{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Truong P"],"funding":["NIGMS NIH HHS"],"pagination":["2093-2096"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3080702"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["52(17)"],"pubmed_abstract":["DMDO oxidation of functionalized α-diazo-β-ketoacetates, formed by zinc triflate catalyzed Mukaiyama-aldol condensation of methyl diazoacetoacetate with aldehydes, occurred in quantitative yield to form dihydrofuranols that undergo acid catalyzed dehydration under mild conditions to generate 3-methoxyfuran-2-carboxylates in good yield."],"journal":["Tetrahedron letters"],"pubmed_title":["An efficient methodology to substituted furans via oxidation of functionalized α-diazo-β-ketoacetates."],"pmcid":["PMC3080702"],"funding_grant_id":["R37 GM046503-18","R37 GM046503","R01 GM046503"],"pubmed_authors":["Doyle MP","Xu X","Truong P"],"additional_accession":[]},"is_claimable":false,"name":"An efficient methodology to substituted furans via oxidation of functionalized α-diazo-β-ketoacetates.","description":"DMDO oxidation of functionalized α-diazo-β-ketoacetates, formed by zinc triflate catalyzed Mukaiyama-aldol condensation of methyl diazoacetoacetate with aldehydes, occurred in quantitative yield to form dihydrofuranols that undergo acid catalyzed dehydration under mild conditions to generate 3-methoxyfuran-2-carboxylates in good yield.","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Apr","modification":"2025-04-25T21:45:08.736Z","creation":"2019-03-27T00:40:54Z"},"accession":"S-EPMC3080702","cross_references":{"pubmed":["21516185"],"doi":["10.1016/j.tetlet.2010.11.166"]}}