Organic Letters · 2017 · 28 citations · 19 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsHeterocyclic ChemistryOrganic SynthesisCross-coupling CatalysisPalladium-catalyzed Cross-couplingPyrrolidine SynthesisStereoselective Cross-couplingStereospecific Reactions
A palladium-catalyzed cross-coupling of 2-alkylaziridines with alkenylboronic acids to give homoallylamines is presented. The reaction is highly regioselective and stereospecific and provides convenient access to enantioenriched amines with 1,1-disubstituted, 1,2-disubstituted, and trisubstituted alkenes. The modular synthesis of a 2,5-disubstituted pyrrolidine natural product was completed in three steps and 67% overall yield.
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Nucleophilic ring opening of aziridines
Xiaoyan Hu · Tetrahedron · 2004 · 881 citations
Youhei Takeda, Yuki Ikeda, Akinobu Kuroda et al. · Journal of the American Chemical Society · 2014 · 170 citations