FP7Individual fellowship2012–2014

AuPdCHARYL · Gold(I)-catalyzed decarboxylation in direct decarboxylative C-H arylation

FP7 — People (Marie Curie Actions)

Duration
2012-09-01 → 2014-08-31
EU contribution
€200,372
Participants
1
Scheme
MC-IEF

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Results in brief

Gold(I)-catalyzed decarboxylation in direct decarboxylative C-H arylation

The project PdAuCHAryl was designed to provide a new method for the synthesis of biaryls, a type of chemical compounds of great importance in a wide range of applications including pharmaceutical and agrochemical industries, materials science and optoelectronics, related compounds being used as fundamental components in light-emitting diodes (a research area that has been recently recognised with the award of the Nobel Prize in physics to three of its main contributors). Our proposed strategy focused on developing a method that would be more simple, efficient and environmentally friendly (i.e. with reduced use of energy and resources and less waste products) than currently available technologies. For this, we planned to build up on previous results from our group and others on the reactivity between gold compounds and aromatic compounds, which we hypothesised would allow for gold to catalyse the direct coupling of two arenes to provide a biaryl (Figure 1). During the first year of the project, we were able to develop and report a proof-of-concept study showing the formation of biaryls from the reaction of aromatic compounds with arylgold compouns (Figure 2a). This study served to prove the feasibility of our approach and encouraged us to continue for the development of a reaction which would use gold only as a catalyst and couple both arenes directly without any previous functionalisation. During the second year we have made significant progress towards achieving such objective. Through extensive experimentation we have identified conditions that allow the coupling of two different arenes with minimal or no formation of undesired by-products (Figure 2b). Work directed to extending the range of starting materials to which it is applicable and to finish optimising the efficiency of the method is ongoing and we expect to be able to publish it soon. The methodology developed, once the optimisation is finished, will open a new route for the preparation of biaryls in a more efficient and simple manner than currently available methods. This is expected to have immediate academic impact by facilitating access to chemical compounds needed for research in other areas, such as medicinal chemistry and molecular biology, materials science, etc. In a longer term, it could be applied in the preparation of industrially useful compounds such as drugs or agrochemicals. The use of this methodology in industrial applications would reduce the number of operations necessary for the preparation of a target compound, thus reducing the cost and favouring the sustainability of the overall process.

Data: CORDIS, © European Union

Project objective

In the present research project we propose the development of new and innovative methodologies for organic synthesis, namely biaryl synthesis, by the combination of different metal-promoted processes. More specifically, the project will be built up on the very efficient procedure for gold-promoted decarboxylation of aromatic carboxylic acids, recently developed by the host group, giving place easily to arylgold(I) species.As we detail below, the transmetallation of these aryl units from gold to other metal (likely palladium) capable of performing an orthogonal transformation as C–H activation would allow the direct cross-coupling of (hetero)arenes (via C–H activation) and aromatic carboxylic acids (via C–CO2H activation, see Scheme 1) without any pre-functionalization.Such a methodology will significantly improve the current methodologies for the synthesis of biaryl motifs (ubiquitous in natural products, pharmaceuticals and organic materials) offering a more direct, economic and significantly greener approach. Replacing the use of organometallic compounds (frequently expensive, not trivial to prepare and giving place to large amounts of metal salt residues) by carboxylic acids (common functional groups in organic compounds, giving place to only CO2 as side product) will make cross-coupling processes more applicable both at laboratory and industrial scales and will very importantly reduce –virtually eliminate– their environmental impact.

Original text from CORDIS.

Participants

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Data: CORDIS, © European Union