-
1
-
-
0001108788
-
-
For selected reviews on C-H bond functionalization, see : a) G. Dyker, Angew. Chem. 1999, 111, 1808-1822;
-
(1999)
Angew. Chem.
, vol.111
, pp. 1808-1822
-
-
Dyker, G.1
-
2
-
-
0033553817
-
-
Angew. Chem. Int. Ed. 1999, 38, 1698-1712;
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 1698-1712
-
-
-
4
-
-
0034867872
-
-
c) C. Jia, T. Kitamura, Y. Fujiwara, Acc. Chem. Res. 2001, 34, 633-639;
-
(2001)
Acc. Chem. Res.
, vol.34
, pp. 633-639
-
-
Jia, C.1
Kitamura, T.2
Fujiwara, Y.3
-
5
-
-
0036589261
-
-
d) V. Ritleng, C. Sirlin, M. Pfeffer, Chem. Rev. 2002, 102, 1731-1770;
-
(2002)
Chem. Rev.
, vol.102
, pp. 1731-1770
-
-
Ritleng, V.1
Sirlin, C.2
Pfeffer, M.3
-
13
-
-
51649122191
-
-
l) J. C. Lewis, R. G. Bergman, J. A. Ellman, Ace. Chem. Res. 2008, 41, 1013-1025;
-
(2008)
Ace. Chem. Res.
, vol.41
, pp. 1013-1025
-
-
Lewis, J.C.1
Bergman, R.G.2
Ellman, J.A.3
-
15
-
-
0037134813
-
-
a) J. A. Johnson, N. Li, D. Sames, J. Am. Chem. Soc. 2002, 124, 6900-6903;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6900-6903
-
-
Johnson, J.A.1
Li, N.2
Sames, D.3
-
17
-
-
25844469333
-
-
c) S. J. O'Malley, K. L. Tan, A. Watzke, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc. 2005, 127, 13496-13497;
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13496-13497
-
-
O'Malley, S.J.1
Tan, K.L.2
Watzke, A.3
Bergman, R.G.4
Ellman, J.A.5
-
18
-
-
33748480130
-
-
d) U. K. Tambar, D. C. Ebner, B. M. Stoltz, J. Am. Chem. Soc. 2006, 128, 11752-11753;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 11752-11753
-
-
Tambar, U.K.1
Ebner, D.C.2
Stoltz, B.M.3
-
19
-
-
60749126307
-
-
e) E. M. Beck, R. Hatley, M. J. Gaunt, Angew. Chem. 2008, 120, 3046-3049;
-
(2008)
Angew. Chem.
, vol.120
, pp. 3046-3049
-
-
Beck, E.M.1
Hatley, R.2
Gaunt, M.J.3
-
20
-
-
44949166937
-
-
Angew. Chem. Int. Ed. 2008, 47, 3004-3007.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 3004-3007
-
-
-
21
-
-
38749146550
-
-
For a leading review on enantioselective nitrenoid and carbenoid and C-H insertions, see: a) H. M. L. Davies, J. R. Manning, Nature 2008, 451, 417-424; for examples of enantioselective rhodium-catalyzed hydro ary lation see:
-
(2008)
Nature
, vol.451
, pp. 417-424
-
-
Davies, H.M.L.1
Manning, J.R.2
-
22
-
-
2942528733
-
-
b) R. K. Thalji, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc. 2004, 126, 7192-7193;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 7192-7193
-
-
Thalji, R.K.1
Bergman, R.G.2
Ellman, J.A.3
-
23
-
-
51549113576
-
-
c) H. Harada, R. K. Thalji, R. G. Bergman, J. A. Ellman, J. Org. Chem. 2008, 73, 6772-6779.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 6772-6779
-
-
Harada, H.1
Thalji, R.K.2
Bergman, R.G.3
Ellman, J.A.4
-
24
-
-
53349092963
-
-
B.-F. Shi, N. Maugel, Y.-H. Zhang, J.-Q. Yu, Angew. Chem. 2008, 120, 4960-4964;
-
(2008)
Angew. Chem.
, vol.120
, pp. 4960-4964
-
-
Shi, B.-F.1
Maugel, N.2
Zhang, Y.-H.3
Yu, J.-Q.4
-
25
-
-
48849108176
-
-
Angew. Chem. Int. Ed. 2008, 47, 4882-4886;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4882-4886
-
-
-
26
-
-
70449581791
-
-
Angew. Chem. 2008, 120, 4960-4964.
-
(2008)
, vol.120
, pp. 4960-4964
-
-
Chem, A.1
-
27
-
-
0037138675
-
-
For examples of enantioselective palladium-catalyzed arylation of activated carbon nucleophiles, see : a) T. Hamada, A. Chieffi, J.Åhman, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 1261-1268;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 1261-1268
-
-
Hamada, T.1
Chieffi, A.2
Åhman, J.3
Buchwald, S.L.4
-
28
-
-
54049104732
-
-
b) E. P. Kündig, T. M. Seidel, Y. Jia, G. Bernardinelli, Angew. Chem. 2007, 119, 8636-8639;
-
(2007)
Angew. Chem.
, vol.119
, pp. 8636-8639
-
-
Kündig, E.P.1
Seidel, T.M.2
Jia, Y.3
Bernardinelli, G.4
-
29
-
-
36148933735
-
-
Angew. Chem. Int. Ed. 2007, 46, 8484-8487;
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 8484-8487
-
-
-
30
-
-
67650539084
-
-
c) S. Würtz, C. Lohre, R. Fröhlich, K. Bergander, F. Glorius, J. Am. Chem. Soc. 2009, 131, 8344-8345.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8344-8345
-
-
Würtz, S.1
Lohre, C.2
Fröhlich, R.3
Bergander, K.4
Glorius, F.5
-
33
-
-
33746877740
-
-
(Eds.: J. Christof fers, A. Baro), Wiley-VCH, Weinheim
-
c) Quaternary Stereocenters (Eds.: J. Christof fers, A. Baro), Wiley-VCH, Weinheim, 2005;
-
(2005)
Quaternary Stereocenters
-
-
-
35
-
-
56449094610
-
-
Angew. Chem. Int. Ed. 2008, 47, 9294-9297;
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 9294-9297
-
-
-
36
-
-
70449563673
-
-
e) T. Seiser, O. A. Roth, N. Cramer, Angew. Chem. 2009, 121, 6438-6441;
-
(2009)
Angew. Chem.
, vol.121
, pp. 6438-6441
-
-
Seiser, T.1
Roth, O.A.2
Cramer, N.3
-
37
-
-
70349944361
-
-
Angew. Chem. Int. Ed. 2009, 48, 6320-6323.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 6320-6323
-
-
-
39
-
-
33846918696
-
-
b) D. Alberico, M. E. Scott, M. Lautens, Chem. Rev. 2007, 107, 174-238;
-
(2007)
Chem. Rev.
, vol.107
, pp. 174-238
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
41
-
-
84891012324
-
-
(Ed.: L. Ackermann), Wiley-VCH, Weinheim
-
M. Miura in Modern Arylation Methods (Ed.: L. Ackermann), Wiley-VCH, Weinheim, 2009, pp. 335-361;
-
(2009)
Modern Arylation Methods
, pp. 335-361
-
-
Miura, M.1
-
43
-
-
31944442069
-
-
a) D. Garcia-Cuadrado, A. A. C. Braga, F. Maseras, A. M. Echavarren, J. Am. Chem. Soc. 2006, 128, 1066-1067;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 1066-1067
-
-
Garcia-Cuadrado, D.1
Braga, A.A.C.2
Maseras, F.3
Echavarren, A.M.4
-
44
-
-
34249793676
-
-
b) D. Garcia-Cuadrado, P. de Mendoza, A. A. C. Braga, F. Maseras, A. M. Echavarren, J. Am. Chem. Soc. 2007, 129, 6880-6886;
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 6880-6886
-
-
Garcia-Cuadrado, D.1
De Mendoza, P.2
Braga, A.A.C.3
Maseras, F.4
Echavarren, A.M.5
-
45
-
-
84891029841
-
-
(Ed.: L. Ackermann), Wiley-VCH, Weinheim
-
c) P. de Mendoza, A. M. Echavarren in Modem Arylation Methods (Ed.: L. Ackermann), Wiley-VCH, Weinheim, 2009, pp. 363-399;
-
(2009)
Modem Arylation Methods
, pp. 363-399
-
-
De Mendoza, P.1
Echavarren, A.M.2
-
46
-
-
31544455027
-
-
d) L.-C. Campeau, M. Parisien, A. Jean, K. Fagnou, J. Am. Chem. Soc. 2006, 128, 581-590;
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 581-590
-
-
Campeau, L.-C.1
Parisien, M.2
Jean, A.3
Fagnou, K.4
-
48
-
-
43849112641
-
-
f) M. Lafrance, D. Lapointe, K. Fagnou, Tetrahedron 2008, 64, 6015-6020.
-
(2008)
Tetrahedron
, vol.64
, pp. 6015-6020
-
-
Lafrance, M.1
Lapointe, D.2
Fagnou, K.3
-
50
-
-
35548943629
-
-
b) A. C. F. Cruz, N. D. Miller, M. C. Willis, Org. Lett. 2007, 9, 4391-4393.
-
(2007)
Org. Lett.
, vol.9
, pp. 4391-4393
-
-
Cruz, A.C.F.1
Miller, N.D.2
Willis, M.C.3
-
51
-
-
35048823480
-
-
C. Defieber, M. A. Ariger, P. Moriel, E. M. Carreira, Angew. Chem. 2007, 119, 3200-3204;
-
(2007)
Angew. Chem.
, vol.119
, pp. 3200-3204
-
-
Defieber, C.1
Ariger, M.A.2
Moriel, P.3
Carreira, E.M.4
-
52
-
-
34250166800
-
-
Angew. Chem. Int. Ed. 2007, 46, 3139-3143.
-
(2007)
Angew. Chem. Int. Ed.
, vol.46
, pp. 3139-3143
-
-
-
53
-
-
0001855867
-
-
For a review on taddol, see: a) D. Seebach, A. K. Beck, A. Heckel, Angew. Chem. 2001, 113, 96-142;
-
(2001)
Angew. Chem.
, vol.113
, pp. 96-142
-
-
Seebach, D.1
Beck, A.K.2
Heckel, A.3
-
54
-
-
33746354232
-
-
Angew. Chem. Int. Ed. 2001, 40, 92-138; For examples of taddol-based phosphoramidites in palladium-catalyzed reactions, see:
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 92-138
-
-
-
55
-
-
0037116510
-
-
b) R. Imbos, A. J. Minnaard, B. L. Feringa, J. Am. Chem. Soc. 2002, 124, 184-185;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 184-185
-
-
Imbos, R.1
Minnaard, A.J.2
Feringa, B.L.3
-
56
-
-
11444261871
-
-
c) N. F. Pelz, A. R. Woodward, H. E. Burks, J. D. Sieber, J. P. Morken, J. Am. Chem. Soc. 2004, 126, 16328-16329;
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 16328-16329
-
-
Pelz, N.F.1
Woodward, A.R.2
Burks, H.E.3
Sieber, J.D.4
Morken, J.P.5
-
57
-
-
34548396841
-
-
d) H. E. Burks, S. Liu, J. P. Morken, J. Am. Chem. Soc. 2007, 129, 8766-8773;
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 8766-8773
-
-
Burks, H.E.1
Liu, S.2
Morken, J.P.3
-
58
-
-
33750350817
-
-
e) T. Ohmura, H. Taniguchi, M. Suginome, J. Am. Chem. Soc. 2006, 128, 13682-13683.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 13682-13683
-
-
Ohmura, T.1
Taniguchi, H.2
Suginome, M.3
-
59
-
-
70449596627
-
-
In general, electron-poor substrates react faster, which is in agreement with the described mechanism of reference [8].
-
In general, electron-poor substrates react faster, which is in agreement with the described mechanism of reference [8].
-
-
-
-
60
-
-
70449575179
-
-
See the Supporting Information. CCDC 745459 (5j) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
See the Supporting Information. CCDC 745459 (5j) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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