Ambient-Temperature Carbon–Oxygen Bond Cleavage of an α‑Aryloxy Ketone with Cp2Ti(BTMSA) and Selective Protonolysis of the Resulting Ti–OR Bonds
收藏Figshare2016-02-20 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Ambient_Temperature_Carbon_Oxygen_Bond_Cleavage_of_an_Aryloxy_Ketone_with_Cp_sub_2_sub_Ti_BTMSA_and_Selective_Protonolysis_of_the_Resulting_Ti_OR_Bonds/2470477
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Reaction of Cp2Ti[η2-(CSiMe3)2] with an α-aryloxy ketone produces a Ti(IV) enolate aryloxide complex. Selective protonolysis of the enolate ligand or both Ti–OR bonds can be achieved with various acids. The reaction of the enolate aryloxide with 1-phenyl-2-phenoxyethanol is catalyzed by a mixture of NEt3 and [HNEt3]X (X = OTf, BPh4).
创建时间：
2016-02-20
