The formation of acetals and ketals from aldehydes and ketones represents one of the most fundamental transformations in organic chemistry. Being useful protecting groups, these acetals also represent a source of ethers through selective reduction of one of the C-O bonds. This chapter covers advances in this process, with a particular focus on the development of a mechanistic understanding of the factors that control regioselective reduction, and on methods which enable highly selective reduction under mild and functional group-tolerant conditions. © 2014 Elsevier Ltd. All rights reserved
We describe DFT computations that address the regioselective preference toward the five-membered rin...
The scope and limitations of reagents for the cleavage of ethers are discussed. The reagents are con...
Acyclic or cyclic O,O-acetals and O,S-acetals underwent reductive cleavage to give primary alcohols ...
The formation of acetals and ketals from aldehydes and ketones represents one of the most fundamenta...
The development of methods to easily synthesize chemical structures is of great importance in the fi...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
Ether derivatives have myriad applications in several areas of chemical industry and academia. Hence...
We report an efficient two step process for the reduction of non-aromatic esters to the correspondin...
The use of benzylidene acetals as protecting groups in carbohydrate chemistry is utterly important. ...
International audienceA simple and practical procedure for the reduction of acetals to ethers is des...
A well-defined cationic Ru–H complex catalyzes reductive etherification of aldehydes and ketones wit...
Chemoselective reductions are valuable in organic synthesis and are routinely discussed in a sophomo...
Gröger H, Hummel W, Borchert S, Kraußer M. Reduction of Ketones and Aldehydes to Alcohols. In: Drauz...
The prevalence of metal-based reducing reagents, including metals, metal complexes, and metal salts,...
The use of enolate anions as protecting groups in order to effect the selective reduction of dicarbo...
We describe DFT computations that address the regioselective preference toward the five-membered rin...
The scope and limitations of reagents for the cleavage of ethers are discussed. The reagents are con...
Acyclic or cyclic O,O-acetals and O,S-acetals underwent reductive cleavage to give primary alcohols ...
The formation of acetals and ketals from aldehydes and ketones represents one of the most fundamenta...
The development of methods to easily synthesize chemical structures is of great importance in the fi...
The transformation of epoxides into other compounds by exploiting the reactivity of the oxirane ring...
Ether derivatives have myriad applications in several areas of chemical industry and academia. Hence...
We report an efficient two step process for the reduction of non-aromatic esters to the correspondin...
The use of benzylidene acetals as protecting groups in carbohydrate chemistry is utterly important. ...
International audienceA simple and practical procedure for the reduction of acetals to ethers is des...
A well-defined cationic Ru–H complex catalyzes reductive etherification of aldehydes and ketones wit...
Chemoselective reductions are valuable in organic synthesis and are routinely discussed in a sophomo...
Gröger H, Hummel W, Borchert S, Kraußer M. Reduction of Ketones and Aldehydes to Alcohols. In: Drauz...
The prevalence of metal-based reducing reagents, including metals, metal complexes, and metal salts,...
The use of enolate anions as protecting groups in order to effect the selective reduction of dicarbo...
We describe DFT computations that address the regioselective preference toward the five-membered rin...
The scope and limitations of reagents for the cleavage of ethers are discussed. The reagents are con...
Acyclic or cyclic O,O-acetals and O,S-acetals underwent reductive cleavage to give primary alcohols ...