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1
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33745079610
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For recent examples, see: J.S. Carey, D. Laffan, C. Thomson, and M.T. Wiliams Org. Biomol. Chem. 4 2006 2337
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Carey, J.S.1
Laffan, D.2
Thomson, C.3
Wiliams, M.T.4
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4
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61449159817
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For recent examples, see: J.Z. Deng, D.V. Paone, A.T. Ginnetti, H. Kurihara, S.D. Dreher, S.A. Weissman, S.R. Stauffer, and C.S. Burgey Org. Lett. 11 2009 345
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Deng, J.Z.1
Paone, D.V.2
Ginnetti, A.T.3
Kurihara, H.4
Dreher, S.D.5
Weissman, S.A.6
Stauffer, S.R.7
Burgey, C.S.8
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5
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61449215236
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D.X. Yang, S.L. Colletti, K. Wu, M. Song, G.Y. Li, and H.C. Shen Org. Lett. 11 2009 381
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Yang, D.X.1
Colletti, S.L.2
Wu, K.3
Song, M.4
Li, G.Y.5
Shen, H.C.6
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6
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57349119776
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A.S. Voisin-Chiret, A. Bouillon, G. Burzicki, M. Celant, R. Legay, H. El-Kashef, and S. Rault Tetrahedron 65 2009 607
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Voisin-Chiret, A.S.1
Bouillon, A.2
Burzicki, G.3
Celant, M.4
Legay, R.5
El-Kashef, H.6
Rault, S.7
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13
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12344249681
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J.J. Song, N.K. Yee, Z. Tan, J. Xu, S.R. Kapadia, and C.H. Senanayake Org. Lett. 6 2004 4905
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Song, J.J.1
Yee, N.K.2
Tan, Z.3
Xu, J.4
Kapadia, S.R.5
Senanayake, C.H.6
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22
-
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0037131349
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Preparation of 2-bromo-5-pyridylboronic acid via lithiation of 2,5-dibromopyridine, see: P.R. Parry, C. Wang, A.S. Batsanov, M.R. Bryce, and B. Tarbit J. Org. Chem. 67 2002 7541
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Parry, P.R.1
Wang, C.2
Batsanov, A.S.3
Bryce, M.R.4
Tarbit, B.5
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23
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0036532565
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A. Bouillon, J.-C. Lancelot, V. Collot, P.R. Bovy, and S. Rault Tetrahedron 58 2002 2885
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(2002)
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Bouillon, A.1
Lancelot, J.-C.2
Collot, V.3
Bovy, P.R.4
Rault, S.5
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24
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0034622027
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X. Wang, P. Rabbat, P. O'Shea, R. Tillyer, E.J. Grabowski, and P.J. Reider Tetrahedron Lett. 41 2000 4335
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Wang, X.1
Rabbat, P.2
O'shea, P.3
Tillyer, R.4
Grabowski, E.J.5
Reider, P.J.6
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25
-
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0033522827
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F. Trecourt, G. Breton, V. Bonnet, F. Mongin, F. Marsais, and G. Queguiner Tetrahedron Lett. 40 1999 4339
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Trecourt, F.1
Breton, G.2
Bonnet, V.3
Mongin, F.4
Marsais, F.5
Queguiner, G.6
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26
-
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0035812684
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-
T. Mase, I.N. Houpis, A. Akao, I.K. Dorziotis, T. Hoang, T. Iida, T. Itoh, K. Kamei, S. Kato, Y. Kato, M. Kawasaki, F. Lang, J. Lee, J. Lynch, P. Maligres, A. Monila, T. Nemoto, S. Okada, R. Reamer, J.Z. Song, D. Tschaen, T. Wada, D. Zewge, R.P. Volante, P.J. Reider, and K. Tomimoto J. Org. Chem. 66 2001 6775
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Mase, T.1
Houpis, I.N.2
Akao, A.3
Dorziotis, I.K.4
Hoang, T.5
Iida, T.6
Itoh, T.7
Kamei, K.8
Kato, S.9
Kato, Y.10
Kawasaki, M.11
Lang, F.12
Lee, J.13
Lynch, J.14
Maligres, P.15
Monila, A.16
Nemoto, T.17
Okada, S.18
Reamer, R.19
Song, J.Z.20
Tschaen, D.21
Wada, T.22
Zewge, D.23
Volante, R.P.24
Reider, P.J.25
Tomimoto, K.26
more..
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28
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11844280304
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A recent example of coupling reaction with aminopyridine, see; A.E. Thompson, G. Hughes, A.S. Batsanov, M.R. Bryce, P.R. Parry, and B. Tarbit J. Org. Chem. 70 2005 388
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(2005)
J. Org. Chem.
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-
-
Thompson, A.E.1
Hughes, G.2
Batsanov, A.S.3
Bryce, M.R.4
Parry, P.R.5
Tarbit, B.6
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29
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78650012171
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a values (in DMSO); range between 10 and 19 for phenols, 20-30 for anilines, source from
-
a values (in DMSO); range between 10 and 19 for phenols, 20-30 for anilines, source from http://www.chem.wisc.edu/areas/reich/pkatable/ index.htm.
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-
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32
-
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78650002584
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note
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6, 125 MHz): δ 159.17, 153.18, 149.34, 145.99, 138.32, 134.70, 122.12, 119.12, 116.92, 107.38.
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