<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Molander GA</submitter><funding>NCRR NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>PHS HHS</funding><pagination>5052-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3820111</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(19)</volume><pubmed_abstract>The synthesis of β,γ-alkynyl esters and amides using air-stable potassium alkynyltrifluoroborates as nucleophilic partners in a mild Suzuki-Miyaura cross-coupling reaction has been achieved. Propargyl esters and amides were obtained in high yields using a low catalyst loading, and the substrate scope of the reaction has been significantly improved over previous methods.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Pd-catalyzed alkynylation of 2-chloroacetates and 2-chloroacetamides with potassium alkynyltrifluoroborates.</pubmed_title><pmcid>PMC3820111</pmcid><funding_grant_id>R01 GM035249</funding_grant_id><funding_grant_id>S10 RR016640</funding_grant_id><funding_grant_id>R01 035249</funding_grant_id><pubmed_authors>Traister KM</pubmed_authors><pubmed_authors>Molander GA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pd-catalyzed alkynylation of 2-chloroacetates and 2-chloroacetamides with potassium alkynyltrifluoroborates.</name><description>The synthesis of β,γ-alkynyl esters and amides using air-stable potassium alkynyltrifluoroborates as nucleophilic partners in a mild Suzuki-Miyaura cross-coupling reaction has been achieved. Propargyl esters and amides were obtained in high yields using a low catalyst loading, and the substrate scope of the reaction has been significantly improved over previous methods.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Oct</publication><modification>2025-04-04T07:25:02.298Z</modification><creation>2019-03-27T03:08:11Z</creation></dates><accession>S-EPMC3820111</accession><cross_references><pubmed>24040828</pubmed><doi>10.1021/ol402391z</doi></cross_references></HashMap>