Regioselective and Redox-Neutral Cp*IrIII-Catalyzed Allylic C-H Alkynylation

Mondal, Shobhan; Pinkert, Tobias; Daniliuc, Constantin G.; Glorius, Frank

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Herein, we report a Cp*IrIII-catalyzed highly regioselective and redox-neutral protocol for the construction of 1,4-enynes from unactivated olefins and bromoalkynes via intermolecular allylic C−H alkynylation. The developed mild reaction conditions tolerate a broad range of common functional groups, even enabling selective alkynylation of allylic C−H bonds in the presence of other prominent directing groups. Mechanistic experiments including the isolation of a catalytically active IrIII-allyl species support an intermolecular allylic C−H activation followed by an electrophilic alkynylation.

Details zur Publikation

FachzeitschriftAngewandte Chemie International Edition (Angew. Chem. Int. Ed.)
Jahrgang / Bandnr. / Volume60
Ausgabe / Heftnr. / Issue11
Seitenbereich5688-5692
StatusVeröffentlicht
Veröffentlichungsjahr2021
DOI10.1002/anie.202015249
Link zum Volltexthttps://onlinelibrary.wiley.com/doi/10.1002/anie.202015249
Stichwörter1,4-enynes; alkynylation; allylic C-H activation; allyl-iridium complex; regioselectivity; Iridium

Autor*innen der Universität Münster

Daniliuc, Constantin-Gabriel
Organisch-Chemisches Institut
Glorius, Frank
Professur für Organische Chemie (Prof. Glorius)
Mondal, Shobhan
Professur für Organische Chemie (Prof. Glorius)
Pinkert, Tobias
Professur für Organische Chemie (Prof. Glorius)