Xinliang LiYi WangZhi‐Zhen Huang2026-03-222026-03-22200510.1071/ch05157https://doi.org/10.1071/ch05157https://andeanlibrary.org/handle/123456789/49792Citaciones: 16Optically pure selenonium salts 3 as the precursors of two new chiral selenonium ylides 4 can be synthesized stereoselectively from natural d-camphor in good yields. It is found that the reaction of the selenonium salt 3b, an aldehyde, and potassium tert-butoxide can take place smoothly in ‘one-pot’ via the formation of selenonium ylide 4b, to give chiral trans-diaryl epoxides 5 in good yields with good diastereoselectivities and enantioselectivities.enChemistryYlideCamphorBiocatalysisEnantioselective synthesisAldehydeGreen chemistryOrganic chemistryIonic liquidSalt (chemistry)New Camphor-Derived Selenonium Ylides: Enantioselective Synthesis of Chiral Epoxidesarticle