<?xml version="1.0" encoding="UTF-8"?>

<modsCollection xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://www.loc.gov/mods/v3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd">
<mods version="3.3">

<genre>article</genre>

<titleInfo><title>Unified synthesis of unconventional α-polyhalogenated amines through hydroaminoalkylation</title></titleInfo>


<note type="publicationStatus">epub_ahead</note>


<note type="qualityControlled">yes</note>

<name type="personal">
  <namePart type="given">Angela K.</namePart>
  <namePart type="family">Hofmeister</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Giulia</namePart>
  <namePart type="family">Iannelli</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Péter</namePart>
  <namePart type="family">Angyal</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Augustin</namePart>
  <namePart type="family">Malandain</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Daniel</namePart>
  <namePart type="family">Kaiser</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Boris</namePart>
  <namePart type="family">Maryasin</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Hanspeter</namePart>
  <namePart type="family">Kählig</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>
<name type="personal">
  <namePart type="given">Matteo</namePart>
  <namePart type="family">Barel</namePart>
  <role><roleTerm type="text">author</roleTerm> </role><identifier type="local">8959927b-2236-11ed-bd6e-ea83d94ade0e</identifier></name>
<name type="personal">
  <namePart type="given">Gaia</namePart>
  <namePart type="family">Novarino</namePart>
  <role><roleTerm type="text">author</roleTerm> </role><identifier type="local">3E57A680-F248-11E8-B48F-1D18A9856A87</identifier><description xsi:type="identifierDefinition" type="orcid">0000-0002-7673-7178</description></name>
<name type="personal">
  <namePart type="given">Nuno</namePart>
  <namePart type="family">Maulide</namePart>
  <role><roleTerm type="text">author</roleTerm> </role></name>







<name type="corporate">
  <namePart></namePart>
  <identifier type="local">GaNo</identifier>
  <role>
    <roleTerm type="text">department</roleTerm>
  </role>
</name>

<name type="corporate">
  <namePart></namePart>
  <identifier type="local">GradSch</identifier>
  <role>
    <roleTerm type="text">department</roleTerm>
  </role>
</name>








<abstract lang="eng">We report a unified method for the synthesis of α-polyhalomethyl amines from alkenes and alkynes, enabled by readily available hemiaminal reagents. This operationally simple transformation allows for the introduction of not only well-established CF3 and CF2H groups, but also the synthetically (and medicinally) underexplored CF2Cl and CFClH motifs—thereby broadening access to previously inaccessible chemical space of halogenated amine scaffolds. The method displays broad substrate scope and functional-group tolerance while operating under mild conditions. Late-stage functionalization of drug-like derivatives of Oxaprozin, Erlotinib, and Ibuprofen (among others) is reported.</abstract>

<originInfo><publisher>Wiley</publisher><dateIssued encoding="w3cdtf">2026</dateIssued>
</originInfo>
<language><languageTerm authority="iso639-2b" type="code">eng</languageTerm>
</language>



<relatedItem type="host"><titleInfo><title>Angewandte Chemie International Edition</title></titleInfo>
  <identifier type="issn">1433-7851</identifier>
  <identifier type="eIssn">1521-3773</identifier>
  <identifier type="MEDLINE">42429166</identifier><identifier type="doi">10.1002/anie.1233707</identifier>
<part>
</part>
</relatedItem>


<extension>
<bibliographicCitation>
<ieee>A. K. Hofmeister &lt;i&gt;et al.&lt;/i&gt;, “Unified synthesis of unconventional α-polyhalogenated amines through hydroaminoalkylation,” &lt;i&gt;Angewandte Chemie International Edition&lt;/i&gt;. Wiley, 2026.</ieee>
<chicago>Hofmeister, Angela K., Giulia Iannelli, Péter Angyal, Augustin Malandain, Daniel Kaiser, Boris Maryasin, Hanspeter Kählig, Matteo Barel, Gaia Novarino, and Nuno Maulide. “Unified Synthesis of Unconventional α-Polyhalogenated Amines through Hydroaminoalkylation.” &lt;i&gt;Angewandte Chemie International Edition&lt;/i&gt;. Wiley, 2026. &lt;a href=&quot;https://doi.org/10.1002/anie.1233707&quot;&gt;https://doi.org/10.1002/anie.1233707&lt;/a&gt;.</chicago>
<short>A.K. Hofmeister, G. Iannelli, P. Angyal, A. Malandain, D. Kaiser, B. Maryasin, H. Kählig, M. Barel, G. Novarino, N. Maulide, Angewandte Chemie International Edition (2026).</short>
<apa>Hofmeister, A. K., Iannelli, G., Angyal, P., Malandain, A., Kaiser, D., Maryasin, B., … Maulide, N. (2026). Unified synthesis of unconventional α-polyhalogenated amines through hydroaminoalkylation. &lt;i&gt;Angewandte Chemie International Edition&lt;/i&gt;. Wiley. &lt;a href=&quot;https://doi.org/10.1002/anie.1233707&quot;&gt;https://doi.org/10.1002/anie.1233707&lt;/a&gt;</apa>
<ista>Hofmeister AK, Iannelli G, Angyal P, Malandain A, Kaiser D, Maryasin B, Kählig H, Barel M, Novarino G, Maulide N. 2026. Unified synthesis of unconventional α-polyhalogenated amines through hydroaminoalkylation. Angewandte Chemie International Edition., e1233707.</ista>
<ama>Hofmeister AK, Iannelli G, Angyal P, et al. Unified synthesis of unconventional α-polyhalogenated amines through hydroaminoalkylation. &lt;i&gt;Angewandte Chemie International Edition&lt;/i&gt;. 2026. doi:&lt;a href=&quot;https://doi.org/10.1002/anie.1233707&quot;&gt;10.1002/anie.1233707&lt;/a&gt;</ama>
<mla>Hofmeister, Angela K., et al. “Unified Synthesis of Unconventional α-Polyhalogenated Amines through Hydroaminoalkylation.” &lt;i&gt;Angewandte Chemie International Edition&lt;/i&gt;, e1233707, Wiley, 2026, doi:&lt;a href=&quot;https://doi.org/10.1002/anie.1233707&quot;&gt;10.1002/anie.1233707&lt;/a&gt;.</mla>
</bibliographicCitation>
</extension>
<recordInfo><recordIdentifier>22370</recordIdentifier><recordCreationDate encoding="w3cdtf">2026-07-19T22:01:48Z</recordCreationDate><recordChangeDate encoding="w3cdtf">2026-07-21T07:19:26Z</recordChangeDate>
</recordInfo>
</mods>
</modsCollection>
