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Foldmetcat SIGNED

Bioinspired Catalytic Metallofoldamers

Total Cost €

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EC-Contrib. €

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Partnership

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 Foldmetcat project word cloud

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

enantioselectively    metals    sites    donor    substrate    phosphonite    digold    hydrogen    enzymes    stereogenic    attain    generate    prepare    anion    rooted    single    pairing    c2    activation    inspired    polyunsaturated    inherent    series    initiated    reactive    unprecedented    gold    arrangement    clusters    larger    unconventional    delineate    cyclase    cavitant    efficient    modes    carbocyclic    catalysts    containing    polyenes    simultaneously    carbocation    mixed    ligands    bond    intrinsic    supramolecular    close    mimicking    paradigm    ophiobolin    site    zinc    organometallic    explore    cascades    catalytic    prototypes    purpose    terpenoid    chiral    transition    activate    heterobimetallic    heterocyclic    types    translocation    first    chemistry    carbenes    skeletons    cyclization    intramolecular    metallic    distant    diphosphines    polyenynes    structurally    reaction    metal    cyclizations    fundamental    reactivity    centers    folding    complexes    resorcinarene    electrophilic    substrates    initial    fold    taxol   

Project "Foldmetcat" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO PRIVADA INSTITUT CATALA D'INVESTIGACIO QUIMICA 

Organization address
address: AVENIDA PAISSOS CATALANS 16
city: TARRAGONA
postcode: 43007
website: www.iciq.es

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 Spain [ES]
 Total cost 2˙500˙000 €
 EC max contribution 2˙500˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-ADG
 Funding Scheme ERC-ADG
 Starting year 2019
 Duration (year-month-day) from 2019-09-01   to  2024-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO PRIVADA INSTITUT CATALA D'INVESTIGACIO QUIMICA ES (TARRAGONA) coordinator 2˙500˙000.00

Map

 Project objective

Inspired by mimicking the characteristics of terpenoid cyclase enzymes, the goal of this proposal is to design new types of catalysts containing electrophilic transition metal centers that could simultaneously fold and activate polyunsaturated substrates promoting non-inherent cyclization modes. Our goal is unprecedented, although it is rooted on fundamental organometallic chemistry, in particular, on the known activation of polyunsaturated substrates by highly electrophilic transition metals. These unconventional cyclizations cascades challenge the paradigm that the intrinsic reactivity of the substrate is the relevant factor in carbocation-initiated processes and would provide access to large carbocyclic skeletons such as those present in taxol and ophiobolin enantioselectively in a single step under catalytic conditions. Although the initial work will be carried out with gold catalysts, a major goal of this research is to develop other general-purpose efficient chiral electrophilic catalysts based on zinc. To attain our goal, we will study more simple catalysts to delineate the factors that control the folding of polyenynes and polyenes. Thus, we will prepare new series of C2-chiral catalysts in which the stereogenic elements are close to the reaction site. Related C2-chiral systems will be generated by supramolecular hydrogen-bond pairing. A similar chiral arrangement could also be achieved by an intramolecular chiral anion translocation from the metal to a distant hydrogen-bond donor site. In addition, we will explore larger systems based on structurally well-defined metallic clusters to generate highly electrophilic chiral reactive sites. The folding and activation of polyunsaturated substrates will be studied first with a series of catalytic prototypes based on digold or heterobimetallic complexes with N-heterocyclic carbenes, diphosphines, mixed ligands of these types, as well as resorcinarene-phosphonite cavitant ligands.

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

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