M
Martin Gazvoda
Researcher at University of Ljubljana
Publications - 34
Citations - 572
Martin Gazvoda is an academic researcher from University of Ljubljana. The author has contributed to research in topics: Catalysis & Reagent. The author has an hindex of 11, co-authored 29 publications receiving 436 citations.
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Journal ArticleDOI
Synthesis of 1,4-Benzodiazepine-2,5-diones by Base Promoted Ring Expansion of 3-Aminoquinoline-2,4-diones
Filip Křemen,Martin Gazvoda,Stanislav Kafka,Karel Proisl,Anna Srholcová,Antonín Klásek,Damijana Urankar,Janez Košmrlj +7 more
TL;DR: An unprecedented reactivity of 3-aminoquinoline-2, 4-diones is reported and a proposed mechanism of the rearrangement and the conformational equilibrium of 1,4-benzodiazepine- 2,5-dione rings are discussed.
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Copper-Catalyzed Azide–Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles
TL;DR: A copper-catalyzed cycloaddition of hydrogen azide with terminal alkynes to form 4-substituted-1H-1,2,3-triazoles in a sustainable manner is reported, showing diverse functional group tolerance and applicable for late-stage functionalization synthetic strategies.
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Systematic Evaluation of 2-Arylazocarboxylates and 2-Arylazocarboxamides as Mitsunobu Reagents.
TL;DR: SC-DSC analysis of representative 2-arylazocarboxylate and 2- Daryl azocar boxamide derivatives has shown high thermal stability, indicating that these azo reagents possess lower chemical hazard compared with typical azoReagents.
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Versatile Coordination of Azocarboxamides: Redox‐Triggered Change of the Chelating Binding Pocket in Ruthenium Complexes
Johannes Klein,Julia Beerhues,David Schweinfurth,Margarethe van der Meer,Martin Gazvoda,Goutam Kumar Lahiri,Janez Košmrlj,Biprajit Sarkar +7 more
TL;DR: The first instance in which a redox-driven change in the complete chelating binding pocket has been observed in a ruthenium complex as well as with azo-based ligands is observed, showing the potential of these versatile azocarboxamide ligands to act as red ox-driven switches with possible relevance to electrocatalysis.
Journal ArticleDOI
Completely Stereocontrolled Aldol Reaction of Chiral β-Amino Acids
Martin Gazvoda,Kathrin Höferl-Prantz,Roland Barth,Wolfgang Felzmann,Andrej Pevec,Janez Košmrlj +5 more
TL;DR: A general protocol to independently access stereoisomerically pure β'-hydroxy-β-amino acid derivatives that is based on dibutylboron triflate-mediated aldol reaction of suitably protected β-aminos acids bearing chiral oxazolidinone auxiliary is reported.