ORGMET. CARB.

Organometallic Reactions in Carbohydrate Chemistry

 Coordinatore STOCKHOLMS UNIVERSITET 

 Organization address address: Universitetsvaegen 10
city: STOCKHOLM
postcode: 10691

contact info
Titolo: Dr.
Nome: Ian
Cognome: Cumpstey
Email: send email
Telefono: 0046 8 674 7263
Fax: 0046 8 15 49 08

 Nazionalità Coordinatore Sweden [SE]
 Totale costo 171˙831 €
 EC contributo 171˙831 €
 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-2007-2-1-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-02-15   -   2010-01-14

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    STOCKHOLMS UNIVERSITET

 Organization address address: Universitetsvaegen 10
city: STOCKHOLM
postcode: 10691

contact info
Titolo: Dr.
Nome: Ian
Cognome: Cumpstey
Email: send email
Telefono: 0046 8 674 7263
Fax: 0046 8 15 49 08

SE (STOCKHOLM) coordinator 0.00

Mappa


 Word cloud

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

transition    carbohydrate    amine    forming    reactions    plan    cyclisation    coupling    complexes    primary    carbocyclisation    metal    reaction    alkene    alkyne       amines   

 Obiettivo del progetto (Objective)

'The aim of this project is to apply some state of the art transition metal catalysed reactions to carbohydrate systems. We plan to investigate the possibilities of using transition metals to catalyse C-C fond forming cyclisations and C-N bond forming cyclisation and cross-coupling reactions. In carbocyclisation reactions, we will be focussing on ene-yne systems, which will be synthesised from carbohydrate starting materials. Electrophilic transition metal complexes such as gold complexes can induce cyclisation of an alkene onto an activated alkyne. Alternatively, debenzylative etherification may be favoured. Ruthenium complexes can carry out one-pot oxidation-reductive-amination to form secondary amines from primary amines and alcohols. We plan to apply this reaction to the synthesis of amine-linked disaccharides, and also to cyclisation reactions where a carbohydrate-derived diol can cyclise with a primary amine, giving an N-substituted iminosugar or azasugar. A combination approach where alkene and alkyne functionalities are introduced to a molecule by the amine coupling reaction followed by a carbocyclisation will be investigated. The polyhydroxylated products of these reactions will be new or known glycomimetics. The new compounds will be tested for their biological activity by our collaborators.'

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