<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>45</viewCount><searchCount>0</searchCount></scores><additional><submitter>Sam B</submitter><funding>NIGMS NIH HHS</funding><pagination>3790-3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3779475</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(14)</volume><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.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers.</pubmed_title><pmcid>PMC3779475</pmcid><funding_grant_id>R01 GM069445</funding_grant_id><pubmed_authors>Krische MJ</pubmed_authors><pubmed_authors>Montgomery TP</pubmed_authors><pubmed_authors>Sam B</pubmed_authors><view_count>45</view_count></additional><is_claimable>false</is_claimable><name>Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers.</name><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.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Jul</publication><modification>2020-10-29T11:45:51Z</modification><creation>2019-03-27T01:16:23Z</creation></dates><accession>S-EPMC3779475</accession><cross_references><pubmed>23841678</pubmed><doi>10.1021/ol401771a</doi></cross_references></HashMap>