Hola,
¿eres nuevo aquí?

Regístrate gratis y conecta tu empresa con financiación pública, partners y proyectos.

Tengo cuenta

Regístrate

Ver video

LAB-SMART

Financiado

Cerrado

Lewis Acidic Borocations improving Suzuki couplings Material synthesis Alky...

Lewis Acidic Borocations improving Suzuki couplings Material synthesis Alkylation and Radical Transformations "Carbon-carbon bond formation is arguably the most important reaction in synthetic chemistry, exemplified by the award of five noble prizes. The most recent Nobel prize was awarded for the development of palladium catalysed cross... ver más

30/09/2017

UNIVERSITY OF MANC...

1M€

Presupuesto del proyecto: 1M€

Líder del proyecto

THE UNIVERSITY OF MANCHESTER No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo FP7 notifico la concesión del proyecto el día 2017-09-30 No tenemos la información de la convocatoria

0% 100%

Información adicional privada

No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

UNIVERSITY OF MANCHESTER

0.00€ | Lider

Proyectos interesantes

EMTECS

Chemical Engine...

Materials Scien...

195K€ Cerrado

FUNTASTIC

Chemical Engine...

Materials Scien...

231K€ Cerrado

NewBorN

Chemical Engine...

Materials Scien...

195K€ Cerrado

DECOCHEM

Chemical Engine...

Materials Scien...

183K€ Cerrado

BRADOCO

Chemical Engine...

Materials Scien...

174K€ Cerrado

CTQ2017-85203-P

Chemical Engine...

Materials Scien...

97K€ Cerrado

Conecta tu I+D

¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video

Líder del proyecto

THE UNIVERSITY OF MANCHESTER No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 1M€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto "Carbon-carbon bond formation is arguably the most important reaction in synthetic chemistry, exemplified by the award of five noble prizes. The most recent Nobel prize was awarded for the development of palladium catalysed cross coupling, of which Suzuki cross coupling is the most widely applied version in industry and academia and utilizes organo-boronates (RB(OR)2) as the nucleophilic component. The aims of this project are; (i) to simplify the synthesis of organo-boron compounds that are utilized in (a) Suzuki cross coupling and (b) as boron containing materials for organic electronic applications. (ii) Reduce the dependency on expensive and toxic palladium by a) extending the Friedel Crafts C-C bond forming reaction to broad scope, electrophilic trifluoromethylation and electrophilic arylation (b) generating and applying efficient iron catalysts in an iron analogue of the Suzuki Reaction. To achieve each of our aims we will utilise the unique properties of electrophilic borocations. Previously we have used boro-cations that combine a coordinatively unsaturated and electrophilic boron centre with a ‘masked’ form of a strong base to develop fundamentally new reactivity. These borocations enabled the sequential one pot activation of a substrate by a strong Lewis acid (the boro-cation) and then release of the masked Lewis base for a subsequent step (e.g., deprotonation). This concept of a boron reagent enabling sequential reactivity by subsequent dissociation of a group is a continual theme through this proposal. This property of borocations will be combined with appropriate leaving groups on the nucleophile to tackle the important challenges outlined above. Key to expanding the synthetic utility is design of the borocation to enable the release not only of a neutral Lewis base (for direct borylation, including the synthesis of RB(OR)2) but also an anionic group (for arylation/alkenylation) or a cationic moiety (for alkylation)."

Conecta tu I+D

Entra hoy

¿Olvidé mi contraseña?

Financiación

Empresas

CTIs/Universidades

Proyectos

Investigadores