Continuous flow enantioselective arylation of aldehydes with ArZnEt using triarylboroxins as the ultimate source of aryl groups
Beilstein J. Org. Chem. 2009, 5, 56.
A highly selective, polymer-supported organocatalyst for Michael additions with enzyme-like behavior
Adv. Synth. Catal. 2009, 351, 3051-3056.
A highly active catalyst for Huisgen 1,3-dipolar cycloadditions based on the tris(triazolyl)methanol-Cu(I) structure
Org. Lett. 2009, 11, 4680-4683.
A solid-supported organocatalyst for highly stereoselective, batch, and continuous-flow Mannich reactions
Chem. Eur. J. 2009, 15, 10167-10172.
Towards continuous flow, highly enantioselective allylic amination: Ligand design, optimization and supporting
Adv. Synth. Catal. 2009, 351, 1539-1556.
Synthesis of highly modular bis(oxazoline) ligands by Suzuki cross-coupling and evaluation as catalytic ligands
Tetrahedron 2009, 65, 8199-8205.
Amino thiols versus amino alcohols in the asymmetric alkynylzinc addition to aldehydes
Tetrahedron Asymmetr. 2009, 20, 1413-1418.
Functionalized nanoparticles as catalysts for enantioselective processes
Org. Biomol. Chem. 2009, 7, 2669-2677.
Di-platinum complexes containing thiolato-urea ligands: Structural and anion binding studies
Dalton Trans. 2009, 2974-2985.