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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.

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

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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