Development of Tartaric Acid Derived Chiral Guanidines and Their Application to Catalytic Enantioselective 伪-Hydroxylation of 尾-Dicarbonyl Compounds
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文摘
A novel library of chiral guanidines featuring a tartaric acid skeleton was developed from diethyl l-tartrate. These guanidines are easily accessed with tunable steric and electronic properties. The utilities of the guanidines were highlighted by their ability to catalyze the 伪-hydroxylation of 尾-ketoesters and 尾-diketones with remarkable efficiency and excellent enantioselectivity.

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