Pieterjan Winant
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Pieterjan Winant has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Wim Dehaen
Department of Chemistry KU Leuven Leuven Belgium
2 shared publications - Flavio da Silva Emery
University of São Paulo
1 shared publication - Shaiani Maria Gil de Melo
Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences at Ribeirao Preto of the University of Sao Paulo, Ribeirao Preto 14040903, SP, Brazil
1 shared publication - Tomas Horsten
Max-Planck-Institute for Chemical Energy Conversion, Stiftstrasse 34–36, 45470 Mülheim an der Ruhr, Germany
1 shared publication
Latest Publications
- Open Access
- 6 September 2021
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 17, 2315-2320
A visible-light-induced, metal-free bis-arylation of 2,5-dichlorobenzoquinone
A metal-free protocol for the direct bis-arylation of 2,5-dichlorobenzoquinone with aryldiazonium salts is reported. The reactive salts are generated in situ and converted to radicals through irradiation with visible light. Reaction products precipitate from the solvent, eliminating the need for purification and thus providing a novel green method for the synthesis of versatile bis-electrophiles.
- 6 September 2021
- Published by Beilstein Institut in Beilstein Journal of Organic Chemistry
- Vol. 17, 2315-2320
Open AccessA visible-light-induced, metal-free bis-arylation of 2,5-dichlorobenzoquinone
A metal-free protocol for the direct bis-arylation of 2,5-dichlorobenzoquinone with aryldiazonium salts is reported. The reactive salts are generated in situ and converted to radicals through irradiation with visible light. Reaction products precipitate from the solvent, eliminating the need for purification and thus providing a novel green method for the synthesis of versatile bis-electrophiles.
- Open Access
A Review of the Synthetic Strategies toward Dihydropyrrolo[1,2-a]Pyrazinones
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 provides an overview of these synthetic pathways. The literature is covered up until 2020 and is organized according to the specific strategies used to construct the scaffold: fusing a pyrazinone to an existing pyrrole, employing a pyrazinone-first strategy, an array of multicomponent reactions and some miscellaneous reactions.
Open AccessA Review of the Synthetic Strategies toward Dihydropyrrolo[1,2-a]Pyrazinones
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 provides an overview of these synthetic pathways. The literature is covered up until 2020 and is organized according to the specific strategies used to construct the scaffold: fusing a pyrazinone to an existing pyrrole, employing a pyrazinone-first strategy, an array of multicomponent reactions and some miscellaneous reactions.