{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,15]],"date-time":"2026-09-15T03:02:47Z","timestamp":1789441367935,"version":"build-2803163510"},"reference-count":26,"publisher":"Wiley","issue":"9","license":[{"start":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T00:00:00Z","timestamp":1788998400000},"content-version":"vor","delay-in-days":9,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"},{"start":{"date-parts":[[2026,9,1]],"date-time":"2026-09-01T00:00:00Z","timestamp":1788220800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chirality"],"published-print":{"date-parts":[[2026,9]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>\n                    The ability of\n                    <jats:italic>threo<\/jats:italic>\n                    \u20102\u2010amino\u20101,2\u2010diphenylethanol (\n                    <jats:bold>1t<\/jats:bold>\n                    ) as a resolving agent for the enantioseparation of carboxylic acids via diastereomeric salt formation was investigated. Although (\u2212)\u2010\n                    <jats:bold>1t<\/jats:bold>\n                    was not applicable to the enantioseparation of racemic 2\u2010arylalkanoic acids and mandelic acid, enantiomers of tropic acid and 2\u2010halomandelic acids were efficiently separated by salt formation with (\u2212)\u2010\n                    <jats:bold>1t<\/jats:bold>\n                    . This resolving ability was complementary to that of the corresponding\n                    <jats:italic>erythro<\/jats:italic>\n                    \u2010isomer (\n                    <jats:bold>1e<\/jats:bold>\n                    ). The hydrogen\u2010bonding patterns and molecular packing mode of the less\u2010soluble diastereomeric salts of (\u2212)\u2010\n                    <jats:bold>1t<\/jats:bold>\n                    were revealed based on the crystallographic analysis.\n                  <\/jats:p>","DOI":"10.1002\/chir.70149","type":"journal-article","created":{"date-parts":[[2026,9,11]],"date-time":"2026-09-11T00:31:02Z","timestamp":1789086662000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Application of\n                    <i>threo<\/i>\n                    \u20102\u2010amino\u20101,2\u2010diphenylethanol as a Resolving Agent for Racemic Carboxylic Acids via Diastereomeric Salt Formation"],"prefix":"10.1002","volume":"38","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8567-9360","authenticated-orcid":false,"given":"Koichi","family":"Kodama","sequence":"first","affiliation":[{"name":"Graduate School of Science and Engineering Saitama University  Saitama Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kosei","family":"Katayama","sequence":"additional","affiliation":[{"name":"Graduate School of Science and Engineering Saitama University  Saitama Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4121-0963","authenticated-orcid":false,"given":"Takuji","family":"Hirose","sequence":"additional","affiliation":[{"name":"Graduate School of Science and Engineering Saitama University  Saitama 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