Abstract:
:Recent years have witnessed the growing interest in the remote functionalization of alkenes for it offers a strategy to activate the challenging C-H bonds distant from the initiation point via alkene isomerization/functionalization. However, the catalytic enantioselective isomerization/functionalization with one single transition metal catalyst remains rare. Here we report a highly regio- and enantioselective cobalt-catalyzed remote C-H bond borylation of internal alkenes via sequential alkene isomerization/hydroboration. A chiral ligand featured twisted pincer, anionic, and non-rigid characters is designed and used for this transformation. This methodology, which is operationally simple using low catalyst loading without additional activator, shows excellent enantioselectivity and can be used to convert various internal alkenes with regio- and stereoisomers to valuable chiral secondary organoboronates with good functional group tolerance.
journal_name
Nat Communjournal_title
Nature communicationsauthors
Chen X,Cheng Z,Guo J,Lu Zdoi
10.1038/s41467-018-06240-ysubject
Has Abstractpub_date
2018-09-26 00:00:00pages
3939issue
1issn
2041-1723pii
10.1038/s41467-018-06240-yjournal_volume
9pub_type
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