-
2
-
-
4444376920
-
-
b) F. Alonso, I. P. Heletskaya, M. Yus, Chem. Rev. 2004, 104, 3079;
-
(2004)
Chem. Rev.
, vol.104
, pp. 3079
-
-
Alonso, F.1
Heletskaya, I.P.2
Yus, M.3
-
3
-
-
0037060980
-
-
c) D. Prim, J. Campagne, D. Joseph, R Andrioletti, Tetrahedron 2002, 58, 2041;
-
(2002)
Tetrahedron
, vol.58
, pp. 2041
-
-
Prim, D.1
Campagne, J.2
Joseph, D.3
Andrioletti, R.4
-
9
-
-
68749102180
-
-
b) R.J. Less, R.L. Melen, V. Naseri, D.S. Wright, Chem. Commun. 2009, 4929;
-
(2009)
Chem. Commun.
, vol.4929
-
-
Less, R.J.1
Melen, R.L.2
Naseri, V.3
Wright, D.S.4
-
13
-
-
1542664933
-
-
e) A.R. McWilliams, H. Dorn, I. Manners, Top. Curr. Chem 2002, 220,141.
-
(2002)
Top. Curr. Chem
, vol.220
, pp. 141
-
-
McWilliams, A.R.1
Dorn, H.2
Manners, I.3
-
14
-
-
22944472711
-
-
3 under an oxygen-free inert atmosphere are known. Selected examples
-
3 under an oxygen-free inert atmosphere are known. Selected examples: a) T. L. Clark, J. M. Rodezno, S. R Clendenning, S. Aouba, P. M. Brodersen, A. J. Lough, H. E. Ruda, I. Manners, Chem. Eur. J. 2005, 11, 4526;
-
(2005)
Chem. Eur. J.
, vol.11
, pp. 4526
-
-
Clark, T.L.1
Rodezno, J.M.2
Clendenning, S.R.3
Aouba, S.4
Brodersen, P.M.5
Lough, A.J.6
Ruda, H.E.7
Manners, I.8
-
15
-
-
0000286706
-
-
b) H. Dorn, R. A. Singh, J. A. Massey, A. J. Lough, I. Manners, Angew. Chem. 1999, 111, 3540;
-
(1999)
Angew. Chem.
, vol.111
, pp. 3540
-
-
Dorn, H.1
Singh, R.A.2
Massey, J.A.3
Lough, A.J.4
Manners, I.5
-
17
-
-
0034686732
-
-
c) H. Dorn, R. A. Singh, J.A. Massey, J.M. Nelson, C. A., Jaska, A. J. Lough, I. Manners, J. Am. Chem. Soc. 2000, 122, 6669;
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 6669
-
-
Dorn, H.1
Singh, R.A.2
Massey, J.A.3
Nelson, J.M.4
Jaska, C.A.5
Lough, A.J.6
Manners, I.7
-
18
-
-
0032539218
-
-
d) R. H. Shu, L. J. Hao, J. F. Harrod, H. G. Woo, E. Samuel, J. Am. Chem. Soc. 1998, 120,12988;
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 12988
-
-
Shu, R.H.1
Hao, L.J.2
Harrod, J.F.3
Woo, H.G.4
Samuel, E.5
-
19
-
-
34548222512
-
-
e) A. J. Roering, S. N. MacMillian, J. M. Tanski, R. Waterman, Inorg. Chem. 2007, 46, 6855;
-
(2007)
Inorg. Chem.
, vol.46
, pp. 6855
-
-
Roering, A.J.1
MacMillian, S.N.2
Tanski, J.M.3
Waterman, R.4
-
20
-
-
33845227451
-
-
f) D. Masuda, A. J. Hoskin, T. W. Graham, C Beddie, M. C. Fermin, N. Etkin, D. W. Stephan, Chem. Eur. J. 2006, 12, 8696;
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 8696
-
-
Masuda, D.1
Hoskin, A.J.2
Graham, T.W.3
Beddie, C.4
Fermin, M.C.5
Etkin, N.6
Stephan, D.W.7
-
25
-
-
71549170228
-
-
For metal-catalyzed dehydrocoupling reactions of other heteroatom compounds, see also: j) D. Miles, J. Ward, D. A. Foucher, Macromolecules 2009, 42, 9199;
-
(2009)
Macromolecules
, vol.42
, pp. 9199
-
-
Miles, D.1
Ward, J.2
Foucher, D.A.3
-
26
-
-
33845233424
-
-
k) T. J. Clark, K. Lee, I. Manners, Chem. Eur. J. 2006, 12, 8634;
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 8634
-
-
Clark, T.J.1
Lee, K.2
Manners, I.3
-
27
-
-
0001362970
-
-
l) F. Gauvin, J. F. Harrod, H. G. Woo, Adv. Organomet. Chem 1998, 42, 363.
-
(1998)
Adv. Organomet. Chem
, vol.42
, pp. 363
-
-
Gauvin, F.1
Harrod, J.F.2
Woo, H.G.3
-
28
-
-
0037190859
-
-
a) R. W. Kinas, A. Okruszek, W. J. Stec, Tetrahedron Lett. 2002, 43, 7875;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 7875
-
-
Kinas, R.W.1
Okruszek, A.2
Stec, W.J.3
-
29
-
-
0010646818
-
-
b) W. J. Stec, A. Zwierzak, J. Michalski, Bull. Acad. PoL Sci. Ser. Sci. Chim. 1970, 18, 23;
-
(1970)
Bull. Acad. PoL Sci. Ser. Sci. Chim.
, vol.18
, pp. 23
-
-
Stec, W.J.1
Zwierzak, A.2
Michalski, J.3
-
32
-
-
0010733368
-
-
a) N. Suzuki, T. Kawai, S. Inoue, N. Sano, Y. Izawa, Bull. Chem. Soc. Jpn 1980, 53, 1421;
-
(1980)
Bull. Chem. Soc. Jpn
, vol.53
, pp. 1421
-
-
Suzuki, N.1
Kawai, T.2
Inoue, S.3
Sano, N.4
Izawa, Y.5
-
33
-
-
21844478979
-
-
b) Y. Rutsugan, K. Nagai, F. Nagaya, H. Tabuchi, K. Yamada, S. Araki, Bull. Chem. Soc. Jpn. 1988, 61, 1707;
-
(1988)
Bull. Chem. Soc. Jpn.
, vol.61
, pp. 1707
-
-
Rutsugan, Y.1
Nagai, K.2
Nagaya, F.3
Tabuchi, H.4
Yamada, K.5
Araki, S.6
-
34
-
-
6344240581
-
-
c)Z. M. Jaszay, I. Petnehazy, L. Toke, Heteroat. Chem. 2004, 15, 447;
-
(2004)
Heteroat. Chem.
, vol.15
, pp. 447
-
-
Jaszay, Z.M.1
Petnehazy, I.2
Toke, L.3
-
37
-
-
46449103920
-
-
a) A. V. Mukovnya, V. L. Tunitskaya, A. L. Khandazhinskaya, N. A. Golubeva, N. F. Zakirova, A. V. Ivanov, M. K. Kukhanova, S. N. Kochetkov, Biochemistry 2008, 73, 660;
-
(2008)
Biochemistry
, vol.73
, pp. 660
-
-
Mukovnya, A.V.1
Tunitskaya, V.L.2
Khandazhinskaya, A.L.3
Golubeva, N.A.4
Zakirova, N.F.5
Ivanov, A.V.6
Kukhanova, M.K.7
Kochetkov, S.N.8
-
38
-
-
27744599638
-
-
b) M. K. Kukhanova, N. F. Zakirova, A, V. Ivanov, L. A. Alexandrova, M. V. Jasco, A. R. Khomutov, Biochem. Biophys Res Commun 2005, 338, 1335;
-
(2005)
Biochem. Biophys Res Commun
, vol.338
, pp. 1335
-
-
Kukhanova, M.K.1
Zakirova, N.F.2
Ivanov, A.V.3
Alexandrova, L.A.4
Jasco, M.V.5
Khomutov, A.R.6
-
39
-
-
0036217711
-
-
c) M.G. Rose, M. P. Farrell, J.C. Schmitz, Clin Colorectal Cancer 2002,1, 220.
-
(2002)
Clin Colorectal Cancer
, vol.1
, pp. 220
-
-
Rose, M.G.1
Farrell, M.P.2
Schmitz, J.C.3
-
40
-
-
71649102139
-
-
a) R. Peng, M. Li, D. Li, Coord. Chem. Rev. 2010, 254,1;
-
(2010)
Coord. Chem. Rev.
, vol.254
, pp. 1
-
-
Peng, R.1
Li, M.2
Li, D.3
-
41
-
-
27644535493
-
-
b) A. Grodzicki, I. Lakomska, P. Piszczek, I. Szymanska, E. Szlyk, Coord. Chem. Rev. 2005, 249, 2232;
-
(2005)
Coord. Chem. Rev.
, vol.249
, pp. 2232
-
-
Grodzicki, A.1
Lakomska, I.2
Piszczek, P.3
Szymanska, I.4
Szlyk, E.5
-
42
-
-
0001064610
-
-
c) D. M. Roundhill, R. P. Sperline, W. R Reaulieu, Coord. Chem. Rev. 1978, 26, 263.
-
(1978)
Coord. Chem. Rev.
, vol.26
, pp. 263
-
-
Roundhill, D.M.1
Sperline, R.P.2
Reaulieu, W.R.3
-
43
-
-
77956579277
-
-
2P(O)OH+ 2AcOH. However, the exact pathway for the formation of 3 is not clear
-
2P(O)OH+ 2AcOH. However, the exact pathway for the formation of 3 is not clear.
-
-
-
-
44
-
-
77956575610
-
-
CCDC 777312 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
-
CCDC 777312 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc. cam.ac.uk/data-request/cit.
-
-
-
-
45
-
-
77249138324
-
-
a) A. S. Filatov, O. Hietsoi, Y. Sevryugina, N. N. Gerasimchuk, M. A. Petrukhina, Inorg. Chem. 2010, 49, 1626;
-
(2010)
Inorg. Chem.
, vol.49
, pp. 1626
-
-
Filatov, A.S.1
Hietsoi, O.2
Sevryugina, Y.3
Gerasimchuk, N.N.4
Petrukhina, M.A.5
-
47
-
-
77956587304
-
-
a) S. Sculfort, P. Croizat, A. Messaoudi, M. Benard, M. M. Rohmer, R. Welter, P. Braunstein, Angew. Chem. 2009, 121, 9843;
-
(2009)
Angew. Chem.
, vol.121
, pp. 9843
-
-
Sculfort, S.1
Croizat, P.2
Messaoudi, A.3
Benard, M.4
Rohmer, M.M.5
Welter, R.6
Braunstein, P.7
-
50
-
-
77956579527
-
-
2→1 + 2 Cu(OAc) + 2 AcOH
-
2→1 + 2 Cu(OAc) + 2 AcOH.
-
-
-
-
51
-
-
77956567714
-
-
For details of the experiments, see the Supporting Information. A separate experiment using isolated la showed that compound la is stable under the reaction conditions for the formation of 2a, indicating that 2a was not formed by further oxidation of 1a
-
For details of the experiments, see the Supporting Information. A separate experiment using isolated la showed that compound la is stable under the reaction conditions for the formation of 2a, indicating that 2a was not formed by further oxidation of 1a.
-
-
-
-
52
-
-
0034852386
-
-
a) A. G. Pokrovsky, T. R. Pronayeva, N. V. Fedyuk, E. A. Shirokova, A. L. Khandazhinskaya, N. B. Tarusova, I. L. Karpenko, A. A. Krayevsky, Nucleosides Nucleotides Nucleic Acids 2001, 20, 767;
-
(2001)
Nucleosides Nucleotides Nucleic Acids
, vol.20
, pp. 767
-
-
Pokrovsky, A.G.1
Pronayeva, T.R.2
Fedyuk, N.V.3
Shirokova, E.A.4
Khandazhinskaya, A.L.5
Tarusova, N.B.6
Karpenko, I.L.7
Krayevsky, A.A.8
-
56
-
-
0000414557
-
-
c) J. Iqbal, B. Bhatia, N. K. Nayyar, Chem. Rev. 1994, 94, 519;
-
(1994)
Chem. Rev.
, vol.94
, pp. 519
-
-
Iqbal, J.1
Bhatia, B.2
Nayyar, N.K.3
-
58
-
-
61349164417
-
-
Cu-catalyzed oxidative couplings are of high interest, but their mechanisms are not well understood
-
Cu-catalyzed oxidative couplings are of high interest, but their mechanisms are not well understood: a) K. Kamata, S. Yamaguchi, M. Kotani, K. Yamaguchi, N. Mizuno, Angew. Chem. 2008, 120, 2441;
-
(2008)
Angew. Chem.
, vol.120
, pp. 2441
-
-
Kamata, K.1
Yamaguchi, S.2
Kotani, M.3
Yamaguchi, K.4
Mizuno, N.5
-
60
-
-
33544463640
-
-
b) P. Siemsen, R. C. Livingston, F. Diederich, Angew. Chem. Int. Ed. 2000, 39, 2633;
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 2633
-
-
Siemsen, P.1
Livingston, R.C.2
Diederich, F.3
-
61
-
-
77950411612
-
-
c) Y. Wei, H. Q. Zhao, J. Kan, W. P. Su, M. C. Hong, J. Am. Chem. Soc 2010, 132, 2522;
-
(2010)
J. Am. Chem. Soc
, vol.132
, pp. 2522
-
-
Wei, Y.1
Zhao, H.Q.2
Kan, J.3
Su, W.P.4
Hong, M.C.5
-
63
-
-
38349095933
-
-
e) T. Hamada, X. Ye, & S. Stahl, J. Am. Chem. Soc. 2008, 130, 833;
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 833
-
-
Hamada, T.1
Ye, X.2
Stahl, S.3
-
64
-
-
67650528785
-
-
f) Y. X. Gao, G. Wang, L. Chen, P. X. Xu, Y. F. Zhao, Y. H. Zhou, L.-B. Han, J. Am. Chem Soc 2009, 131, 7956.
-
(2009)
J. Am. Chem Soc
, vol.131
, pp. 7956
-
-
Gao, Y.X.1
Wang, G.2
Chen, L.3
Xu, P.X.4
Zhao, Y.F.5
Zhou, Y.H.6
Han, L.-B.7
|