-
3
-
-
27444440607
-
-
Laschat, S.; Becheanu, A.; Bell, T.; Baro, A. Synlett 2005, 2547
-
(2005)
Synlett
, pp. 2547
-
-
Laschat, S.1
Becheanu, A.2
Bell, T.3
Baro, A.4
-
5
-
-
0012759546
-
-
In;, Eds.; Thieme: Stuttgart,; Vol. 1, p
-
Malacria, M.; Aubert, C.; Renaud, J. L. In Science of Synthesis: Houben-Weyl Methods of Molecular Transformations; Lautens, M.; Trost, B. M., Eds.; Thieme: Stuttgart, 2001; Vol. 1, p 439.
-
(2001)
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations
, pp. 439
-
-
Malacria, M.1
Aubert, C.2
Renaud, J.L.3
Lautens, M.4
Trost, B.M.5
-
8
-
-
0000463815
-
-
Ojima, I.; Tzamarioudaki, M.; Li, Z.; Donovan, R. J. Chem. Rev. 1996, 96, 635
-
(1996)
Chem. Rev.
, vol.96
, pp. 635
-
-
Ojima, I.1
Tzamarioudaki, M.2
Li, Z.3
Donovan, R.J.4
-
9
-
-
0002110351
-
-
Lautens, M.; Klute, W.; Tam, W. Chem. Rev. 1996, 96, 49
-
(1996)
Chem. Rev.
, vol.96
, pp. 49
-
-
Lautens, M.1
Klute, W.2
Tam, W.3
-
11
-
-
78049491294
-
-
Kersten, L.; Roesner, S.; Hilt, G. Org. Lett. 2010, 12, 4920
-
(2010)
Org. Lett.
, vol.12
, pp. 4920
-
-
Kersten, L.1
Roesner, S.2
Hilt, G.3
-
12
-
-
77955166413
-
-
Arndt, M.; Reinhold, A.; Hilt, G. J. Org. Chem. 2010, 75, 5203
-
(2010)
J. Org. Chem.
, vol.75
, pp. 5203
-
-
Arndt, M.1
Reinhold, A.2
Hilt, G.3
-
15
-
-
36148991424
-
-
Hilt, G.; Treutwein, J. Angew. Chem., Int. Ed. 2007, 46, 8500
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 8500
-
-
Hilt, G.1
Treutwein, J.2
-
16
-
-
77950224100
-
-
Hilt, G.; Paul, A.; Treutwein, J. Org. Lett. 2010, 12, 1536
-
(2010)
Org. Lett.
, vol.12
, pp. 1536
-
-
Hilt, G.1
Paul, A.2
Treutwein, J.3
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17
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78651518861
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2(dppp)] = cobalt(1,2-bis(diphenylphosphino)propane) dibromide
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2(dppp)] = cobalt(1,2-bis(diphenylphosphino)propane) dibromide.
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18
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78651495821
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2(dppe)] = cobalt(1,2-bis(diphenylphosphino)ethane) dibromide
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2(dppe)] = cobalt(1,2-bis(diphenylphosphino)ethane) dibromide.
-
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19
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78651498587
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When terminal alkynes were used the cyclotrimerization of the alkynes to the corresponding 1,2,4-trisubstituted benzene derivatives became the predominent reaction pathway, see
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When terminal alkynes were used the cyclotrimerization of the alkynes to the corresponding 1,2,4-trisubstituted benzene derivatives became the predominent reaction pathway, see
-
-
-
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22
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27644487954
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Hilt, G.; Hess, W.; Vogler, T.; Hengst, C. J. Organomet. Chem. 2005, 690, 5170
-
(2005)
J. Organomet. Chem.
, vol.690
, pp. 5170
-
-
Hilt, G.1
Hess, W.2
Vogler, T.3
Hengst, C.4
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23
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78651484088
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For cobalt-catalyzed reactions involving borylated partners, see
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For cobalt-catalyzed reactions involving borylated partners, see
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24
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34547371164
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Geny, A.; Leboef, D.; Rouquié, G.; Vollhardt, K. P. C.; Malacria, M.; Gandon, V.; Aubert, C. Chem.-Eur. J. 2007, 13, 5408
-
(2007)
Chem.-Eur. J.
, vol.13
, pp. 5408
-
-
Geny, A.1
Leboef, D.2
Rouquié, G.3
Vollhardt, K.P.C.4
Malacria, M.5
Gandon, V.6
Aubert, C.7
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25
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77955126518
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-
Leboef, D.; Iannazzo, L.; Geny, A.; Malacria, M.; Vollhardt, K. P. C.; Aubert, C.; Gandon, V. Chem.-Eur. J. 2010, 16, 8904
-
(2010)
Chem.-Eur. J.
, vol.16
, pp. 8904
-
-
Leboef, D.1
Iannazzo, L.2
Geny, A.3
Malacria, M.4
Vollhardt, K.P.C.5
Aubert, C.6
Gandon, V.7
-
26
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69149096020
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Reddipalli, G.; Venkataiah, M.; Mishra, M. K.; Fadnavis, N. W. Tetrahedron: Asymmetry 2009, 20, 1802
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1802
-
-
Reddipalli, G.1
Venkataiah, M.2
Mishra, M.K.3
Fadnavis, N.W.4
-
28
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58049194312
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-
Tortosa, M.; Yakelis, N. A.; Roush, W. R. J. Org. Chem. 2008, 73, 9657
-
(2008)
J. Org. Chem.
, vol.73
, pp. 9657
-
-
Tortosa, M.1
Yakelis, N.A.2
Roush, W.R.3
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29
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77953001833
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For a recent reference, see
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For a recent reference, see: Auvinet, A.-L.; Harrity, J. P. A.; Hilt, G. J. Org. Chem. 2010, 75, 3893
-
(2010)
J. Org. Chem.
, vol.75
, pp. 3893
-
-
Auvinet, A.-L.1
Harrity, J.P.A.2
Hilt, G.3
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30
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78651491901
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The crystal structure has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 798849
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The crystal structure has been deposited at the Cambridge Crystallographic Data Centre and allocated the deposition number CCDC 798849.
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