{"database":"biostudies-other","file_versions":[],"scores":null,"additional":{"submitter":["Molander GA"],"funding":["NCRR NIH HHS","NIGMS NIH HHS"],"pagination":["9198-202"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2515367"],"abstract":["[reaction: see text] The palladium-catalyzed cross-coupling of potassium aryltrifluoroborates with benzylic halides occurs in good yield with high functional group tolerance. The increased stability of potassium aryltrifluoroborates compared to other boron coupling partners makes this an effective route to functionalized methylene-linked biaryl systems."],"repository":["biostudies-other"],"data_source":["Europe PMC"],"omics_type":["Unknown"],"volume":["71(24)"],"journal":["The Journal of organic chemistry"],"pmcid":["PMC2515367"],"funding_grant_id":["R01 GM035249","R01 GM035249-22","GM35249","S10 RR016640","S10 RR016640-01"],"pubmed_authors":["Elia MD","Molander GA"],"additional_accession":[]},"is_claimable":false,"name":"Suzuki-Miyaura cross-coupling reactions of benzyl halides with potassium aryltrifluoroborates.","description":"[reaction: see text] The palladium-catalyzed cross-coupling of potassium aryltrifluoroborates with benzylic halides occurs in good yield with high functional group tolerance. The increased stability of potassium aryltrifluoroborates compared to other boron coupling partners makes this an effective route to functionalized methylene-linked biaryl systems.","dates":{"release":"2006-01-01T00:00:00Z","publication":"2006 Nov","modification":"2019-03-26T23:28:27Z","creation":"2019-03-26T23:28:27Z"},"accession":"S-EPMC2515367","cross_references":{"pubmed":["17109547"],"doi":["10.1021/jo061699f "]}}