Find in Library
Search millions of books, articles, and more
Indexed Open Access Databases
Dearomatization of 3-Aminophenols for Synthesis of Spiro[chromane-3,1′-cyclohexane]-2′,4′-dien-6′-ones via Hydride Transfer Strategy-Enabled [5+1] Annulations
oleh: Jia-Cheng Ge, Yufeng Wang, Feng-Wei Guo, Xiangyun Kong, Fangzhi Hu, Shuai-Shuai Li
Format: | Article |
---|---|
Diterbitkan: | MDPI AG 2024-02-01 |
Deskripsi
The Sc(OTf)<sub>3</sub>-catalyzed dearomative [5+1] annulations between readily available 3-aminophenols and <i>O</i>-alkyl <i>ortho</i>-oxybenzaldehydes were developed for synthesis of spiro[chromane-3,1′-cyclohexane]-2′,4′-dien-6′-ones. The “two-birds-with-one-stone” strategy was disclosed by the dearomatization of phenols and direct α-C(sp<sup>3</sup>)–H bond functionalization of oxygen through cascade condensation/[1,5]-hydride transfer/dearomative-cyclization process. In addition, the antifungal activity assay and derivatizations of products were conducted to further enrich the utility of the structure.