{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ortiz-Marciales M"],"funding":["NIGMS NIH HHS"],"pagination":["3447-9"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2811074"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["5(19)"],"pubmed_abstract":["[reaction: see text] Representative B-butyl- and B-methyl-1,3,2-oxazaborolidines derived from ephedrine and norephedrine were prepared in good yield and excellent purity by one-pot treatment of B-H oxazaborolidines with the corresponding organolithium reagent and subsequent hydrolysis of the cyclic borohydride intermediate with anhydrous ammonium chloride."],"journal":["Organic letters"],"pubmed_title":["Efficient synthesis of B-alkylated oxazaborolidines derived from ephedrine and norephedrine."],"pmcid":["PMC2811074"],"funding_grant_id":["GM59829","S06 GM008216-200016","R15 GM059829-01","GM08216","S06 GM008216"],"pubmed_authors":["Gonzalez E","Martinez J","Espinosa S","De Jesus M","Figueroa R","Ortiz-Marciales M","Correa W"],"additional_accession":[]},"is_claimable":false,"name":"Efficient synthesis of B-alkylated oxazaborolidines derived from ephedrine and norephedrine.","description":"[reaction: see text] Representative B-butyl- and B-methyl-1,3,2-oxazaborolidines derived from ephedrine and norephedrine were prepared in good yield and excellent purity by one-pot treatment of B-H oxazaborolidines with the corresponding organolithium reagent and subsequent hydrolysis of the cyclic borohydride intermediate with anhydrous ammonium chloride.","dates":{"release":"2003-01-01T00:00:00Z","publication":"2003 Sep","modification":"2025-04-05T11:31:36.083Z","creation":"2019-03-26T22:30:10Z"},"accession":"S-EPMC2811074","cross_references":{"pubmed":["12967296"],"doi":["10.1021/ol0352153"]}}