{"database":"biostudies-literature","file_versions":[],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":46,"searchCount":0},"additional":{"submitter":["Tarselli MA"],"funding":["NIGMS NIH HHS"],"pagination":["4596-9"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2818175"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(20)"],"pubmed_abstract":["A procedure for the coupling of aliphatic imines with allylic and allenic alkoxides is described. The success of these studies was enabled by a unique reactivity profile of Ti(IV) isopropoxide/n-BuLi compared to well-known Ti(IV) isopropoxide/RMgX systems."],"journal":["Organic letters"],"pubmed_title":["Aliphatic imines in titanium-mediated reductive cross-coupling: unique reactivity of Ti(O-i-Pr)4/n-BuLi."],"pmcid":["PMC2818175"],"funding_grant_id":["R01 GM080266-01","R01 GM080266","R01 GM080266-03","R01 GM080266-02","R01 GM080266-04","R01 GM080266-04S1","GM80266"],"pubmed_authors":["Tarselli MA","Micalizio GC"],"view_count":["46"],"additional_accession":[]},"is_claimable":false,"name":"Aliphatic imines in titanium-mediated reductive cross-coupling: unique reactivity of Ti(O-i-Pr)4/n-BuLi.","description":"A procedure for the coupling of aliphatic imines with allylic and allenic alkoxides is described. The success of these studies was enabled by a unique reactivity profile of Ti(IV) isopropoxide/n-BuLi compared to well-known Ti(IV) isopropoxide/RMgX systems.","dates":{"release":"2009-01-01T00:00:00Z","publication":"2009 Oct","modification":"2024-10-15T21:24:01.843Z","creation":"2019-03-27T00:28:25Z"},"accession":"S-EPMC2818175","cross_references":{"pubmed":["19810765"],"doi":["10.1021/ol901870n"]}}