Enamine activation concept has been successfully extended to the asymmetric introduction of Selenium-based compounds into aldehydes. The main features of this novel organocatalytic transformation rely on the high levels of reaction efficiency and stereocontrol (ee ranging from 95% to 99%) obtained using easily available chiral secondary amines along with the high synthetic utility of the chiral alfa-seleno aldehydes, versatile chiral intermediates for a variety of different synthetic transformations
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
omega-Transaminases have been evaluated as biocatalysts in the reductive amination of organoselenium...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to <...
Enamine activation concept has been successfully extended to the asymmetric introduction of Selenium...
In the last decades, organoselenium chemistry has been developed as an important tool for synthetic ...
The discovery and synthetic applications of novel organoselenium compounds and their reactions proce...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
Selenium plays a crucial role in different biological processes, being necessary for theproper funct...
Selenium-based methods have developed rapidly over the past few years asnd organoselenium chemistry ...
(Chemical Equation Presented) Effective discrimination: Efficient lithium amide-induced terminal epo...
Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficien...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The first part of this dissertation serves as an introduction to the current state of electrophilic ...
The synthesis of chiral-centered selenium compounds is presented. Enantioselective oxidations of the...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
omega-Transaminases have been evaluated as biocatalysts in the reductive amination of organoselenium...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to <...
Enamine activation concept has been successfully extended to the asymmetric introduction of Selenium...
In the last decades, organoselenium chemistry has been developed as an important tool for synthetic ...
The discovery and synthetic applications of novel organoselenium compounds and their reactions proce...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
Selenium plays a crucial role in different biological processes, being necessary for theproper funct...
Selenium-based methods have developed rapidly over the past few years asnd organoselenium chemistry ...
(Chemical Equation Presented) Effective discrimination: Efficient lithium amide-induced terminal epo...
Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficien...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to p...
The first part of this dissertation serves as an introduction to the current state of electrophilic ...
The synthesis of chiral-centered selenium compounds is presented. Enantioselective oxidations of the...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
omega-Transaminases have been evaluated as biocatalysts in the reductive amination of organoselenium...
The organocatalytic asymmetric α-alkylation of aldehydes by 1,6-conjugated addition of enamines to <...