-
1
-
-
0036589259
-
-
Hassan J, Svignon M, Gozzi C, Schulz E, Lemaire M, Chem. Rev. 2002 102 1359
-
(2002)
Chem. Rev.
, vol.102
, pp. 1359
-
-
Hassan, J.1
Svignon, M.2
Gozzi, C.3
Schulz, E.4
Lemaire, M.5
-
6
-
-
47249143370
-
-
For selected reviews, see:, Bellina F, Cauteruccio S, Rossi R, Curr. Org. Chem. 2008 12 774
-
(2008)
Curr. Org. Chem.
, vol.12
, pp. 774
-
-
Bellina, F.1
Cauteruccio, S.2
Rossi, R.3
-
13
-
-
79952676713
-
-
Liu C, Zhang H, Shi W, Lei A, Chem. Rev. 2011 111 1780
-
(2011)
Chem. Rev.
, vol.111
, pp. 1780
-
-
Liu, C.1
Zhang, H.2
Shi, W.3
Lei, A.4
-
16
-
-
34547960227
-
-
Dwight T A., Rue N R., Charyk D, Josselyn R, DeBoef B, Org. Lett. 2007 9 3137
-
(2007)
Org. Lett.
, vol.9
, pp. 3137
-
-
Dwight, T.A.1
Rue, N.R.2
Charyk, D.3
Josselyn, R.4
Deboef, B.5
-
17
-
-
43449139728
-
-
Potavathri S, Dumas A S., Dwight T A., Naumiec G R., Hammann [nl]J M., DeBoef B, Tetrahedron Lett. 2008 49 4050
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 4050
-
-
Potavathri, S.1
Dumas, A.S.2
Dwight, T.A.3
Naumiec, G.R.4
Hammann, J.M.5
Deboef, B.6
-
18
-
-
77958036325
-
-
Potavathri S, Pereira K C., Gorelsky S I., Pike A, LeBris A P., DeBoef B, J. Am. Chem. Soc. 2010 132 14676
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 14676
-
-
Potavathri, S.1
Pereira, K.C.2
Gorelsky, S.I.3
Pike, A.4
Lebris, A.P.5
Deboef, B.6
-
19
-
-
79952590882
-
-
For a recent heteroarene-arene cross-coupling with dual C-H bond cleavage, see:, Malakar C C., Schmidt D, Conrad J, Beifuss U, Org. Lett. 2011 13 1378
-
(2011)
Org. Lett.
, vol.13
, pp. 1378
-
-
Malakar, C.C.1
Schmidt, D.2
Conrad, J.3
Beifuss, U.4
-
20
-
-
79951816256
-
-
For a palladium-free, copper-mediated biaryl coupling of azoles with 2-arylazines, see:, Kitahara M, Umeda N, Hirano K, Satoh T, Miura M, J. Am. Chem. Soc. 2011 133 2160
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 2160
-
-
Kitahara, M.1
Umeda, N.2
Hirano, K.3
Satoh, T.4
Miura, M.5
-
22
-
-
77249107844
-
-
Xi P, Yang F, Qin S, Zhao D, Lan J, Gao G, Hu C, You J, 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
-
25
-
-
79953227751
-
-
Gong X, Song G, Zhang H, Li X, Org. Lett. 2011 13 1766
-
(2011)
Org. Lett.
, vol.13
, pp. 1766
-
-
Gong, X.1
Song, G.2
Zhang, H.3
Li, X.4
-
26
-
-
79956346739
-
-
Yamaguchi A D., Mandal D, Yamaguchi J, Itami K, Chem. Lett. 2011 40 555
-
(2011)
Chem. Lett.
, vol.40
, pp. 555
-
-
Yamaguchi, A.D.1
Mandal, D.2
Yamaguchi, J.3
Itami, K.4
-
27
-
-
79957461555
-
-
Wang Z, Li K, Zhao D, Lan J, You J, Angew. Chem. Int. Ed. 2011 50 5365
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 5365
-
-
Wang, Z.1
Li, K.2
Zhao, D.3
Lan, J.4
You, J.5
-
28
-
-
72949117197
-
-
Li Y, Jin J, Qian W, Bao W, Org. Biomol. Chem. 2010 8 326
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 326
-
-
Li, Y.1
Jin, J.2
Qian, W.3
Bao, W.4
-
29
-
-
77949840558
-
-
Truong T, Alvarado J, Tran L D., Daugulis O, Org. Lett. 2010 12 1200
-
(2010)
Org. Lett.
, vol.12
, pp. 1200
-
-
Truong, T.1
Alvarado, J.2
Tran, L.D.3
Daugulis, O.4
-
30
-
-
73049108954
-
-
Monguchi D, Yamamura A, Fujiwara T, Somete T, Mori A, Tetrahedron Lett. 2010 51 850
-
(2010)
Tetrahedron Lett.
, vol.51
, pp. 850
-
-
Monguchi, D.1
Yamamura, A.2
Fujiwara, T.3
Somete, T.4
Mori, A.5
-
40
-
-
64349115758
-
-
Akhmadullina N S., Cherkashina N V., Kozitsyna N Y., Stolarov I P., Perova E V., Gekhman [nl]A E., Nefedov S E., Vargaftik M N., Moiseev I I., Inorg. Chim. Acta 2009 362 1943
-
(2009)
Inorg. Chim. Acta
, vol.362
, pp. 1943
-
-
Akhmadullina, N.S.1
Cherkashina, N.V.2
Kozitsyna, N.Y.3
Stolarov, I.P.4
Perova, E.V.5
Gekhman, A.E.6
Nefedov, S.E.7
Vargaftik, M.N.8
Moiseev, I.I.9
-
41
-
-
67650645824
-
-
Akhmadullina N S., Cherkashina N V., Kozitsyna N Y., Gekhman A E., Vargaftik M N., Kinet. Catal. 2009 50 396
-
(2009)
Kinet. Catal.
, vol.50
, pp. 396
-
-
Akhmadullina, N.S.1
Cherkashina, N.V.2
Kozitsyna, N.Y.3
Gekhman, A.E.4
Vargaftik, M.N.5
-
43
-
-
33846064670
-
-
For pKa values (in DMSO) calculated by DFT methods, see: Fu, Y.; Li, J.-N.; Liu, L.; Guo, Q.-X. Tetrahedron 2007, 63, 1568.
-
(2007)
Tetrahedron
, vol.63
, pp. 1568
-
-
Fu, Y.1
Li, J.-N.2
Liu, L.3
Guo, Q.-X.4
-
44
-
-
33745959757
-
-
[nl]
-
Lafrance M, Rowley C N., Woo T K., Fagnou K, [nl] J. Am. Chem. Soc. 2006 128 8754
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 8754
-
-
Lafrance, M.1
Rowley, C.N.2
Woo, T.K.3
Fagnou, K.4
-
47
-
-
57149120979
-
-
Nakao Y, Kashihara N, Kanyiva K S., Hiyama T, [nl]J. Am. Chem. Soc. 2008 130 16170
-
(2008)
[Nl]J. Am. Chem. Soc.
, vol.130
, pp. 16170
-
-
Nakao, Y.1
Kashihara, N.2
Kanyiva, K.S.3
Hiyama, T.4
-
49
-
-
77950796637
-
-
Zhang X, Fan S, He C.-Y, Wan X, Min Q.-Q, Yang J, Jiang [nl]Z.-X, J. Am. Chem. Soc. 2010 132 4506
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4506
-
-
Zhang, X.1
Fan, S.2
He, C.-Y.3
Wan, X.4
Min, Q.-Q.5
Yang, J.6
Jiang, Z.-X.7
-
50
-
-
80052069034
-
-
Ref. 15 shows a product from the 3,5-linkage of [nl]N -methylindole and a thiazole
-
Ref. 15 shows a product from the 3,5-linkage of [nl]N -methylindole and a thiazole
-
-
-
-
51
-
-
80052040592
-
-
Ref. 17 reports one example for the 2,5-linkage of oxazoles
-
Ref. 17 reports one example for the 2,5-linkage of oxazoles.
-
-
-
-
52
-
-
67849129077
-
-
For metal-free heteroaryl-heteroaryl cross-couplings, see:, Kita Y, Morimoto K, Ito M, Ogawa C, Goto A, Dohi T, J. Am. Chem. Soc. 2009 131 1668
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 1668
-
-
Kita, Y.1
Morimoto, K.2
Ito, M.3
Ogawa, C.4
Goto, A.5
Dohi, T.6
-
54
-
-
41449090176
-
-
Such concepts have been developed for direct arylations [nl]of heteroarenes, see for example:, Campeau L.-C, Bertrand-Laperle M, Leclerc J.-P, Villemure E, Gorelsky S, Fagnou K, J. Am. Chem. Soc. 2008 130 3276
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 3276
-
-
Campeau, L.-C.1
Bertrand-Laperle, M.2
Leclerc, J.-P.3
Villemure, E.4
Gorelsky, S.5
Fagnou, K.6
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