<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Feng WJ</submitter><funding>Natural Science Foundation of Anhui Province (Anhui Provincial Natural Science Foundation)</funding><funding>Natural Science Foundation of Anhui Province</funding><funding>Youth Innovation Promotion Association of the Chinese Academy of Sciences (Youth Innovation Promotion Association CAS)</funding><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><funding>Youth Innovation Promotion Association of the Chinese Academy of Sciences</funding><pagination>2390</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11893763</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Deuterium labeling has found extensive applications across various research fields, including organic synthesis, drug design, and molecular imaging. Electrocatalytic semi-hydrogenation of alkynes offers a viable route for the synthesis of Z-alkenes, yet it falls short in achieving the semi-deuteration of these compounds. In this study, we report an electrochemical cobalt-catalyzed transfer deuteration reaction that proficiently accomplishes the semi-deuteration of alkynes, yielding Z-configuration deuterated alkene products. This reaction utilizes cost-effective cobalt salts as catalysts and employs D&lt;sub>2&lt;/sub>O and AcOD (acetic acid-d) as economical and efficient deuterium sources, underscoring its practicality and feasibility. The reaction demonstrates a broad alkyne substrate scope, h</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Electrochemical cobalt-catalyzed semi-deuteration of alkynes to access deuterated Z-alkenes.</pubmed_title><pmcid>PMC11893763</pmcid><funding_grant_id>22371273</funding_grant_id><funding_grant_id>22293011, T2341001</funding_grant_id><funding_grant_id>2208085J26</funding_grant_id><funding_grant_id>2023476</funding_grant_id><pubmed_authors>Feng WJ</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Fu Y</pubmed_authors><pubmed_authors>Chang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical cobalt-catalyzed semi-deuteration of alkynes to access deuterated Z-alkenes.</name><description>Deuterium labeling has found extensive applications across various research fields, including organic synthesis, drug design, and molecular imaging. Electrocatalytic semi-hydrogenation of alkynes offers a viable route for the synthesis of Z-alkenes, yet it falls short in achieving the semi-deuteration of these compounds. In this study, we report an electrochemical cobalt-catalyzed transfer deuteration reaction that proficiently accomplishes the semi-deuteration of alkynes, yielding Z-configuration deuterated alkene products. This reaction utilizes cost-effective cobalt salts as catalysts and employs D&lt;sub>2&lt;/sub>O and AcOD (acetic acid-d) as economical and efficient deuterium sources, underscoring its practicality and feasibility. The reaction demonstrates a broad alkyne substrate scope, h</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-04T02:54:21.343Z</modification><creation>2025-04-04T02:54:21.343Z</creation></dates><accession>S-EPMC11893763</accession><cross_references><pubmed>40064911</pubmed><doi>10.1038/s41467-025-57782-x</doi></cross_references></HashMap>