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

Información del proyecto

N-STRAINED

Identificador del acuerdo de subvención: 842422

DOI

10.3030/842422

Proyecto cerrado

Fecha de la firma de la CE 22 Marzo 2019

Fecha de inicio 1 Abril 2019

Fecha de finalización 31 Marzo 2021

Financiado con arreglo a

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Coste total

€ 212 933,76

Aportación de la UE

€ 212 933,76

Coordinado por

THE UNIVERSITY OF MANCHESTER
United Kingdom

Periodic Reporting for period 1 - N-STRAINED (Nitrogen-Radical-Based Radical Strain-Release Strategies for the Divergent Assembly of Polyfunctionalized 3D-Building Blocks)

Período documentado: 2019-04-01 hasta 2021-03-31

Resumen del contexto y de los objetivos generales del proyecto

• What is the problem/issue being addressed?
This Fellowship aimed at delivering transformative advances towards the assembly of nitrogenate molecules of interest to the pharmaceutical and agrochemical sectors. The project was based on the use of visible-light as the source of energy for the generation and use of nitrogen radicals in catalysis. A relevant part of the project was based on achieving strai-release amination using [1.1.1]propellane and obtain in one single chemical step bicyclo[1.1.1]pentylamines.

• Why is it important for society?
This project aims at delivering fundamental advances for the preparation of nitrogenated molecules, which are fundamental to the discovery and evolution of drugs, agrochemicals and food additives. Improving the way we make these molecules underpins the manufacture of high-value materials that impact positively our lives.

• What are the overall objectives?
1) Develop novel starin-release startegies of nitrogen radicals to achieva aminochlorination.
2) Develop novel divergent and multicomponent processes for the single step assembly of bicyclo[1.1.1]pentylamines
3) Apply the starin-release experimentation in transition metal catalysis with nickel to expand the pool of divergent functionalizations.

Trabajo realizado desde el comienzo del proyecto hasta el final del período abarcado por el informe y los principales resultados hasta la fecha

• We started our work identifying conditions for the succesful preparation of [1.1.1]propellane in different organic solvents compatible for integration with photoredox catalysis.
• We then prepared a broad range of nitrogen radical precursors for the generation of amidyl radicals under photoredox conditions.
• We have spent considerable time optimising the key strain-release functionalization which meant solving problems of reactivity.
• Once the key reactions were optimised we evaluated the scope of the process trying to identify full applicability and also limiting factors
• Once the key substrates were prepared and purified we conducted detailed X-ray crystallography studies to determine the structural features of these building blocks. This information proved to be pivotal for understanding their ability of acting as aromatic bioisosteres.
• This work has been published in the peer-reviewed journal Angew. Chem. Int. Ed. 2020,59, 8225 and was highlighted in Synfact 2020, 16, 423.

Avances que van más allá del estado de la técnica e impacto potencial esperado (incluida la repercusión socioeconómica y las implicaciones sociales más amplias del proyecto hasta la fecha)

• The results obtained in this Fellowship have demonstrated, for the first time, that nitrogen radicals can be used in radical strain-release amination reactions.
• the transformation that we have developed are a unique class of multicomponent processes that enable the divergent preparation of many high-value building block in one singlke chemical step.
• the mechanistic work that we have performed has shed light on many of the fundamental parameters that control both strain release chemistry but also the chemical nature of bicyclo[1.1.1]pentylamines

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