-
1
-
-
77149164746
-
-
R. Jazzar, J. Hitce, A. Renaudat, J. Sofack-Kreutzer, O. Baudoin, Chem. Eur. J. 2010, 16, 2654
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 2654
-
-
Jazzar, R.1
Hitce, J.2
Renaudat, A.3
Sofack-Kreutzer, J.4
Baudoin, O.5
-
3
-
-
33746236405
-
-
O. Baudoin, A. Herrbach, F. Guéritte, Angew. Chem. 2003, 115, 5914
-
(2003)
Angew. Chem.
, vol.115
, pp. 5914
-
-
Baudoin, O.1
Herrbach, A.2
Guéritte, F.3
-
5
-
-
33846521293
-
-
J. Hitce, P. Retailleau, O. Baudoin, Chem. Eur. J. 2007, 13, 792
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 792
-
-
Hitce, J.1
Retailleau, P.2
Baudoin, O.3
-
6
-
-
57349192903
-
-
M. Chaumontet, R. Piccardi, N. Audic, J. Hitce, J.-L. Peglion, E. Clot, O. Baudoin, J. Am. Chem. Soc. 2008, 130, 15157
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 15157
-
-
Chaumontet, M.1
Piccardi, R.2
Audic, N.3
Hitce, J.4
Peglion, J.-L.5
Clot, E.6
Baudoin, O.7
-
7
-
-
77955393861
-
-
S. Rousseaux, M. Davi, J. Sofack-Kreutzer, C. Pierre, C. E. Kefalidis, E. Clot, K. Fagnou, O. Baudoin, J. Am. Chem. Soc. 2010, 132, 10706
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 10706
-
-
Rousseaux, S.1
Davi, M.2
Sofack-Kreutzer, J.3
Pierre, C.4
Kefalidis, C.E.5
Clot, E.6
Fagnou, K.7
Baudoin, O.8
-
10
-
-
84859250819
-
-
N. Martin, C. Pierre, M. Davi, R. Jazzar, O. Baudoin, Chem. Eur. J. 2012, 18, 4480
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 4480
-
-
Martin, N.1
Pierre, C.2
Davi, M.3
Jazzar, R.4
Baudoin, O.5
-
11
-
-
84890804011
-
-
J. Sofack-Kreutzer, N. Martin, A. Renaudat, R. Jazzar, O. Baudoin, Angew. Chem. 2012, 124, 10545
-
(2012)
Angew. Chem.
, vol.124
, pp. 10545
-
-
Sofack-Kreutzer, J.1
Martin, N.2
Renaudat, A.3
Jazzar, R.4
Baudoin, O.5
-
13
-
-
84906784518
-
-
For pioneering work, see
-
For pioneering work, see
-
-
-
-
23
-
-
36749003741
-
-
M. Lafrance, S. I. Gorelsky, K. Fagnou, J. Am. Chem. Soc. 2007, 129, 14570
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 14570
-
-
Lafrance, M.1
Gorelsky, S.I.2
Fagnou, K.3
-
24
-
-
48849113342
-
-
T. Watanabe, S. Oishi, N. Fujii, H. Ohno, Org. Lett. 2008, 10, 1759
-
(2008)
Org. Lett.
, vol.10
, pp. 1759
-
-
Watanabe, T.1
Oishi, S.2
Fujii, N.3
Ohno, H.4
-
25
-
-
77955405522
-
-
S. Rousseaux, S. I. Gorelsky, B. K. W. Chung, K. Fagnou, J. Am. Chem. Soc. 2010, 132, 10692
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 10692
-
-
Rousseaux, S.1
Gorelsky, S.I.2
Chung, B.K.W.3
Fagnou, K.4
-
26
-
-
80155170211
-
-
M. Nakanishi, D. Katayev, C. Besnard, E. P. Kündig, Angew. Chem. 2011, 123, 7576
-
(2011)
Angew. Chem.
, vol.123
, pp. 7576
-
-
Nakanishi, M.1
Katayev, D.2
Besnard, C.3
Kündig, E.P.4
-
28
-
-
84867069406
-
-
T. Saget, S. J. Lemouzy, N. Cramer, Angew. Chem. 2012, 124, 2281
-
(2012)
Angew. Chem.
, vol.124
, pp. 2281
-
-
Saget, T.1
Lemouzy, S.J.2
Cramer, N.3
-
30
-
-
84875311188
-
-
T. Piou, L. Neuville, J. Zhu, Angew. Chem. 2012, 124, 11729
-
(2012)
Angew. Chem.
, vol.124
, pp. 11729
-
-
Piou, T.1
Neuville, L.2
Zhu, J.3
-
32
-
-
84875778287
-
-
E. Larionov, M. Nakanishi, D. Katayev, C. Besnard, E. P. Kündig, Chem. Sci. 2013, 4, 1995.
-
(2013)
Chem. Sci.
, vol.4
, pp. 1995
-
-
Larionov, E.1
Nakanishi, M.2
Katayev, D.3
Besnard, C.4
Kündig, E.P.5
-
33
-
-
0027969994
-
-
B. D. Dorsey, R. B. Levin, S. L. McDaniel, J. P. Vacca, J. P. Guare, P. L. Darke, J. A. Zugay, E. A. Emini, W. A. Schleif, J. C. Quintero, J. H. Lin, I.-W. Chen, M. K. Holloway, P. M. D. Fitzgerald, M. G. Axel, D. Ostovic, P. S. Anderson, J. R. Huff, J. Med. Chem. 1994, 37, 3443.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3443
-
-
Dorsey, B.D.1
Levin, R.B.2
McDaniel, S.L.3
Vacca, J.P.4
Guare, J.P.5
Darke, P.L.6
Zugay, J.A.7
Emini, E.A.8
Schleif, W.A.9
Quintero, J.C.10
Lin, J.H.11
Chen, I.-W.12
Holloway, M.K.13
Fitzgerald, P.M.D.14
Axel, M.G.15
Ostovic, D.16
Anderson, P.S.17
Huff, J.R.18
-
34
-
-
0001361308
-
-
P. Kraft, J. A. Bajgrowicz, C. Denis, G. Fráter, Angew. Chem. 2000, 112, 3106
-
(2000)
Angew. Chem.
, vol.112
, pp. 3106
-
-
Kraft, P.1
Bajgrowicz, J.A.2
Denis, C.3
Fráter, G.4
-
36
-
-
84906785439
-
-
(Bayer CropScience AG), US Pat. Appl. Publ., 20040157739A1 20040812.
-
H. Ahrens, H. Dietrich, K. Minn, T. Auler, H. Bieringer, M. Hills, H. Kehne, H. Menne, (Bayer CropScience AG), US Pat. Appl. Publ., 20040157739A1 20040812, 2004.
-
(2004)
-
-
Ahrens, H.1
Dietrich, H.2
Minn, K.3
Auler, T.4
Bieringer, H.5
Hills, M.6
Kehne, H.7
Menne, H.8
-
37
-
-
33750853326
-
-
P. R. Carlier, Y. Zhang, C. Slebodnick, M. M.-C. Lo, I. D. Williams, J. Org. Chem. 2006, 71, 8835.
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8835
-
-
Carlier, P.R.1
Zhang, Y.2
Slebodnick, C.3
Lo, M.M.-C.4
Williams, I.D.5
-
39
-
-
33746427066
-
-
N. I. Bowers, D. R. Boyd, N. D. Sharma, P. A. Goodrich, M. R. Groocock, A. J. Blacker, P. Goode, H. Dalton, J. Chem. Soc. Perkin Trans. 1 1999, 1453
-
(1999)
J. Chem. Soc. Perkin Trans. 1
, pp. 1453
-
-
Bowers, N.I.1
Boyd, D.R.2
Sharma, N.D.3
Goodrich, P.A.4
Groocock, M.R.5
Blacker, A.J.6
Goode, P.7
Dalton, H.8
-
40
-
-
0037131143
-
-
C. Cadot, P. I. Dalko, J. Cossy, C. Ollivier, R. Chuard, P. Renaud, J. Org. Chem. 2002, 67, 7193.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 7193
-
-
Cadot, C.1
Dalko, P.I.2
Cossy, J.3
Ollivier, C.4
Chuard, R.5
Renaud, P.6
-
41
-
-
84906783019
-
-
0-catalyzed intramolecular C-H arylation of cyclopropanes, see
-
0-catalyzed intramolecular C-H arylation of cyclopropanes, see
-
-
-
-
42
-
-
82455174224
-
-
S. Rousseaux, B. Liégault, K. Fagnou, Chem. Sci. 2012, 3, 244
-
(2012)
Chem. Sci.
, vol.3
, pp. 244
-
-
Rousseaux, S.1
Liégault, B.2
Fagnou, K.3
-
45
-
-
84876679305
-
-
C. L. Ladd, D. Sustac Roman, A. B. Charette, Tetrahedron 2013, 69, 4479
-
(2013)
Tetrahedron
, vol.69
, pp. 4479
-
-
Ladd, C.L.1
Sustac Roman, D.2
Charette, A.B.3
-
46
-
-
84875199921
-
-
C. L. Ladd, D. Sustac Roman, A. B. Charette, Org. Lett. 2013, 15, 1350
-
(2013)
Org. Lett.
, vol.15
, pp. 1350
-
-
Ladd, C.L.1
Sustac Roman, D.2
Charette, A.B.3
-
48
-
-
0035819953
-
-
For a seminal example in C-H insertion chemistry, see.
-
For a seminal example in C-H insertion chemistry, see:, H. M. L. Davies, P. Ren, J. Am. Chem. Soc. 2001, 123, 2070.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2070
-
-
Davies, H.M.L.1
Ren, P.2
-
49
-
-
84906787748
-
-
For selected examples, see
-
For selected examples, see
-
-
-
-
50
-
-
0001501076
-
-
K. Morikawa, J. Park, P. G. Andersson, T. Hashiyama, K. B. Sharpless, J. Am. Chem. Soc. 1993, 115, 8463
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 8463
-
-
Morikawa, K.1
Park, J.2
Andersson, P.G.3
Hashiyama, T.4
Sharpless, K.B.5
-
52
-
-
4644286223
-
-
S. Ishikawa, T. Hamada, K. Manabe, S. Kobayashi, J. Am. Chem. Soc. 2004, 126, 12236
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 12236
-
-
Ishikawa, S.1
Hamada, T.2
Manabe, K.3
Kobayashi, S.4
-
53
-
-
33846613821
-
-
N. Takenaka, J. P. Abell, H. Yamamoto, J. Am. Chem. Soc. 2007, 129, 742
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 742
-
-
Takenaka, N.1
Abell, J.P.2
Yamamoto, H.3
-
54
-
-
53549095018
-
-
T. Poisson, V. Dalla, F. Marsais, G. Dupas, S. Oudeyer, V. Levacher, Angew. Chem. 2007, 119, 7220
-
(2007)
Angew. Chem.
, vol.119
, pp. 7220
-
-
Poisson, T.1
Dalla, V.2
Marsais, F.3
Dupas, G.4
Oudeyer, S.5
Levacher, V.6
-
56
-
-
84906783119
-
-
CCDC-986266 (2 t), 986267 (A1), and 990781 (A2) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
-
CCDC-986266 (2 t), 986267 (A1), and 990781 (A2) contain 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.
-
-
-
-
57
-
-
84906786526
-
-
These low-to-moderate yields are mainly attributed to the formation of insoluble material during the reaction. The protodebrominated product was the only observed soluble compound in the reaction of 1 t. In addition, an independently prepared cis/trans diastereoisomeric mixture of 2 t was stable under the reaction conditions, with no change in the diastereomeric ratio.
-
These low-to-moderate yields are mainly attributed to the formation of insoluble material during the reaction. The protodebrominated product was the only observed soluble compound in the reaction of 1 t. In addition, an independently prepared cis/trans diastereoisomeric mixture of 2 t was stable under the reaction conditions, with no change in the diastereomeric ratio.
-
-
-
-
58
-
-
34249850201
-
-
R. Fernández, A. Ros, A. Magriz, H. Dietrich, J. M. Lassaletta, Tetrahedron 2007, 63, 6755.
-
(2007)
Tetrahedron
, vol.63
, pp. 6755
-
-
Fernández, R.1
Ros, A.2
Magriz, A.3
Dietrich, H.4
Lassaletta, J.M.5
-
60
-
-
84906779683
-
-
[2c,d, 18] respectively, through DFT calculations.
-
[2c,d, 18] respectively, through DFT calculations.
-
-
-
-
61
-
-
78049327465
-
-
For a study on the effect of the base and ligand on the CMD mechanism, see.
-
For a study on the effect of the base and ligand on the CMD mechanism, see:, C. E. Kefalidis, O. Baudoin, E. Clot, Dalton Trans. 2010, 39, 10528.
-
(2010)
Dalton Trans.
, vol.39
, pp. 10528
-
-
Kefalidis, C.E.1
Baudoin, O.2
Clot, E.3
|