Nome |
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Thermal Stability Evaluation of Nitroalkanes with Differential Scanning Calorimetry, file 6d2272d5-c5ae-48dc-849f-cc1b31a3beb0
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206
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A new fully heterogeneous synthesis of pyrrole-2-acetic acid derivatives, file e0ff0072-8966-9bac-e053-1705fe0af019
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206
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Visible Light Promoted Metal- and Photocatalyst-Free Synthesis of Allylarenes, file e0ff0072-fdbe-9bac-e053-1705fe0af019
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178
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A new one-pot synthesis of quinoline-2-carboxylates under heterogeneous conditions, file e0ff0072-c0a8-9bac-e053-1705fe0af019
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157
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Nitroaldol (Henry) reaction of 2-oxoaldehydes with nitroalkanes as a strategic step for a useful, one-pot synthesis of 1,2-diketones, file e0ff0072-6093-9bac-e053-1705fe0af019
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119
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A New Valuable Synthesis of Polyfunctionalized Furans Starting from β-Nitroenones and Active Methylene Compounds, file e0ff0073-fb79-9bac-e053-1705fe0af019
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115
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3-Alkylated indoles by reduction of sulfonyl indoles under flow chemical conditions, file e0ff0073-d2a2-9bac-e053-1705fe0af019
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98
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Synthesis of Unsymmetrical Bisindolylmethanes by Reaction of Indolylmagnesium Bromides with Sulfonyl Indoles, file e0ff0074-24cf-9bac-e053-1705fe0af019
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93
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β-Nitroacrylates: New Key Precursors of Indole-2-Carboxylates via Fischer Indole Synthesis, file e0ff0073-fb77-9bac-e053-1705fe0af019
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89
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One-pot synthesis of alkyl pyrrole-2-carboxylates starting from β-nitroacrylates and primary amines, file e0ff0072-5fe8-9bac-e053-1705fe0af019
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76
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Reaction of alpha-amido sulfones with functionalized nitrocompounds: a new two-step synthesis of Nalkoxycarbonyl-2,5-disubstituted pyrroles, file e0ff0073-53bc-9bac-e053-1705fe0af019
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49
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Synthesis of Nitro Alcohols by Riboflavin Promoted Tandem Nef-Henry Reactions on Nitroalkanes, file e0ff0074-a5c9-9bac-e053-1705fe0af019
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37
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Catalysts’ evolution in the asymmetric conjugate addition of nitroalkanes to electron-poor alkenes, file 3638ccf0-c2aa-406d-97f4-2cf001c5682a
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18
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Sustainable and fast synthesis of functionalized quinoxalines promoted by natural deep eutectic solvents (NADESs), file cc3f8065-8576-4adc-be14-2f06e2e29ef1
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16
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A New and Effective One-Pot Synthesis of Polysubstituted Carbazoles Starting from β-Nitro-β,γ-Unsaturated-Ketones and Indoles, file e0ff0074-d4e1-9bac-e053-1705fe0af019
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11
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Synthetic Approaches to the Challenging Direct C-Alkylation and C-Allylation of Unactivated Nitroalkanes, file ed71da63-b097-4455-af3f-22f6263b4e33
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10
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A microfluidic flow chemistry platform for organic synthesis: the Hofmann rearrangement, file e0ff0072-4c09-9bac-e053-1705fe0af019
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9
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Total Synthesis of 1”- and 2”-Hydroxycannabidiol Metabolites, file 5ed708e7-7636-453f-a9df-7af57ac18fd1
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8
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Enantioselective Catalyzed Synthesis of Amino Derivatives Using Electrophilic Open-Chain N-Activated Ketimines, file 91a1c1ce-93d5-46de-80eb-d492a2e82875
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7
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Boosting Conjugate Addition to Nitroolefins Using Lithium Tetraorganozincates: Synthetic Strategies and Structural Insights, file 77a3d0ba-9771-41b1-86ac-240e38348d5a
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6
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Overcoming the Usual Reactivity of β-Nitroenones: Synthesis of Polyfunctionalized Homoallylic Alcohols and Conjugated Nitrotriene Systems, file 26c045bb-f9df-41fd-8585-de2a43c3ec7a
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5
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Synthesis and use of nitrocyclopropane derivatives, file e0ff0072-46d9-9bac-e053-1705fe0af019
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5
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Boosting Conjugate Addition to Nitroolefins Using Lithium Tetraorganozincates: Synthetic Strategies and Structural Insights, file e0ff0074-9231-9bac-e053-1705fe0af019
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5
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Synthesis of carlina oxide analogues and evaluation of their insecticidal efficacy and cytotoxicity, file 4734393e-1db5-4630-9610-1795131cf7a3
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4
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A New One-Pot Synthesis of 3,6-Disubstituted Pyridazines Starting from β-Nitro-β,γ-Unsaturated Ketones, file 67ce252a-51b9-48eb-9440-432c9ef2130c
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4
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More Chips to Nitroolefins: Decatungstate Photocatalysed Hydroalkylation Under Batch and Flow Conditions, file ccc0b3ee-a82d-4686-9532-3b3b76d6f0a0
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4
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Eco-friendly synthesis of beta-nitro ketones from conjugated enones: an important improvement of the Miyakoshi procedure, file e0ff0072-471d-9bac-e053-1705fe0af019
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4
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Continuous flow based catch and release protocol for the synthesis of α-Ketoesters, file e0ff0072-4c0b-9bac-e053-1705fe0af019
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3
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A Practical and Efficient Conversion of Luteolin into Luteoloside, file e0ff0074-e3ed-9bac-e053-1705fe0af019
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3
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Reaction of carbon nucleophiles with alkylideneindazolium and indolium ions generated from 3-(1-arylsulfonylalkyl)indazoles and indoles, file e0ff0072-4aef-9bac-e053-1705fe0af019
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2
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Arylsulfonyl Group: Activating Properties and Recent Synthetic Applications, file e0ff0072-4c39-9bac-e053-1705fe0af019
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2
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Sulfonyl Azoles in the Synthesis of 3-Functionalized Azole Derivatives, file e0ff0072-9af5-9bac-e053-1705fe0af019
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2
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Synthesis of β-Nitro Ketones by Chemoselective Reduction of β-Nitro Enones under Solid Heterogeneous Catalysis, file e0ff0072-fcbf-9bac-e053-1705fe0af019
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2
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A Practical and Efficient Synthesis of (±)-Anatabine, file e0ff0073-17df-9bac-e053-1705fe0af019
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2
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Synthetic Approach to the Preparation of (2-Acetoxy)allyl Nitro Compounds, file e0ff0073-8559-9bac-e053-1705fe0af019
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2
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Tryptophol and derivatives: natural occurrence and applications to the synthesis of bioactive compounds, file e0ff0073-cea5-9bac-e053-1705fe0af019
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2
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Diastereoselective Isomerization of (E)-β-Nitroenones into β-Nitro-β,γ-Unsaturated Ketones under Microwave Conditions, file e0ff0074-9229-9bac-e053-1705fe0af019
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2
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Synthesis of Heterocyclic Systems Starting from Carbonyl and Carboxyl Functionalized Nitro Compounds by One-Pot Processes, file e0ff0074-922d-9bac-e053-1705fe0af019
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2
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Three-Step Synthesis of Highly Substituted Phenols from 1,3-Dinitropropanes, file e0ff0072-46db-9bac-e053-1705fe0af019
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1
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Synthesis of 3-(Tosylalkyl) Indazoles and their Desulfonylation Reaction. A New Entry to 3-Substituted Indazoles by an Unprecedented Friedel–Crafts Process, file e0ff0072-486f-9bac-e053-1705fe0af019
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1
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Reaction of 3-(1-arylsulfonylalkyl)-indoles with easily enolisable derivatives promoted by potassium fluoride on basic alumina, file e0ff0072-491a-9bac-e053-1705fe0af019
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1
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Synthesis of 3-substituted indoles via reactive alylideneindolenine intermediates, file e0ff0072-4af0-9bac-e053-1705fe0af019
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1
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Regioselective Synthesis of 3-Substituted Pyrroles by Nucleophilic Addition of 3-(1-Arylsulfonylalkyl) Pyrroles Activated under Basic or Acid Conditions, file e0ff0072-4c27-9bac-e053-1705fe0af019
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1
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Nitroalkanes as Key compounds for the Synthesis of Amino Derivatives, file e0ff0072-4d23-9bac-e053-1705fe0af019
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1
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A Two step Synthesis of Unsymmetrical 1,4-Disubstituted Carbazoles from Sulfonyl Indoles Under Heterogeneous Catalysis, file e0ff0072-4e4c-9bac-e053-1705fe0af019
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1
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Double functionalization of N-Boc-3-(tosylmethyl)indole exploiting the activating properties of the tosyl group, file e0ff0072-5019-9bac-e053-1705fe0af019
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1
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Ketosulfonyl indoles in the regiodefined synthesis of tryptophols and related indole derivatives, file e0ff0072-515b-9bac-e053-1705fe0af019
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1
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Solvent-Free Non-Covalent Organocatalysis: EnantioselectiveAddition of Nitroalkanes to Alkylideneindolenines as a FlexibleGateway to Optically Active Tryptamine Derivatives, file e0ff0072-517c-9bac-e053-1705fe0af019
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1
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Metal-free synthesis of imido derivatives by direct oxidation of α-amido sulfones, file e0ff0072-5265-9bac-e053-1705fe0af019
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1
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Synthetic Approaches to 3‑(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds, file e0ff0072-5d83-9bac-e053-1705fe0af019
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1
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Synthesis and Functionalization of Unsymmetrical Arylsulfonyl Bisindoles and Bisbenzazoles, file e0ff0072-6002-9bac-e053-1705fe0af019
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1
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A Photochemical Route to Benzo[a]carbazoles via Domino Elimination/Electrocyclization of 2-Aryl-3-(1-tosylalkyl)indoles, file e0ff0072-6073-9bac-e053-1705fe0af019
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1
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A New Synthesis of Polyfunctionalized 2-Alkyl-1,4-diketones, file e0ff0072-6092-9bac-e053-1705fe0af019
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1
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Synthesis of 3-(2-Nitroalkyl)pyrroles from Sulfonylpyrroles and their Conversion to 6-Azaindole Derivatives, file e0ff0072-62a2-9bac-e053-1705fe0af019
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1
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Two-Step Synthesis of Polysubstituted 6-Nitroindoles under Flow Chemical and Microwave Conditions, file e0ff0072-f6cc-9bac-e053-1705fe0af019
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1
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A new, low impact and efficient synthesis of ω-nitro esters under solid heterogeneous catalysis, file e0ff0072-fcc3-9bac-e053-1705fe0af019
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1
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Oxidative Conversion of Sulfonyl Indoles into 3-Alkylidene-2-oxindoles under Flow Chemical Conditions, file e0ff0073-16fc-9bac-e053-1705fe0af019
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1
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Aliphatic Nitro Compounds as Key Precursors for the Eco-Friendly Synthesis of Fine Chemicals under Solvent-Free Conditions, file e0ff0073-baf8-9bac-e053-1705fe0af019
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1
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Recent Advances in the Synthesis of Unsymmetrical Bisindolylmethane Derivatives, file e0ff0073-ca0f-9bac-e053-1705fe0af019
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1
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Outstanding insecticidal activity and sublethal effects of Carlina acaulis root essential oil on the housefly, Musca domestica, with insights on its toxicity on human cells, file e0ff0073-f3a1-9bac-e053-1705fe0af019
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1
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Formation of Carbon-Carbon Double Bonds: Recent Developments via Nitrous Acid Elimination (NAE) from Aliphatic Nitro Compounds, file e0ff0074-0172-9bac-e053-1705fe0af019
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1
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Development of new and efficient copper(II) complexes of hexyl bis(pyrazolyl)acetate ligands as catalysts for allylic oxidation, file e0ff0074-90d5-9bac-e053-1705fe0af019
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1
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A Novel and Practical Continuous Flow Chemical Synthesis of Cannabidiol (CBD) and its CBDV and CBDB Analogues, file e0ff0074-dcf5-9bac-e053-1705fe0af019
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1
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Diastereoselective Conversion of β-Nitro-β,γ-Unsaturated Ketones into Conjugated (E,E)-Dienones, file e6733c5a-b037-4f15-af83-130e17dbe2e0
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1
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Totale |
1.589 |