The Essential Guide to Lewis Acids

Oliver M. Sandes (Editor)
Series: Chemistry Research and Applications
BISAC: SCI013010



Volume 10

Issue 1

Volume 2

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Special issue: Resilience in breaking the cycle of children’s environmental health disparities
Edited by I Leslie Rubin, Robert J Geller, Abby Mutic, Benjamin A Gitterman, Nathan Mutic, Wayne Garfinkel, Claire D Coles, Kurt Martinuzzi, and Joav Merrick


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Lewis acids have been utilized to activate molecules, whether it be the generation of a simple Lewis acid-base adduct or the coordination and activation of a substrate molecule in a catalytic transformation. When designing new Lewis acids, a synthetic chemist has to consider the properties of the Lewis acid. As such, this compilation describes the methods used in measuring Lewis acid strength, including a ladder diagram comparing the Lewis acid strength of both main group and metal-based Lewis acids.

Since carboxylic acid derivatives are commercially available, non-toxic, cheap and normally stable to air and moisture, carboxylic acid derivatives are ideal reactants for synthetic strategy. The decarboxylative coupling reaction is discussed as one of the most important tools for organic synthesis, and remarkable progress has been made in this field.

In conclusion, the authors highlight recent advances achieved in the development of processes for esters production from glycerol and terpenic alcohols in metal salts-catalyzed reactions, using acetic acid as the carbonylic reactant. The effects of main reaction parameters such as concentration, temperature and reactants stoichiometry are assessed. A comparison with traditional acid catalysts used in these reactions is also performed.
(Imprint: Nova)


Chapter 1. Influence of Lewis Acid Strength on Molecule Activation
(Z. M. Heiden and B. L. Thompson, Department of Chemistry, Washington State University, Pullman, WA, US)

Chapter 2. Decarboxylative Oxidative Coupling Reaction
(Nai-Xing Wang Tong Zhang and Yalan Xing, Technical Institute of Physics and Chemistry
Chinese Academy of Sciences, Beijing, China, and others)

Chapter 3. Metal Salts-Catalyzed Terpenic Esters Synthesis
(Marcio Jose da Silva, Chemistry Department, Federal University of Vicosa, Vicosa, Minas Gerais State, Brazil)


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