A catalytic asymmetric conjugate addition reaction of organocopper reagents, generated from copper salt, a chiral phosphine, and Grignard reagent, with cyclohexenone is highly dependent on the counter anion of copper species, solvents, Grignard reagents, and the structure of the chiral phosphine. Th
Catalytic Conjugate Addition of Heterocyclic Compounds to α,β-Unsaturated Carbonyl Compounds by Hafnium Salts and Scandium Salts.
✍ Scribed by Motoi Kawatsura; Sachiko Aburatani; Junichi Uenishi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 34 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
Catalytic Enantioselective Conjugate Addition of Grignard Reagents to Cyclic α,β-Unsaturated Carbonyl Compounds. -The outcome of the title reaction is influenced by many factors such as amount and structure of the chiral phosphine, copper salt, Grignard reagent, as well as the solvent used.
Stimulated by the efficiency exhibited by enzymes, chemists have sought not only to understand the mechanistic basis for enzymatic reactions, but also to reproduce and even surpass their capabilities. The complementary fields of enzymatic catalysis and transition metal based asymmetric catalysis hav
Stimulated by the efficiency exhibited by enzymes, chemists have sought not only to understand the mechanistic basis for enzymatic reactions, but also to reproduce and even surpass their capabilities. The complementary fields of enzymatic catalysis and transition metal based asymmetric catalysis hav