MCCYC

METAL CATALYZED STRATEGIES FOR C-H BOND ACTIVATION AND CYCLOADDITION. SYNTHETIC APPLICATIONS AND DISCOVERY OF NON CONVETIONAL TRANSFORMATIONS

 Coordinatore UNIVERSIDADE DE SANTIAGO DE COMPOSTELA 

 Organization address address: "PAZO DE SAN XEROME, PRAZA DO OBRADOIRO S/N"
city: SANTIAGO DE COMPOSTELA
postcode: 15782

contact info
Titolo: Dr.
Nome: Fernando
Cognome: Sedano Arnaez
Email: send email
Telefono: +34 981 547050
Fax: +34 981 528019

 Nazionalità Coordinatore Spain [ES]
 Totale costo 45˙000 €
 EC contributo 45˙000 €
 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-2009-RG
 Funding Scheme MC-ERG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-04-01   -   2013-03-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSIDADE DE SANTIAGO DE COMPOSTELA

 Organization address address: "PAZO DE SAN XEROME, PRAZA DO OBRADOIRO S/N"
city: SANTIAGO DE COMPOSTELA
postcode: 15782

contact info
Titolo: Dr.
Nome: Fernando
Cognome: Sedano Arnaez
Email: send email
Telefono: +34 981 547050
Fax: +34 981 528019

ES (SANTIAGO DE COMPOSTELA) coordinator 45˙000.00

Mappa


 Word cloud

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

bond    synthesis   

 Obiettivo del progetto (Objective)

'Metal catalyzed C-H bond functionalization reactions is an area of organic synthesis having an exponential development and a great acceptation in the chemist community because meets the ideals of green chemistry. In this proposal we present a project research based on the development of new strategies of C-H bond activation/cycloaddition that leads to the formation of functionalized heterocycles. Furthermore the methodology is proposed to be applied to the synthesis of piperidine acid analogs, known prenyltransferase inhibitors. The inhibition of prenyltransferases could prevent the proper functioning of the Ras (protein), which is commonly abnormally active in cancer, and it could be key for the development of new therapeutics in the fight against this widespread illness.'

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