In 2018,Chemical Communications (Cambridge, United Kingdom) included an article by Fieser, Megan E.; Schimler, Sydonie D.; Mitchell, Lauren A.; Wilborn, Emily G.; John, Alex; Hogan, Levi T.; Benson, Brooke; LaPointe, Anne M.; Tolman, William B.. Application In Synthesis of 2-(2-Hydroxyethyl)pyridine. The article was titled 《Dual-catalytic decarbonylation of fatty acid methyl esters to form olefins》. The information in the text is summarized as follows:
The homogeneous dehydrative decarbonylation of fatty acid Me esters (FAMEs) to form olefins was reported. In order to facilitate cleavage of the unactivated acyl C-O bond of the alkyl ester, a one pot dual-catalytic directing group strategy was developed through optimization of the individual transesterification and decarbonylation reaction steps. The experimental part of the paper was very detailed, including the reaction process of 2-(2-Hydroxyethyl)pyridine(cas: 103-74-2Application In Synthesis of 2-(2-Hydroxyethyl)pyridine)
2-(2-Hydroxyethyl)pyridine(cas: 103-74-2) belongs to pyridine. Pyridine derivatives lend themselves to many roles in the spirited field of supramolecular chemistry – whether as the ligand backbone of metal-organic polymers or presiding over the key electronic stations of nanodevices. In biochemistry, pyridine-containing cofactors are necessary nutrients on which our lives depend. Application In Synthesis of 2-(2-Hydroxyethyl)pyridine