Journal of the American Chemical Society · 2022 · 81 citations · 79 references
Natural SciencesChemistryCatalysisIndustrial ChemistryOrganic ChemistryCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisAlkyl Cross-couplingAlkylation ReactionsCopper-catalyzed CouplingStereoselective Cross-couplingTransition-metal-catalyzed Functionalization
Copper-catalyzed stereospecific cross-couplings of boronic esters are reported. Boron “ate” complexes derived from pinacol boronic esters and tert-butyl lithium undergo stereospecific transmetalation to copper cyanide, followed by coupling with alkynyl bromides, allyl halides, propargylic halides, β-haloenones, hydroxylamine esters, and acyl chlorides. Through this simple transformation, commercially available inexpensive compounds can be employed to convert primary and secondary alkylboronic esters to a wide array of synthetically useful compounds.
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Enantiospecific sp2–sp3 coupling of secondary and tertiary boronic esters
Amadeu Bonet, Marcin Odachowski, Daniele Leonori et al. · Nature Chemistry · 2014 · 429 citations · Full text
Iron-Catalyzed Suzuki−Miyaura Coupling of Alkyl Halides
Takuji Hatakeyama, Toru Hashimoto, Yoshiyuki Kondo et al. · Journal of the American Chemical Society · 2010 · 344 citations