Chemoselective Claisen–Schmidt bis-substitutional condensation catalyzed by an alkoxy-bridged dinuclear Ti(IV) cluster
The highly efficient and chemoselective α,α′-bis-substitution of alkanones is important in organic synthesis. Herein, a dimeric titanium cluster, Ti 2 Cl 2 (OPr i ) 6 ·2HOPr i ( Ti 2 ), is used in the Claisen–Schmidt condensation reaction, for the selectively activation of symmetrical ketones containing α,α′-methylene groups and production of α,α′-bis-substituted alkanones in high efficiency and chemoselectivity. The high efficiency and chemoselectivity can be extended to a variety of typical alkanones and aromatic aldehydes . Both of the oxo-bridged dimeric motif of Ti 2 and the ionic Ti–Cl bond are responsible for the high efficiency and chemoselectivity.
研究领域:
有机化学
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催化
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无机化学
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高影响因子
危险品化学品经营许可证（带存储）