Tetrahedron

Efficient electrochemical dicarboxylations of arylacetylenes with carbon dioxide using nickel as the cathode

GQ Yuan, HF Jiang, C Lin

Index: Yuan, Gao-Qing; Jiang, Huan-Feng; Lin, Chang Tetrahedron, 2008 , vol. 64, # 25 p. 5866 - 5872

Full Text: HTML

Citation Number: 27

Abstract

The electrochemical dicarboxylation of arylacetylenes with carbon dioxide could be smoothly achieved in an undivided cell using Ni as the cathode and Al as the anode with n- Bu4NBr–DMF as the supporting electrolyte, at a constant current under CO2 pressure of 3MPa and room temperature in the absence of additional catalysts. The corresponding aryl- maleic anhydrides and 2-arylsuccinic acids were afforded in excellent total yields (82–94 ...

CuCl-catalyzed radical cyclisation of N-α-perchloroacyl-ketene-N, S-acetals: a new way to prepare disubstituted maleic anhydrides

[Cornia, Andrea; Felluga, Fulvia; Frenna, Vincenzo; Ghelfi, Franco; Parsons, Andrew F.; Pattarozzi, Mariella; Roncaglia, Fabrizio; Spinelli, Domenico Tetrahedron, 2012 , vol. 68, # 29 p. 5863 - 5881]

A simple, convenient method for the synthesis of maleic anhydrides from α-keto esters and alkanoic acid anhydrides using the TiCl 4/n-Bu 3 N reagent system

[Kishorebabu, Neela; Periasamy, Mariappan Tetrahedron Letters, 2006 , vol. 47, # 13 p. 2107 - 2109]

Heterocyclic Studies. VII. The Preparation and Reactions of 2-Amino-5-hydroxypyridines; the Formation of an Azaquinone1

[Moore; Marascia Journal of the American Chemical Society, 1959 , vol. 81, p. 6049,6053]

CuCl-catalyzed radical cyclisation of N-α-perchloroacyl-ketene-N, S-acetals: a new way to prepare disubstituted maleic anhydrides

Diaryl-substituted maleic anhydrides

[Fields, E. K.; Behrend, S. J.; Meyerson, S.; Winzenburg, M. L.; Ortega, B. R.; Hall, H. K. Journal of Organic Chemistry, 1990 , vol. 55, # 17 p. 5165 - 5170]

Efficient electrochemical dicarboxylations of arylacetylenes with carbon dioxide using nickel as the cathode

Abstract

Related Articles:

More Articles...