<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Duarte de Almeida L</submitter><funding>European Research Council</funding><pagination>4177-4181</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8519145</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>363(17)</volume><pubmed_abstract>Several manganese-PNP pincer catalysts for the formal hydroamination of allylic alcohols are presented. The resulting γ-amino alcohols are selectively obtained in high yields applying &lt;b>Mn-1&lt;/b> in a tandem process under mild conditions.</pubmed_abstract><journal>Advanced synthesis &amp; catalysis</journal><pubmed_title>Catalytic Formal Hydroamination of Allylic Alcohols Using Manganese PNP-Pincer Complexes.</pubmed_title><pmcid>PMC8519145</pmcid><funding_grant_id>NoNaCat 670986</funding_grant_id><funding_grant_id>670986</funding_grant_id><pubmed_authors>Beller M</pubmed_authors><pubmed_authors>Duarte de Almeida L</pubmed_authors><pubmed_authors>Bourriquen F</pubmed_authors><pubmed_authors>Junge K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Catalytic Formal Hydroamination of Allylic Alcohols Using Manganese PNP-Pincer Complexes.</name><description>Several manganese-PNP pincer catalysts for the formal hydroamination of allylic alcohols are presented. The resulting γ-amino alcohols are selectively obtained in high yields applying &lt;b>Mn-1&lt;/b> in a tandem process under mild conditions.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2025-05-18T12:29:57.503Z</modification><creation>2025-05-18T12:29:57.503Z</creation></dates><accession>S-EPMC8519145</accession><cross_references><pubmed>34690626</pubmed><doi>10.1002/adsc.202100081</doi></cross_references></HashMap>