-
5
-
-
24644462889
-
-
G. Bringmann A. J. Price Mortimer P. A. Keller M. J. Gresser J. Garner M. Breuning Angew. Chem., Int. Ed. 2005 44 5384
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 5384
-
-
Bringmann, G.1
Price Mortimer, A.J.2
Keller, P.A.3
Gresser, M.J.4
Garner, J.5
Breuning, M.6
-
13
-
-
84890973385
-
-
Wiley-VCH, Weinheim, For reviews on decarboxylative biaryl formation, see
-
L. Ackermann, Modern Arylation Methods, Wiley-VCH, Weinheim, 2009
-
(2009)
Modern Arylation Methods
-
-
Ackermann, L.1
-
16
-
-
0027913099
-
-
For selected reviews on C-H functionalization, see
-
S. Murai F. Kakiuchi S. Sekine Y. Tanaka A. Kamatani M. Sonoda N. Chatani 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
-
34
-
-
0003607021
-
-
Pergamon, Oxford
-
A. R. Katritzky, C. W. Rees and E. F. Scriven, Comprehensive Heterocyclic Chemistry III, Pergamon, Oxford, 1999, vol. 1
-
(1999)
Comprehensive Heterocyclic Chemistry III
, vol.1
-
-
Katritzky, A.R.1
Rees, C.W.2
Scriven, E.F.3
-
36
-
-
70349967829
-
-
D. Ma S. Xie P. Xue X. Zhang J. Dong Y. Jiang Angew. Chem., Int. Ed. 2009 48 4222
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 4222
-
-
Ma, D.1
Xie, S.2
Xue, P.3
Zhang, X.4
Dong, J.5
Jiang, Y.6
-
68
-
-
70349784952
-
-
D. Zhao W. Wang F. Yang J. Lan L. Yang G. Gao J. You Angew. Chem., Int. Ed. 2009 48 3296
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 3296
-
-
Zhao, D.1
Wang, W.2
Yang, F.3
Lan, J.4
Yang, L.5
Gao, G.6
You, J.7
-
79
-
-
79952050537
-
-
S. Kirchberg S. Tani K. Ueda J. Yamaguchi A. Studer K. Itami Angew. Chem., Int. Ed. 2011 50 2387
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 2387
-
-
Kirchberg, S.1
Tani, S.2
Ueda, K.3
Yamaguchi, J.4
Studer, A.5
Itami, K.6
-
86
-
-
77249107844
-
-
P. Xi F. Yang S. Qin D. Zhao J. Lan G. Gao C. Hu J. You J. Am. Chem. Soc. 2010 132 1822
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 1822
-
-
Xi, P.1
Yang, F.2
Qin, S.3
Zhao, D.4
Lan, J.5
Gao, G.6
Hu, C.7
You, J.8
-
96
-
-
80051704102
-
-
J. Park E. Park A. Kim Y. Lee K. Chi J. Kwak Y. Jung I. Kim Org. Lett. 2011 13 4390
-
(2011)
Org. Lett.
, vol.13
, pp. 4390
-
-
Park, J.1
Park, E.2
Kim, A.3
Lee, Y.4
Chi, K.5
Kwak, J.6
Jung, Y.7
Kim, I.8
-
118
-
-
82355163559
-
-
2 as oxidant, see
-
H. Wang L. Wang J. Shang X. Li H. Wang J. Gui A. Lei Chem. Commun. 2012 48 76
-
(2012)
Chem. Commun.
, vol.48
, pp. 76
-
-
Wang, H.1
Wang, L.2
Shang, J.3
Li, X.4
Wang, H.5
Gui, J.6
Lei, A.7
-
119
-
-
62249124735
-
-
A 1 mmol scale reaction in a 100 mL pressure tube afforded in 86% isolated yield For related iron-catalyzed oxidative reactions, see
-
K. Bahrami M. Khodaei F. Naali Synlett 2009 569
-
(2009)
Synlett
, vol.3
, pp. 569
-
-
Bahrami, K.1
Khodaei, M.2
Naali, F.3
|