| Nome |
# |
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Pirazoli ed isossazoli funzionalizzati: nuove strategie di sintesi, file e1dc1a2d-0b64-1507-e053-3a05fe0ac7a3
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40
|
|
Metal-Free Oxidative Cross Esterification of Alcohols via Acyl Chloride Formation, file e1dc1a2b-52f4-1507-e053-3a05fe0ac7a3
|
37
|
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Trichloroisocyanuric Acid: a Versatile and Efficient Chlorinating and Oxidizing Reagent, file e1dc1a2c-0a83-1507-e053-3a05fe0ac7a3
|
14
|
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Triclorotriazina: un nuovo reattivo per antiche reazioni, file e1dc1a2d-0847-1507-e053-3a05fe0ac7a3
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12
|
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Synthesis and characterization of the chemical properties of new classes of NO donors as potential dopamine releasers in the treatment of Parkinson’s disease, file e1dc1a2a-64c9-1507-e053-3a05fe0ac7a3
|
8
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A Mechanochemical-Assisted Oxidation of Amines to Carbonyl Compounds and Nitriles, file e1dc1a2d-daca-1507-e053-3a05fe0ac7a3
|
7
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Metal-Free Direct Oxidation of Aldehydes to Esters Using TCCA, file e1dc1a2a-492f-1507-e053-3a05fe0ac7a3
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4
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Mechanically induced oxidation of alcohols to aldehydes and ketones in ambient air: Revisiting TEMPO-assisted oxidations, file e1dc1a2b-5500-1507-e053-3a05fe0ac7a3
|
4
|
|
Recovery, Purification, Analysis and Chemical Modification of a Waste Cooking Oil, file de058484-064a-4ffe-8293-e76fa35e405b
|
3
|
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Mild and Highly Selective Formyl Protection of Primary Hydroxyl
Groups, file e1dc1a2a-4569-1507-e053-3a05fe0ac7a3
|
3
|
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“Microwave-assisted synthesis of sulfonamides”., file e1dc1a2a-5d63-1507-e053-3a05fe0ac7a3
|
3
|
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Clorurazione di ammine ed ammidi: l'acido tricloroisocianurico, un reattivo blando ma efficace, file e1dc1a2d-0844-1507-e053-3a05fe0ac7a3
|
3
|
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Glycerol Acetalization in Cyclopentyl Methyl Ether with Mild Acid Catalysts, file 0e3f950e-9f93-45a7-9cba-d879715c1bd6
|
2
|
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A Chemoselective, Easy Bromination of(Hydroxymethyl)Phenols, file e1dc1a2a-42e1-1507-e053-3a05fe0ac7a3
|
2
|
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“Quick and click” assembly of functionalised indole rings via metal-promoted cyclative tandem reactions, file e1dc1a2a-47a3-1507-e053-3a05fe0ac7a3
|
2
|
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A very mild and chemoselective oxidation of alcohols to carbonyl compounds, file e1dc1a2a-4e8c-1507-e053-3a05fe0ac7a3
|
2
|
|
One-pot syntehsis of hydroxamic acids from aldehydes and hydroxylamine, file e1dc1a2a-4f8d-1507-e053-3a05fe0ac7a3
|
2
|
|
Preparation of pyrazole and isoxazole libraries on cellulose beads:
a new cheap and versatile biopolymer, file e1dc1a2a-5827-1507-e053-3a05fe0ac7a3
|
2
|
|
An Easy Microwave-Assisted Synthesis of
Sulfonamides Directly from Sulfonic Acids, file e1dc1a2a-5883-1507-e053-3a05fe0ac7a3
|
2
|
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“Microwave-assisted synthesis of sulfonamides”., file e1dc1a2a-5d64-1507-e053-3a05fe0ac7a3
|
2
|
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Synthesis of Nitric Oxide Donors Derived from Piloty’s Acid and Study of Their Effects on Dopamine Secretion from PC12 Cells, file e1dc1a2b-090b-1507-e053-3a05fe0ac7a3
|
2
|
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Nenitzescu Synthesis of 5-Hydroxyindoles with Zinc, Iron and Magnesium Salts in Cyclopentyl Methyl Ether, file e1dc1a2c-d6ce-1507-e053-3a05fe0ac7a3
|
2
|
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Iron-catalysed oxidative amidation of alcohols with amines, file e1dc1a2c-f462-1507-e053-3a05fe0ac7a3
|
2
|
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Sintesi di librerie di benzofurani e indoli mediante strategia "catch and release", file e1dc1a2c-fd34-1507-e053-3a05fe0ac7a3
|
2
|
|
Nuovi amminoacidi chirali contenenti nuclei eterociclici: mimesi di legamicis-ammidici, file e1dc1a2d-0869-1507-e053-3a05fe0ac7a3
|
2
|
|
Bromurazione selettiva di idrossibenzilalcoli, file e1dc1a2d-0bda-1507-e053-3a05fe0ac7a3
|
2
|
|
Aquivion perfluorosulfonic superacid as an effective catalyst for selective epoxidation of vegetable oils, file e1dc1a2d-a896-1507-e053-3a05fe0ac7a3
|
2
|
|
Trichloroisocyanuric Acid: a Versatile and Efficient Chlorinating and Oxidizing Reagent, file e1dc1a2d-d274-1507-e053-3a05fe0ac7a3
|
2
|
|
A Visible-Light Driven Esterification of Aldehydes Catalyzed by VOSO4, file 6bfc4e45-b59c-4a88-ae5b-0657ec7869a6
|
1
|
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PROCESS FOR THE HALOGENATION AT THE ALPHA-H POSITION OF ALKYLARENES VARIOUSLY SUBSTITUTED ON THE AROMATIC RING, file 93bc50e7-3412-44ff-99ee-f26cb8a68b89
|
1
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Ammonium salts catalyzed acetalization reactions in green ethereal solvents, file c16ebadb-68bb-4387-a26c-3b5005ca9314
|
1
|
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Mechanochemistry Frees Thiourea Dioxide (TDO) from the ‘Veils’ of Solvent, Exposing All Its Reactivity, file d46888aa-44d4-4817-bb6c-3ef7a0453ad6
|
1
|
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A mild and efficient synthesis of substituted quinolines via a cross-dehydrogenative coupling of (Bio)available alcohols and aminoarenes, file e1dc1a2a-3f33-1507-e053-3a05fe0ac7a3
|
1
|
|
An Insight of the Reactions of Amines with Trichloroisocyanuric acid, file e1dc1a2a-443f-1507-e053-3a05fe0ac7a3
|
1
|
|
An easy and convenient synthesis of Weinreb amides and hydroxamates, file e1dc1a2a-456b-1507-e053-3a05fe0ac7a3
|
1
|
|
A Mild and Efficient Alternative to the
Classical Swern Oxidation, file e1dc1a2a-45be-1507-e053-3a05fe0ac7a3
|
1
|
|
Microwave-Assisted Synthesis of N-Monosubstituted Urea Derivatives, file e1dc1a2a-493e-1507-e053-3a05fe0ac7a3
|
1
|
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A Mild Procedure for the Preparation of 3-Aryl-4-formylpyrazoles, file e1dc1a2a-497c-1507-e053-3a05fe0ac7a3
|
1
|
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A two-step tandem reaction to prepare hydroxamic acids directly from alcohols, file e1dc1a2a-4dfe-1507-e053-3a05fe0ac7a3
|
1
|
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Some Recent Approaches to the Synthesis of 2-Substituted Benzofurans, file e1dc1a2a-515c-1507-e053-3a05fe0ac7a3
|
1
|
|
[1,3,5]-Triazine: A Versatile Heterocycle in Current Applications of
Organic Chemistry, file e1dc1a2a-5197-1507-e053-3a05fe0ac7a3
|
1
|
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A Mild and Inexpensive Procedure for the Synthesis of N-N'-Di-Boc-Protected Guanidines, file e1dc1a2a-5308-1507-e053-3a05fe0ac7a3
|
1
|
|
Cellulose Beads: a New Versatile Solid Support for Microwave-
Assisted Synthesis. Preparation of Pyrazole and Isoxazole Libraries, file e1dc1a2a-5799-1507-e053-3a05fe0ac7a3
|
1
|
|
A New, Simple Procedure for the Synthesis of Formyl Amides, file e1dc1a2a-57ef-1507-e053-3a05fe0ac7a3
|
1
|
|
A Facile Approach to the Synthesis of Chiral
2-Substituted Benzofurans, file e1dc1a2a-57fc-1507-e053-3a05fe0ac7a3
|
1
|
|
A new supported reagent for the photochemical generation of radicals in solution, file e1dc1a2a-5897-1507-e053-3a05fe0ac7a3
|
1
|
|
Solid-phase synthesis of isoxazole-based amino acids: a new scaffold for molecular diversity, file e1dc1a2a-5898-1507-e053-3a05fe0ac7a3
|
1
|
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Recent approaches to the
solid-phase synthesis of
N- and O-heterocycles, file e1dc1a2a-5cae-1507-e053-3a05fe0ac7a3
|
1
|
|
Microwave-assisted synthesis of sulfonamides, file e1dc1a2a-5eaa-1507-e053-3a05fe0ac7a3
|
1
|
|
A Fast and Efficient One-Pot Microwave Assisted Synthesis of Variously Di-substituted 1,2,4-Oxadiazoles, file e1dc1a2a-61a1-1507-e053-3a05fe0ac7a3
|
1
|
|
Formic acid: A promising bio-renewable feedstock for fine chemicals, file e1dc1a2a-633f-1507-e053-3a05fe0ac7a3
|
1
|
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Preparation of Benzimidazoles via Oxidation of Tertiary Amines, file e1dc1a2a-6343-1507-e053-3a05fe0ac7a3
|
1
|
|
Mono-N-Alkylation of Anilines with R3N Using Pd/C under Microwave Irradiation, file e1dc1a2a-6344-1507-e053-3a05fe0ac7a3
|
1
|
|
Synthesis of 1-Alkyl-4-imidazolecarboxylates: a catch and release strategy, file e1dc1a2b-4ebc-1507-e053-3a05fe0ac7a3
|
1
|
|
Size Selectivity in the Hydroxylation of Esters of Unsaturated Fatty Acids, file e1dc1a2d-7dd8-1507-e053-3a05fe0ac7a3
|
1
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| Totale |
197 |