Issue 9, 1990

Stereoselective formation of malefic acid diester from two diazo acetic acid esters on a Raney nickel surface. Evidence for dipod-chemisorbed carbenes

Abstract

The N2 elimination from diazo acetic acid esters, heterogeneously catalysed by Raney Nickel, yields as chemidesorbed main product up to 93% malefic acid diester, cis-stereoselectivity is observed and additional methyl/ethyl ester crossing experiments provide evidence for dipod-chemisorbed surface carbene intermediates.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 690-692

Stereoselective formation of malefic acid diester from two diazo acetic acid esters on a Raney nickel surface. Evidence for dipod-chemisorbed carbenes

H. Bock and H. P. Wolf, J. Chem. Soc., Chem. Commun., 1990, 690 DOI: 10.1039/C39900000690

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