<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Han J</submitter><funding>National Natural Science Foundation of China</funding><pagination>E1828</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6539882</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(9)</volume><pubmed_abstract>This work discloses a new procedure for the resolution of commercially available racemic rimantadine hydrochloride to enantiomerically pure (S)-rimantadine using (R)-phenoxypropionic acid as a recyclable resolving reagent. Good chemical yields, operational ease, and low-cost structure underscore the preparative value of this method for the production of enantiomerically pure rimantadine for medicinal or synthetic studies.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Optical Resolution of Rimantadine.</pubmed_title><pmcid>PMC6539882</pmcid><funding_grant_id>21761132021 and 21606133</funding_grant_id><pubmed_authors>Izawa K</pubmed_authors><pubmed_authors>Sato T</pubmed_authors><pubmed_authors>Takeda R</pubmed_authors><pubmed_authors>Moriwaki H</pubmed_authors><pubmed_authors>Han J</pubmed_authors><pubmed_authors>Abe H</pubmed_authors><pubmed_authors>Soloshonok VA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optical Resolution of Rimantadine.</name><description>This work discloses a new procedure for the resolution of commercially available racemic rimantadine hydrochloride to enantiomerically pure (S)-rimantadine using (R)-phenoxypropionic acid as a recyclable resolving reagent. Good chemical yields, operational ease, and low-cost structure underscore the preparative value of this method for the production of enantiomerically pure rimantadine for medicinal or synthetic studies.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2025-04-04T09:36:08.493Z</modification><creation>2019-07-01T13:56:23Z</creation></dates><accession>S-EPMC6539882</accession><cross_references><pubmed>31083636</pubmed><doi>10.3390/molecules24091828</doi></cross_references></HashMap>