{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ralph G"],"funding":["Division of Chemistry","City College of New York","National Institute of General Medical Sciences","NIGMS NIH HHS"],"pagination":["3912-3915"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8021098"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["38(20)"],"pubmed_abstract":["We report the preparation of enantioenriched secondary alkylcarbastannatranes via a stereoinvertive S<sub>N</sub>2 reaction of enantioenriched alkyl mesylates and carbastannatranyl anion equivalents. Using this process, enantioenriched secondary alcohols may be converted into highly enantioenriched alkylcarbastannatranes, which are useful in stereospecific cross-coupling reactions."],"journal":["Organometallics"],"pubmed_title":["Preparation of Enantioenriched Alkylcarbastannatranes via Nucleophilic Inversion of Alkyl Mesylates for Use in Stereospecific Cross-Coupling Reactions."],"pmcid":["PMC8021098"],"funding_grant_id":["CHE-1665189","R01GM131079","R01 GM131079"],"pubmed_authors":["Ralph G","Biscoe MR"],"additional_accession":[]},"is_claimable":false,"name":"Preparation of Enantioenriched Alkylcarbastannatranes via Nucleophilic Inversion of Alkyl Mesylates for Use in Stereospecific Cross-Coupling Reactions.","description":"We report the preparation of enantioenriched secondary alkylcarbastannatranes via a stereoinvertive S<sub>N</sub>2 reaction of enantioenriched alkyl mesylates and carbastannatranyl anion equivalents. Using this process, enantioenriched secondary alcohols may be converted into highly enantioenriched alkylcarbastannatranes, which are useful in stereospecific cross-coupling reactions.","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 Oct","modification":"2025-04-04T14:55:27.281Z","creation":"2022-02-09T14:16:49.778Z"},"accession":"S-EPMC8021098","cross_references":{"pubmed":["33824546"],"doi":["10.1021/acs.organomet.9b00467"]}}