| Nome |
# |
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Synthesis of NH-sulfoximines from sulfides by chemoselective one-pot N- and O-transfers, file dd9e0c69-00b7-1e9c-e053-3a05fe0a45ef
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165
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A Convenient, Mild, and Green Synthesis of NH-Sulfoximines in Flow Reactors, file dd9e0c66-8d07-1e9c-e053-3a05fe0a45ef
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140
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1,3-Dibromo-1,1-difluoro-2-propanone as a Useful Synthon for a Chemoselective Preparation of 4-Bromodifluoromethyl Thiazoles, file dd9e0c68-e113-1e9c-e053-3a05fe0a45ef
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131
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Benchmarking acidic and basic catalysis for a robust production of biofuel from waste cooking oil, file dd9e0c68-9c1a-1e9c-e053-3a05fe0a45ef
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96
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Highly Chemoselective NH- and O-Transfer to Thiols Using Hypervalent Iodine Reagents: Synthesis of Sulfonimidates and Sulfonamides, file dd9e0c6a-61b6-1e9c-e053-3a05fe0a45ef
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96
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Titanium dioxide as a catalyst in biodiesel production, file dd9e0c68-9bfd-1e9c-e053-3a05fe0a45ef
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86
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Recent advances in the chemistry of metallated azetidines, file dd9e0c6c-36bf-1e9c-e053-3a05fe0a45ef
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80
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Transfer of Electrophilic NH Using Convenient Sources of Ammonia: Direct Synthesis of NH Sulfoximines from Sulfoxides, file dd9e0c68-eb9c-1e9c-e053-3a05fe0a45ef
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68
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Contribution of microreactor technology and flow chemistry to the development of green and sustainable synthesis, file dd9e0c68-e89c-1e9c-e053-3a05fe0a45ef
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66
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Stereo-and enantioselective addition of organolithiums to 2-oxazolinylazetidines as a synthetic route to 2-acylazetidines, file dd9e0c68-9a4b-1e9c-e053-3a05fe0a45ef
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58
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Sequential α-lithiation and aerobic oxidation of an arylacetic acid - continuous-flow synthesis of cyclopentyl mandelic acid, file dd9e0c68-a4bc-1e9c-e053-3a05fe0a45ef
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52
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Flow microreactor synthesis of 2,2-disubstituted oxetanes via 2-phenyloxetan-2-yl lithium, file dd9e0c68-eb96-1e9c-e053-3a05fe0a45ef
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51
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A direct and sustainable synthesis of tertiary butyl esters enabled by flow microreactors, file dd9e0c6c-27e4-1e9c-e053-3a05fe0a45ef
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45
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Synthesis and use of halodifluoromethyl heterocycles, file dd9e0c68-986d-1e9c-e053-3a05fe0a45ef
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28
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Azetidine-Borane Complexes: Synthesis, Reactivity and Stereoselective Functionalization, file dd9e0c6b-405e-1e9c-e053-3a05fe0a45ef
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28
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External Trapping of Halomethyllithium Enabled by Flow Microreactors, file dd9e0c6c-3e59-1e9c-e053-3a05fe0a45ef
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18
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Exploiting a "Beast" in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy, file dd9e0c6c-2415-1e9c-e053-3a05fe0a45ef
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14
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Exploiting a "Beast" in Carbenoid Chemistry: Development of a Straightforward Direct Nucleophilic Fluoromethylation Strategy, file dd9e0c68-986a-1e9c-e053-3a05fe0a45ef
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6
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A direct and sustainable synthesis of tertiary butyl esters enabled by flow microreactors, file dd9e0c69-031f-1e9c-e053-3a05fe0a45ef
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5
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Flow Technology for Telescoped Generation, Lithiation and Electrophilic (C3) Functionalization of Highly Strained 1-Azabicyclo[1.1.0]butanes, file dd9e0c6a-dfd5-1e9c-e053-3a05fe0a45ef
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4
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Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file 7d5864c9-7a94-4172-b574-768edbd384c0
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3
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Pharmaceutical development of novel lactate-based 6-fluoro-L-DOPA formulations, file dd9e0c63-fbdc-1e9c-e053-3a05fe0a45ef
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3
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(S)-ethyl 2-(tert-butoxycarbonylamino)-3-(2-iodo-4,5-methylenedioxyphenyl)propanoate, file dd9e0c68-05e8-1e9c-e053-3a05fe0a45ef
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3
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Synthesis of Sulfonimidamides from Sulfenamides via an Alkoxy-amino-λ6-sulfanenitrile Intermediate, file dd9e0c68-aa2e-1e9c-e053-3a05fe0a45ef
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3
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Recent advances in the chemistry of metallated azetidines, file dd9e0c68-e8a4-1e9c-e053-3a05fe0a45ef
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3
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Use of Flow Technologies and Photochemical Methods for the Preparation and Synthetic Manipulation of Functionalized Azetines, file 15a0563b-2c1a-4394-884c-584985be04f1
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2
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The synthetic versatility of fluoroiodomethane: recent applications as monofluoromethylation platform, file aeec7f52-2857-46e4-908a-9050db30b510
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2
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Asymmetric Synthesis of alpha,beta-Substituted beta-Aminoalkanamides and Stereochemical Determination, file dd9e0c62-4af2-1e9c-e053-3a05fe0a45ef
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2
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Lithiated oxazolinyloxiranes and oxazolinylaziridines, file dd9e0c62-5ddd-1e9c-e053-3a05fe0a45ef
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2
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null, file dd9e0c63-3cfa-1e9c-e053-3a05fe0a45ef
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2
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A greener and efficient access to substituted four- and six-membered sulfur-bearing heterocycles, file dd9e0c64-4758-1e9c-e053-3a05fe0a45ef
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2
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2-Arylazetidines as ligands for nicotinic acetylcholine receptors, file dd9e0c64-e49b-1e9c-e053-3a05fe0a45ef
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2
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Straightforward chemo- and stereoselective fluorocyclopropanation of allylic alcohols: Exploiting the electrophilic nature of the not so elusive fluoroiodomethyllithium, file dd9e0c68-9c16-1e9c-e053-3a05fe0a45ef
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2
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External Trapping of Halomethyllithium Enabled by Flow Microreactors, file dd9e0c68-9cfe-1e9c-e053-3a05fe0a45ef
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2
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Flow technology for organometallic-mediated synthesis, file dd9e0c68-a4be-1e9c-e053-3a05fe0a45ef
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2
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Easy access to constrained peptidomimetics and 2,2-disubstituted azetidines by the unexpected reactivity profile of α-lithiated N-Boc-azetidines, file dd9e0c68-eb93-1e9c-e053-3a05fe0a45ef
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2
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Azetidine-Borane Complexes: Synthesis, Reactivity and Stereoselective Functionalization, file dd9e0c6a-60fd-1e9c-e053-3a05fe0a45ef
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2
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Synthesis of Sulfinamidines and Sulfinimidate Esters by Transfer of Nitrogen to Sulfenamides, file dd9e0c6a-dfdf-1e9c-e053-3a05fe0a45ef
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2
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Flow Microreactor Technology for Taming Highly Reactive Chloroiodomethyllithium Carbenoid: Direct and Chemoselective Synthesis of α-Chloroaldehydes, file dd9e0c6a-efcc-1e9c-e053-3a05fe0a45ef
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2
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Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file f97ef6ac-a816-42f5-9f0e-4d13dc4255a2
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2
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FLOW MICROREATOR TECHONOLOGY AS UNIQUE TOOL FOR THE GENERATION AND USE OF (HIGHLY) REACTIVE ORGANOLITHIUM REAGENTS, file 3744079c-2bdb-4046-a128-83dca252214e
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1
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Microreactor as enabling technology for taming highly reactive metal fluorocarbenoids, file 757b24ae-4795-4d46-8627-28017a504c12
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1
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Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file 78d5bc70-5d02-4cc1-b4d8-35c81ed08d00
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1
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Use of Flow Technologies and Photochemical Methods for the Preparation and Synthetic Manipulation of Functionalized Azetines, file a91be0d2-e0c3-4914-97fc-50e7b2b94152
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1
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Development of a continuous flow synthesis of propranolol: tackling a competitive side reaction, file dd9e0c68-9c14-1e9c-e053-3a05fe0a45ef
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1
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Functionalization of four-membered cyclic sulfoximines by a convenient lithiation/trapping sequence, file dd9e0c68-9d00-1e9c-e053-3a05fe0a45ef
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1
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Nitrogen Stereodynamics and Complexation Phenomena as Key Factors in the Deprotonative Dynamic Resolution of Alkylideneaziridines: A Spectroscopic and Computational Study, file dd9e0c68-b6e1-1e9c-e053-3a05fe0a45ef
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1
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Straightforward Strategies for the Preparation of NH-Sulfox-imines: A Serendipitous Story, file dd9e0c68-d6f1-1e9c-e053-3a05fe0a45ef
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1
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A Practical 11B NMR Evaluation of BH3 Titer in Commercial Solutions, file dd9e0c68-d6f4-1e9c-e053-3a05fe0a45ef
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1
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Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles, file dd9e0c68-e115-1e9c-e053-3a05fe0a45ef
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1
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Targeting a Mirabegron precursor by BH3-mediated continuous flow reduction process, file dd9e0c68-e117-1e9c-e053-3a05fe0a45ef
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1
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A Study of Graphene-Based Copper Catalysts: Copper(I) Nanoplatelets for Batch and Continuous-Flow Applications, file dd9e0c68-e11b-1e9c-e053-3a05fe0a45ef
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1
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A convenient enantioselective CBS-reduction of arylketones in flow-microreactor systems, file dd9e0c68-e897-1e9c-e053-3a05fe0a45ef
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1
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Enantioselective carbolithiation of S-alkenyl-N-aryl thiocarbamates: Kinetic and thermodynamic control, file dd9e0c68-eb8c-1e9c-e053-3a05fe0a45ef
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1
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Exploiting structural and conformational effects for a site-selective lithiation of azetidines, file dd9e0c68-eb99-1e9c-e053-3a05fe0a45ef
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1
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Chiral Switchable Catalysts for Dynamic Control of Enantioselectivity, file dd9e0c69-00ab-1e9c-e053-3a05fe0a45ef
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1
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[InlineMediaObject not available: see fulltext.] Use of azetidine scaffolds in stereoselective transformations (microreview), file dd9e0c69-00b0-1e9c-e053-3a05fe0a45ef
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1
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Modular and Chemoselective Strategy for the Direct Access to α-Fluoroepoxides and Aziridines via the Addition of Fluoroiodomethyllithium to Carbonyl-Like Compounds, file dd9e0c69-00b9-1e9c-e053-3a05fe0a45ef
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1
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Regio- and Stereoselective Synthesis of Sulfur-Bearing Four-Membered Heterocycles: Direct Access to 2,4-Disubstituted Thietane 1-Oxides, file dd9e0c69-0313-1e9c-e053-3a05fe0a45ef
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1
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Computational NMR as Useful Tool for Predicting Structure and Stereochemistry of Four-Membered Sulfur Heterocycles, file dd9e0c69-0322-1e9c-e053-3a05fe0a45ef
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1
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Fluoro-Substituted Methyllithium Chemistry: External Quenching Method Using Flow Microreactors, file dd9e0c6a-d48d-1e9c-e053-3a05fe0a45ef
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1
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Continuous flow synthesis of heterocycles: A recent update on the flow synthesis of indoles, file dd9e0c6a-efd3-1e9c-e053-3a05fe0a45ef
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1
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N−N Bond Formation Using an Iodonitrene as an Umpolung of Ammonia: Straightforward and Chemoselective Synthesis of Hydrazinium Salts, file dd9e0c6b-0ab1-1e9c-e053-3a05fe0a45ef
|
1
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|
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file df16cb67-ceac-49b5-b23e-30b5196eb45d
|
1
|
| Totale |
1.306 |