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Nickel‐Catalyzed Anionic Cross‐Coupling Reaction of Lithium Sulfonimidoyl Alkylidene Carbenoids With Organolithiums

Authors :
Jürgen Decker
Mu-Hyun Baik
Gerd Bülow
Steve Park
Irene Erdelmeier
Hans‐Joachim Gais
Joonghee Won
Source :
Chemistry (Weinheim an Der Bergstrasse, Germany), Chemistry-a European journal 26(13), 2914-2926 (2020). doi:10.1002/chem.201904862
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

The mechanistic platform for a novel nickel0‐catalyzed anionic cross‐coupling reaction (ACCR) of lithium sulfonimidoyl alkylidene carbenoids (metalloalkenyl sulfoximines) with organometallic reagents is reported herein, affording substituted alkenylmetals and lithium sulfinamides. The Ni0‐catalyzed ACCR of three different types of metalloalkenyl sulfoximines, including acyclic, axially chiral and exocyclic derivatives, with sp2 organolithiums and sp2 and sp3 Grignard reagents has been studied. The ACCR of metalloalkenyl sulfoximines with PhLi in the presence of the Ni0‐catalyst and precatalyst Ni(PPh3)2Cl2 afforded alkenyllithiums, under inversion of configuration at the C atom and complete retention at the S atom. In a combination of experimental and DFT studies, we propose a catalytic cycle of the Ni0‐catalyzed ACCR of lithioalkenyl sulfoximines. Computational studies reveal two distinctive pathways of the ACCR, depending on whether a phosphine or 1,5‐cyclooctadiene (COD) is the ligand of the Ni atom. They rectify the underlying importance of forming the key Ni0‐vinylidene intermediate through an indispensable electron‐rich Ni0‐center coordinated by phosphine ligands. Fundamentally, we present a mechanistic study in controlling the diastereoselectivity of the alkenyllithium formation via the key lithium sulfinamide coordinated Ni0‐vinylidene complex, which consequently avoids an unselective formation of an alkylidene carbene Ni‐complex and ultimately racemic alkenyllithium.<br />The nickel0‐catalyzed anionic cross‐coupling reaction (ACCR) of lithium sulfonimidoyl alkylidene carbenoids (metalloalkenyl sulfoximines) with organometallic reagents affords substituted alkenylmetals and lithium sulfinamides. The Ni0‐catalyzed ACCR of three different types of metalloalkenyl sulfoximines, including acyclic, axially chiral, and exocyclic derivatives, with sp2 organolithiums and sp2 and sp3 Grignard reagents has been experimentally and theoretically studied.

Details

ISSN :
15213765 and 09476539
Volume :
26
Database :
OpenAIRE
Journal :
Chemistry – A European Journal
Accession number :
edsair.doi.dedup.....b01add5e521af0e1cda99e7e876f1d84
Full Text :
https://doi.org/10.1002/chem.201904862