Faïza DIABA

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Associate Professor

University of Barcelona

Spain

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Faïza DIABA is an Associate Professor at the University of Barcelona, Spain. Her research areas focus on the biological activity profiles of lactams, using techniques such as in vitro cytotoxicity and in vivo zebrafish assays. Recent publications include studies on palladium-catalyzed reactions and the synthesis of complex organic molecules. She is dedicated to advancing the field of synthetic chemistry with an emphasis on practical applications and assessments of cytotoxicity.

Recent Grants

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Photocatalysis in C-C and C-heteroatom bond formation towards the synthesis of natural compounds-IP Faïza Diaba

Open Date: 2020-01-01

Close Date: 2026-01-01

Grant: Close

Synthesis of natural compounds with cytotoxic activity - IP: Faïza Diaba

Open Date: 2018-01-01

Close Date: 2021-01-01

Faïza DIABA

Research Interests

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Recent Grants

Articles (16)

From In Vitro Cytotoxicity to In Vivo Zebrafish Assays: A Study on 3,3-Dichloro β-, γ- and δ-Lactams and Their Biological Activity Profiles

From In Vitro Cytotoxicity to In Vivo Zebrafish Assays: A Study on 3,3-Dichloro β-, γ- and δ-Lactams and Their Biological Activity Profiles

Palladium-Catalyzed α-Arylation of Esters: Synthesis of the Tetrahydroisoquinoline Ring

Palladium-Catalyzed α-Arylation of Esters: Synthesis of the Tetrahydroisoquinoline Ring

Synthesis of the ABC Core of Daphniphyllum Alkaloids with a [5–6–7] Azatricyclic Scaffold via Ring Expansion of Azabicyclic and Azatricyclic Building Blocks

Microwave-Assisted Atom Transfer Radical Cyclization in the Synthesis of 3,3-Dichloro-γ- and δ-Lactams from N-Alkenyl-Tethered Trichloroacetamides Catalyzed by RuCl2(PPh3)3 and Their Cytotoxic Evaluation

Microwave-Assisted Atom Transfer Radical Cyclization in the Synthesis of 3,3-Dichloro-γ- and δ-Lactams from <i>N</i>-Alkenyl-Tethered Trichloroacetamides Catalyzed by RuCl<sub>2</sub>(PPh<sub>3</sub>)<sub>3</sub> and Their Cytotoxic Evaluation

Catalyst-free photo-induced aerobic radical synthesis of lactams from N-alkenyl trichloroacetamides in 2-methyltetrahydrofuran as the radical initiator under violet light

Cytotoxic Assessment of 3,3-Dichloro-β-Lactams Prepared through Microwave-Assisted Benzylic C-H Activation from Benzyl-Tethered Trichloroacetamides Catalyzed by RuCl2(PPh3)3

Cytotoxic Assessment of 3,3-Dichloro-beta-Lactams Prepared through Microwave-Assisted Benzylic C-H Activation from Benzyl-Tethered Trichloroacetamides Catalyzed by RuCl2(PPh3)(3)

Synthesis of the ABC Ring of Calyciphylline A-Type Alkaloids by a Stereocontrolled Aldol Cyclization: Formal Synthesis of (±)-Himalensine A

Synthesis of the ABC Ring of Calyciphylline A-Type Alkaloids by a Stereocontrolled Aldol Cyclization: Formal Synthesis of (?)-Himalensine A

Photoredox catalysis in the synthesis of γ- and δ-lactams from N-alkenyl trichloro- and dichloroacetamides

Synthesis and reactivity of hydroindole enelactams leading to densely functionalized scaffolds

Radical Reactions in Alkaloid Synthesis: A Perspective from Carbon Radical Precursors

Radical Reactions in Alkaloid Synthesis: A Perspective from Carbon Radical Precursors

Collaborators (2)

Elisabet Teixido

Enrique Gomez Bengoa

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