A vicarious, one-pot synthesis of benzo- and naphthofurans: Applications to the syntheses of stereumene B and paeoveitols was written by Rashid, Showkat;Bhat, Bilal A.;Mehta, Goverdhan. And the article was included in Tetrahedron Letters in 2019.Reference of 52010-89-6 The following contents are mentioned in the article:
An interesting albeit unexpected deviation during attempted Tanabe γ-lactone annulation on 4-hydroxycyclohexanones has led to a general, one-pot synthesis of benzofurans and naphtho[2,3-b]furans from readily assembled precursors. The utility of this adaptable methodol. has been demonstrated through concise syntheses of natural products, stereumene B, paeoveitol D and (±)-paeoveitol. This study involved multiple reactions and reactants, such as 2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6Reference of 52010-89-6).
2,5-Dihydroxy-4-methylbenzaldehyde (cas: 52010-89-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Reference of 52010-89-6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts