{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T13:22:18Z","timestamp":1788355338755,"version":"build-2803163510"},"reference-count":29,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-017"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-012"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-004"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Analytica Chimica Acta"],"published-print":{"date-parts":[[2023,10]]},"DOI":"10.1016\/j.aca.2023.341811","type":"journal-article","created":{"date-parts":[[2023,9,11]],"date-time":"2023-09-11T05:33:00Z","timestamp":1694410380000},"page":"341811","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"special_numbering":"C","title":["Virtual chiral recognition of eugenol derivatives on amylose tris(3-chloro-5-methylphenylcarbamate) chiral stationary phase in unusual normal-phase mode"],"prefix":"10.1016","volume":"1279","author":[{"ORCID":"https:\/\/orcid.org\/0009-0004-7284-8366","authenticated-orcid":false,"given":"Gaia","family":"Pulitelli","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Francesca Romana","family":"Mammone","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0808-7644","authenticated-orcid":false,"given":"Daniele","family":"Sadutto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Damiano","family":"Tanini","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roberto","family":"Cirilli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.aca.2023.341811_bib1","doi-asserted-by":"crossref","DOI":"10.1016\/j.trac.2019.115709","article-title":"Recent trends in preparation, investigation and application of polysaccharide-based chiral stationary phases for separation of enantiomers in high-performance liquid chromatography","volume":"122","author":"Chankvetadze","year":"2020","journal-title":"Trends Anal. Chem."},{"key":"10.1016\/j.aca.2023.341811_bib2","doi-asserted-by":"crossref","first-page":"6077","DOI":"10.1021\/cr8005558","article-title":"Structure control of polysaccharide derivatives for efficient separation of enantiomers by chromatography","volume":"109","author":"Ikai","year":"2009","journal-title":"Chem. Rev."},{"key":"10.1016\/j.aca.2023.341811_bib3","doi-asserted-by":"crossref","DOI":"10.1016\/j.trac.2019.115639","article-title":"Chiral recognition in separation sciences. Part I: polysaccharide and cyclodextrin selectors","volume":"120","author":"Scriba","year":"2019","journal-title":"TrAC, Trends Anal. Chem."},{"key":"10.1016\/j.aca.2023.341811_bib4","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2021.462085","article-title":"Evaluation of a polysaccharide-based chiral reversed-phase liquid chromatography screen strategy in pharmaceutical analysis","volume":"1645","author":"Lin","year":"2021","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib5","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/0021-9673(94)00729-S","article-title":"Dimethyl-, dichloro- and chloromethylphenylcarbamates of amylose as chiral stationary phases for high-performance liquid chromatography","volume":"694","author":"Chankvetadze","year":"1995","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib6","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2020.461244","article-title":"Method screening strategies of stereoisomers of compounds with multiple chiral centers and a single chiral center","volume":"1624","author":"Lin","year":"2020","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib7","first-page":"320","article-title":"Multimodal HPLC screening of polysaccharide-based chiral stationary phases","volume":"20","author":"Huybrechts","year":"2007","journal-title":"LC-GC Eur."},{"key":"10.1016\/j.aca.2023.341811_bib8","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2021.461878","article-title":"Chiral chromatography method screening strategies: past, present and future","volume":"1638","author":"Tarafder","year":"2021","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib9","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1016\/S0021-9673(97)00648-1","article-title":"3-Fluoro-, 3-chloro- and 3-bromo-5-methylphenylcarbamates of cellulose and amylose as chiral stationary phases for high-performance liquid chromatographic enantioseparation","volume":"787","author":"Chankvetadze","year":"1997","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib10","doi-asserted-by":"crossref","first-page":"194e205","DOI":"10.1016\/j.aca.2020.10.050","article-title":"The molecular bases of chiral recognition in 2-(benzylsulfinyl)benzamide enantioseparation","volume":"1141","author":"Peluso","year":"2021","journal-title":"Anal. Chim. Acta"},{"key":"10.1016\/j.aca.2023.341811_bib11","doi-asserted-by":"crossref","first-page":"39","DOI":"10.1016\/0021-9673(94)80278-5","article-title":"Chloromethylphenylcarbamate derivatives of cellulose as chiral stationary phases for high-performance liquid chromatography","volume":"670","author":"Chankvetadze","year":"1994","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib12","author":"Cantatore","year":"2022","journal-title":"Sep. Sci. plus"},{"key":"10.1016\/j.aca.2023.341811_bib13","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1002\/cber.19901230432","volume":"123","author":"Hopf","year":"1990","journal-title":"Chem. Ber."},{"key":"10.1016\/j.aca.2023.341811_bib14","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1016\/j.chroma.2017.11.049","article-title":"Enantioselective separation of racemates using CHIRALPAK IG amylose-based chiral stationary phase under normal standard, non-standard and reversed phase high performance liquid chromatography","volume":"1532","author":"Ghanem","year":"2018","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib15","doi-asserted-by":"crossref","DOI":"10.1016\/j.aca.2022.339880","article-title":"ON\/OFF receptor-like enantioseparation of planar chiral 1,2-ferrocenes on an amylose-based chiral stationary phase: the role played by 2-propanol","volume":"1211","author":"Cantatore","year":"2022","journal-title":"Anal. Chim. Acta"},{"key":"10.1016\/j.aca.2023.341811_bib16","doi-asserted-by":"crossref","first-page":"3569","DOI":"10.1080\/00268976.2019.1647360","article-title":"Molecular dynamics simulations of the chiral recognition mechanism for a polysaccharide chiral stationary phase in enantiomeric chromatographic separations","volume":"117","author":"Wang","year":"2019","journal-title":"Mol. Phys."},{"key":"10.1016\/j.aca.2023.341811_bib17","doi-asserted-by":"crossref","first-page":"5877","DOI":"10.1021\/ac034714e","volume":"75","author":"Wang","year":"2003","journal-title":"Anal. Chem."},{"key":"10.1016\/j.aca.2023.341811_bib18","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1016\/j.chroma.2016.07.034","article-title":"3-(Phenyl-4-oxy)-5-phenyl-4,5-dihydro-(1H)-pyrazole: a fascinating molecular framework to study the enantioseparation ability of the amylose (3,5-dimethylphenylcarbamate) chiral stationary phase. Part I. Structure-enantioselectivity relationships","volume":"1467","author":"Carradori","year":"2016","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib19","doi-asserted-by":"crossref","first-page":"140","DOI":"10.1016\/j.chroma.2017.04.001","article-title":"3-(Phenyl-4-oxy)-5-phenyl- 4,5-dihydro-(1H)-pyrazole: a fascinating molecular framework to study the enantioseparation ability of the amylose (3,5-dimethylphenylcarbamate) chiral stationary phase. Part II. Solvophobic effects in enantiorecognition process","volume":"1499","author":"Pierini","year":"2017","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib20","article-title":"Enantioseparation of new axially chiral carboxylic acids on polysaccharide-based chiral stationary phases under normal phase elution conditions","volume":"1","author":"Sechi","year":"2023","journal-title":"J. Pharm. Biomed. Anal."},{"key":"10.1016\/j.aca.2023.341811_bib21","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2019.460445","article-title":"Separation of enantiomers of chiral sulfoxides in high-performanceliquid chromatography with cellulose-based chiral selectors usingacetonitrile and acetonitrile-water mixtures as mobile phases","volume":"1609","author":"Shedania","year":"2020","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib22","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1016\/j.chroma.2017.11.037","article-title":"A chromatographic study on the exceptional chiral recognition of 2-(benzylsulfinyl)benzamide by an immobilized-type chiral stationary phase based on cellulose tris(3,5-dichlorophenylcarbamate)","volume":"1531","author":"Carradori","year":"2018","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib23","doi-asserted-by":"crossref","first-page":"649","DOI":"10.1021\/ci200592h","article-title":"Computer-aided molecular design of asymmetric pyrazole derivatives with exceptional enantioselective recognition toward the Chiralcel OJ-H stationary phase","volume":"52","author":"Alcaro","year":"2012","journal-title":"J. Chem. Inf. Model."},{"key":"10.1016\/j.aca.2023.341811_bib24","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1016\/j.jpha.2019.04.002","article-title":"Temperature and eluent composition effects on enantiomer separation of carvedilol by high-performance liquid chromatography on immobilized amylose-based chiral stationary phases","volume":"9","author":"Panella","year":"2019","journal-title":"J. Pharm. Anal."},{"key":"10.1016\/j.aca.2023.341811_bib25","doi-asserted-by":"crossref","first-page":"6554e6560","DOI":"10.1016\/j.chroma.2011.06.068","article-title":"Enantiomer elution order reversal of fluorenylmethoxycarbonyl-isoleucine in high-performance liquid chromatography by changing the mobile phase temperature and composition","volume":"1218","author":"Chankvetadze","year":"2011","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib26","doi-asserted-by":"crossref","first-page":"228","DOI":"10.1016\/j.chroma.2019.05.026","article-title":"Chromatographic and thermodynamic comparison of amylosetris(3-chloro-5-methylphenylcarbamate) coated or covalentlyimmobilized on silica in high-performance liquid chromatographicseparation of the enantiomers of select chiral weak acids","volume":"1602","author":"Maisuradze","year":"2019","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib27","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1016\/S0021-9673(96)00888-6","article-title":"Description and prediction of retention in normal-phase high-performance liquid chromatography with binary and ternary mobile phases","volume":"762","author":"Jandera","year":"1997","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib28","doi-asserted-by":"crossref","DOI":"10.1016\/j.chroma.2023.464161","article-title":"Exploitation of the enantioselectivity space of coated amylose tris(3,5-dimethylphenylcarbamate) in mixtures of 2-propanol and acetonitrile","volume":"1705","author":"Horv\u00e1th","year":"2023","journal-title":"J. Chromatogr. A"},{"key":"10.1016\/j.aca.2023.341811_bib29","doi-asserted-by":"crossref","first-page":"309","DOI":"10.1016\/j.chroma.2007.12.032","article-title":"Apparent and true enntioselectivity of single- and binary-selector chiral stationary phases in gas chromatography","volume":"1184","author":"Levkin","year":"2008","journal-title":"J. Chromatogr. A"}],"container-title":["Analytica Chimica Acta"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003267023010322?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0003267023010322?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,12]],"date-time":"2025-09-12T20:06:56Z","timestamp":1757707616000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0003267023010322"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,10]]},"references-count":29,"alternative-id":["S0003267023010322"],"URL":"https:\/\/doi.org\/10.1016\/j.aca.2023.341811","relation":{},"ISSN":["0003-2670"],"issn-type":[{"value":"0003-2670","type":"print"}],"subject":[],"published":{"date-parts":[[2023,10]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Virtual chiral recognition of eugenol derivatives on amylose tris(3-chloro-5-methylphenylcarbamate) chiral stationary phase in unusual normal-phase mode","name":"articletitle","label":"Article Title"},{"value":"Analytica Chimica Acta","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.aca.2023.341811","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2023 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}],"article-number":"341811"}}