Reductive Cleavage of Allyllic Ketals by an Arene-Catalysed Lithiation: A Simple and Direct Route to Masked Lithium Homoenolates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
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1. Generation, Stability, and Utility of Lithium 4,4′-Di-tert-butylbiphenylide (LiDBB);The Journal of Organic Chemistry;2016-10-27
2. Fundamental Difference in Reductive Lithiations with Preformed Radical Anions versus Catalytic Aromatic Electron-Transfer Agents: N ,N- Dimethylaniline as an Advantageous Catalyst;Angewandte Chemie International Edition;2015-11-18
3. Fundamental Difference in Reductive Lithiations with Preformed Radical Anions versus Catalytic Aromatic Electron-Transfer Agents: N ,N- Dimethylaniline as an Advantageous Catalyst;Angewandte Chemie;2015-11-18
4. Reductive Lithiation in the Absence of Aromatic Electron Carriers. A Steric Effect Manifested on the Surface of Lithium Metal Leads to a Difference in Relative Reactivity Depending on Whether the Aromatic Electron Carrier Is Present or Absent;The Journal of Organic Chemistry;2015-08-14
5. Lithium 4,4′-Di-tert-butylbiphenylide;Encyclopedia of Reagents for Organic Synthesis;2014-05-27
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