Chiral aldehyde catalysis is a useful strategy in the catalytic asymmetric α-functionalization of amino methyl compounds but these reaction types are limited. Here, the authors report two chiral aldehyde-catalysed diastereodivergent reactions, namely, a 1,6-conjugate addition and a bio-inspired Mannich reaction
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
Over the last 20 years asymmetric aminocatalysis has emerged as highly useful and reliable method of...
Small organic molecules recently emerged as a third class of broadly useful asymmetric catalysts tha...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Stereoselective Mannich reactions of aldehydes with ketimines provide chiral β-amino aldehydes that ...
Amine acid transformation is an important chemical process in biological systems. As a well-develope...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The organocatalytic asymmetric \u3b1-alkylation of aldehydes by 1,6-conjugated addition of enamines ...
A highly enantioselective catalytic route to carbamate- and benzoate-protected β-amino aldehydes and...
Organocatalytic asymmetric amine conjugate additions to ?,?-unsaturated aldehydes catalyzed by prote...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
Over the last 20 years asymmetric aminocatalysis has emerged as highly useful and reliable method of...
Small organic molecules recently emerged as a third class of broadly useful asymmetric catalysts tha...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Stereoselective Mannich reactions of aldehydes with ketimines provide chiral β-amino aldehydes that ...
Amine acid transformation is an important chemical process in biological systems. As a well-develope...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The organocatalytic asymmetric \u3b1-alkylation of aldehydes by 1,6-conjugated addition of enamines ...
A highly enantioselective catalytic route to carbamate- and benzoate-protected β-amino aldehydes and...
Organocatalytic asymmetric amine conjugate additions to ?,?-unsaturated aldehydes catalyzed by prote...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
The direct catalytic α-amidoalkylation of dihydroquinolines with aldehydes bearing oxygen functional...
Over the last 20 years asymmetric aminocatalysis has emerged as highly useful and reliable method of...
Small organic molecules recently emerged as a third class of broadly useful asymmetric catalysts tha...