Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficient synthesis of such compounds including the determination of their absolute configuration is described
A series of chiral acetals were prepared from 7-hydroxyindan- 1 -one and a variety of substituted c...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
Phenyl and methyls (1) have found increasing interest in organic synthesis. They have been prepared ...
Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficien...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
Enamine activation concept has been successfully extended to the asymmetric introduction of Selenium...
Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH ...
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...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
The research, to be discussed in three chapters, involves the development of new synthetic methods w...
A wide range of precursors for selenium electrophiles is already known, but the requirements for the...
a,ß-Ethylenic chiral acetals react regio- and stereoselectively with organolithium reagents. The obt...
A catalytic enantioselective transacetalization has been developed. The chiral phosphoric acid TRIP ...
New chiral non-racemic diselenides were prepared and their corresponding selenium electrophiles were...
A series of chiral acetals were prepared from 7-hydroxyindan- 1 -one and a variety of substituted c...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
Phenyl and methyls (1) have found increasing interest in organic synthesis. They have been prepared ...
Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficien...
Very simple, chiral, non-racemic diselenides were prepared and their corresponding selenium electrop...
Enamine activation concept has been successfully extended to the asymmetric introduction of Selenium...
Achiral as well as chiral 2,3-olefinic acetals are converted into 2- and 3- hydroxy acetals via LAH ...
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...
New chiral diselenides were prepared in a few steps from readily available starting materials. The s...
The research, to be discussed in three chapters, involves the development of new synthetic methods w...
A wide range of precursors for selenium electrophiles is already known, but the requirements for the...
a,ß-Ethylenic chiral acetals react regio- and stereoselectively with organolithium reagents. The obt...
A catalytic enantioselective transacetalization has been developed. The chiral phosphoric acid TRIP ...
New chiral non-racemic diselenides were prepared and their corresponding selenium electrophiles were...
A series of chiral acetals were prepared from 7-hydroxyindan- 1 -one and a variety of substituted c...
Organoselenium reagents have found varied applications throughout organic chemistry. Like many trans...
Phenyl and methyls (1) have found increasing interest in organic synthesis. They have been prepared ...
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