Functional Group Interconversion: Decarbonylative Borylation of Esters for the Synthesis of Organoboronates
KAUST DepartmentChemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Online Publication Date2016-10-11
Print Publication Date2016-11-14
Permanent link to this recordhttp://hdl.handle.net/10754/622118
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AbstractA new and efficient nickel-catalyzed decarbonylative borylation reaction of carboxylic acid esters with bis(pinacolato)-diboron has been developed. This transformation allows access to structurally diverse aryl as well as alkenyl and alkyl boronate esters with high reactivity, broad substrate scope, and excellent functional-group tolerance. Further experiments show that this protocol can be carried out on a gram scale and applied to orthogonal synthetic strategies.
CitationGuo L, Rueping M (2016) Functional Group Interconversion: Decarbonylative Borylation of Esters for the Synthesis of Organoboronates. Chemistry - A European Journal 22: 16787–16790. Available: http://dx.doi.org/10.1002/chem.201604504.
SponsorsL.G. was supported by the China Scholarship Council.
JournalChemistry - A European Journal