<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tong X</submitter><funding>Natural Science Foundation of Yunnan Province</funding><funding>National Natural Science Foundation of China</funding><funding>Natural Science Foundation of Yunnan Province (Yunnan Provincial Natural Science Foundation)</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>8985</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12511331</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>The streamlined dual-functional group transfer (streamlined dual-FGT) strategy represents an efficient and sustainable approach for difunctionalization reactions, where all atoms or functional groups from the starting materials are fully incorporated into the final products without generating by-products. Pyridine and nitrile functionalities are prevalent and highly valued structural motifs found in a myriad of natural products, pharmaceuticals, agrochemicals, and polymers. The simultaneous incorporation of these groups via the streamlined dual-FGT strategy is thus of considerable significance in synthetic chemistry. Herein, we report a regioselective pyridylcyanation of internal alkynes enabled by an oxalate-based photocatalytic system, employing cyanopyridine as a streamlined dual-functi</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Photocatalytic streamlined dual-functional group transfer from cyanopyridine to internal alkynes.</pubmed_title><pmcid>PMC12511331</pmcid><funding_grant_id>22371200</funding_grant_id><funding_grant_id>202201AT070205</funding_grant_id><funding_grant_id>21933005</funding_grant_id><funding_grant_id>22473014</funding_grant_id><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Jie J</pubmed_authors><pubmed_authors>Tong X</pubmed_authors><pubmed_authors>Ang HT</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Tian D</pubmed_authors><pubmed_authors>Yuan M</pubmed_authors><pubmed_authors>Su H</pubmed_authors><pubmed_authors>Yu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photocatalytic streamlined dual-functional group transfer from cyanopyridine to internal alkynes.</name><description>The streamlined dual-functional group transfer (streamlined dual-FGT) strategy represents an efficient and sustainable approach for difunctionalization reactions, where all atoms or functional groups from the starting materials are fully incorporated into the final products without generating by-products. Pyridine and nitrile functionalities are prevalent and highly valued structural motifs found in a myriad of natural products, pharmaceuticals, agrochemicals, and polymers. The simultaneous incorporation of these groups via the streamlined dual-FGT strategy is thus of considerable significance in synthetic chemistry. Herein, we report a regioselective pyridylcyanation of internal alkynes enabled by an oxalate-based photocatalytic system, employing cyanopyridine as a streamlined dual-functi</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-04T07:41:24.012Z</modification><creation>2026-06-01T03:06:28.698Z</creation></dates><accession>S-EPMC12511331</accession><cross_references><pubmed>41068130</pubmed><doi>10.1038/s41467-025-64029-2</doi></cross_references></HashMap>