Synthesis and reactivity of aminofuroxans
DM Bystrov, LL Fershtat, NN Makhova - Chemistry of Heterocyclic …, 2019 - Springer
In this review article, we provide general information on the known methods for directed
synthesis of 3-and 4-aminofuroxans, as well as analyze the main aspects of their reactivity …
synthesis of 3-and 4-aminofuroxans, as well as analyze the main aspects of their reactivity …
Recent developments in ruthenium–nitrosoarene chemistry: Unconventional synthetic strategies, new ligand designs, and exploration of ligands redox non-innocence
This review describes the recent advances in ruthenium–nitrosoarene chemistry. The
preparations of Ru–nitrosoarene complexes by (1) intermolecular nitrosonium insertion into …
preparations of Ru–nitrosoarene complexes by (1) intermolecular nitrosonium insertion into …
Ruthenium-Chelated Non-Innocent Bis (heterocyclo) methanides: A Mimicked β-Diketiminate
The unexplored substrate-based reactivity profile of newly designed bis (heterocyclo)
methanide (BHM, L1–L3), a structural mimic of ubiquitous β-diketiminate, was demonstrated …
methanide (BHM, L1–L3), a structural mimic of ubiquitous β-diketiminate, was demonstrated …
Electronically Triggered Switchable Binding Modes of the C-Organonitroso (ArNO) Moiety on the {Ru(acac)2} Platform
This work evaluated the switchable binding profile of the biochemically relevant and redox
non-innocent C-organonitroso (ArNO) moiety with the selective {Ru (acac) 2}(acac …
non-innocent C-organonitroso (ArNO) moiety with the selective {Ru (acac) 2}(acac …
Divergent oriented synthesis of 2H-1, 2, 3-triazoles via rearrangement of furoxanylhydrazones
VA Sereda, LL Fershtat - Mendeleev Communications, 2023 - Elsevier
Divergent oriented synthesis of 2H-1,2,3-triazoles via rearrangement of
furoxanylhydrazones Page 1 Mendeleev Commun., 2023, 33, 764–766 – 764 – Mendeleev …
furoxanylhydrazones Page 1 Mendeleev Commun., 2023, 33, 764–766 – 764 – Mendeleev …
The (Dioximate)NiII/I2 System: Ligand Oxidation and Binding Modes of Triiodide Species
ZM Efimenko, AS Novikov, DM Ivanov… - Inorganic …, 2020 - ACS Publications
Reinvestigation of (o-benzoquinonedioximate) 2Ni/I2 systems demonstrated that the
reaction itself and also the crystallization conditions dramatically affect the identity of …
reaction itself and also the crystallization conditions dramatically affect the identity of …
Isolation of ruthenium–indoline and− indole zwitterion complexes: insight into the metal-induced cyclization of aniline-tethered alkynes and strategy to lower the …
Isolation of the first examples of Ru (II)–indoline and− indole zwitterion complexes derived
from reactions between [Ru ([14] aneS4) Cl2]([14] aneS4= 1, 4, 8, 11 …
from reactions between [Ru ([14] aneS4) Cl2]([14] aneS4= 1, 4, 8, 11 …
Ruthenium derivatives of in situ generated redox-active 1, 2-dinitrosobenzene and 2-nitrosoanilido. Diverse structural and electronic forms
The article describes one-pot synthesis and structural elucidation of tc-[RuII (pap) 2 (L•–)]
ClO4 [1] ClO4 and tc-[RuII (pap) 2 (L′–)] ClO4 [2] ClO4, which were obtained from tc-[RuII …
ClO4 [1] ClO4 and tc-[RuII (pap) 2 (L′–)] ClO4 [2] ClO4, which were obtained from tc-[RuII …
Synthesis, spectroscopic, electrochemistry and antioxidant properties of benzofuroxan and 2H-benzimidazole 1, 3-dioxide derivatives: Effects of conjugation with …
JCP Mayer, PC Pereira, PL Sagrilo, BA Iglesias… - Journal of Molecular …, 2024 - Elsevier
A series of novel benzofuroxan and of 2, 2-dimethyl-2H-benzimidazole 1, 3-dioxide
derivatives conjugated to the strong electron-withdrawing 1, 2, 4-oxadiazole ring and to the …
derivatives conjugated to the strong electron-withdrawing 1, 2, 4-oxadiazole ring and to the …
Solvent‐Mediated Functionalization of Benzofuroxan on Electron‐Rich Ruthenium Complex Platform
An unprecedented reactivity profile of biochemically relevant R‐benzofuroxan (R= H, Me,
Cl), with high structural diversity and molecular complexity on a selective {Ru (acac) …
Cl), with high structural diversity and molecular complexity on a selective {Ru (acac) …