DASCA

Direct Alkylation of Saturated Cyclic Amines via catalytic C-H Functionalization

 Coordinatore UNIVERSITEIT ANTWERPEN 

 Organization address address: PRINSSTRAAT 13
city: ANTWERPEN
postcode: 2000

contact info
Titolo: Mrs.
Nome: Anne
Cognome: Adams
Email: send email
Telefono: +32 3 265 30 28
Fax: +32 3 265 30 11

 Nazionalità Coordinatore Belgium [BE]
 Totale costo 169˙800 €
 EC contributo 169˙800 €
 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-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-03-01   -   2015-02-28

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITEIT ANTWERPEN

 Organization address address: PRINSSTRAAT 13
city: ANTWERPEN
postcode: 2000

contact info
Titolo: Mrs.
Nome: Anne
Cognome: Adams
Email: send email
Telefono: +32 3 265 30 28
Fax: +32 3 265 30 11

BE (ANTWERPEN) coordinator 169˙800.00

Mappa


 Word cloud

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

bonds    groups    functional    direct   

 Obiettivo del progetto (Objective)

'Direct conversion of C-H into C-C bonds is arguably indispensable in modern organic chemistry, as it allows for obtaining target compounds which are otherwise only accessible via lengthy procedures involving multi-step synthesis. Catalytic C-H functionalization is the most attractive approach to achieve this goal, as it does not require stoichiometric amounts of activating reagent. This research proposal aims to develop direct transition metal-catalyzed functionalizations of C(sp3)–H bonds in saturated nitrogen-based heterocycles, with a particular focus on compatibility with a very broad range of functional groups, regioselectivity and stereoselectivity. Towards this goal, insertion reactions with substituted alkenes featuring a variety of functional groups will be explored. The development of such a technology offers an important contribution to novel, improved and more sustainable synthetic pathways and is expected to be highly warranted for drug discovery purposes.'

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