-
5
-
-
41449108079
-
-
Palladium-catalyzed dioxygenation: a
-
Palladium-catalyzed dioxygenation: a) Y. Li, D. Song, V.M. Dong, Z Am. Chem. Soc 2008, 130, 2962;
-
(2008)
Z Am. Chem. Soc
, vol.130
, pp. 2962
-
-
Li, Y.1
Song, D.2
Dong, V.M.3
-
6
-
-
72249086147
-
-
b) K. H. Jensen, T. P. Pathak, Y. Zhang, M. S. Sigman, Z Am. Chem. Soc 2009, 131, 17074;
-
(2009)
Z Am. Chem. Soc
, vol.131
, pp. 17074
-
-
Jensen, K.H.1
Pathak, T.P.2
Zhang, Y.3
Sigman, M.S.4
-
7
-
-
67749110109
-
-
c) A. Wang, H. Jiang, H. Chen, J. Am. Chem. Soc 2009, 757, 3846;
-
(2009)
J. Am. Chem. Soc
, vol.757
, pp. 3846
-
-
Wang, A.1
Jiang, H.2
Chen, H.3
-
8
-
-
76849116840
-
-
d) W. Wang, F. Wang, M. Shi, Organometallics 2010, 29, 928.
-
(2010)
Organometallics
, vol.29
, pp. 928
-
-
Wang, W.1
Wang, F.2
Shi, M.3
-
9
-
-
27144440348
-
-
Palladium-catalyzed diamidation: a) J. Streuff, CH. Hövelmann, M. Nieger, K. Muñiz, Z Am. Chem. Soc. 2005, 127, 14586;
-
(2005)
Z Am. Chem. Soc.
, vol.127
, pp. 14586
-
-
Streuff, J.1
Hövelmann, Ch.2
Nieger, M.3
Muñiz, K.4
-
10
-
-
34748841069
-
-
b) H. Du, W. Yuan, B. Zhao, Y. Shi, Z Am, Chem. Soc 2007, 129, 11688;
-
(2007)
Z Am, Chem. Soc
, vol.129
, pp. 11688
-
-
Du, H.1
Yuan, W.2
Zhao, B.3
Shi, Y.4
-
11
-
-
70349925643
-
-
c) R. Wang, H. Du, Y. Shi, Angew. Chem 2008, 720, 8348;
-
(2008)
Angew. Chem
, vol.720
, pp. 8348
-
-
Wang, R.1
Du, H.2
Shi, Y.3
-
16
-
-
19744375923
-
-
c) E. J. Alexanian, C. Lee, E. J. Sorensen, Z Am. Chem. Soc 2005, 727, 7690.
-
(2005)
Z Am. Chem. Soc
, vol.727
, pp. 7690
-
-
Alexanian, E.J.1
Lee, C.2
Sorensen, E.J.3
-
17
-
-
33846644502
-
-
Some recent publications
-
The intramolecular oxidative carbofunctional ization of olefins has been far more intensively investigated than the intermolecular variants. For a review, see: J. P. Wolfe, Eur. J. Org. Chem. 2007, 571. Some recent publications:
-
(2007)
Eur. J. Org. Chem.
, pp. 571
-
-
Wolfe, J.P.1
-
18
-
-
33644933443
-
-
a) K.-T. Yip, M. Yang, K.-L. Law, N.-Y. Zhu, D. Yang, Z Am. Chem. Soc 2006, 128, 3130;
-
(2006)
Z Am. Chem. Soc
, vol.128
, pp. 3130
-
-
Yip, K.-T.1
Yang, M.2
Law, K.-L.3
Zhu, N.-Y.4
Yang, D.5
-
21
-
-
48749120080
-
-
d) C. E. Houlden, C. D. Hailey, J. G. Ford, M. R. Gagné, G. C. LloydJones, K. I. Hooker-Milbum, Z Am Chem. Soc 2008, 130, 10066;
-
(2008)
Z Am Chem. Soc
, vol.130
, pp. 10066
-
-
Houlden, C.E.1
Hailey, C.D.2
Ford, J.G.3
Gagné, M.R.4
LloydJones, G.C.5
Hooker-Milbum, K.I.6
-
22
-
-
67650507268
-
-
e) C. F. Rosewall, P. A. Sibbald, D. V. Listin, F. E. Michael, Z Am. Chem. Soc 2009, 131, 9488.
-
(2009)
Z Am. Chem. Soc
, vol.131
, pp. 9488
-
-
Rosewall, C.F.1
Sibbald, P.A.2
Listin, D.V.3
Michael, F.E.4
-
23
-
-
39549088712
-
-
Intermolecular oxidative carbofunctionalization of olefins: a) D. Kalyani, M. S. Sanford, Z Am. Chem. Soc 2008, 130, 2150;
-
(2008)
Z Am. Chem. Soc
, vol.130
, pp. 2150
-
-
Kalyani, D.1
Sanford, M.S.2
-
24
-
-
67649460736
-
-
b) K. Cheng, L. Huang, Y. Zhang, Org. Lett. 2009, 11, 2908.
-
(2009)
Org. Lett.
, vol.11
, pp. 2908
-
-
Cheng, K.1
Huang, L.2
Zhang, Y.3
-
25
-
-
0035896265
-
-
Radical carboaminoxylations: a) A. Studer, Chem. Eur. J. 2001, 7, 1159;
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 1159
-
-
Studer, A.1
-
31
-
-
70349897059
-
-
c) J. Guin, S. De Sarkar, S. Grimme, A. Studer, Angew. Chem. 2008, 120, 8855;
-
(2008)
Angew. Chem.
, vol.120
, pp. 8855
-
-
Guin, J.1
De Sarkar, S.2
Grimme, S.3
Studer, A.4
-
33
-
-
65949098700
-
-
d) M. S. Maji, T. Pfeifer, A. Studer, Angew. Chem. 2008, 720 ,9690;
-
(2008)
Angew. Chem.
, vol.720
, pp. 9690
-
-
Maji, M.S.1
Pfeifer, T.2
Studer, A.3
-
35
-
-
77952418757
-
-
e) M. S. Maji, T. Pfeifer, A. Studer, Chem. Eur. J. 2010, 16, 5872.
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 5872
-
-
Maji, M.S.1
Pfeifer, T.2
Studer, A.3
-
36
-
-
0033096995
-
-
For a review, see: H. Gao, J. A. Katzenellenbogen, R. Garg, C Hansen, Chem. Rev. 1999, 99, 723.
-
(1999)
Chem. Rev.
, vol.99
, pp. 723
-
-
Gao, H.1
Katzenellenbogen, J.A.2
Garg, R.3
Hansen, C.4
-
37
-
-
0029935522
-
-
a) H. Hu, S. P. Hollinshead, S. E. Hall, K. Kalter, L. M. Rallas, Bioorg. Med. Chem. Lett 1996, 6, 973;
-
(1996)
Bioorg. Med. Chem. Lett
, vol.6
, pp. 973
-
-
Hu, H.1
Hollinshead, S.P.2
Hall, S.E.3
Kalter, K.4
Rallas, L.M.5
-
38
-
-
34247332707
-
-
b) M. F. Gross, S. Reaudoin, G. McNaughton-Smith, G. S. Amato, N. A. Castle, C. Huang, A. Zou, W. Yu, Bioorg. Med. Chem. Lett. 2007, 17, 2849;
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 2849
-
-
Gross, M.F.1
Reaudoin, S.2
McNaughton-Smith, G.3
Amato, G.S.4
Castle, N.A.5
Huang, C.6
Zou, A.7
Yu, W.8
-
39
-
-
48649108672
-
-
c) S. Hudson, M. Kiankarimi, W. Eccles, Y. S. Mostofi, M. J. Genicot, W. Dwight, R A. Fleck, K. Gogas, W. Wade, Bioorg. Med. Chem. Lett. WS, 18, 4495;
-
Bioorg. Med. Chem. Lett. WS
, vol.18
, pp. 4495
-
-
Hudson, S.1
Kiankarimi, M.2
Eccles, W.3
Mostofi, Y.S.4
Genicot, M.J.5
Dwight, W.6
Fleck, R.A.7
Gogas, K.8
Wade, W.9
-
40
-
-
14944355617
-
-
d) S. Ulmschneider, U. Müller-Vieira, C. D. Klein, I. Antes, T. Lengauer, R. W. Hartmann, J. Med. Chem. 2005, 48, 1563;
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1563
-
-
Ulmschneider, S.1
Müller-Vieira, U.2
Klein, C.D.3
Antes, I.4
Lengauer, T.5
Hartmann, R.W.6
-
41
-
-
45749135895
-
-
e) P. Camps, X. Formosa, C. Galdeano, T. Gómez, D. Muñoz-Torrero, M. Scarpellini, E. Viayna, A. Radia, M. V. Qos, A. Camins, M. Pallas, M. Rartobni, F. Mancini. V. Andrisano, J. Estelrich, M. Lizondo, A. RidonChanal, F. J. Luque, Z Med. Chem. 2008, 57, 3588.
-
(2008)
Z Med. Chem.
, vol.57
, pp. 3588
-
-
Camps, P.1
Formosa, X.2
Galdeano, C.3
Gómez, T.4
Muñoz-Torrero, D.5
Scarpellini, M.6
Viayna, E.7
Radia, A.8
Qos, M.V.9
Camins, A.10
Pallas, M.11
Rartobni, M.12
Mancini V Andrisano, F.13
Estelrich, J.14
Lizondo, M.15
RidonChanal, A.16
Luque, F.J.17
-
42
-
-
56849128233
-
-
a) S. Kirchberg, T. Vogler, A. Studer, Synlett 2008, 18, 2841;
-
(2008)
Synlett
, vol.18
, pp. 2841
-
-
Kirchberg, S.1
Vogler, T.2
Studer, A.3
-
44
-
-
77649172795
-
-
S. Kirchberg, R. Fröhlich, A. Studer, Angew. Chem. 2009, 121, 4299;
-
(2009)
Angew. Chem.
, vol.121
, pp. 4299
-
-
Kirchberg, S.1
Fröhlich, R.2
Studer, A.3
-
46
-
-
77956599570
-
-
As a side product, the product of a double phenylation oxidation reaction was isolated in 9% yield (see the Supporting Information)
-
As a side product, the product of a double phenylation oxidation reaction was isolated in 9% yield (see the Supporting Information).
-
-
-
-
48
-
-
0000423547
-
-
b) N. E. Grimmer, N. J. Coville, C. B. de Koning, J. M. Smith, L. M. Cook, Z Organomet Chem. 2000, 616, 112;
-
(2000)
Z Organomet Chem.
, vol.616
, pp. 112
-
-
Grimmer, N.E.1
Coville, N.J.2
De Koning, C.B.3
Smith, J.M.4
Cook, L.M.5
-
49
-
-
0000688113
-
-
c) I. Hoppe, D. Hoppe, G. Roche, M. Marsch, K. Harms, Angew. Chem. 1995, 107, 2328;
-
(1995)
Angew. Chem.
, vol.107
, pp. 2328
-
-
Hoppe, I.1
Hoppe, D.2
Roche, G.3
Marsch, M.4
Harms, K.5
-
51
-
-
77956578994
-
-
CCDC 771860 (3a) and CCDC 771861 (9) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC 771860 (3a) and CCDC 771861 (9) 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.
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