Expedient access to -alkylphthalimides redox-neutral photocatalysed Giese-type reactions.

Org Biomol Chem

School of Fundamental Science, Zhejiang Pharmaceutical University, No. 666 Siming Road, Ningbo 315500, China.

Published: July 2022

The photoredox-catalysed Giese-type reaction has emerged as a useful and powerful platform for radical-based transformations. Herein, a novel protocol for the preparation of -alkylphthalimides has been successfully developed the reactions of -vinylphthalimides with radicals using alkyl silicates or Hantzsch esters as the radical precursors. According to the result of deuteration experiments, a mechanism involving a radical addition/SET reduction/protonation process has been proposed. The synthetic application of -alkylphthalimide has also been demonstrated by deprotecting the phthalimido group using the Ing-Manske procedure.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d2ob00769jDOI Listing

Publication Analysis

Top Keywords

expedient access
4
access -alkylphthalimides
4
-alkylphthalimides redox-neutral
4
redox-neutral photocatalysed
4
photocatalysed giese-type
4
giese-type reactions
4
reactions photoredox-catalysed
4
photoredox-catalysed giese-type
4
giese-type reaction
4
reaction emerged
4

Similar Publications

Objective: To assess the perceived impact of state and institutional policies on managing pregnancies of unknown location (PUL) at U.S. Ryan residency programs.

View Article and Find Full Text PDF

Lewis acid-catalyzed [2π+2σ] cycloaddition of dihydropyridines with bicyclobutanes.

Chem Commun (Camb)

January 2025

Organisch-Chemisches Institut, Universität Münster, Corrensstraße 40, 48149 Münster, Germany.

Herein we report a simple BF-catalyzed cycloaddition of dihydropyridines with bicyclobutanes for the expedient synthesis of novel three-dimensional azacycle-fused bicyclo[2.1.1]hexane scaffolds.

View Article and Find Full Text PDF
Article Synopsis
  • The study presents a method using TMSOTf to create spiroketal derivatives through hydroalkoxylation and cycloaddition reactions involving hydroxy cyclopropenes and aldehydes.
  • This process generates a donor-acceptor cyclopropane intermediate, allowing for the efficient synthesis of [5.5]- and [6.5]-spiroketals.
  • The resulting spirocyclic compounds can be further modified to produce complex polycyclic heterocycles through metal halogen exchange and copper-catalyzed reactions, with a decarboxylation step that introduces a fourth chiral center.
View Article and Find Full Text PDF

Case report: Treatment of non-medical tetrahydrocannabinol toxicosis with transmucosal cannabidiol-infused dissolving sheets in six dogs.

Front Vet Sci

December 2024

Department of Small Animal Clinical Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL, United States.

Increased cases of canine tetrahydrocannabinol (THC) toxicosis have been reported in North America in recent years. Cases are often evaluated on an emergency basis and treatment has relied upon supportive care which can be costly and prohibitive for some pet owners. The purpose of this report is to describe the clinical findings and outcomes in dogs with non-medical, presumptive THC toxicosis treated by administration of a cannibidiol (CBD)-infused transmucosal dissolving sheet.

View Article and Find Full Text PDF

A rare case of a pure yolk sac testicular tumour presenting in an adult with learning difficulties is presented. Pure yolk sac tumours are much more common in children, but when they do occur in adults, onset can be both insidious and aggressive. The best practice for identification involves the precise use of ultrasound, blood tests for tumour markers and FDG-PET/CT imaging for staging.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!