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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.

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

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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