<?xml version="1.0" encoding="UTF-8"?>
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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.2174/1570178614666171121144234</dc:identifier><dc:language>eng</dc:language><dc:creator>Merino, P.</dc:creator><dc:creator>Tejero, T.</dc:creator><dc:creator>Delso, I.</dc:creator><dc:creator>Juste, V.</dc:creator><dc:creator>Pedron, M.</dc:creator><dc:creator>Orta, S.</dc:creator><dc:creator>Matute, R.</dc:creator><dc:title>Direct Hydroxymethylation of C=N Double Bonds</dc:title><dc:identifier>ART-2018-105854</dc:identifier><dc:description>Direct hydroxymethylation of C=N double bonds including imines, nitrones, oximes, hydrazones and iminium salts is a less explored synthetic approach to 1, 2-amino alcohols that provides good alternatives to the classical methods. The review deals with nucleophilic additions of organometallic hydroxymethyl reagents and lithiated alkoxyallenes to C=N double bonds. Reductive cross couplings between C=N double bonds and aldehydes or ketones are also discussed.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/163905</dc:source><dc:doi>10.2174/1570178614666171121144234</dc:doi><dc:identifier>http://zaguan.unizar.es/record/163905</dc:identifier><dc:identifier>oai:zaguan.unizar.es:163905</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E10</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2016-76155-R</dc:relation><dc:identifier.citation>LETTERS IN ORGANIC CHEMISTRY 15, 5 (2018), 375-386</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights></dc:dc>

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