YLIDXCHEM

DEVELOPMENT AND APPLICATIONS OF NEW YLID CHEMISTRY

 Coordinatore THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Linda
Cognome: Pialek
Email: send email
Telefono: +44 1865 289811
Fax: +44 1865 289801

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 171˙867 €
 EC contributo 171˙867 €
 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-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-07-01   -   2011-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD

 Organization address address: University Offices, Wellington Square
city: OXFORD
postcode: OX1 2JD

contact info
Titolo: Ms.
Nome: Linda
Cognome: Pialek
Email: send email
Telefono: +44 1865 289811
Fax: +44 1865 289801

UK (OXFORD) coordinator 171˙867.62

Mappa


 Word cloud

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

sigmatropic    tandem    oxonium    ylide    cross    rearrangement    pot    metathesis    enantioselective    strategies    methodology    synthesis   

 Obiettivo del progetto (Objective)

'The aims of this research are to develop efficient synthetic methodology for one-pot catalytic cross-metathesis/tandem oxonium ylide formation– [2,3] sigmatropic rearrangement of unsaturated diazocarbonyl substrates, to establish a pool of useful chiral catalysts for this chemistry, and to apply this methodology in strategies for the enantioselective synthesis of selected biologically active natural product classes. The objectives are: Development and scope of one-pot cross-metathesis/tandem oxonium ylide formation– [2,3] sigmatropic rearrangement New catalyst preparation and evaluation in enantioselective tandem ylide formation – rearrangement Development of asymmetric synthesis strategies to hyperolactone anti-HIV agents'

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