{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Cheng G"],"funding":["NIGMS NIH HHS"],"pagination":["4545-8"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2596068"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["8(20)"],"pubmed_abstract":["The high facioselectivity in the epoxidation of 4-deoxypentenosides (4-DPs) by dimethyldioxirane (DMDO) correlates with a stereoelectronic bias in the 4-DPs' ground-state conformations, as elucidated by polarized-pi frontier molecular orbital (PPFMO) analysis."],"journal":["Organic letters"],"pubmed_title":["Stereoselective epoxidation of 4-deoxypentenosides: a polarized-pi model."],"pmcid":["PMC2596068"],"funding_grant_id":["R01 GM069862","GM-06982-01","R01 GM069862-04"],"pubmed_authors":["Wenthold PG","Wei A","Shi Q","Cheng G","Boulineau FP","Liew ST"],"additional_accession":[]},"is_claimable":false,"name":"Stereoselective epoxidation of 4-deoxypentenosides: a polarized-pi model.","description":"The high facioselectivity in the epoxidation of 4-deoxypentenosides (4-DPs) by dimethyldioxirane (DMDO) correlates with a stereoelectronic bias in the 4-DPs' ground-state conformations, as elucidated by polarized-pi frontier molecular orbital (PPFMO) analysis.","dates":{"release":"2006-01-01T00:00:00Z","publication":"2006 Sep","modification":"2020-11-01T08:15:40Z","creation":"2019-03-27T00:19:38Z"},"accession":"S-EPMC2596068","cross_references":{"pubmed":["16986946"],"doi":["10.1021/ol0617401"]}}