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Lemonnier, G., Poisson, T., Couve-Bonnaire, S., Jubault, P., Pannecoucke, X., Eur. J. Org. Chem., 2013, 3278–3289.
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(2013)
Eur. J. Org. Chem.
, pp. 3278-3289
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Lemonnier, G.1
Poisson, T.2
Couve-Bonnaire, S.3
Jubault, P.4
Pannecoucke, X.5
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83
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84876710551
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Lemonnier, G., Poisson, T., Couve-Bonnaire, S., Pannecoucke, X., Tetrahedron Lett. 54 (2013), 2821–2824.
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(2013)
Tetrahedron Lett.
, vol.54
, pp. 2821-2824
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-
Lemonnier, G.1
Poisson, T.2
Couve-Bonnaire, S.3
Pannecoucke, X.4
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84
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-
85128621725
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The reaction did not proceed in the absence of base or copper salt.
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The reaction did not proceed in the absence of base or copper salt.
-
-
-
-
85
-
-
85128597867
-
-
In our previous communications regarding the introduction of the CF2CO2Et moiety with BrCF2CO2Et, both CuI and CuII salts were efficient, see ref.[6b–6d]
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In our previous communications regarding the introduction of the CF2CO2Et moiety with BrCF2CO2Et, both CuI and CuII salts were efficient, see ref.[6b–6d].
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-
-
-
86
-
-
85128611590
-
-
Bathophenanthroline, neocuproine, BINAP [2,2′-bis(diphenylphosphino)-1,1′-binaphthyl], dppe [1,2-bis(diphenylphosphino)ethane], and terpyridine were screened without improvement of the reaction yield.
-
Bathophenanthroline, neocuproine, BINAP [2,2′-bis(diphenylphosphino)-1,1′-binaphthyl], dppe [1,2-bis(diphenylphosphino)ethane], and terpyridine were screened without improvement of the reaction yield.
-
-
-
-
87
-
-
85128589845
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-
A similar trend has been previously observed, see ref.[8c]
-
A similar trend has been previously observed, see ref.[8c].
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