BIOPYRR

New Methodology for the Synthesis of Bioactive Pyrrolidines and Pyrrolidinones

 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: 441865000000
Fax: 441865000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 130˙430 €
 EC contributo 130˙430 €
 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-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-03-01   -   2011-08-31

 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: 441865000000
Fax: 441865000000

UK (OXFORD) coordinator 130˙430.60

Mappa

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 Word cloud

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privileged    methodology    motif    biologically    synthesis    transition    structures    natural    metal    efficient    synthetic    biological    pyrrolidinone   

 Obiettivo del progetto (Objective)

'The development of new and efficient methodology for the synthesis of privileged structures of biological importance is an ever important goal for organic chemists. Natural products continue to provide a source of such important chemical entities for the treatment of human diseases. In particular the pyrrolidine and pyrrolidinone motif are biologically privileged structures which are present in over 9000 natural products, many of which possess important biological activity. The aim of this proposal is to develop a range of new transition metal mediated and transition metal catalysed synthetic methodologies for the efficient synthesis of pyrrolidines and pyrrolidinones which will be applied to the total synthesis of a biologically important natural product which contains a lactone-pyrrolidinone as its core heterocyclic motif. The developed synthetic methodology will also be applicable to the synthesis of a wide range of biologically active natural product targets.'

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