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OLECAT SIGNED

Development of Stereoselective Olefin Functionalization Methods

Total Cost €

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EC-Contrib. €

0

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.

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

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

Map

 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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