<b>Chelation as a Driving Force in Organic Reactions. IV.<sup>1</sup> Synthesis of α-Nitro Acids by Control of the Carboxylation-Decarboxylation Equilibrium</b><sup>2</sup>
作者:Herman L. Finkbeiner、Martin. Stiles
DOI:10.1021/ja00888a031
日期:1963.3
Steinkopf; Supan, Chemische Berichte, 1910, vol. 43, p. 3249
作者:Steinkopf、Supan
DOI:——
日期:——
Synthesis of geminal dinitro compounds
申请人:The United States of America as represented by the Secretary of the Air
公开号:US04910322A1
公开(公告)日:1990-03-20
Geminal dinitro compounds are prepared by reacting an organic nitro compound having a replaceable hydrogen on the carbon to which the nitro group is attached with a source of nitrite ions in the presence of an oxidizing agent and a catalytic amount of an alkali metal ferricyanide.