99463-13-5Relevant academic research and scientific papers
Pd-Catalysed Decarbonylation Free Approach to Carbonylative Esterification of 5-HMF to Its Aryl Esters Synthesis Using Aryl Halides and Oxalic Acid as C1 Source
Singh Chauhan, Arvind,Kumar, Ajay,Kumar Sharma, Ajay,Das, Pralay
, p. 12971 - 12975 (2021)
A decarbonylation free, polystyrene-supported, Pd (Pd@PS)-catalysed carbonylative esterification of the hydroxy group of 5-hydroxymethyl furfural (5-HMF) to its corresponding aryl esters has been developed. The use of Pd@PS, oxalic acid as CO source, and aryl halides was first explored for the aryl ester of 5-HMF synthesis. Here, we investigated the vital role of a polystyrene support to avoid the commonly known decarbonylation of 5-HMF. The reaction exhibits vast substrate scope with comparably good yield and catalyst recyclability.
Synthesis of Some Furfural and Syringic Acid Derivatives
Jogia, Madhu K.,Vakamoce, Veikila,Weavers, Rex T.
, p. 1009 - 1016 (2007/10/02)
The formation of several derivatives of furfural and syringic acid, including some incorporating both components, is described.Assignments of the 1H and 13C n.m.r. spectra are also included.
