113 results on '"Mantellini, Fabio"'
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2. Easy one-pot synthesis of multifunctionalized indole–pyrrole hybrids as a new class of antileishmanial agents
3. Tailored Aza-Michael Addition as Key Feature of Novel Approach to 1H-imidazo[5,1-c][1,4]oxazine Scaffolds
4. Synthesis of Azacarbolines via PhIO2-Promoted Intramolecular Oxidative Cyclization of α-Indolylhydrazones
5. Experimental and Theoretical DFT Investigations in the [2,3]-Wittig-Type Rearrangement of Propargyl/Allyl-Oxy-Pyrazolones
6. Synthesis of new polyazines by 1,4 photochemical or anionic polymerization of 1,2-diaza-1,3-butadienes
7. Synthesis of Novel Tryptamine Derivatives and Their Biological Activity as Antitumor Agents
8. Straightforward entry into 5-hydroxy-1-aminopyrrolines and the corresponding pyrroles from 1,2-diaza-1,3-butadienes
9. Construction of Unusual Indole-Based Heterocycles from Tetrahydro-1H-pyridazino[3,4-b]indoles
10. Synthesis of Polycyclic Fused Indoline Scaffolds through a Substrate-Guided Reactivity Switch
11. Synthesis of new dihydroberberine and tetrahydroberberine analogues and evaluation of their antiproliferative activity on NCI-H1975 cells
12. 2-Oxohydrazones, 4-hydrazono-1H-pyrazol-5-ones, and derived products by air oxidation of 1,2-hydrazino-hydrazones
13. Easy access to (E,Z)-beta-nitro-alpha, beta-olefinated hydrazones, 6-oxo-1,6-dihydropyridazines, and 4-chloro-1-aminopyrroles by domino reactions of 1,2-diaza-1,3-butadienes with halogen-coactivated methylene or methine compounds
14. Synthesis of Azacarbolines via PhIO2‑Promoted Intramolecular Oxidative Cyclization of α‑Indolylhydrazones.
15. Reaction of some 1,2-diaza-1,3-butadienes with activated methine compounds. A straightforward entry to 1,4-dihydropyridazine, pyridazine, and 4,5(4H,5H)-cyclopropylpyrazole derivatives
16. 1,2-Diaza-1,3-dienes-based Multi-component Reactions in Sequential Protocols to Synthesize Arylamino 5-hydrazono thiophene-3 carboxylates
17. Sequential MCR via Staudinger/Aza-Wittig versus Cycloaddition Reaction to Access Diversely Functionalized 1-Amino-1H-Imidazole-2(3H)-Thiones
18. Metal and Oxidant-Free Brønsted Acid-Mediated Cascade Reaction to Substituted Benzofurans
19. Unexpected synthesis of 2,3,5,6-tetrahydro-1H-pyrrolo[3,4-c]pyridine-1,3,6-triones via double Michael addition/CS2 extrusion/double cyclization sequence
20. Unprecedented Heteroring Annulated Pyrrolino-tetrahydroberberine Analogues
21. One-Pot Synthesis of Biheterocycles Based on Indole and Azole Scaffolds Using Tryptamines and 1,2-Diaza-1,3-dienes as Building Blocks
22. Reactivity of 1,2-Diaza-1,3-dienes with Azomethine Ylides: [3+4] versus [3+2] Cycloadditions
23. Straightforward access of pyrazines, piperazinones, and quinoxalines by reactions of 1,2-diaza-1,3-butadienes with 1,2-diamines under solution, solvent-free, or solid-phase conditions
24. Solvent-free reaction of some 1,2-diaza-1,3-butadienes with phosphites: Environmentally friendly access to new diazaphospholes and E-hydrazonophosphonates
25. Divergent Approach to Thiazolylidene Derivatives: A Perspective on the Synthesis of a Heterocyclic Skeleton from β-Amidothioamides Reactivity
26. Access to new 2-oxofuro[2,3-b]pyrroles and 2-methylenepyrroles through the reaction of 1,2-diaza-1,3-butadienes and gamma-ketoesters
27. Regioselective [1N+2C+2C] assembly of fully decorated pyrroles from primary amines, 1,2-diaza-1,3-dienes and 2,3-allenoates
28. Expeditious synthesis of new 1,2,3-thiadiazoles and 1,2,3-selenadiazoles from 1,2-diaza-1,3-butadienes via Hurd-Mori-type reactions
29. Divergent Approach to Thiazolylidene Derivatives: A Perspective on the Synthesis of a Heterocyclic Skeleton from β-Amidothioamides Reactivity
30. Reactivity of 1,2-Diaza-1,3-dienes with Azomethine Ylides: [3+4] versus [3+2] Cycloadditions
31. Aza-Diels-Alder Reaction Between 1,2-Diaza-1,3-dienes and beta-Aryl-alpha,beta-unsaturated Carbonyl Compounds. Easy One-pot Entry to 2’-Oxo-imidazo[1’,5’- f]tetrahydropyridazine
32. Diversity-oriented synthesis of functionalized 1-aminopyrroles by regioselective ZnCl2-catalyzed one-Pot conjugate addition/cyclization reactions of 1,3-bis(silyl enol ethers) with 1,2-diaza-1,3-butadienes
33. Interceptive [4 + 1] Annulation of in Situ Generated 1,2-Diaza-1,3-dienes with Diazo Esters: Direct Access to Substituted Mono-, Bi-, and Tricyclic 4,5-Dihydropyrazoles
34. Expeditious synthesis of new 1,2,3-thiadiazoles and 1,2,3-selenadiazoles from 1,2-diaza-1,3-butadienes via Hurd-Mori reactions
35. Improved synthesis of substituted quinoxalines from new N=N-polymer-bound 1,2-diaza-1,3-butadienes
36. Eclectic 1-aryl-1,2-diaza-1,3-butadienes: valuable tools for the preparation of pyrrol-2-ones, 1-arylpyrazoles, 2-(3-oxopyrazol-4-yl)malonates and 4-(2-oxopyrrol-3-yl)pyrazol-3-ones
37. Inverse electron-demand Diels-Alder reactions of (E)-3-diazenylbut-2-enes in water
38. Solid-phase synthesis of triphenylphosphoranylidene-4,5-dihydropyrazol-5-ones, 4-aminocarbonyl-pyrroles, 4-methoxy-1H-pyrazol-5(2H)-ones and 1,2-thiazolin-4-ones from polymer-bound 1,2-diaza-1,3-butadienes
39. 2-Oxohydrazones, 4-Hydrazono-1H-pyrazol-5-ones, and derived products by air oxidation of 1,2-hydrazino-hydrazones
40. Easy access to (E,Z)-β-nitro-α-β-olefinated hydrazones, 6-oxo-1,6-dihydropyridazines, and 4-chloro-1-aminopyrroles by domino reactions of 1,2-diaza-1,3-butadienes with halogen-coactivated methylene or methine compounds
41. First preparation and reaction of polymer-bound 1,2-diaza-1,3-butadienes. A convenient entry to 4-triphenylphosphoranilidene-4,5-dihydropyrazol-5-ones
42. Chemo, regio, and stereoselectivity in the olefination of hydrazone 1,4-adducts between conjugated azoalkenes and sulphur co-activated methylene compounds
43. Reaction of some 1,2-diaza-1,3-butadienes with activated methine compounds. A straightforward entry to 1,4-dihydropyridazine, pyridazine, and 4,5(4H,5H)-cyclopropylpyrazole derivatives
44. Novel and convenient synthesis of 1,4-dihydropyridazines and pyridazines from conjugated azoalkenes
45. Synthesis and reactions of some 4-chloro-4-alkoxycarbonyl-1,2-diaza-1,3-butadienes
46. Divergent Regioselective Synthesis of 2,5,6,7-Tetrahydro-1H-1,4-diazepin-2-ones and 5H-1,4-Benzodiazepines
47. Synthesis of Functionalized Pyrroles via Catalyst- and Solvent-Free Sequential Three-Component Enamine−Azoene Annulation
48. Straightforward Access to Pyrazines, Piperazinones, and Quinoxalines by Reactions of 1,2-Diaza-1,3-butadienes with 1,2-Diamines under Solution, Solvent-Free, or Solid-Phase Conditions
49. Solvent-Free Reaction of Some 1,2-Diaza-1,3-butadienes with Phosphites: Environmentally Friendly Access to New Diazaphospholes andE-Hydrazonophosphonates
50. Access to New 2-Oxofuro[2,3-b]pyrroles and 2-Methylenepyrroles through the Reaction of 1,2-Diaza-1,3-butadienes and γ-Ketoesters
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