{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["13(4)"],"submitter":["Liao S"],"pubmed_abstract":["A simple, efficient and mild methodology for the synthesis of 1,3,2-benzodiazaborininones [R-B(aam)] from boronic acids and anthranilamides on ethyl acetate is described. A series of 1,3,2-benzodiazaborininones were prepared in moderate to excellent yields at room temperature without dehydrating agents, metal catalysts, corrosive acids or other additives. Meanwhile, a multi-gram scale reaction is also performed to ensure the scalability of the reaction, and the product can be conveniently isolated by simple filtration."],"journal":["RSC advances"],"pagination":["2570-2573"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9847347"],"repository":["biostudies-literature"],"pubmed_title":["A rapid construction of 1,3,2-benzodiazaborininones [R-B(aam)] from boronic acids and anthranilamides."],"pmcid":["PMC9847347"],"pubmed_authors":["Li Y","Liu K","Kuang Q","Lu H","Hu X","Liao S","Yuan J","Wu H"],"additional_accession":[]},"is_claimable":false,"name":"A rapid construction of 1,3,2-benzodiazaborininones [R-B(aam)] from boronic acids and anthranilamides.","description":"A simple, efficient and mild methodology for the synthesis of 1,3,2-benzodiazaborininones [R-B(aam)] from boronic acids and anthranilamides on ethyl acetate is described. A series of 1,3,2-benzodiazaborininones were prepared in moderate to excellent yields at room temperature without dehydrating agents, metal catalysts, corrosive acids or other additives. Meanwhile, a multi-gram scale reaction is also performed to ensure the scalability of the reaction, and the product can be conveniently isolated by simple filtration.","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Jan","modification":"2025-04-05T13:31:10.546Z","creation":"2025-04-05T13:31:10.546Z"},"accession":"S-EPMC9847347","cross_references":{"pubmed":["36741161"],"doi":["10.1039/d2ra06573h"]}}