<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(24)</volume><submitter>Brol A</submitter><pubmed_abstract>Deamination of 1-aminoalkylphosphonic acids in the reaction with HNO&lt;sub>2&lt;/sub> (generated "in situ" from NaNO&lt;sub>2&lt;/sub>) yields a mixture of substitution products (1-hydroxyalkylphosphonic acids), elimination products (vinylphosphonic acid derivatives), rearrangement and substitution products (2-hydroxylkylphosphonic acids) as well as H&lt;sub>3&lt;/sub>PO&lt;sub>4&lt;/sub>. The variety of formed reaction products suggests that 1-phosphonoalkylium ions may be intermediates in such deamination reactions.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>8849</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9783495</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Deamination of 1-Aminoalkylphosphonic Acids: Reaction Intermediates and Selectivity.</pubmed_title><pmcid>PMC9783495</pmcid><pubmed_authors>Brol A</pubmed_authors><pubmed_authors>Olszewski TK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deamination of 1-Aminoalkylphosphonic Acids: Reaction Intermediates and Selectivity.</name><description>Deamination of 1-aminoalkylphosphonic acids in the reaction with HNO&lt;sub>2&lt;/sub> (generated "in situ" from NaNO&lt;sub>2&lt;/sub>) yields a mixture of substitution products (1-hydroxyalkylphosphonic acids), elimination products (vinylphosphonic acid derivatives), rearrangement and substitution products (2-hydroxylkylphosphonic acids) as well as H&lt;sub>3&lt;/sub>PO&lt;sub>4&lt;/sub>. The variety of formed reaction products suggests that 1-phosphonoalkylium ions may be intermediates in such deamination reactions.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-22T13:16:33.382Z</modification><creation>2025-04-06T00:39:05.914Z</creation></dates><accession>S-EPMC9783495</accession><cross_references><pubmed>36557979</pubmed><doi>10.3390/molecules27248849</doi></cross_references></HashMap>