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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.

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

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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