HIPOCAT

High Performance Lewis Acid Organocatalysis

 Coordinatore MAX PLANCK INSTITUT FUER KOHLENFORSCHUNG 

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 Nazionalità Coordinatore Germany [DE]
 Totale costo 2˙490˙000 €
 EC contributo 2˙490˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2010-AdG_20100224
 Funding Scheme ERC-AG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-02-01   -   2016-01-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    MAX PLANCK INSTITUT FUER KOHLENFORSCHUNG

 Organization address address: KAISER WILHELM PLATZ 1
city: MUELHEIM AN DER RUHR
postcode: 45470

contact info
Titolo: Mrs.
Nome: Salome
Cognome: Marenya
Email: send email
Telefono: 492083000000
Fax: 492083000000

DE (MUELHEIM AN DER RUHR) hostInstitution 2˙490˙000.00
2    MAX PLANCK INSTITUT FUER KOHLENFORSCHUNG

 Organization address address: KAISER WILHELM PLATZ 1
city: MUELHEIM AN DER RUHR
postcode: 45470

contact info
Titolo: Prof.
Nome: Benjamin
Cognome: List
Email: send email
Telefono: 492083000000
Fax: 492083000000

DE (MUELHEIM AN DER RUHR) hostInstitution 2˙490˙000.00

Mappa


 Word cloud

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

organocatalysts    chiral    bases    metal    acid    catalysis    organic    recently    asymmetric    molecules    made    acids    industrial    lewis    catalysts    organocatalysis    active   

 Obiettivo del progetto (Objective)

'Although the demand for chiral enantiomerically pure molecules as pharmaceuticals, agrochemicals, and liquid crystals is growing strongly, the use of asymmetric catalysis for their production is rare. The most common industrial method to produce enantiopure compounds is still chiral resolution, which wastes half of the material. This surprises considering that catalytic methods are potentially cost-, energy, and resource-saving, have a lesser impact on the environment, and are in line with the general concepts of green chemistry and sustainability. Recently organocatalysis has grown into one of three fundamental classes of asymmetric catalysts complementing metal- and biocatalysis. In principle, organocatalysts have many beneficial features such as air and moisture stability, non-toxicity, and easy accessibility, making them attractive for industrial applications. However, most organocatalysts are insufficiently active and require high catalysts loadings, counterbalancing these positive features. Remarkably, of the four types of organocatalysts, Brønsted bases and acids, and Lewis bases, and acids, organic Lewis acid catalysts have been almost entirely ignored. Very recently though, within the group of the applicant, the finding was made that such catalysts can be extremely active and enantioselective, suggesting the possibility for truly high performance organocatalysis. This proposal therefore aims at the design of novel organic Lewis acid catalysts, their exploration in asymmetric catalysis, and their mechanistic understanding. The program is expected to lead the way towards the next generation organocatalysts, which will rival the efficiency of the most active metal- and biocatalysts, and have the potential to profoundly change the way chiral molecules are made.'

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