Publication | Closed Access
Design, Generation, and Synthetic Application of Borylzincate: Borylation of Aryl Halides and Borylzincation of Benzynes/Terminal Alkyne
166
Citations
40
References
2013
Year
Materials ScienceAryl HalidesChemical EngineeringSuccessive Reaction SequenceEngineeringAlkene MetathesisEnantioselective SynthesisBenzynes/terminal AlkyneZn-catalyzed BorylationOrganic ChemistryOrganometallic CatalysisCatalysisChemistrySynthesis MethodModel Dft CalculationsSynthetic ChemistrySynthetic ApplicationBorophene
Borylzincate was generated in situ from dialkylzinc, diboron, and metal alkoxide. Model DFT calculations showed that although the formation of borylzincate is kinetically favorable, it is thermodynamically unfavorable. Therefore, we designed a successive reaction sequence that would provide a compensating energy gain. This enabled Zn-catalyzed borylation of aryl halides and borylzincation of benzynes and terminal alkyne from diborons without the need for any cocatalyst.
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