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PHOTO ORGANO-GOLD SIGNED

Driving asymmetric photoreactions by merging organo- and gold-catalysis

Total Cost €

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EC-Contrib. €

0

Partnership

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 PHOTO ORGANO-GOLD project word cloud

Explore the words cloud of the PHOTO ORGANO-GOLD project. It provides you a very rough idea of what is the project "PHOTO ORGANO-GOLD" about.

comprising    readily    otherwise    bromide    excellent    molecule    company    photoreactions    competencies    structures    ing    catalysts    remarkable    visible    move    privileged    community    fellow    chemical    activation    unachievable    strategies    date    pharma    cultural    compounds    frameworks    libraries    molecules    small    position    modern    host    mediated    screening    amino    acid    candidate    triggered    lundbeck    photoredox    prosperity    chiral    ir    dk    natural    chemistry    play    perception    unactivated    easily    platform    aryl    activated    assembling    disubstituted    powerful    photo    ideal    oxindole    organic    drug       discovery    chloride    gold    rh    alkyl    alpha    world    unrelated    bearing    avenues    facilitated    optimal    pharmaceutical    organocatalysis    era    broaden    nature    copenhagen    synthesis    probability    desirable    yields    asymmetric    light    changing    basic    catalysis    seven    career    enantiopure    combine    generating    collection    reactions    remained    catalytic    biological    place   

Project "PHOTO ORGANO-GOLD" 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]
 Project website http://www.iciq.org/research/research_group/prof-paolo-melchiorre/
 Total cost 158˙121 €
 EC max contribution 158˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-05-06   to  2018-05-05

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO PRIVADA INSTITUT CATALA D'INVESTIGACIO QUIMICA ES (TARRAGONA) coordinator 158˙121.00

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 Project objective

We are in a changing era for drug discovery: the growing perception is that basic chemical research will play a greater role in pharmaceutical development. One current challenge is to develop a new kind of chemistry that yields a screening collection comprising optimal chiral molecules that increase the probability of success in identifying drug-candidate structures. Also, the chemistry community has recently recognized how visible light-mediated photoreactions can open new avenues in modern organic synthesis and the past seven years have witnessed its remarkable prosperity. Therefore, developing photo-facilitated asymmetric reactions focusing on rapidly generating privileged chiral natural-like compounds for drug discovery are highly desirable. The proposed research aims to combine the fellow’s experience in gold catalysis and the host’s experience in photo-triggered organocatalysis (two powerful fields of molecule activation, which have to date remained unrelated) to develop otherwise unachievable catalytic asymmetric photoreactions. Specifically, we will focus on using readily available, unactivated aryl/alkyl chloride or bromide, which cannot be easily activated by the commonly used Rh- or Ir-based photoredox catalysts. The resulting strategies will be used as an ideal platform for assembling libraries comprising enantiopure chiral small molecules bearing α,α-disubstituted α-amino acid & 3,3-disubstituted oxindole frameworks, which, along with biological screening carried out in collaboration with a world-wide recognized pharma-company (Lundbeck A/S, Copenhagen, DK), will increase the probability of success in identifying drug-candidate structures. The multi-cultural nature of this project will greatly contribute to broaden the fellow competencies and will place him in an excellent position for the next career move

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