Phosphonium Ionic Liquid–Catalyzed Michael Addition of Mercaptans to α,β-Unsaturated Ketones

Green Procedure for the Synthesis of β-Nitro Sulfides by Michael Addition of Thiols to Nitroolefins

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Epi-Cinchona Based Thiourea Organocatalyst Family as an Efficient Asymmetric Michael Addition Promoter: Enantioselective Conjugate Addition of Nitroalkanes to Chalcones and α,β-UnsaturatedN-Acylpyrroles

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Rapid, efficient and selective conjugate addition of thiols to α, β-unsaturated carbonyl compounds using silica supported sodium hydrogen sulfate under solvent-free conditions†

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KF/Al2O3as a Highly Efficient, Green, Heterogeneous, and Reusable Catalytic System for the Solvent-Free Synthesis of Carboacyclic Nucleosides via Michael Addition Reaction

(2008) Abdolkarim Zare et al.   SYNTHETIC COMMUNICATIONS

Efficient Iron‐Catalyzed Sakurai–Michael Addition of Allyltrimethylsilane to Chalcones

(2008) Li‐Wen Xu et al.   SYNTHETIC COMMUNICATIONS

Organocatalytic Asymmetric Sulfa-Michael Addition to α,β-Unsaturated Ketones

(2007) Paolo Ricci et al.   ADVANCED SYNTHESIS & CATALYSIS

Ammonium chloride-catalyzed carbon–sulfur bond formation in water

(2007) WeiYi Chen et al.   CATALYSIS COMMUNICATIONS