
, pp. 4687
-
-
Lim, Y.G.1
Ahn, J.A.2
Jun, C.H.3
-
13
-
-
2942528733
-
-
(e) Thalji, R. K.; Ellman, J. A.; Bergman, R. G. J. Am. Chem. Soc. 2004, 126, 7192.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 7192
-
-
Thalji, R.K.1
Ellman, J.A.2
Bergman, R.G.3
-
14
-
-
0037181051
-
-
(f) Boele, M. D. K.; van Strijdonck, G. P. R.; de Vries, A. H. M.; Kamer, P. C. J.; de Vries, J. G.; van Leeuwen, P. W. N. M. J. Am. Chem. Soc. 2002, 124, 1586.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 1586
-
-
Boele, M.D.K.1
van Strijdonck, G.P.R.2
de Vries, A.H.M.3
Kamer, P.C.J.4
de Vries, J.G.5
van Leeuwen, P.W.N.M.6
-
17
-
-
19744365933
-
-
(i) Kalyani, D.; Deprez, N. R.; Desai, L. V.; Sanford, M. S. J. Am. Chem. Soc. 2005, 127, 7330.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 7330
-
-
Kalyani, D.1
Deprez, N.R.2
Desai, L.V.3
Sanford, M.S.4
-
18
-
-
1542345322
-
-
(j) Dick, A. R.; Hull, K. L.; Sanford, M. S. J. Am. Chem. Soc. 2004, 126, 2300.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 2300
-
-
Dick, A.R.1
Hull, K.L.2
Sanford, M.S.3
-
19
-
-
17044366225
-
-
(k) Giri, R.; Chen, X.; Yu, J. Q. Angew. Chem., Int. Ed. 2005, 44, 2112.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 2112
-
-
Giri, R.1
Chen, X.2
Yu, J.Q.3
-
20
-
-
28044468663
-
-
Giri, R.; Liang, J.; Lei, J. G.; Li, J. J.; Wang, D. H.; Chen, X.; Naggar, I. C.; Guo, C.; Foxman, B. M.; Yu, J. Q. Angew. Chem., Int. Ed. 2005, 44, 7420.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 7420
-
-
Giri, R.1
Liang, J.2
Lei, J.G.3
Li, J.J.4
Wang, D.H.5
Chen, X.6
Naggar, I.C.7
Guo, C.8
Foxman, B.M.9
Yu, J.Q.10
-
21
-
-
33748515918
-
-
(m) Yanagisawa, S.; Sudo, T.; Noyori, R.; Itami, K. J. Am. Chem. Soc. 2006, 128, 11748.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 11748
-
-
Yanagisawa, S.1
Sudo, T.2
Noyori, R.3
Itami, K.4
-
22
-
-
0346850026
-
-
(n) Murahashi, S. I.; Komiya, N.; Terai, H.; Nakae, T. J. Am. Chem. Soc. 2003, 125, 15312.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 15312
-
-
Murahashi, S.I.1
Komiya, N.2
Terai, H.3
Nakae, T.4
-
23
-
-
27544488753
-
-
(o) Murahashi, S. I.; Komiya, N.; Terai, H. Angew. Chem., Int. Ed. 2005, 44, 6931.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 6931
-
-
Murahashi, S.I.1
Komiya, N.2
Terai, H.3
-
24
-
-
30744445455
-
-
(p) Chen, X.; Li, J. J.; Hao, X. S.; Goodhue, C. E.; Yu, J. Q. J. Am. Chem. Soc. 2006, 128, 78.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 78
-
-
Chen, X.1
Li, J.J.2
Hao, X.S.3
Goodhue, C.E.4
Yu, J.Q.5
-
25
-
-
33749509027
-
-
(q) Chen, X.; Goodhue, C. E.; Yu, J. Q. J. Am. Chem. Soc. 2006, 128, 12634.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 12634
-
-
Chen, X.1
Goodhue, C.E.2
Yu, J.Q.3
-
26
-
-
33947644069
-
-
(r) Giri, R.; Maugel, N.; Li, J. J.; Wang, D. H.; Breazzano, S. P.; Saunders, L. B.; Yu, J. Q. J. Am. Chem. Soc. 2007, 129, 3510.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 3510
-
-
Giri, R.1
Maugel, N.2
Li, J.J.3
Wang, D.H.4
Breazzano, S.P.5
Saunders, L.B.6
Yu, J.Q.7
-
27
-
-
21244438753
-
-
(s) Daugulis, O.; Zaitsev, V. G. Angew. Chem., Int. Ed. 2005, 44, 4046.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 4046
-
-
Daugulis, O.1
Zaitsev, V.G.2
-
28
-
-
25444458063
-
-
(t) Zaitesv, V. G.; Shabashov, D.; Daugulis, O. J. Am. Chem. Soc. 2005, 127, 13154.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 13154
-
-
Zaitesv, V.G.1
Shabashov, D.2
Daugulis, O.3
-
38
-
-
33645464350
-
-
@ (h) Zhang, Y.; Li, C.-J. Angew. Chem., Int. Ed. 2006, 45, 1949.
-
@ (h) Zhang, Y.; Li, C.-J. Angew. Chem., Int. Ed. 2006, 45, 1949.
-
-
-
-
40
-
-
33745157509
-
-
(j) Li, Z.; Bohle, D. S.; Li, C.-J. Proc. Natl. Acad. Sci. U. S. A. 2006, 103, 8928.
-
(2006)
Proc. Natl. Acad. Sci. U. S. A
, vol.103
, pp. 8928
-
-
Li, Z.1
Bohle, D.S.2
Li, C.-J.3
-
41
-
-
34548356423
-
-
Li, Z.; Cao, L.; Li, C.-J. Angew. Chem., Int. Ed. 2007, 46, 6505. For an account, see: Li, C.-J. Acc. Chem. Res. 2009, ASAP.
-
(k) Li, Z.; Cao, L.; Li, C.-J. Angew. Chem., Int. Ed. 2007, 46, 6505. For an account, see: Li, C.-J. Acc. Chem. Res. 2009, ASAP.
-
-
-
-
44
-
-
1942521272
-
-
(c) Masui, K.; Ikegami, H.; Mori, A. J. Am. Chem. Soc. 2004, 126, 5074.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 5074
-
-
Masui, K.1
Ikegami, H.2
Mori, A.3
-
46
-
-
35048815950
-
-
(e) Stuart, D. R.; Villemure, E.; Fagnou, K. J. Am. Chem. Soc. 2007, 129, 12072.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12072
-
-
Stuart, D.R.1
Villemure, E.2
Fagnou, K.3
-
47
-
-
41249083170
-
-
(f) Dohi, T.; Ito, M.; Morimoto, K.; Iwata, M.; Kita, Y. Angew Chem., Int. Ed. 2008, 47, 1301.
-
(2008)
Angew Chem., Int. Ed
, vol.47
, pp. 1301
-
-
Dohi, T.1
Ito, M.2
Morimoto, K.3
Iwata, M.4
Kita, Y.5
-
48
-
-
34547960227
-
-
(g) Dwight, T. A.; Rue, N. R.; Charyk, D.; Josselyn, R.; DeBoef, B. Org. Lett. 2007, 9, 3137.
-
(2007)
Org. Lett
, vol.9
, pp. 3137
-
-
Dwight, T.A.1
Rue, N.R.2
Charyk, D.3
Josselyn, R.4
DeBoef, B.5
-
49
-
-
38849126856
-
-
(h) Li, B.; Tian, S.; Fang, Z.; Shi, Z. Angew Chem., Int. Ed. 2008, 47, 1115.
-
(2008)
Angew Chem., Int. Ed
, vol.47
, pp. 1115
-
-
Li, B.1
Tian, S.2
Fang, Z.3
Shi, Z.4
-
51
-
-
34948824004
-
-
Xia, J.-B.; You, S.-L. Organomet al.lics 2007, 26, 4869.
-
(j) Xia, J.-B.; You, S.-L. Organomet al.lics 2007, 26, 4869.
-
-
-
-
52
-
-
34250861444
-
-
(k) Cai, G.; Fu, Y.; Li, Y.; Wan, X.; Shi, Z.-J. J. Am. Chem. Soc. 2007, 129, 7666.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 7666
-
-
Cai, G.1
Fu, Y.2
Li, Y.3
Wan, X.4
Shi, Z.-J.5
-
54
-
-
34247882697
-
-
For recent successful examples of direct functionalization of pyridines and quinolines, see: a
-
For recent successful examples of direct functionalization of pyridines and quinolines, see: (a) Lewis, J. C.; Bergman, R. G.; Ellman, J. A. J. Am. Chem. Soc. 2007, 129, 5332.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 5332
-
-
Lewis, J.C.1
Bergman, R.G.2
Ellman, J.A.3
-
55
-
-
57349094283
-
-
(b) Berman, A. M.; Lewis, J. C.; Bergman, R. G.; Ellman, J. A. J. Am. Chem. Soc. 2008, 130, 14926.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 14926
-
-
Berman, A.M.1
Lewis, J.C.2
Bergman, R.G.3
Ellman, J.A.4
-
56
-
-
39749196066
-
-
(c) Nakao, Y.; Kanyiva, K. S.; Hiyama, T. J. Am. Chem. Soc. 2008, 130, 2448.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 2448
-
-
Nakao, Y.1
Kanyiva, K.S.2
Hiyama, T.3
-
57
-
-
58449085051
-
-
(d) Yanagisawa, S.; Ueda, K.; Taniguchi, T.; Itami, K. Org. Lett. 2008, 10, 4673.
-
(2008)
Org. Lett
, vol.10
, pp. 4673
-
-
Yanagisawa, S.1
Ueda, K.2
Taniguchi, T.3
Itami, K.4
-
58
-
-
29844433863
-
-
For recent examples of direct functionalization of pyridine N-oxide and N-iminopyridinum ylide, see: (a) Campeau, L. C.; Rousseaux, S.; Fagnou, K. J. Am. Chem. Soc. 2005, 127, 18020.
-
For recent examples of direct functionalization of pyridine N-oxide and N-iminopyridinum ylide, see: (a) Campeau, L. C.; Rousseaux, S.; Fagnou, K. J. Am. Chem. Soc. 2005, 127, 18020.
-
-
-
-
59
-
-
33845320517
-
-
(b) Leclerc, J. P.; Fagnou, K. Angew. Chem., Int. Ed. 2006, 45, 7781.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 7781
-
-
Leclerc, J.P.1
Fagnou, K.2
-
60
-
-
36749074391
-
-
(c) Kanyiva, K. S.; Nakao, Y.; Hiyama, T. Angew. Chem., Int. Ed. 2007, 46, 8872.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 8872
-
-
Kanyiva, K.S.1
Nakao, Y.2
Hiyama, T.3
-
61
-
-
47749125841
-
-
(d) Cho, S. H.; Hwang, S. J.; Chang, S. J. Am. Chem. Soc. 2008, 130, 9254.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 9254
-
-
Cho, S.H.1
Hwang, S.J.2
Chang, S.3
-
62
-
-
38348998675
-
-
(e) Larivée, A.; Mousseau, J. J.; Charette, A. B. J. Am. Chem. Soc. 2008, 130, 52.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 52
-
-
Larivée, A.1
Mousseau, J.J.2
Charette, A.B.3
-
64
-
-
53549084027
-
-
(b) Deng, G. J.; Zhao, L.; Li, C.-J. Angew. Chem., Int. Ed. 2008, 47, 6278.
-
(2008)
Angew. Chem., Int. Ed
, vol.47
, pp. 6278
-
-
Deng, G.J.1
Zhao, L.2
Li, C.-J.3
-
65
-
-
58449108832
-
-
Deng, G. J.; Ueda, K.; Yanagisawa, S.; Itami, K.; Li, C.-J. Chem.-Eur. J. 2009, 15, 333.
-
(2009)
Chem.-Eur. J
, vol.15
, pp. 333
-
-
Deng, G.J.1
Ueda, K.2
Yanagisawa, S.3
Itami, K.4
Li, C.-J.5
-
67
-
-
64349098740
-
-
Tetrahydroisoquinoline also reacted with cyclooctane and gave 4b in 64% yield when 3 equiv of tert-butyl peroxide was used.
-
Tetrahydroisoquinoline also reacted with cyclooctane and gave 4b in 64% yield when 3 equiv of tert-butyl peroxide was used.
-
-
-
-
68
-
-
64349100903
-
-
In all cases, no alkylation of pyridine and quinoline derivatives at the meta-position of nitrogen was observed. For quinoline, a trace amount of monoalkylation product was observed with alkylation occurring at the ortho position of nitrogen
-
In all cases, no alkylation of pyridine and quinoline derivatives at the meta-position of nitrogen was observed. For quinoline, a trace amount of monoalkylation product was observed with alkylation occurring at the ortho position of nitrogen.
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