NIGOCAT
Nature-Inspired Gold Catalytic Tools
| Coordinatore | UNIVERSITAET ZUERICH
Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie. |
| Nazionalità Coordinatore | Switzerland [CH] |
| Totale costo | 1˙500˙000 € |
| EC contributo | 1˙500˙000 € |
| Programma | FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) |
| Code Call | ERC-2012-StG_20111012 |
| Funding Scheme | ERC-SG |
| Anno di inizio | 2012 |
| Periodo (anno-mese-giorno) | 2012-10-01 - 2017-09-30 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
UNIVERSITAET ZUERICH
Organization address
address: Raemistrasse 71 contact info |
CH (ZURICH) | hostInstitution | 1˙500˙000.00 |
Mappa
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Obiettivo del progetto (Objective)
'The study of biologically relevant processes heavily relays on “small molecules”. Thus, the demand for novel chemical probes is of highest importance not only for chemistry, but also for closely related disciplines such as biology, medicine or material science. As the construction of complex molecular architectures from chemical building blocks still remains a far-from-routine task, the development of methodologies to increase the control over chemical reactivity and achieve molecular complexity with higher levels of efficiency has become one of the frontier challenges of chemistry in the 21st century. NIGOCAT aims to substantially contribute towards this goal. The general objective of this proposal is the design, synthesis and application in catalysis of novel, nature-inspired gold(I) and gold(III)-catalytic tools able to mimic nature´s efficiency and exquisite taste for the synthesis and stereoselective functionalization of “small molecules”. The proposed research tackles three main challenges faced by current synthetic methods: 1. Efficient generation of structural complexity; 2. Selective C-H bond functionalization; 3. High levels of stereocontrol in asymmetric catalysis. We aim to streamline the construction of molecular complexity based on modular, unprecedented multi-center gold factories. Our hypothesis is that the assembly of different reactive sites within a single catalyst will provide an increased level of efficiency in gold-orchestrated catalytic cascades from simple starting materials, thus mimicking the way nature assembles its complex primary metabolites. Second, we aim to tackle the flexible, selective functionalization of C-H bonds using novel metaloenzyme-inspired ligands on gold. Third, we aim to develop novel gold peptide-based catalytic systems as general tools able to provide high levels of absolute stereocontrol in gold catalysis.'