During the last six years the asymmetric catalysis of carbonyl transformations via iminium ion and enamine intermediates using chiral amines as organocatalysts has grown most remarkably. In this personal account an overview of this area is given. The field can be divided into two sub areas: (a) Iminium catalysis, which is typically used for cycloadditions and conjugate additions to enals and enones and (b) Enamine catalysis, which is commonly used in electrophilic α-substitution reactions of ketones and aldehydes. A common origin of the two catalysis principles is proposed and their recent merger in tandem sequences is discussed
Our laboratory has been engaged in the design of broadly useful new strategies for enantioselective ...
Abstract—Siloxy amino acid lithium salt, O-tert-butyldiphenylsilyl L-serine lithium salt, was found ...
An asymmetric catalytic synthesis of chiral amines using a chiral base catalysed [1,3]-proton shift ...
The catalysis by primary and secondary amines of electrophilic substitution reactions in the α-posit...
Organocatalysis—the branch of catalysis featuring small organic molecules as the catalysts—has, in t...
Over the last 20 years asymmetric aminocatalysis has emerged as highly useful and reliable method of...
The chemistry of preformed enamines, especially their use as enolate equivalents, has been a well-in...
Chiral molecules play a central role in our daily life and in nature, for instance the different ena...
Review on a very fast moving area of research: Catalysis with chiral secondary amines (asymmetric am...
We report a new strategy for organocatalytic cascade reactions. Accordingly, enamine catalysis, imin...
Formation of iminium ions from the condensation of chiral secondary or primary amines with α,β-unsat...
In this review the principal enantioselective methodologies merging transition-metal catalysis and a...
Amine acid transformation is an important chemical process in biological systems. As a well-develope...
Disclosed herein is a new catalytic approach for an efficient access to cyclic β-amino acids widely ...
In this work, we exposed a brief report about the development of the asymmetric aminocatalysis by us...
Our laboratory has been engaged in the design of broadly useful new strategies for enantioselective ...
Abstract—Siloxy amino acid lithium salt, O-tert-butyldiphenylsilyl L-serine lithium salt, was found ...
An asymmetric catalytic synthesis of chiral amines using a chiral base catalysed [1,3]-proton shift ...
The catalysis by primary and secondary amines of electrophilic substitution reactions in the α-posit...
Organocatalysis—the branch of catalysis featuring small organic molecules as the catalysts—has, in t...
Over the last 20 years asymmetric aminocatalysis has emerged as highly useful and reliable method of...
The chemistry of preformed enamines, especially their use as enolate equivalents, has been a well-in...
Chiral molecules play a central role in our daily life and in nature, for instance the different ena...
Review on a very fast moving area of research: Catalysis with chiral secondary amines (asymmetric am...
We report a new strategy for organocatalytic cascade reactions. Accordingly, enamine catalysis, imin...
Formation of iminium ions from the condensation of chiral secondary or primary amines with α,β-unsat...
In this review the principal enantioselective methodologies merging transition-metal catalysis and a...
Amine acid transformation is an important chemical process in biological systems. As a well-develope...
Disclosed herein is a new catalytic approach for an efficient access to cyclic β-amino acids widely ...
In this work, we exposed a brief report about the development of the asymmetric aminocatalysis by us...
Our laboratory has been engaged in the design of broadly useful new strategies for enantioselective ...
Abstract—Siloxy amino acid lithium salt, O-tert-butyldiphenylsilyl L-serine lithium salt, was found ...
An asymmetric catalytic synthesis of chiral amines using a chiral base catalysed [1,3]-proton shift ...