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- W2336700997 endingPage "1273" @default.
- W2336700997 startingPage "1256" @default.
- W2336700997 abstract "The catalytic enantioselective carbonyl addition reaction has long attracted the interest of chemists because of its synthetic importance. Although many highly enantioselective reactions have been developed, with few exceptions the reactions are carried out at relatively high catalyst loadings, making them less practical for scale-up applications. In addition, organometallic reagents employed as carbon nucleophiles have been limited to those with relatively low reactivity, such as diorganozincs and arylboronic acids. In an effort to enhance the practicality, a highly active and enantioselective chiral titanium catalyst system was recently developed in our laboratory, enabling the enantioselective carbonyl addition reaction to aldehydes using various organometallic reagents (RM; M = MgX, Li, BY2, ZnX, AlMe2) at lower catalyst loadings (≤5 mol %)." @default.
- W2336700997 created "2016-06-24" @default.
- W2336700997 creator A5076717033 @default.
- W2336700997 date "2016-04-20" @default.
- W2336700997 modified "2023-10-18" @default.
- W2336700997 title "Development of Highly Active Chiral Titanium Catalysts for the Enantioselective Addition of Various Organometallic Reagents to Aldehydes" @default.
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