<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lin H</submitter><funding>National Natural Science Foundation of China</funding><funding>Central University Basic Research Fund of China</funding><pagination>24232-24237</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9036638</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(39)</volume><pubmed_abstract>In this study, we found a green method to obtain aryl nitriles from aromatic aldehyde in water. This simple process was modified from a conventional method. Compared with those approaches, we used water as the solvent instead of harmful chemical reagents. In this one-pot conversion, we got twenty-five aryl nitriles conveniently with pollution to the environment being minimized. Furthermore, we confirmed the reaction mechanism by capturing the intermediates, aldoximes.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment.</pubmed_title><pmcid>PMC9036638</pmcid><funding_grant_id>21702100</funding_grant_id><funding_grant_id>21907051</funding_grant_id><funding_grant_id>U1903201</funding_grant_id><funding_grant_id>020814380151</funding_grant_id><funding_grant_id>020814380140</funding_grant_id><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Qi J</pubmed_authors><pubmed_authors>Ma X</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Han H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>One pot synthesis of aryl nitriles from aromatic aldehydes in a water environment.</name><description>In this study, we found a green method to obtain aryl nitriles from aromatic aldehyde in water. This simple process was modified from a conventional method. Compared with those approaches, we used water as the solvent instead of harmful chemical reagents. In this one-pot conversion, we got twenty-five aryl nitriles conveniently with pollution to the environment being minimized. Furthermore, we confirmed the reaction mechanism by capturing the intermediates, aldoximes.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2025-04-19T12:59:37.294Z</modification><creation>2025-04-19T12:59:37.294Z</creation></dates><accession>S-EPMC9036638</accession><cross_references><pubmed>35479036</pubmed><doi>10.1039/d1ra03559b</doi></cross_references></HashMap>