<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ramachandran PV</submitter><funding>Herbert C. Brown Center for Borane Research</funding><pagination>268</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10780903</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>Borane-pyridine acts as an efficient (5 mol%) liquid catalyst, providing improved solubility for the direct amidation of a wide range of aromatic and aliphatic carboxylic acids and amines to form secondary and tertiary carboxamides. Tolerance of potentially incompatible halo, nitro, and alkene functionalities has been demonstrated.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Borane-Pyridine: An Efficient Catalyst for Direct Amidation.</pubmed_title><pmcid>PMC10780903</pmcid><funding_grant_id>N/A</funding_grant_id><pubmed_authors>Ramachandran PV</pubmed_authors><pubmed_authors>Singh A</pubmed_authors><pubmed_authors>Hamann HJ</pubmed_authors><pubmed_authors>Walker H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Borane-Pyridine: An Efficient Catalyst for Direct Amidation.</name><description>Borane-pyridine acts as an efficient (5 mol%) liquid catalyst, providing improved solubility for the direct amidation of a wide range of aromatic and aliphatic carboxylic acids and amines to form secondary and tertiary carboxamides. Tolerance of potentially incompatible halo, nitro, and alkene functionalities has been demonstrated.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-22T10:37:58.44Z</modification><creation>2025-04-05T23:39:10.477Z</creation></dates><accession>S-EPMC10780903</accession><cross_references><pubmed>38202849</pubmed><doi>10.3390/molecules29010268</doi></cross_references></HashMap>