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CombiCat

Combined Catalysis: Enhancing Asymmetric Synthesis

Total Cost €

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EC-Contrib. €

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Partnership

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Project "CombiCat" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD 

Organization address
address: WELLINGTON SQUARE UNIVERSITY OFFICES
city: OXFORD
postcode: OX1 2JD
website: www.ox.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website http://anderson.chem.ox.ac.uk
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-10-01   to  2018-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK (OXFORD) coordinator 183˙454.00

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 Project objective

The stereoselective synthesis of small organic molecules depends on robust catalytic methods. Despite many advances in enantioselective synthesis, an unsolved challenge in catalysis is the translation of enantioselective catalytic reactions to diastereoselective reactions – where a chiral catalyst controls the outcome of reaction of a chiral substrate.

In this proposal, we seek to investigate this 'double stereodifferentiation' in various organocatalytic reactions, and in transition metal-catalyzed cycloisomerization, two fields which take advantage of the expertise of the host group and the experienced researcher. We further aim to explore the union of these two fields using 'Combined catalysis' – specifically, in dual catalytic processes through which we seek to improve stereoselective syntheses of small organic molecules attractive to the pharmaceutical industry. The culmination of the project will be cascade dual catalytic processes, where the organocatalyst serves to activate the substrate towards metal-catalyzed cycloisomerization, and also to mediate a further asymmetric synthetic transformation.

The successful completion of these goals will require the combined expertise of the two project partners: in metal catalysis (the host group) and organocatalysis (the ER), with the proposal being based on preliminary results in both areas.

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The information about "COMBICAT" are provided by the European Opendata Portal: CORDIS opendata.

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