ACTIVATION OF CARBON-DIOXIDE - NICKEL-CATALYZED ELECTROCHEMICAL CARBOXYLATION OF DIYNES

被引:56
作者
DERIEN, S
CLINET, JC
DUNACH, E
PERICHON, J
机构
[1] LAB ELECTROCHIM CATALYSE & SYNTHESE ORGAN,CNRS,F-94320 THIAIS,FRANCE
[2] UNIV PARIS 11,INST CHIM MOLEC,F-91405 ORSAY,FRANCE
关键词
D O I
10.1021/jo00061a038
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The simultaneous activation of carbon dioxide and diynes by electrogenerated LNi(0) complexes (L = bpy, pentamethyldiethylenetriamine: PMDTA) enables the selective incorporation of one molecule of CO2 into the unsaturated systems and the preparative-scale electrosyntheses of carboxylic acids. A series of nonconjugated diynes afforded selectively linear or cyclic adducts depending on the ligand. Diynes bearing both a terminal and an internal triple bond gave exclusive CO2 incorporation into the terminal alkynyl group, regioselectively at the 2-position. The electrocarboxylation of 1,3-diynes with the Ni-PMDTA catalytic system yielded, regio- and stereoselectively, (E)-2-vinylidene-3-yne carboxylic acids in one step. The electrosyntheses were carried out in single-compartment cells fitted with a consumable magnesium anode, and utilized a catalytic amount of an air-stable Ni(II) complex as the catalyst precursor. Cyclic voltammetry studies revealed that both carbon dioxide and the diynes are able to coordinate to LNi(0)-generated species in DMF.
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页码:2578 / 2588
页数:11
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