Wu, Xiao-Feng published the artcileA General and Efficient Palladium-Catalyzed Alkoxycarbonylation of Phenols To Form Esters through In Situ Formed Aryl Nonaflates, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol, the publication is Chemistry – A European Journal (2012), 18(13), 3831-3834, S3831/1-S3831/27, database is CAplus and MEDLINE.
A novel process for the palladium catalyzed alkoxycarbonylation of phenols is presented. Activation of the phenols occurs via convenient in situ generation of aryl nonaflates. Electron-withdrawing or electron-donating substituents on the aryl or ester moiety are tolerated amongst the varied functional groups. Notably, not only homoesterification, but also cross-coupling of two different phenols (alcs.) are possible under these conditions.
Chemistry – A European Journal published new progress about 23351-09-9. 23351-09-9 belongs to alcohols-buliding-blocks, auxiliary class Pyrrole,Benzene,Alcohol, name is 4-(1H-Pyrrol-1-yl)phenol, and the molecular formula is C22H18O2, Recommanded Product: 4-(1H-Pyrrol-1-yl)phenol.
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