Answers are grounded in this paper and cite their sources.
The combination of a urea catalyst and an α-nitro-α-diazo ester gives rise to a reactive species able to undergo insertion into the N-H bonds of anilines. This new strategy to achieve N-H insertion reactivity is in contrast to typical metal-catalyzed conditions for the generation of carbenoids from α-diazocarbonyl compounds. This report includes the extension of the insertion reaction to a three-component coupling for the construction of α-amino-α-aryl esters in high yield.
No takes yet. Share an insight, caveat, or question.
So et al. (2012) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: