{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ramachandran PV"],"funding":["Herbert C. Brown Center for Borane Research"],"pagination":["268"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10780903"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["29(1)"],"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."],"journal":["Molecules (Basel, Switzerland)"],"pubmed_title":["Borane-Pyridine: An Efficient Catalyst for Direct Amidation."],"pmcid":["PMC10780903"],"funding_grant_id":["N/A"],"pubmed_authors":["Ramachandran PV","Singh A","Hamann HJ","Walker H"],"additional_accession":[]},"is_claimable":false,"name":"Borane-Pyridine: An Efficient Catalyst for Direct Amidation.","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.","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jan","modification":"2025-04-22T10:37:58.44Z","creation":"2025-04-05T23:39:10.477Z"},"accession":"S-EPMC10780903","cross_references":{"pubmed":["38202849"],"doi":["10.3390/molecules29010268"]}}