Lithium Diisopropylamide: Solution Kinetics and Implications for Organic Synthesis
- 12 April 2007
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 46 (17), 3002-3017
- https://doi.org/10.1002/anie.200603038
Abstract
Lithium diisopropylamide (LDA) is a prominent reagent used in organic synthesis. In this Review, rate studies of LDA‐mediated reactions are placed in the broader context of organic synthesis in three distinct segments. The first section provides a tutorial on solution kinetics, emphasizing the characteristic rate behavior caused by dominant solvation and aggregation effects. The second section summarizes substrate‐ and solvent‐dependent mechanisms that reveal basic principles of solvation and aggregation. The final section suggests how an understanding of mechanism might be combined with empirical methods to optimize yields, rates, and selectivities of organolithium reactions and applied to organic synthesis.Keywords
This publication has 80 references indexed in Scilit:
- Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl Carbamates: Role of Aggregates and Mixed AggregatesJournal of the American Chemical Society, 2006
- Organolithium Reagents in Pharmaceutical Asymmetric ProcessesChemical Reviews, 2006
- Reaction of Ketones with Lithium Hexamethyldisilazide: Competitive Enolizations and 1,2-AdditionsJournal of the American Chemical Society, 2004
- Lithium Diisopropylamide-Mediated Lithiations of Imines: Insights into Highly Structure-Dependent Rates and SelectivitiesJournal of the American Chemical Society, 2003
- Using a Graphing Calculator to Determine a First-Order Rate Constant When the Infinity Reading Is UnknownJournal of Chemical Education, 2002
- Structure and Reactivity of Lithium Diisopropylamide Solvated by Polyamines: Evidence of Monomer- and Dimer-Based DehydrohalogenationsJournal of the American Chemical Society, 1998
- Mechanisms of the Base-Induced Isomerizations of Cyclopentene and Cyclohexene Oxides: Influence of Structure and Solvent on α and β Proton RemovalThe Journal of Organic Chemistry, 1996
- Synthesis, isolation, and structure of an LDA-THF complexThe Journal of Organic Chemistry, 1993
- Metalation of imines by lithium diisopropylamide solvated by N,N,N',N'-tetramethylethylenediamine: evidence for solvent-free open dimer reactive intermediatesJournal of the American Chemical Society, 1993
- The structure of lithium tetramethylpiperidide and lithium diisopropylamide in the presence of hexamethylphosphoramide: structure-dependent distribution of cyclic and open dimers, ion triplets, and monomersJournal of the American Chemical Society, 1991