{"database":"biostudies-literature","file_versions":[],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":45,"searchCount":0},"additional":{"submitter":["Sam B"],"funding":["NIGMS NIH HHS"],"pagination":["3790-3"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3779475"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(14)"],"pubmed_abstract":["Trifluoromethyl substituted allenes engage in ruthenium catalyzed reductive couplings with paraformaldehyde to form products of hydrohydroxymethylation as single regioisomers. This method enables generation of CF3-bearing all-carbon quaternary stereocenters."],"journal":["Organic letters"],"pubmed_title":["Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers."],"pmcid":["PMC3779475"],"funding_grant_id":["R01 GM069445"],"pubmed_authors":["Krische MJ","Montgomery TP","Sam B"],"view_count":["45"],"additional_accession":[]},"is_claimable":false,"name":"Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers.","description":"Trifluoromethyl substituted allenes engage in ruthenium catalyzed reductive couplings with paraformaldehyde to form products of hydrohydroxymethylation as single regioisomers. This method enables generation of CF3-bearing all-carbon quaternary stereocenters.","dates":{"release":"2013-01-01T00:00:00Z","publication":"2013 Jul","modification":"2020-10-29T11:45:51Z","creation":"2019-03-27T01:16:23Z"},"accession":"S-EPMC3779475","cross_references":{"pubmed":["23841678"],"doi":["10.1021/ol401771a"]}}