{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Tian Y"],"funding":["National Natural Science Foundation of China","Hubei Provincial Natural Science Foundation of China"],"pagination":["3341"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10140953"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["28(8)"],"pubmed_abstract":["A highly regioselective reaction of 2-indolylmethanols with enamides has been developed at room temperature by using AlCl<sub>3</sub> as a catalyst. A wide range of hybrids (40 examples) of indoles and enamides were obtained in moderate to good yields (up to 98% yield). This transformation represents the efficient way to introduce biologically important indoles and enamides skeleton into structurally complex hybrids."],"journal":["Molecules (Basel, Switzerland)"],"pubmed_title":["Regioselective Reaction of 2-Indolylmethanols with Enamides."],"pmcid":["PMC10140953"],"funding_grant_id":["81973208, 52173279","2019CFB624"],"pubmed_authors":["Liu X","Zou Y","Liang E","Zheng Y","He D","Wang Q","Tian Y","Gao L"],"additional_accession":[]},"is_claimable":false,"name":"Regioselective Reaction of 2-Indolylmethanols with Enamides.","description":"A highly regioselective reaction of 2-indolylmethanols with enamides has been developed at room temperature by using AlCl<sub>3</sub> as a catalyst. A wide range of hybrids (40 examples) of indoles and enamides were obtained in moderate to good yields (up to 98% yield). This transformation represents the efficient way to introduce biologically important indoles and enamides skeleton into structurally complex hybrids.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Apr","modification":"2025-05-18T13:25:56.911Z","creation":"2024-10-18T18:32:18.136Z"},"accession":"S-EPMC10140953","cross_references":{"pubmed":["37110576"],"doi":["10.3390/molecules28083341"]}}