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ELDORADO SIGNED

Electrophilicity-Lifting Directed by Organochalcogen Redox-Auxiliaries and Diversiform Organocatalysis

Total Cost €

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EC-Contrib. €

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Partnership

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 ELDORADO project word cloud

Explore the words cloud of the ELDORADO project. It provides you a very rough idea of what is the project "ELDORADO" about.

realization    superordinate    identification    proper    coupling    lastingly    reactions    utility    societal    innovative    individual    routine    lines    electrophilic    practices    energy    site    catalysis    ecologically    regimes    sciences    bonds    cooperative    prime    efficient    oxidation    regenerative    protocols    biologically    ecological    multiple    rank    inexpensive    heretofore    modern    array    action    economic    source    background    synthesis    polyatomic    opportunity    deficit    technologies    consumption    diverse    hydrocarbons    21st    scientific    sustainable    technological    transform    profound    century    frameworks    visible    enormous    single    despite    air    unprecedented    integral    pressing    context    compounds    redox    renewable    organic    momentous    benefits    certain    catalyst    aromatic    oxidant    chemical    consequently    oxidative    strikingly    consideration    sources    derivatization    cognizant    abundant    rational    chalcogen    put    enantioselective    methodological    manipulation    becomes    components    light    activation    syntheses    pertinence    rearrangement    isolated    natural    polyketide    molecules    issue    regard    limited    aerobic    carbon    modular    gratuitous    metallic    chemoselective   

Project "ELDORADO" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAET REGENSBURG 

Organization address
address: UNIVERSITATSSTRASSE 31
city: REGENSBURG
postcode: 93053
website: http://www.uni-regensburg.de/

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 Germany [DE]
 Total cost 1˙499˙953 €
 EC max contribution 1˙499˙953 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-08-01   to  2024-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAET REGENSBURG DE (REGENSBURG) coordinator 1˙499˙953.00
2    GEORG-AUGUST-UNIVERSITAT GOTTINGENSTIFTUNG OFFENTLICHEN RECHTS DE (GOTTINGEN) participant 0.00

Map

 Project objective

The implementation of viable practices for the ecologically cognizant production and consumption of energy and renewable resources rank among the most pressing societal challenges of the 21st century. Against this background, the design and development of innovative concepts for the sustainable use of energy and energy-rich compounds from regenerative sources becomes a matter of profound technological and scientific pertinence. A promising approach that has been put forward in the context of chemical synthesis is the application of visible light as an inexpensive source of energy and air as an abundant and gratuitous oxidant for the derivatization of certain hydrocarbons. Despite the enormous economic and ecological benefits associated with the use of light and air as integral components of redox reactions, the realization of such processes is strikingly limited to very isolated applications. Consequently, this methodological deficit represents a momentous opportunity for modern chemical sciences to lastingly transform the routine lines of action for the oxidative manipulation of organic molecules. A key issue that needs to be taken into consideration for the design of efficient light-driven aerobic oxidation protocols is the identification of proper catalyst systems that allow for the site- and chemoselective activation of individual bonds within polyatomic frameworks. In this regard, the prime objective of the proposed research program is the rational design of non-metallic and in part cooperative catalysis regimes as enabling technologies for the electrophilic activation of non-aromatic carbon–carbon multiple- and carbon-chalcogen single bonds to facilitate a wide and diverse array of heretofore unprecedented oxidative coupling-, addition-, and rearrangement reactions. To demonstrate its utility in a superordinate context, this methodological concept will be applied in highly modular enantioselective syntheses of biologically relevant polyketide natural products.

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

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