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OLECAT SIGNED

Development of Stereoselective Olefin Functionalization Methods

Total Cost €

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EC-Contrib. €

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Partnership

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 OLECAT project word cloud

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

acyclic    collection    structures    beneficial    discovery    fe    hydrazines    bicyclic    medicines    olefinic    pyrans    acids    serve    patterns    chemical    small    azides    catalysts    economically    co    discover    sustainable    catalyst    preparation    unsaturated    enantioselective    settings    active    optically    metals    catalytic    utilize    easily    molecule    abundant    regard    convenient    blocks    boronic    routes    efficient    pyrrolidines    strategies    carboxylic    time    convert    building    earth    environmentally    reactions    chemo    boric    found    readily    enantioselectivity    nutraceuticals    executed    functionalization    fragments    materials    agents    chiral    oxidation    aldol    piperidines    carnitine    incorporate    allylation    trienes    furans    mn    cyclic    stereochemical    dienes    tenable    structural    ligands    diastereo    pharma    substantially    stereochemically    bioactive    starting    olefin    classes    form    convergent    regio    amines    synthesis    polyols    saturated    alcohols    nitriles   

Project "OLECAT" data sheet

The following table provides information about the project.

Coordinator
EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH 

Organization address
address: Raemistrasse 101
city: ZUERICH
postcode: 8092
website: https://www.ethz.ch/de.html

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 Switzerland [CH]
 Total cost 2˙498˙635 €
 EC max contribution 2˙498˙635 € (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    EIDGENOESSISCHE TECHNISCHE HOCHSCHULE ZUERICH CH (ZUERICH) coordinator 2˙498˙635.00

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 Project objective

The ability toThe ability to readily access small-molecule building blocks at will has important consequences for the discovery and development of novel medicines and materials. It is particularly beneficial when the chemical methods are convenient while at the same time economically and environmentally tenable and sustainable. We are especially interested in catalytic processes that are easily executed and utilize readily available starting materials to produce optically active products with high regio, chemo, diastereo, and enantioselectivity. The proposal aims to discover, develop, and study a collection of enantioselective olefin functionalization reactions that provide access to useful building blocks, such as amines, azides, hydrazines, nitriles, alcohols, involving acyclic, cyclic and bicyclic structures. The catalyst will be derived from earth abundant metals, such as Fe, Mn, and Co and incorporate novel chiral ligands. The study includes the design and preparation of two structural classes of novel, chiral boric acids that are expected to serve as catalyst for the enantioselective functionalization of unsaturated carboxylic acids and boronic acids. The methods are expected to substantially impact the development of novel strategies for complex molecule synthesis. In this regard, we propose to use the catalysts form this study to convert dienes and trienes into polyols with characteristic stereochemical and oxidation patterns found in bioactive agents, including pharma- and nutraceuticals (carnitine). Such advances enable new approaches that go beyond the well-established methods such as aldol/allylation for the preparation of stereochemically complex fragments. Catalysts will also be developed that convert acyclic olefinic alcohols and amines into optically active, saturated furans, pyrans, pyrrolidines, and piperidines. The implementation of the various catalytic methods in complex settings enables efficient, convergent routes to bioactive agents.

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

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