1 publication
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Copper–Phthalocyanine Conjugates of Serum Albumins as Enantioselective Catalysts in Diels–Alder Reactions
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Angew. Chem. Int. Ed. 2006, 45, 2416-2419, 10.1002/anie.200504561
Chirality from blood: Serum albumins form strong complexes with CuII–phthalocyanines, leading to protein conjugates. These hybrid catalysts promote enantioselective Diels–Alder reactions, such as that of azachalcones 1 with cyclopentadiene (2) to give products 3 with 85–98 % ee.
Metal: CuLigand type: PhthalocyanineHost protein: Bovine serum albumin (BSA)Anchoring strategy: SupramolecularOptimization: ChemicalNotes: Chirality from blood: Serum albumins form strong complexes with CuII–phthalocyanines, leading to protein conjugates. These hybrid catalysts promote enantioselective Diels–Alder reactions, such as that of azachalcones 1 with cyclopentadiene (2) to give products 3 with 85–98 % ee.