National Repository of Grey Literature 7 records found  Search took 0.01 seconds. 
Stereoslective addition reaction to ketimines
Franc, Michael
This diploma thesis deals with the stereoselective addition reaction of benzothiophenone derivatives to ketimines derived from isatin using bifunctional organocatalysis. The stereoselective addition reaction was optimized to provide the appropriate reaction conditions which were subsequently used to study the scope of the reaction. Keywords Organocatalysis, stereoselective synthesis, bifunctional organocatalysts, ketimines, sulphur heterocykles.
Preparation of H-bonding organocatalysts
Franc, Michael ; Veselý, Jan (advisor) ; Jindřich, Jindřich (referee)
This bachelor thesis deals with the preparation of chiral (thio)urea and squaramide derivatives, that can act as H-bonding organocatalysts. The catalytic efficiency of the prepared organocatalysts was explored in asymmetric Morita-Baylis-Hillman and aza-Henry reaction.
Synthesis of cycles using organocatalysis and catalysis with metal complexes
Hurný, David ; Veselý, Jan (advisor) ; Trnka, Tomáš (referee)
This thesis deals with an enantioselective synthesis of cyclic compounds by using a combination of organocatalysis and transition metal catalysis. The thesis deals mainly with usage of aminocatalyst for activation of aldehydes and copper catalyst for activation of terminal triple bond. The first part is focused on the preparation of starting compounds for cyclizations (α-oxoesters, α- substituted nitroalkanes and α-substituted aldehydes). The second part concerns carbocyclization itself and optimization of reaction conditions to achieve highly stereoselective reaction. Powered by TCPDF (www.tcpdf.org)
The preparation of chiral NHC carbene precatalysts
Krejčířová, Kateřina ; Veselý, Jan (advisor) ; Míšek, Jiří (referee)
This bachelor thesis is focused on the preparation of chiral NHC carbene precatalysts, which are used as organocatalysts in a variety of organic transformations leading to the formation of optically active compounds. In the course of this work, several triazolium salts were prepared from suitable starting materials using six reaction steps. Triazolium salts derived from oxazolidinone were obtained from well available starting materials, arylhydrazines and phenylalanine.
Stereoslective addition reaction to ketimines
Franc, Michael ; Veselý, Jan (advisor) ; Kotora, Martin (referee)
This diploma thesis deals with the stereoselective addition reaction of benzothiophenone derivatives to ketimines derived from isatin using bifunctional organocatalysis. The stereoselective addition reaction was optimized to provide the appropriate reaction conditions which were subsequently used to study the scope of the reaction. Keywords Organocatalysis, stereoselective synthesis, bifunctional organocatalysts, ketimines, sulphur heterocykles.
Synthesis of cycles using organocatalysis and catalysis with metal complexes
Hurný, David ; Veselý, Jan (advisor) ; Trnka, Tomáš (referee)
This thesis deals with an enantioselective synthesis of cyclic compounds by using a combination of organocatalysis and transition metal catalysis. The thesis deals mainly with usage of aminocatalyst for activation of aldehydes and copper catalyst for activation of terminal triple bond. The first part is focused on the preparation of starting compounds for cyclizations (α-oxoesters, α- substituted nitroalkanes and α-substituted aldehydes). The second part concerns carbocyclization itself and optimization of reaction conditions to achieve highly stereoselective reaction. Powered by TCPDF (www.tcpdf.org)
Preparation of H-bonding organocatalysts
Franc, Michael ; Veselý, Jan (advisor) ; Jindřich, Jindřich (referee)
This bachelor thesis deals with the preparation of chiral (thio)urea and squaramide derivatives, that can act as H-bonding organocatalysts. The catalytic efficiency of the prepared organocatalysts was explored in asymmetric Morita-Baylis-Hillman and aza-Henry reaction.

Interested in being notified about new results for this query?
Subscribe to the RSS feed.