Carlos Díez-Poza
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Carlos Díez-Poza has a total of 34 co-authors. Here are the top co-authors by number of shared publications:
- Asunción Barbero
Department of Organic Chemistry Faculty of Science University of Valladolid (UVa) Campus Miguel Delibes 47011 Valladolid Spain
17 shared publications - Laura Fernández-Peña
Faculty of Pharmacy, University of Castilla-La Mancha. Calle Almansa 14 - Edif. Bioincubadora, 02008, Albacete, Spain
7 shared publications - Christopher J. Whiteoak
Departamento de Química Orgánica y Química Inorgánica, Instituto de Investigación en Química “Andrés M. Del Río” (IQAR) Universidad De Alcalá, Campus Universitario Madrid Spain
3 shared publications - Héctor Barbero
GIR MIOMeT, IU CINQUIMA/Química Inorgánica, Facultad de Ciencias, Universidad de Valladolid, Valladolid E47011, Spain
3 shared publications - Marta Elena Gonzalez Mosquera
Departamento de Química Orgánica y Química Inorgánica, Instituto de Investigación en Química “Andrés M. del Río” (IQAR), Universidad de Alcalá, Campus Universitario, Alcalá de Henares, Madrid 28871, Spain
3 shared publications - Paula González-Andrés
Department of Organic Chemistry, Campus Miguel Delibes, University of Valladolid, 47011 Valladolid, Spain
3 shared publications
Latest Publications
- Open Access
- 7 November 2025
- Published by Springer Nature in Communications Chemistry
- Vol. 8 (1) , 1-30
Homogeneous catalysis in continuous flow integrating photocatalysis, electrocatalysis, and automation technologies
In recent years, homogeneous catalysis in continuous flow has undergone remarkable advances, driving significant progress across a broad range of chemical transformations. In this review, we examine how novel synthetic tools such as photo- and electrocatalysis have been merged with catalytic processes to unlock synthetic opportunities and enable transformations in flow that are challenging under conventional batch conditions. Furthermore, we discuss the integration of automation and high-throughput methodologies, emphasizing their roles in synthesis, catalyst screening and reaction optimization in homogeneous flow catalysis. By providing a unified perspective on these developments, we highlight the impact of modern technologies and the potential for interdisciplinary innovation.
- 7 November 2025
- Published by Springer Nature in Communications Chemistry
- Vol. 8 (1) , 1-30
Open AccessHomogeneous catalysis in continuous flow integrating photocatalysis, electrocatalysis, and automation technologies
In recent years, homogeneous catalysis in continuous flow has undergone remarkable advances, driving significant progress across a broad range of chemical transformations. In this review, we examine how novel synthetic tools such as photo- and electrocatalysis have been merged with catalytic processes to unlock synthetic opportunities and enable transformations in flow that are challenging under conventional batch conditions. Furthermore, we discuss the integration of automation and high-throughput methodologies, emphasizing their roles in synthesis, catalyst screening and reaction optimization in homogeneous flow catalysis. By providing a unified perspective on these developments, we highlight the impact of modern technologies and the potential for interdisciplinary innovation.
- 14 September 2025
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 28 (40)
Exploration of Structure–Property Relationships by Altering Glycol Backbone Unsaturation (Double/Triple Bonds) in Furan‐Based Polyesters
This study highlights both the challenges and opportunities associated with developing bio‐based furanic polyesters. Incorporating unsaturated moieties into glycol chains effectively modulates polymer rigidity and thermal properties, though it requires careful optimization of polymerization conditions. The findings demonstrate the viability of solution polycondensation for synthesizing high‐quality FDCA‐based polyesters with unsaturated glycols and pave the way for further investigations into polymer design strategies that balance flexibility, thermal stability, and environmental sustainability.
- 14 September 2025
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 28 (40)
Exploration of Structure–Property Relationships by Altering Glycol Backbone Unsaturation (Double/Triple Bonds) in Furan‐Based Polyesters
This study highlights both the challenges and opportunities associated with developing bio‐based furanic polyesters. Incorporating unsaturated moieties into glycol chains effectively modulates polymer rigidity and thermal properties, though it requires careful optimization of polymerization conditions. The findings demonstrate the viability of solution polycondensation for synthesizing high‐quality FDCA‐based polyesters with unsaturated glycols and pave the way for further investigations into polymer design strategies that balance flexibility, thermal stability, and environmental sustainability.
- 23 November 2024
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 6 (23) , 14695-14706
Non-Isocyanate Polyurethanes (NIPUs) Incorporating Isomers of Abundant Sugar-Derived 1,4:3,6-Dianhydrohexitols
- 23 November 2024
- Published by American Chemical Society (ACS) in ACS Applied Polymer Materials
- Vol. 6 (23) , 14695-14706
Non-Isocyanate Polyurethanes (NIPUs) Incorporating Isomers of Abundant Sugar-Derived 1,4:3,6-Dianhydrohexitols
- Open Access
- 3 May 2024
- Published by Wiley in Asian Journal of Organic Chemistry
- Vol. 13 (7)
Stereoselective Synthesis of Polysubstituted Tetrahydropyrans by Brønsted Acid‐Mediated Hydroxyalkoxylation of Silylated Alkenols
A convenient route for the preparation of tetrahydropyran (THP) derivatives with a quaternary and tertiary vicinal stereocenters is reported. The atom economy acid‐catalyzed cyclization of allylsilyl alcohols provided polysubstituted tetrahydropyrans in good yields and excellent diastereoselectivities (>95 : 5). In comparison with the traditional oxymercuration procedure, this approach resulted to be more efficient in both yield and stereocontrol.
- 3 May 2024
- Published by Wiley in Asian Journal of Organic Chemistry
- Vol. 13 (7)
Open AccessStereoselective Synthesis of Polysubstituted Tetrahydropyrans by Brønsted Acid‐Mediated Hydroxyalkoxylation of Silylated Alkenols
A convenient route for the preparation of tetrahydropyran (THP) derivatives with a quaternary and tertiary vicinal stereocenters is reported. The atom economy acid‐catalyzed cyclization of allylsilyl alcohols provided polysubstituted tetrahydropyrans in good yields and excellent diastereoselectivities (>95 : 5). In comparison with the traditional oxymercuration procedure, this approach resulted to be more efficient in both yield and stereocontrol.
- Open Access
- 23 May 2023
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 88 (11) , 6776-6783
Changing the Reaction Pathway of Silyl-Prins Cyclization by Switching the Lewis Acid: Application to the Synthesis of an Antinociceptive Compound
Developing new procedures for the synthesis of tetrahydropyrans in a very stereoselective manner is of great importance for the synthesis of THP-containing natural products. Here, we report an interesting protocol for the synthesis of polysubstituted halogenated tetrahydropyrans by silyl-Prins cyclization of vinylsilyl alcohols, in which the nature of the Lewis acid determines the outcome of the process. The methodology has been applied to the synthesis of a known antinociceptive.
- 23 May 2023
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 88 (11) , 6776-6783
Open AccessChanging the Reaction Pathway of Silyl-Prins Cyclization by Switching the Lewis Acid: Application to the Synthesis of an Antinociceptive Compound
Developing new procedures for the synthesis of tetrahydropyrans in a very stereoselective manner is of great importance for the synthesis of THP-containing natural products. Here, we report an interesting protocol for the synthesis of polysubstituted halogenated tetrahydropyrans by silyl-Prins cyclization of vinylsilyl alcohols, in which the nature of the Lewis acid determines the outcome of the process. The methodology has been applied to the synthesis of a known antinociceptive.
- Open Access
- 31 March 2023
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 21 (18) , 3733-3755
Synthesis and applications of the sulfur containing analogues of cyclic carbonates
This review highlights routes for the synthesis of both five- and six-membered cyclic thiocarbonates and presents examples of their reactivities/applications.
- 31 March 2023
- Published by Royal Society of Chemistry (RSC) in Organic & Biomolecular Chemistry
- Vol. 21 (18) , 3733-3755
Open AccessSynthesis and applications of the sulfur containing analogues of cyclic carbonates
This review highlights routes for the synthesis of both five- and six-membered cyclic thiocarbonates and presents examples of their reactivities/applications.
- Open Access
- 22 February 2023
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 52 (18) , 5882-5894
Group 13 salphen compounds (In, Ga and Al): a comparison of their structural features and activities as catalysts for cyclic carbonate synthesis
[InBr(salphen)] is identified as the most active catalyst for conversion of CO2and epoxides to cyclic carbonates compared to the Al and Ga congeners. The elucidated mechanism highlights the importance of both Lewis acidity and ligand fluxionality.
- 22 February 2023
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 52 (18) , 5882-5894
Open AccessGroup 13 salphen compounds (In, Ga and Al): a comparison of their structural features and activities as catalysts for cyclic carbonate synthesis
[InBr(salphen)] is identified as the most active catalyst for conversion of CO2and epoxides to cyclic carbonates compared to the Al and Ga congeners. The elucidated mechanism highlights the importance of both Lewis acidity and ligand fluxionality.
- Open Access
- 15 October 2022
- Published by MDPI AG in Marine Drugs
- Vol. 20 (10) , 642
The Tetrahydrofuran Motif in Marine Lipids and Terpenes
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances, or anticancer drugs. Thus, they have attracted the attention of the synthetics community and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, their isolation, structure determination, and a special focus on their total syntheses and biological profiles.
- 15 October 2022
- Published by MDPI AG in Marine Drugs
- Vol. 20 (10) , 642
Open AccessThe Tetrahydrofuran Motif in Marine Lipids and Terpenes
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances, or anticancer drugs. Thus, they have attracted the attention of the synthetics community and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, their isolation, structure determination, and a special focus on their total syntheses and biological profiles.
- Open Access
- 21 September 2022
- Published by MDPI AG in Preprints.org
The Tetrahydrofuran Motif in Marine Lipids and Terpenes
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances or anticancer drugs. Thus, they have attracted the attention of the synthetic community, and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, with a special focus on their isolation, structure determination, biological profiles and total syntheses.
- 21 September 2022
- Published by MDPI AG in Preprints.org
Open AccessThe Tetrahydrofuran Motif in Marine Lipids and Terpenes
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances or anticancer drugs. Thus, they have attracted the attention of the synthetic community, and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, with a special focus on their isolation, structure determination, biological profiles and total syntheses.
- Open Access
- 3 February 2022
- Published by MDPI AG in Marine Drugs
- Vol. 20 (2) , 120
The Tetrahydrofuran Motif in Polyketide Marine Drugs
Oxygen heterocycles are units that are abundant in a great number of marine natural products. Among them, marine polyketides containing tetrahydrofuran rings have attracted great attention within the scientific community due to their challenging structures and promising biological activities. An overview of the most important marine tetrahydrofuran polyketides, with a focused discussion on their isolation, structure determination, approaches to their total synthesis, and biological studies is provided.
- 3 February 2022
- Published by MDPI AG in Marine Drugs
- Vol. 20 (2) , 120
Open AccessThe Tetrahydrofuran Motif in Polyketide Marine Drugs
Oxygen heterocycles are units that are abundant in a great number of marine natural products. Among them, marine polyketides containing tetrahydrofuran rings have attracted great attention within the scientific community due to their challenging structures and promising biological activities. An overview of the most important marine tetrahydrofuran polyketides, with a focused discussion on their isolation, structure determination, approaches to their total synthesis, and biological studies is provided.