184839-63-2Relevant academic research and scientific papers
Annelation of aromatic oxo compounds
Karady, Sandor,Amato, Joseph S.,Reamer, Robert A.,Weinstock, Leonard M.
, p. 8277 - 8280 (2007/10/03)
The silyl enol ether of α-diazoacetoacetate is used for the annelation of aromatic oxo compounds. The method involves condensation with the oxo compound in the presence of TiCl4 followed by rhodium octanoate-catalyzed ring closure to afford fur
RHODIUM(II) ACETATE-CATALYZED REACTION OF ETHYL 2-DIAZO-3-OXOPENT-4-ENOATES: SIMPLE ROUTES TO 4-ARYL-2-HYDROXY-1-NAPHTHOATES AND β,γ-UNSATURATED ESTERS. THE DIANION OF ETHYL 4-(DIETHYLPHOSPHONO)ACETOACETATE AS A PROPIONATE EQUIVALENT
Taylor, Edward C.,Davies, Huw M. L.
, p. 5453 - 5456 (2007/10/02)
Rhodium(II) acetate-catalyzed decomposition of ethyl 2-diazo-3-oxopent-4-enoates results in the formation of either 4-aryl-2-hydroxy-naphthoates or β,γ-unsaturated esters.In the latter transformation, the dianion of 4-(diethylphosphono)acetoacetate functi
