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2003; Angew. Chem. 2003, 115, 5558 Coord. Chem. Rev. 2004 248 2337 Synlett 2006 1283 Chem. Rev. 2006 106 2651
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Ley S V., Thomas A W., Angew. Chem. Int. Ed. 2003 42 5400; Angew. Chem. 2003, 115, 5558, Beletskaya I P., Cheprakov A V., Coord. Chem. Rev. 2004 248 2337, Hartwig J F., Synlett 2006 1283, Corbet J.-P, Mignani G, Chem. Rev. 2006 106 2651
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Ley, S.V.1
Thomas, A.W.2
Beletskaya, I.P.3
Cheprakov, A.V.4
Hartwig, J.F.5
Corbet, J.-P.6
Mignani, G.7
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3
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35848967589
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For some examples with Pd catalysis, see: 2007 J. Am. Chem. Soc. 2002 124 6043 J. Am. Chem. Soc. 2003 125 6653
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For some examples with Pd catalysis, see:, Ikawa T, Barder T E., Biscoe M R., Buchwald S L., J. Am. Chem. Soc. 2007 129 13001, Yin J, Buchwald S L., J. Am. Chem. Soc. 2002 124 6043, Huang X, Anderson K W., Zim D, Jiang L, Klapars A, Buchwald S L., J. Am. Chem. Soc. 2003 125 6653
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J. Am. Chem. Soc.
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Ikawa, T.1
Barder, T.E.2
Biscoe, M.R.3
Buchwald, S.L.4
Yin, J.5
Buchwald, S.L.6
Huang, X.7
Anderson, K.W.8
Zim, D.9
Jiang, L.10
Klapars, A.11
Buchwald, S.L.12
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4
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16244411305
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For some examples on Cu catalysis, see: 2005 J. Org. Chem. 2007 72 3863 Synlett 2004 1517 Adv. Synth. Catal. 2006 348 2197 Chem. Eur. J. 2004 10 5607 Org. Lett. 2006 8 5609 J. Org. Chem. 2007 72 8943 J.Org. Chem. 2007 72 8969 Tetrahedron Lett. 2007 48 4207 Chem. Eur. J. 2006 12 3636
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For some examples on Cu catalysis, see:, Strieter E R., Blackmond D G., Buchwald S L., J. Am. Chem. Soc. 2005 127 4120, Lv X, Bao W, J. Org. Chem. 2007 72 3863, Hosseinzadeh R, Tajbakhsh M, Mohadjerani M, Mehdinejad H, Synlett 2004 1517, Guo X, Rao H, Fu H, Jiang Y, Zhao Y, Adv. Synth. Catal. 2006 348 2197, Cristau H.-J, Cellier P P., Spindler J.-F, Taillefer M, Chem. Eur. J. 2004 10 5607, Chen Y.-J, Chen H.-H, Org. Lett. 2006 8 5609, Ma H.-C, Jiang X.-Z, J. Org. Chem. 2007 72 8943, Yang M, Liu F, J.Org. Chem. 2007 72 8969, Verma A K., Singh J, Sankar V K., Chaudhary R, Chandra R, Tetrahedron Lett. 2007 48 4207, Rao H, Jin Y, Fu H, Jiang Y, Zhao Y, Chem. Eur. J. 2006 12 3636
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J. Am. Chem. Soc.
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Strieter, E.R.1
Blackmond, D.G.2
Buchwald, S.L.3
Lv, X.4
Bao, W.5
Hosseinzadeh, R.6
Tajbakhsh, M.7
Mohadjerani, M.8
Mehdinejad, H.9
Guo, X.10
Rao, H.11
Fu, H.12
Jiang, Y.13
Zhao, Y.14
Cristau, H.-J.15
Cellier, P.P.16
Spindler, J.-F.17
Taillefer, M.18
Chen, Y.-J.19
Chen, H.-H.20
Ma, H.-C.21
Jiang, X.-Z.22
Yang, M.23
Liu, F.24
Verma, A.K.25
Singh, J.26
Sankar, V.K.27
Chaudhary, R.28
Chandra, R.29
Rao, H.30
Jin, Y.31
Fu, H.32
Jiang, Y.33
Zhao, Y.34
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5
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44349112602
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For Fe-catalyzed reactions, see: 2008 Angew. Chem. Int. Ed. 2007 46 8862; Angew. Chem. 2007, 119, 9018
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For Fe-catalyzed reactions, see:, Correa A, Elmore S, Bolm C, Chem. Eur. J. 2008 14 3527, Correa A, Bolm C, Angew. Chem. Int. Ed. 2007 46 8862; Angew. Chem. 2007, 119, 9018
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Chem. Eur. J.
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Correa, A.1
Elmore, S.2
Bolm, C.3
Correa, A.4
Bolm, C.5
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7
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38649132925
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For examples using TBAB as a reaction medium, see: 2008 J. Org. Chem. 2007 72 6294 J. Org. Chem. 2003 68 2929
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For examples using TBAB as a reaction medium, see:, Jammi S, Barua P, Rout P, Saha P, Punniyamurthy T, Tetrahedron Lett. 2008 49 1484, Tang B.-X, Wang F, Li J.-H, Xie Y.-X, Zhang M.-B, J. Org. Chem. 2007 72 6294, Calo V, Nacci A, Monopoli A, Laera S, Cioffi N, J. Org. Chem. 2003 68 2929
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Tetrahedron Lett.
, vol.49
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Jammi, S.1
Barua, P.2
Rout, P.3
Saha, P.4
Punniyamurthy, T.5
Tang, B.-X.6
Wang, F.7
Li, J.-H.8
Xie, Y.-X.9
Zhang, M.-B.10
Calo, V.11
Nacci, A.12
Monopoli, A.13
Laera, S.14
Cioffi, N.15
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8
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33947202279
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For examples using TBAB as an additive, see: 2007 Synthesis 2006 3955 J. Org. Chem. 2006 71 6834 Org. Lett. 2005 7 2101 Org. Lett. 2009 11 2575 J. Org. Chem. 2003 68 9412 J. Org. Chem. 2008 73 2315
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For examples using TBAB as an additive, see:, Li J.-H, Li J.-L, Wang D.-P, Pi S.-F, Xie Y.-X, Zhang M.-B, Hu X.-C, J. Org. Chem. 2007 72 2053, Zhu X, Ma Y, Su L, Song H, Chen G, Liang D, Wan Y, Synthesis 2006 3955, Mino T, Shirae Y, Sasai Y, Sakamoto M, Fujita T, J. Org. Chem. 2006 71 6834, Arvela R K., Leadbeater N E., Org. Lett. 2005 7 2101, Schmink J R., Leadbeater N E., Org. Lett. 2009 11 2575, Tagata T, Nishida M, J. Org. Chem. 2003 68 9412, Alacid E, Najera C, J. Org. Chem. 2008 73 2315
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J. Org. Chem.
, vol.72
, pp. 2053
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Li, J.-H.1
Li, J.-L.2
Wang, D.-P.3
Pi, S.-F.4
Xie, Y.-X.5
Zhang, M.-B.6
Hu, X.-C.7
Zhu, X.8
Ma, Y.9
Su, L.10
Song, H.11
Chen, G.12
Liang, D.13
Wan, Y.14
Mino, T.15
Shirae, Y.16
Sasai, Y.17
Sakamoto, M.18
Fujita, T.19
Arvela, R.K.20
Leadbeater, N.E.21
Schmink, J.R.22
Leadbeater, N.E.23
Tagata, T.24
Nishida, M.25
Alacid, E.26
Najera, C.27
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