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Wim Dehaen

0000-0002-9597-0629

Publications (5)

Synthetic Pathways to Pyrido[3,4-c]pyridazines and Their Polycyclic Derivatives

Temitayo Omowumi Alegbejo Price, Flavio Emery & Wim Dehaen · Organics · 2022

Pyrido[3,4-c]pyridazines are nitrogen-containing scaffolds that have been described as being promising in medicinal chemistry, but they are rather rare chemicals. In this review article, the literature on synthetic pathways towards pyrido[3,4-c]pyridazines is listed exhaustively,...

Open access Research Article 10.3390/org3040028

Exploration of the Divergent Outcomes for the Nenitzescu Reaction of Piperazinone Enaminoesters

Rebecca Hermans, Max Van Hoof, Luc Van Meervelt & Wim Dehaen · Organics · 2023

The Nenitzescu reaction is a condensation reaction between an enamine and a quinone, which can give rise to a wide variety of reaction products depending on the nature of the starting material and the reaction conditions. The most commonly observed products are 5-hydroxyindoles a...

Open access Research Article 10.3390/org4020012

1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4-carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles

Tomas Opsomer, Kaat Valkeneers, Ana Ratković & Wim Dehaen · Organics · 2021

1,2,3-Triazole-4-carbaldehydes are useful synthetic intermediates which may play an important role in the discovery of novel applications of the 1,2,3-triazole moiety. In this work, a one-step multigram scale synthesis of 4-formyl-1-(4-nitrophenyl)-1H-1,2,3-triazole (FNPT) as a p...

Open access Research Article 10.3390/org2040024

A Review of the Synthetic Strategies toward Dihydropyrrolo[1,2-a]Pyrazinones

Pieterjan Winant, Tomas Horsten, Shaiani Gil de Melo, Flavio Emery & Wim Dehaen · Organics · 2021

Dihydropyrrolo[1,2-a]pyrazinone rings are a class of heterocycles present in a wide range of bioactive natural products and analogues thereof. As a direct result of their bioactivity, the synthesis of this privileged class of compounds has been extensively studied. This review pr...

Open access Research Article 10.3390/org2020011