<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(42)</volume><submitter>Zhang Y</submitter><pubmed_abstract>A Cu-bis(sulfonamide)-diamine complex catalytic system was exploited in asymmetric Henry reactions to construct versatile chiral nitroalcohols with high enantioselectivity from carbamate-acetaldehydes and nitromethane. This elegant approach was further implemented to complete the asymmetric total syntheses of a series of oxazolidone skeleton drugs, such as linezolid (antibiotic) and rivaroxaban (anti-coagulant), in a concise and efficient way.</pubmed_abstract><journal>RSC advances</journal><pagination>35292-35295</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12459656</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cu-diamine ligand-controlled asymmetric Henry reactions and their application in concise total syntheses of linezolid and rivaroxaban.</pubmed_title><pmcid>PMC12459656</pmcid><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cu-diamine ligand-controlled asymmetric Henry reactions and their application in concise total syntheses of linezolid and rivaroxaban.</name><description>A Cu-bis(sulfonamide)-diamine complex catalytic system was exploited in asymmetric Henry reactions to construct versatile chiral nitroalcohols with high enantioselectivity from carbamate-acetaldehydes and nitromethane. This elegant approach was further implemented to complete the asymmetric total syntheses of a series of oxazolidone skeleton drugs, such as linezolid (antibiotic) and rivaroxaban (anti-coagulant), in a concise and efficient way.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T20:18:36.016Z</modification><creation>2026-05-01T03:10:35.952Z</creation></dates><accession>S-EPMC12459656</accession><cross_references><pubmed>41000610</pubmed><doi>10.1039/d5ra05795g</doi></cross_references></HashMap>