Investigation of additive effects in enantioselective copper-catalysed C-H insertion and aromatic addition reactions of α-diazocarbonyl compounds
Data(s) |
16/08/2016
16/08/2016
01/01/2012
08/01/2013
|
---|---|
Resumo |
Significant enhancements in enantioselectivities and reaction efficiencies in asymmetric copper-catalysed C-H insertion and aromatic addition reactions of α-diazocarbonyl compounds in the presence of various group I salts are reported. For the first time in carbenoid chemistry, evidence for the critical role of the metal cation is described. |
Formato |
application/pdf |
Identificador |
Slattery, C. N., Clarke, L. A., O'Neill, S., Ring, A., Ford, A. and Maguire, A. R. (2012) 'Investigation of additive effects in enantioselective copper-catalysed C-H insertion and aromatic addition reactions of α-diazocarbonyl compounds', Synlett, 23(5), pp. 765-767. DOI: 10.1055/s-0031-1290598 23 5 765 767 0936-5214 1437-2096 http://hdl.handle.net/10468/2997 10.1055/s-0031-1290598 Synlett D62911ST |
Idioma(s) |
en |
Publicador |
Georg Thieme Verlag |
Direitos |
© Georg Thieme Verlag Stuttgart · New York |
Palavras-Chave | #C-H insertion #Buchner reaction #Diazocarbonyl #Copper catalysis #Bis(oxazoline) ligands #Carbene insertion #Bonds #Complexes |
Tipo |
Article (peer-reviewed) |