Directing group
In organic chemistry, a directing group (DG) is a substituent on a molecule or ion that facilitates reactions by interacting with a reagent. The term is usually applied to C-H activation of hydrocarbons, where it is defined as a "coordinating moiety (an “internal ligand”), which directs a metal catalyst into the proximity of a certain C–H bond." In a well known example, the ketone group in acetophenone is the DG in the Murai reaction.[1]
The Murai reaction is related to directed ortho metalation, a reaction is typically applied to the lithiation of substituted aromatic rings..[2] .
Transient directing groups
Since directing groups are ligands, their effectiveness correlates with their affinities for metals. Common functional groups such as ketones usually are only weak ligands and thus often are poor DGs. This problem is solved by the use of a transient directing group. Transient DGs reversibly convert weak DGs (e.g., ketones) into strong DG's (e.g., imines) via a Schiff base condensation. Subsequent to serving their role as DGs, the imine can hydrolyze, regenerating the ketone and amine.[3]
References
- ^ "A Comprehensive Overview of Directing Groups Applied in Metal-Catalysed C–H functionalisation chemistry". Chemical Society Reviews. 47 (17): 6603–6743. 2018. doi:10.1039/C8CS00201K. PMC 6113863. PMID 30033454.
{{cite journal}}: Cite uses deprecated parameter|authors=(help) - ^ Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics Victor Snieckus Chem. Rev.; 1990; 90(6); 879-933. Abstract
- ^ "Transient imines as 'next generation' directing groups for the catalytic functionalisation of C–H bonds in a single operation" (PDF). Organic & Biomolecular Chemistry. 16 (25): 4582–4595. 2018. doi:10.1039/C8OB00926K. hdl:10044/1/60231. PMID 29796566.
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