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<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Mol. Biosci.</journal-id>
<journal-title>Frontiers in Molecular Biosciences</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Mol. Biosci.</abbrev-journal-title>
<issn pub-type="epub">2296-889X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1504226</article-id>
<article-id pub-id-type="doi">10.3389/fmolb.2024.1504226</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Molecular Biosciences</subject>
<subj-group>
<subject>Correction</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Corrigendum: A sulfuryl group transfer strategy to selectively prepare sulfated steroids and isotopically labelled derivatives</article-title>
<alt-title alt-title-type="left-running-head">Alshehri et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmolb.2024.1504226">10.3389/fmolb.2024.1504226</ext-link>
</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Alshehri</surname>
<given-names>Jaber A.</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/1479740/overview"/>
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<contrib contrib-type="author">
<name>
<surname>Gill</surname>
<given-names>Daniel M.</given-names>
</name>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Jones</surname>
<given-names>Alan M.</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/1420686/overview"/>
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<aff>
<institution>Molecular Synthesis Laboratory</institution>, <institution>School of Pharmacy</institution>, <institution>Institute of Clinical Sciences</institution>, <institution>University of Birmingham</institution>, <addr-line>Edgbaston</addr-line>, <country>United Kingdom</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited and reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/246647/overview">Gra&#xe7;a Soveral</ext-link>, University of Lisbon, Portugal</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Alan M. Jones, <email>a.m.jones.2@bham.ac.uk</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>19</day>
<month>12</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>11</volume>
<elocation-id>1504226</elocation-id>
<history>
<date date-type="received">
<day>30</day>
<month>09</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>25</day>
<month>11</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Alshehri, Gill and Jones.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Alshehri, Gill and Jones</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
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<related-article id="RA1" related-article-type="corrected-article" journal-id="Front. Mol. Biosci." journal-id-type="nlm-ta" xlink:href="10.3389/fmolb.2021.776900" ext-link-type="doi">A Corrigendum on <article-title>A sulfuryl group transfer strategy to selectively prepare sulfated steroids and isotopically labelled derivatives</article-title> by Alshehri JA, Gill DM and Jones AM (2021). Front. Mol. Biosci. 8:776900. doi: <object-id>10.3389/fmolb.2021.776900</object-id>
</related-article>
<kwd-group>
<kwd>sulfation</kwd>
<kwd>selectivity</kwd>
<kwd>isotopic labelling</kwd>
<kwd>sulfuryl transfer</kwd>
<kwd>TBSAB</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Cellular Biochemistry</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>In the published article, there was an error in <xref ref-type="scheme" rid="sch2">Scheme 2</xref> as published. The stereogenic center in compounds 9-11 was incorrectly depicted. The corrected <xref ref-type="scheme" rid="sch2">Scheme 2</xref> and its caption appear below.</p>
<fig id="sch2" position="float">
<label>SCHEME 2</label>
<caption>
<p>Sulfation of the pregnenolone (6) and pregnendiol (9) steroids.</p>
</caption>
<graphic xlink:href="FMOLB_fmolb-2024-1504226_wc_sch2.tif"/>
</fig>
<p>In the published article, there was an error in <bold>Supplementary Data Sheet 1</bold>, section Compound characterisation. The name of the fourth compound was incorrectly captured as &#x201c;Pregnanediol or (3S,8S,9S,10R,13S,14S,17S)-17-((S)-1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol (<bold>9</bold>).&#x201d;</p>
<p>The correct name appears below:</p>
<p>&#x201c;Pregnanediol or (3<italic>S</italic>,8<italic>S</italic>,9<italic>S</italic>,10<italic>R</italic>,13S,14<italic>S</italic>,17<italic>S</italic>)-17-((<italic>R</italic>)-1-hydroxyethyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1<italic>H</italic>-cyclopenta[<italic>a</italic>]phenanthren-3-ol (<bold>9</bold>).&#x201d;</p>
<p>In the published article, there was an error in <bold>Supplementary Data Sheet 1</bold>, section Compound characterisation. The name of the fifth compound was incorrectly captured as &#x201c;Disodium-3,17-pregnanediol disulfate or sodium (<italic>S</italic>)-1-((3<italic>S</italic>,8<italic>S</italic>,9<italic>S</italic>,10<italic>R</italic>,13<italic>S</italic>,14<italic>S</italic>,17<italic>S</italic>)-10,13-dimethyl-3-(sulfonatooxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[<italic>a</italic>]phenanthren-17-yl)ethyl sulfate (<bold>11</bold>).&#x201d;</p>
<p>The correct name appears below:</p>
<p>&#x201c;Disodium-3,17-pregnanediol disulfate or sodium (3<italic>S</italic>,8<italic>S</italic>,9<italic>S</italic>,10<italic>R</italic>,13<italic>S</italic>,14<italic>S</italic>,17<italic>S</italic>)-10,13-dimethyl-17-((<italic>R</italic>)-1-(sulfonatooxy)ethyl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1<italic>H</italic>-cyclopenta[<italic>a</italic>]phenanthren-3-yl sulfate (<bold>11</bold>).&#x201d;</p>
<p>The authors apologize for these errors and state that these do not change the scientific conclusions of the article in any way. The original article has been updated.</p>
</body>
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<sec sec-type="disclaimer" id="s1">
<title>Publisher&#x2019;s note</title>
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