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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.

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

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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