4749-70-6Relevant articles and documents
Stereoselective Formation of Maleic Acid Diester from Two Diazo Acetic Acid Esters on a Raney Nickel Surface. Evidence for Dipod-chemisorbed Carbenes
Bock, Hans,Wolf, Hans Peter
, p. 690 - 692 (1990)
The N2 elimination from diazo acetic acid esters, heterogeneously catalysed by Raney Nickel, yields as chemidesorbed main product up to 93percent maleic acid diester, cis-stereoselectivity is observed and additional methyl/ethyl ester crossing experiments provide evidence for dipod-chemisorbed surface carbene intermediates.
Cyclopropanation Catalysed by RuCl2(PPh3)3 and OsCl2(PPh3)3
Demonceau, A.,Lemoine, C. A.,Noels, A. F.,Chizhevsky, I. T.,Sorokin, P.V.
, p. 8419 - 8422 (2007/10/02)
OsCl2(PPh3)3 is a cyclopropanation catalyst using ethyl diazoacetate with a variety of activated alkenes; OsCl2(PPh3)3 is however less active than RuCl2(PPh3)3 for the decomposition of the diazo reagent and the subsequent cyclopropanation.