-
1
-
-
0000820085
-
-
a) B. A. Arndsten, R. G. Bergman, T. A. Mobley, T. H. Peterson, Acc. Chem. Res. 1995, 28, 154-162;
-
(1995)
Acc. Chem. Res.
, vol.28
, pp. 154-162
-
-
Arndsten, B.A.1
Bergman, R.G.2
Mobley, T.A.3
Peterson, T.H.4
-
5
-
-
0001108788
-
-
a) G. Dyker, Angew. Chem. 1999, 111, 1808-1822;
-
(1999)
Angew. Chem.
, vol.111
, pp. 1808-1822
-
-
Dyker, G.1
-
6
-
-
0033553817
-
-
Angew. Chem. Int. Ed. 1999, 38, 1698-1712;
-
(1999)
Angew. Chem. Int. Ed.
, vol.38
, pp. 1698-1712
-
-
-
12
-
-
0001568295
-
-
3 to be a viable arylation catalyst in the presence of a carbonate base: S. Pivsa-Art, T. Satoh, Y. Kawamura, M. Miura, M. Nomura, Bull. Chem. Soc. Jpn. 1998, 71, 467-473;
-
(1998)
Bull. Chem. Soc. Jpn.
, vol.71
, pp. 467-473
-
-
Pivsa-Art, S.1
Satoh, T.2
Kawamura, Y.3
Miura, M.4
Nomura, M.5
-
13
-
-
20444370318
-
-
b) B. S. Lane, M. A. Brown, D. Sames, J. Am. Chem. Soc. 2005, 127, 8050-8057.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 8050-8057
-
-
Lane, B.S.1
Brown, M.A.2
Sames, D.3
-
14
-
-
0037442583
-
-
one example
-
a) A. Mori, A. Sekiguchi, K. Masui, T. Shimada, M. Horie, K. Osakada, M. Kawamoto, T. Ikeda, J. Am. Chem. Soc. 2003, 125, 1700-1701 (one example);
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 1700-1701
-
-
Mori, A.1
Sekiguchi, A.2
Masui, K.3
Shimada, T.4
Horie, M.5
Osakada, K.6
Kawamoto, M.7
Ikeda, T.8
-
15
-
-
33746270586
-
-
note
-
b) Scattered examples of heterocycle-aryl bromide couplings are given in ref. [4a];
-
-
-
-
16
-
-
0038306206
-
-
c) A. Yokooji, T. Okazawa, T. Satoh, M. Miura, M. Nomura, Tetrahedron 2003, 59, 5685-5689;
-
(2003)
Tetrahedron
, vol.59
, pp. 5685-5689
-
-
Yokooji, A.1
Okazawa, T.2
Satoh, T.3
Miura, M.4
Nomura, M.5
-
17
-
-
13244262766
-
-
d) Electron-rich aryl bromides were coupled with benzothiazole and benzoxazole in: D. Alagille, R. M. Baldwin, G. D. Tamagnan, Tetrahedron Lett. 2005, 46, 1349-1351.
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1349-1351
-
-
Alagille, D.1
Baldwin, R.M.2
Tamagnan, G.D.3
-
18
-
-
0742321839
-
-
J. C. Lewis, S. H. Wiedemann, R. G. Bergman, J. A. Ellman, Org. Lett. 2004, 6, 35-38.
-
(2004)
Org. Lett.
, vol.6
, pp. 35-38
-
-
Lewis, J.C.1
Wiedemann, S.H.2
Bergman, R.G.3
Ellman, J.A.4
-
19
-
-
0036738330
-
-
a) M. Larhed, C. Moberg, A. Hallberg, Acc. Chem. Res. 2002, 35, 717-727;
-
(2002)
Acc. Chem. Res.
, vol.35
, pp. 717-727
-
-
Larhed, M.1
Moberg, C.2
Hallberg, A.3
-
21
-
-
33746320850
-
-
US Patent 3400163, 1968
-
"Phoban" is commerically available as a technical mixture of [3.3.1] and [4.2.1] isomers and has received limited but continual attention since its original patent in 1968: a) R. G. Mason, J. L. van Winkle (Shell Oil Co.), US Patent 3400163, 1968;
-
-
-
Mason, R.G.1
Van Winkle, J.L.2
-
23
-
-
0000706939
-
-
c) For its use as a ligand, see: H. C. L. Abbenhuis, U. Burckhardt, V. Gramlich, C. Köllner, P. S. Pregosin, R. Salzmann, A. Togni, Organometallics 1995, 14, 759-766;
-
(1995)
Organometallics
, vol.14
, pp. 759-766
-
-
Abbenhuis, H.C.L.1
Burckhardt, U.2
Gramlich, V.3
Köllner, C.4
Pregosin, P.S.5
Salzmann, R.6
Togni, A.7
-
24
-
-
6344253335
-
-
d) G. S. Forman, A. E. McConnell, M. J. Hanton, A. M. Z. Slawin, R. P. Tooze, W. J. van Rensburg, W. H. Meyer, C. Dwyer, M. M. Kirk, D. W. Serfontein, Organometallics, 2004, 23, 4824-4827.
-
(2004)
Organometallics
, vol.23
, pp. 4824-4827
-
-
Forman, G.S.1
McConnell, A.E.2
Hanton, M.J.3
Slawin, A.M.Z.4
Tooze, R.P.5
Van Rensburg, W.J.6
Meyer, W.H.7
Dwyer, C.8
Kirk, M.M.9
Serfontein, D.W.10
-
26
-
-
33746289102
-
-
see ref. [8d]
-
a) see ref. [8d];
-
-
-
-
27
-
-
33746312751
-
-
unpublished results
-
b) C. L. Dwyer, M. M. Kirk, W. H. Meyer, W. J. van Rensburg, G. S. Forman, unpublished results.
-
-
-
Dwyer, C.L.1
Kirk, M.M.2
Meyer, W.H.3
Van Rensburg, W.J.4
Forman, G.S.5
-
28
-
-
33746321129
-
-
note
-
Significant amounts of demethylation were observed for the microwave-mediated arylation using iodoanisole, presumably due to nucleophilic displacement by iodide anion at high temperatures.
-
-
-
-
29
-
-
0001567706
-
-
Z. Chen, Q. Jiang, G. Zhu, D. Xiao, P. Cao, C. Guo, X. Zhang, J. Org. Chem. 1997, 62, 4521-4523.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4521-4523
-
-
Chen, Z.1
Jiang, Q.2
Zhu, G.3
Xiao, D.4
Cao, P.5
Guo, C.6
Zhang, X.7
-
30
-
-
0000778182
-
-
A number of reports have described the phenyl-substituted analogue of 2a. but none have mentioned the endo isomer: a) S. T. Howard, J. P. Foreman, P. G. Edwards, Inorg. Chem. 1996, 35, 5805-5812;
-
(1996)
Inorg. Chem.
, vol.35
, pp. 5805-5812
-
-
Howard, S.T.1
Foreman, J.P.2
Edwards, P.G.3
-
31
-
-
0001822832
-
-
b) S. J. Coles, P. G. Edwards, M. B. Hursthouse, K. M. Abdul Malik, J. L. Thick, R. P. Tooze, J. Chem. Soc. Dalton Trans. 1997, 1821-1830.
-
(1997)
J. Chem. Soc. Dalton Trans.
, pp. 1821-1830
-
-
Coles, S.J.1
Edwards, P.G.2
Hursthouse, M.B.3
Abdul Malik, K.M.4
Thick, J.L.5
Tooze, R.P.6
-
32
-
-
9344240844
-
-
and references therein
-
G. Altenhoff, R. Goddard, C. W. Lehmann, F. Glorius, J. Am. Chem. Soc. 2004, 126, 15195-15201, and references therein.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15195-15201
-
-
Altenhoff, G.1
Goddard, R.2
Lehmann, C.W.3
Glorius, F.4
-
33
-
-
0034629166
-
-
and references therein
-
J. Sisko, A. J. Kassick, M. Mellinger, J. J. Filan, A. Allen, M. A. Olsen, J. Org. Chem. 2000, 65, 1516-1524, and references therein.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 1516-1524
-
-
Sisko, J.1
Kassick, A.J.2
Mellinger, M.3
Filan, J.J.4
Allen, A.5
Olsen, M.A.6
-
34
-
-
0037012428
-
-
a) K. L. Tan, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc. 2002, 124, 3202-3203;
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3202-3203
-
-
Tan, K.L.1
Bergman, R.G.2
Ellman, J.A.3
-
36
-
-
33746270468
-
-
Angew. Chem. Int. Ed. 2006, 45, 1592-1595
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 1592-1595
-
-
|