Investigation of additive effects in enantioselective copper-catalysed C-H insertion and aromatic addition reactions of α-diazocarbonyl compounds


Autoria(s): Slattery, Catherine N.; Clarke, Leslie-Ann; O'Neill, Shane T.; Ring, Aoife; Ford, Alan; Maguire, Anita R.
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)