DIAZOFREE

Efficient Synthesis of N-Heterocycles using Ynamides as Diazo Equivalents

Coordinatore	THE UNIVERSITY OF BIRMINGHAM    more  Organization address address: Edgbaston city: BIRMINGHAM postcode: B15 2TT contact info Titolo: Ms. Nome: May Cognome: Chung Email: send email Telefono: 441214000000
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	200˙371 €
EC contributo	200˙371 €
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-2011-IEF
Funding Scheme	MC-IEF
Anno di inizio	2012
Periodo (anno-mese-giorno)	2012-03-01   -   2014-02-28

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	THE UNIVERSITY OF BIRMINGHAM  Organization address address: Edgbaston city: BIRMINGHAM postcode: B15 2TT contact info Titolo: Ms. Nome: May Cognome: Chung Email: send email Telefono: 441214000000	UK (BIRMINGHAM)	coordinator	200˙371.80

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 Obiettivo del progetto (Objective)

'Diazo groups are the most commonly used precursors for the controlled formation of very widely employed metal carbenes. However, the potential hazards associated with their use, coupled with the synthetic inefficiency and structural and functional group restrictions that are imposed from their installation, are limiting. This project is aimed at developing, studying and applying an alternative diazofree approach to access versatile metal carbenoid intermediates. New methodologies will result in valuable N-heterocyclic structures widely found in functional materials and many biologically active natural products, pharmaceuticals and agrochemicals. The proposed gold-catalysed novel transformations of ynamides will be combined with recent advances in copper catalysis for a short, efficient and general two-step synthetic strategy to prepare a wide variety of functionalised N-heterocycles from simple amine derivatives and (pseudo)alkynes. After establishing the reactivity concept, which will further the understanding of a new area of transition-metal catalysis, the wider synthetic applicability of this strategy will be explored. The potential value and impact of this method will be demonstrated to the wider synthetic community by its specific utility in target-led synthesis. Alongside the scientific impact of the research, the incorporated outreach activities will increase public awareness of the relevance of such research, generate enthusiasm in younger generations to pursue interest in science, and establish a generally accessible resource on gold catalysis. The skills and experience generated in this manner will complement the scientific leadership, communication and knowledge-transfer ability which will be established alongside the practical and intellectual skills and expertise in transition-metal catalysis and methodology that develop from this project.'