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《Tetrahedron letters》2019,60(41):151134
A first chiral strategy for synthesis of (R)-5-hydroxy-3-(4-methoxyphenethyl) cyclohex-2-enone reported. Key transformation includes Barbier allylation, ionic hydrogenation, Jeffery reaction, Katsuki Sharpless asymmetric epoxidation, reductive opening of epoxide and ring closing metathesis. 相似文献
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