Process for the preparation of pyridine-2, 3-dicarboxylic acids

作者: George W. Matcham , Randall A. Roehl , David I. Stirling

DOI:

关键词: MetalDecarboxylationIonic strengthMuconic acidAmine gas treatingPyridineChemistryOrganic chemistryPrimary (chemistry)AmmoniaPolymer chemistry

摘要: Pyridine-2,3-dicarboxylic acids are prepared by the action of 2,3-dihydroxybenzoate-3,4-dioxygenase on 2,3-dihydroxybenzoic in a liquid medium which lacks active decarboxylase and has pH from 4 to 9, an ionic strength below about 1 molar, low concentration metal cations complex anions. In close temporal proximity, the 2-hydroxy-3-carboxy­ muconic acid semialdehyde forms is allowed react with source ammonia or primary amine, avoiding substantial decarboxylation.

参考文章(5)
Alan Fersht, Enzyme structure and mechanism ,(1977)
D.W. Ribbons, P.J. Senior, 2,3-Dihydroxybenzoate 3,4-oxygenase from Pseudomonas fluorescens—Oxidation of a substrate analog Archives of Biochemistry and Biophysics. ,vol. 138, pp. 557- 565 ,(1970) , 10.1016/0003-9861(70)90381-4
Jih-Han Hsieh, Sol J. Barer, Peter C. Maxwell, Muconic acid productivity by a stabilized mutant microorganism population ,(1983)