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N-STRAINED SIGNED

Nitrogen-Radical-Based Radical Strain-Release Strategies for the Divergent Assembly of Polyfunctionalized 3D-Building Blocks

Total Cost €

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EC-Contrib. €

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Partnership

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 N-STRAINED project word cloud

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

saturated    radicals    potency    organic    substantially    propellane    expand    construction    drugs    invention    nitrogenated    chemical    limited    generate    explores    reactivity    polyfunctionalized    replace    lives    hydrocarbons    building    blocks    bicyclo    aromatics    evolve    endeavour    manipulate    release    designing    chemistry    urgent    structural    host    transferring    underpin    introduce    bioisoter    form    3d    plan    compounds    bonds    strained    small    agrochemicals    career    discover    pentylamines    photoredox    react    envisioned    reaction    space    university    motif    materials    valuable    flat    explore    shaped    group    assemble    nitrogen    almost    continuous    architectures    quest    clinical    prepared    severely    preparing       photocatalysis    introducing    central    direct    synthetic    pharmaceutical    preparation    ways    molecules    containing    implications    medicinal    training    facilitated    innovative    manchester    scientific    basis    modifying    difficulties    strain    disseminating    platform    sharing    capitalizes    generating    strategies    pentyl    life    strategic    2d    disclosed    eg    divergent   

Project "N-STRAINED" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF MANCHESTER 

Organization address
address: OXFORD ROAD
city: MANCHESTER
postcode: M13 9PL
website: www.manchester.ac.uk

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 United Kingdom [UK]
 Total cost 212˙933 €
 EC max contribution 212˙933 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF MANCHESTER UK (MANCHESTER) coordinator 212˙933.00

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 Project objective

Nitrogen-containing compounds underpin every aspect of our life: they form the structural basis of almost all drugs, agrochemicals and materials. The invention of methods to form C–N bonds is of strategic importance to discover and evolve molecules with direct implications on our lives. Central to this quest is designing synthetic strategies able to explore novel areas of chemical space. As the pharmaceutical sector is now aware of the greater clinical success of molecules with 3D architectures, developing methods able to assemble 3D-shaped and saturated building blocks is a topic of continuous scientific endeavour. The small and strained bicyclo[1.1.1]pentyl motif has been identified as a valuable bioisoter to replace flat (2D) aromatics and improve the potency of lead molecules. However, difficulties in preparing and modifying this structural element have severely limited its use in medicinal chemistry. There is an urgent need to develop novel methods that can effectively manipulate and introduce this motif into organic compounds. This project seeks to substantially expand the fields of photocatalysis and nitrogen-radicals by introducing the concept of “photoredox strain-release”: a novel reactivity that explores the ability of nitrogen-radicals to react with strained hydrocarbons (eg propellane) and enable a unique preparation of polyfunctionalized bicyclo[1.1.1]pentylamines. This research capitalizes on recent developments of the host group that has disclosed 2 novel ways to effectively generate nitrogen radicals. This reactivity will be integrated with other reaction platform allowing the divergent 1-step construction of many important nitrogenated 3D-building blocks that cannot be prepared by any other method. The development of such an innovative and ambitious project at the University of Manchester will be facilitated by generating, transferring, sharing and disseminating knowledge, and will enhance my future career following the training plan envisioned.

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