FUNCTOPROLASYMMCAT

Application of Functionalised Oligoprolines in Asymmetric Catalysis

 Coordinatore EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZURICH 

 Organization address address: Raemistrasse 101
city: ZUERICH
postcode: 8092

contact info
Titolo: Prof.
Nome: Helma
Cognome: Wennemers
Email: send email
Telefono: +41 44 633 37 77

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 192˙622 €
 EC contributo 192˙622 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-05-01   -   2015-04-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZURICH

 Organization address address: Raemistrasse 101
city: ZUERICH
postcode: 8092

contact info
Titolo: Prof.
Nome: Helma
Cognome: Wennemers
Email: send email
Telefono: +41 44 633 37 77

CH (ZUERICH) coordinator 192˙622.20

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 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

oligoproline    create    catalytic    supramolecular    synthetic    successful    oligoprolines    enantioselective    contribution    area    helical    class   

 Obiettivo del progetto (Objective)

'Although oligoprolines have been known for decades up till the recent years they have only been applied as spacers in the study of energy and electron transfer phenomena. Recently a new methodology for the functionalisation of their backbones has been developed. The great flexibility of the reported synthetic approach both with respect to the number and character of introduced motifs allows for effective fine-tuning of the properties of these helical oligopeptides. Herein we propose to apply functionalised oligoprolines as novel asymmetric organocatalysts and chiral ligands for metal-catalysed transformations. Successful demonstration that the helical chirality can be transferred efficiently into an enantioselective transformation will be a very important contribution to the area and may result in the establishment of new class of catalysts. We also aim at creating switchable systems in which we will control the catalytic activity of these compounds by a simple, external stimuli. This will constitute a major achievement in the fast growing area of modern chemical sciences focusing on mimicking the behaviour of natural catalytic systems. The ultimate goal of the project however is design and operation of a supramolecular catalytic assembly line consisting of oligoproline units. We plan to create a platform which will catalyse the synthesis of an oligomeric specie from monomers in solution, however only when its’ single oligoproline components assemble together to create the ‘active form’ of the catalytic system. Successful accomplishment of this task will be a landmark contribution to the fields enantioselective catalysis, supramolecular chemistry and nanotechnology and could lay the foundations for a new class of functional synthetic systems.'

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