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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.

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

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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