HEИндивидуална стипендия2024–2026

BRAT · Development of a boryl radical-mediated H-atom transfer umpolung blueprint to make nucleophilic radicals behave as electrophilic species

„Хоризонт Европа“ — Действия „Мария Склодовска-Кюри“

Период
2024-06-03 → 2026-06-02
Финансиране от ЕС
189 687 €
Участници
1
Схема
HORIZON-TMA-MSCA-PF-EF

Линиите свързват координатора с партньорите.

Накратко на български

Борилните радикали се използват за промяна на химическото поведение на алкилните радикали, за да реагират те с електронно богати ароматни съединения и олефини. Това улеснява синтеза на ценни алифатични продукти, които в момента са трудни за създаване.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Цел на проекта

Aliphatic molecules are integral to every aspect of chemistry and radical chemistry has strong impact in their preparation. However, radical reactions are heavily influenced by the polarity of these species, which ultimately controls their reactivty profile.Most notably, standard alkyl radicals are nucleophilic and therefore do not react with electron rich aromatics and olefins. Electrophilic radicals display strong reactivity with these species but they are of limited synthetic value.This project seeks to address this challenge by developing an innovative approach for radical ""umpolung"". In particular, we will demonstrate the integration of photoredox catalysis and boryl radical-mediated H-atom transfer catalysis, as a unique blueprint for the activation of alpha,alpha-diborylated alkalnes. This will generate alpha,alpha-diborylated radicals that, owing to their strong electrophilic character, will (i) react with electron rich aromatics and olefins and then (ii) enable diverge functionalization. In this way we will overcome the fundamental issue that nucleophilic alkyl radicals do not react with electron rich olefins/aromatics. This reactivity will streamline the preparation of many high-value but difficult to make aliphatic products, will be used in late-stage functionalizations and will substantially expand the fields of photoredox catalysis and boryl radical chemistry.This research capitalizes on recent developments of the Leonori group that has experience in the design of methodologies based on both H-atom transfer and boryl radical reactivity. The completion of such an innovative and ambitious project at RWTH Aachen University will be facilitated by generating, transferring, sharing and disseminating knowledge, and will enhance my future career following the training plan envisioned.""

Оригинален текст от CORDIS (на английски).

Участници

  • RHEINISCH-WESTFAELISCHE TECHNISCHE HOCHSCHULE AACHEN · AachenКоординаторГермания

Връзки

Данни: CORDIS, © Европейски съюз