Literature DB >> 17387670

Lithium diisopropylamide: solution kinetics and implications for organic synthesis.

David B Collum1, Anne J McNeil, Antonio Ramirez.   

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.

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Year:  2007        PMID: 17387670     DOI: 10.1002/anie.200603038

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  43 in total

1.  Reaction of lithium diethylamide with an alkyl bromide and alkyl benzenesulfonate: origins of alkylation, elimination, and sulfonation.

Authors:  Lekha Gupta; Antonio Ramírez; David B Collum
Journal:  J Org Chem       Date:  2010-11-16       Impact factor: 4.354

2.  Lithium Hexamethyldisilazide-Mediated Enolization of Acylated Oxazolidinones: Solvent, Cosolvent, and Isotope Effects on Competing Monomer- and Dimer-Based Pathways.

Authors:  Gabriel J Reyes-Rodríguez; Russell F Algera; David B Collum
Journal:  J Am Chem Soc       Date:  2017-01-12       Impact factor: 15.419

3.  Disodium Salts of Pseudoephedrine-Derived Myers Enolates: Stereoselectivity and Mechanism of Alkylation.

Authors:  Yuhui Zhou; Ivan Keresztes; Samantha N MacMillan; David B Collum
Journal:  J Am Chem Soc       Date:  2019-10-15       Impact factor: 15.419

4.  Mechanism of Lithium Diisopropylamide-Mediated Ortholithiation of 1,4-Bis(trifluoromethyl)benzene under Nonequilibrium Conditions: Condition-Dependent Rate Limitation and Lithium Chloride-Catalyzed Inhibition.

Authors:  Jun Liang; Alexander C Hoepker; Russell F Algera; Yun Ma; David B Collum
Journal:  J Am Chem Soc       Date:  2015-05-06       Impact factor: 15.419

5.  Computational studies of lithium diisopropylamide deaggregation.

Authors:  Alexander C Hoepker; David B Collum
Journal:  J Org Chem       Date:  2011-09-02       Impact factor: 4.354

6.  Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Alkene Isomerizations and Diene Metalations.

Authors:  Russell F Algera; Yun Ma; David B Collum
Journal:  J Am Chem Soc       Date:  2017-08-14       Impact factor: 15.419

7.  On the nature of the oxidative heterocoupling of lithium enolates.

Authors:  Brian M Casey; Robert A Flowers
Journal:  J Am Chem Soc       Date:  2011-07-08       Impact factor: 15.419

8.  Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.

Authors:  K Cory MacLeod; Fabian S Menges; Sean F McWilliams; Stephanie M Craig; Brandon Q Mercado; Mark A Johnson; Patrick L Holland
Journal:  J Am Chem Soc       Date:  2016-08-29       Impact factor: 15.419

9.  Lithium diisopropylamide-mediated reactions of imines, unsaturated esters, epoxides, and aryl carbamates: influence of hexamethylphosphoramide and ethereal cosolvents on reaction mechanisms.

Authors:  Yun Ma; David B Collum
Journal:  J Am Chem Soc       Date:  2007-11-07       Impact factor: 15.419

10.  Autocatalysis in lithium diisopropylamide-mediated ortholithiations.

Authors:  Kanwal J Singh; Alexander C Hoepker; David B Collum
Journal:  J Am Chem Soc       Date:  2008-12-31       Impact factor: 15.419

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