-
2
-
-
34547883488
-
-
For recent examples, see: (a) Chiong, H. A.; Pham, Q.-N.; Daugulis, O. J. Am. Chem. Soc. 2007, 129, 9879.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9879
-
-
Chiong, H.A.1
Pham, Q.-N.2
Daugulis, O.3
-
3
-
-
0030532360
-
-
(b) Sonoda, M.; Kakiuchi, F.; Kamatani, A.; Chatani, N.; Murai, S. Chem. Lett. 1996, 25, 109.
-
(1996)
Chem. Lett.
, vol.25
, pp. 109
-
-
Sonoda, M.1
Kakiuchi, F.2
Kamatani, A.3
Chatani, N.4
Murai, S.5
-
4
-
-
52449083568
-
-
O'Brien, E. M.; Morgan, B. J.; Kozlowski, M. Angew. Chem., Int. Ed. 2008, 47, 6877.
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6877
-
-
O'Brien, E.M.1
Morgan, B.J.2
Kozlowski, M.3
-
10
-
-
1542295909
-
-
(f) An, J.; Bagnell, L.; Cablewski, T.; Strauss, C. R.; Trainor, R. W. J. Org. Chem. 1997, 62, 2505.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 2505
-
-
An, J.1
Bagnell, L.2
Cablewski, T.3
Strauss, C.R.4
Trainor, R.W.5
-
11
-
-
57849159089
-
-
(g) Sharma, A.; Kumar, R.; Sharma, N.; Kumar, V.; Sinha, A. K. Adv. Synth. Catal. 2008, 350, 2910.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 2910
-
-
Sharma, A.1
Kumar, R.2
Sharma, N.3
Kumar, V.4
Sinha, A.K.5
-
13
-
-
0000102007
-
-
(a) Shepard, A. F.; Winslow, N. R.; Johnson, J. R. J. Am. Chem. Soc. 1930, 52, 2083.
-
(1930)
J. Am. Chem. Soc.
, vol.52
, pp. 2083
-
-
Shepard, A.F.1
Winslow, N.R.2
Johnson, J.R.3
-
16
-
-
0000932560
-
-
(d) Cairncross, A.; Roland, J. R.; Henderson, R. M.; Sheppard, W. A. J. Am. Chem. Soc. 1970, 92, 3187.
-
(1970)
J. Am. Chem. Soc.
, vol.92
, pp. 3187
-
-
Cairncross, A.1
Roland, J.R.2
Henderson, R.M.3
Sheppard, W.A.4
-
18
-
-
33746866185
-
-
(f) Cohen, T.; Berninger, R. W.; Wood, J. T. J. Org. Chem. 1978, 43, 837.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 837
-
-
Cohen, T.1
Berninger, R.W.2
Wood, J.T.3
-
21
-
-
3042797136
-
-
(a) Matsubara, S.; Yokota, Y.; Oshima, K. Org. Lett. 2004, 6, 2071.
-
(2004)
Org. Lett.
, vol.6
, pp. 2071
-
-
Matsubara, S.1
Yokota, Y.2
Oshima, K.3
-
22
-
-
34547152046
-
-
(b) Dickstein, S. J.; Mulrooney, C. A.; O'Brien, E. M.; Morgan, B. J.; Kozlowski, M. C. Org. Lett. 2007, 9, 2441.
-
(2007)
Org. Lett.
, vol.9
, pp. 2441
-
-
Dickstein, S.J.1
Mulrooney, C.A.2
O'Brien, E.M.3
Morgan, B.J.4
Kozlowski, M.C.5
-
23
-
-
0032541559
-
-
For selected examples of copper-mediated decarboxylations, see: (a) Beccalli, E. M.; Clerici, F.; Marchesini, A. Tetrahedron 1998, 54, 11675.
-
(1998)
Tetrahedron
, vol.54
, pp. 11675
-
-
Beccalli, E.M.1
Clerici, F.2
Marchesini, A.3
-
24
-
-
0035977227
-
-
(b) Gaukroger, K.; Hadfield, J. A.; Hepworth, L. A.; Lawrencen, N. J.; McGown, A. T. J. Org. Chem. 2001, 66, 8135.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 8135
-
-
Gaukroger, K.1
Hadfield, J.A.2
Hepworth, L.A.3
Lawrencen, N.J.4
McGown, A.T.5
-
26
-
-
33746929476
-
-
(d) Gooßen, L. J.; Deng, G.; Levy, L. M. Science 2006, 313, 662.
-
(2006)
Science
, vol.313
, pp. 662
-
-
Gooßen, L.J.1
Deng, G.2
Levy, L.M.3
-
28
-
-
35949001662
-
-
(a) Gooßen, L. J.; Thiel, W. R.; Rodriguez, N.; Linder, C.; Melzer, B. Adv. Synth. Catal. 2007, 349, 2241.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 2241
-
-
Gooßen, L.J.1
Thiel, W.R.2
Rodriguez, N.3
Linder, C.4
Melzer, B.5
-
29
-
-
64149104404
-
-
(b) Goossen, L. J.; Manjolinho, F.; Khan, B. A.; Rodriguez, N. J. Org. Chem. 2009, 74, 2620.
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2620
-
-
Goossen, L.J.1
Manjolinho, F.2
Khan, B.A.3
Rodriguez, N.4
-
32
-
-
70450172140
-
-
(a) Cornella, J.; Sanchez, C.; Banawa, D.; Larrosa, I. Chem. Commun. 2009, 7176.
-
(2009)
Chem. Commun.
, pp. 7176
-
-
Cornella, J.1
Sanchez, C.2
Banawa, D.3
Larrosa, I.4
-
33
-
-
70450182929
-
-
For a similar method, see: (b) Goossen, L. J.; Linder, C.; Rodriguez, N.; Lange, C. C.; Fromm, A. Chem. Commun. 2009, 7173.
-
(2009)
Chem. Commun.
, pp. 7173
-
-
Goossen, L.J.1
Linder, C.2
Rodriguez, N.3
Lange, C.C.4
Fromm, A.5
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34
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72849140085
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The origin of this selectivity is unclear at the moment, especially as the reaction seems to be activated by strongly electron -donating and -withdrawing groups, which may indicate that two different mechanisms are in place
-
The origin of this selectivity is unclear at the moment, especially as the reaction seems to be activated by strongly electron -donating and -withdrawing groups, which may indicate that two different mechanisms are in place.
-
-
-
-
35
-
-
72849132282
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-
Longer reaction times did not improve the yield
-
Longer reaction times did not improve the yield.
-
-
-
-
36
-
-
72849108713
-
-
However, indoles and pyrroles were found to be unsuitable for protodecarboxylation under these reaction conditions
-
However, indoles and pyrroles were found to be unsuitable for protodecarboxylation under these reaction conditions.
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