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Nickel‐Catalyzed Anionic Cross‐Coupling Reaction of Lithium Sulfonimidoyl Alkylidene Carbenoids With Organolithiums
- 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.
- Subjects :
- 010402 general chemistry
01 natural sciences
Catalysis
Coupling reaction
nickel–vinylidene
nickel
chemistry.chemical_compound
Sulfinamide
Cross‐Coupling Reactions
Full Paper
organolithium
010405 organic chemistry
Ligand
Organic Chemistry
General Chemistry
Full Papers
diastereoselectivity
Combinatorial chemistry
0104 chemical sciences
chemistry
Catalytic cycle
Reagent
ddc:540
carbenoids
Carbene
Phosphine
Subjects
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