| 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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167
|
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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
|
|
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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Synthesis of Sulfoximine Carbamates by Rhodium-Catalyzed Nitrene Transfer of Carbamates to Sulfoxides, file dd9e0c64-4d88-1e9c-e053-3a05fe0a45ef
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116
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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
|
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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Recent advances in the chemistry of metallated azetidines, file dd9e0c6c-36bf-1e9c-e053-3a05fe0a45ef
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88
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Titanium dioxide as a catalyst in biodiesel production, file dd9e0c68-9bfd-1e9c-e053-3a05fe0a45ef
|
87
|
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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
|
69
|
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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
|
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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52
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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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46
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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
|
28
|
|
External Trapping of Halomethyllithium Enabled by Flow Microreactors, file dd9e0c6c-3e59-1e9c-e053-3a05fe0a45ef
|
19
|
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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
|
6
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A direct and sustainable synthesis of tertiary butyl esters enabled by flow microreactors, file dd9e0c69-031f-1e9c-e053-3a05fe0a45ef
|
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
|
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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Flow Technology for the Genesis and Use of (Highly) Reactive Organometallic Reagents, file dd9e0c66-f822-1e9c-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
|
3
|
|
Recent advances in the chemistry of metallated azetidines, file dd9e0c68-e8a4-1e9c-e053-3a05fe0a45ef
|
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
|
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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Deconstruction of 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline moiety to separate Pglycoprotein (P-gp) activity from σ2 receptor affinity in mixed P-gp/σ2 receptor agents, file dd9e0c62-7e42-1e9c-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
|
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
|
2
|
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External Trapping of Halomethyllithium Enabled by Flow Microreactors, file dd9e0c68-9cfe-1e9c-e053-3a05fe0a45ef
|
2
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Flow technology for organometallic-mediated synthesis, file dd9e0c68-a4be-1e9c-e053-3a05fe0a45ef
|
2
|
|
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
|
2
|
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Azetidine-Borane Complexes: Synthesis, Reactivity and Stereoselective Functionalization, file dd9e0c6a-60fd-1e9c-e053-3a05fe0a45ef
|
2
|
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Synthesis of Sulfinamidines and Sulfinimidate Esters by Transfer of Nitrogen to Sulfenamides, file dd9e0c6a-dfdf-1e9c-e053-3a05fe0a45ef
|
2
|
|
Flow Microreactor Technology for Taming Highly Reactive Chloroiodomethyllithium Carbenoid: Direct and Chemoselective Synthesis of α-Chloroaldehydes, file dd9e0c6a-efcc-1e9c-e053-3a05fe0a45ef
|
2
|
|
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file f97ef6ac-a816-42f5-9f0e-4d13dc4255a2
|
2
|
|
FLOW MICROREATOR TECHONOLOGY AS UNIQUE TOOL FOR THE GENERATION AND USE OF (HIGHLY) REACTIVE ORGANOLITHIUM REAGENTS, file 3744079c-2bdb-4046-a128-83dca252214e
|
1
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Microreactor as enabling technology for taming highly reactive metal fluorocarbenoids, file 757b24ae-4795-4d46-8627-28017a504c12
|
1
|
|
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file 78d5bc70-5d02-4cc1-b4d8-35c81ed08d00
|
1
|
|
Use of Flow Technologies and Photochemical Methods for the Preparation and Synthetic Manipulation of Functionalized Azetines, file a91be0d2-e0c3-4914-97fc-50e7b2b94152
|
1
|
|
Synthesis and Reactivity of Oxazolinyl Allylic Alcohols, file dd9e0c62-48b7-1e9c-e053-3a05fe0a45ef
|
1
|
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Sintesi di Derivati di Baylis-Hillman Mascherati, file dd9e0c62-48c0-1e9c-e053-3a05fe0a45ef
|
1
|
|
Addizioni Nucleofile 1-4 di Alogenoalchilossazoline ed Ossirani Litiati a Complessi Carbenici a,b-Insaturi “tipo Fischer, file dd9e0c62-4a4b-1e9c-e053-3a05fe0a45ef
|
1
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|
alfa-Lithiated Stirene Oxide and Oxazolinyloxiranes: Structure and Dynamics in Solution, file dd9e0c62-4e9a-1e9c-e053-3a05fe0a45ef
|
1
|
|
1-Litio-1-ossazolinil-2,2-dimetilossirano: Struttura in Soluzione, Reattività, Comportamento Dinamico e Stabilità Configurazionale, file dd9e0c62-5208-1e9c-e053-3a05fe0a45ef
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1
|
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Conjugate Nucleophilic Addition of Lithiated Chloroalkyloxazolines and Oxazolinyloxiranes to a,b-Unsatureted Fischer Carbene Complexes, file dd9e0c62-5cbc-1e9c-e053-3a05fe0a45ef
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1
|
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Synthesis of Substituted 3,10b-dihydro-2H-Oxazolo[2,3-A]isoquinolines From Ortho-lithiated Aryl Oxazolinyloxiranes, file dd9e0c62-6642-1e9c-e053-3a05fe0a45ef
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1
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On the Michael Addition of a- and orto- Lithiated Aryloxiranes to a,b-Unsaturated Fischer Carbene Complexes, file dd9e0c62-66c7-1e9c-e053-3a05fe0a45ef
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1
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Ossazolinilossirani a-litiati: Struttura e dinamica in soluzione, file dd9e0c62-71e7-1e9c-e053-3a05fe0a45ef
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1
|
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Synthesis and Reactivity of Oxazolinyl Allylic Alcohols, file dd9e0c62-735e-1e9c-e053-3a05fe0a45ef
|
1
|
|
Arilossirani orto-Litiati nella Sintesi Stereospecifica di Tetraidronaftoli, file dd9e0c62-7af6-1e9c-e053-3a05fe0a45ef
|
1
|
|
a-Lithiated Oxazolinyloxirane: Structure, Configurational Stability and Dynamics in Solution, file dd9e0c62-7b0d-1e9c-e053-3a05fe0a45ef
|
1
|
|
Coupling Reaction of Lithiated Oxiranes with Fischer Carbene Complexes: Stereoselective Synthesis of Substituted Cyclopropanes, file dd9e0c62-8347-1e9c-e053-3a05fe0a45ef
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1
|
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Coupling Reaction of Lithiated Chloroalkiloxazolines with Fischer Carbene Complexes: Synthesis of Substituted Cyclopropanes, file dd9e0c62-838f-1e9c-e053-3a05fe0a45ef
|
1
|
|
Synthesis and Reactivity of Oxazolinyl Allylic Alcohols, file dd9e0c62-872b-1e9c-e053-3a05fe0a45ef
|
1
|
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Ortho-Lithiated Aryloxiranes in the Stereoselective Shyntesis of Phtalanes, file dd9e0c62-8975-1e9c-e053-3a05fe0a45ef
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1
|
|
Expanding the synthetic portfolio of organolithiums: direct use in catalytic cross-coupling reactions, file dd9e0c63-4c9a-1e9c-e053-3a05fe0a45ef
|
1
|
|
Supported Catalysts for Continuous Flow Synthesis, file dd9e0c68-9bff-1e9c-e053-3a05fe0a45ef
|
1
|
|
Development of a continuous flow synthesis of propranolol: tackling a competitive side reaction, file dd9e0c68-9c14-1e9c-e053-3a05fe0a45ef
|
1
|
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Functionalization of four-membered cyclic sulfoximines by a convenient lithiation/trapping sequence, file dd9e0c68-9d00-1e9c-e053-3a05fe0a45ef
|
1
|
|
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
|
1
|
|
Straightforward Strategies for the Preparation of NH-Sulfox-imines: A Serendipitous Story, file dd9e0c68-d6f1-1e9c-e053-3a05fe0a45ef
|
1
|
|
A Practical 11B NMR Evaluation of BH3 Titer in Commercial Solutions, file dd9e0c68-d6f4-1e9c-e053-3a05fe0a45ef
|
1
|
|
Use of Hypervalent Iodine in the Synthesis of Isomeric Dihydrooxazoles, file dd9e0c68-e115-1e9c-e053-3a05fe0a45ef
|
1
|
|
Targeting a Mirabegron precursor by BH3-mediated continuous flow reduction process, file dd9e0c68-e117-1e9c-e053-3a05fe0a45ef
|
1
|
|
A Study of Graphene-Based Copper Catalysts: Copper(I) Nanoplatelets for Batch and Continuous-Flow Applications, file dd9e0c68-e11b-1e9c-e053-3a05fe0a45ef
|
1
|
|
A convenient enantioselective CBS-reduction of arylketones in flow-microreactor systems, file dd9e0c68-e897-1e9c-e053-3a05fe0a45ef
|
1
|
|
Enantioselective carbolithiation of S-alkenyl-N-aryl thiocarbamates: Kinetic and thermodynamic control, file dd9e0c68-eb8c-1e9c-e053-3a05fe0a45ef
|
1
|
|
Exploiting structural and conformational effects for a site-selective lithiation of azetidines, file dd9e0c68-eb99-1e9c-e053-3a05fe0a45ef
|
1
|
|
Chiral Switchable Catalysts for Dynamic Control of Enantioselectivity, file dd9e0c69-00ab-1e9c-e053-3a05fe0a45ef
|
1
|
|
[InlineMediaObject not available: see fulltext.] Use of azetidine scaffolds in stereoselective transformations (microreview), file dd9e0c69-00b0-1e9c-e053-3a05fe0a45ef
|
1
|
|
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
|
1
|
|
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
|
1
|
|
Computational NMR as Useful Tool for Predicting Structure and Stereochemistry of Four-Membered Sulfur Heterocycles, file dd9e0c69-0322-1e9c-e053-3a05fe0a45ef
|
1
|
|
Fluoro-Substituted Methyllithium Chemistry: External Quenching Method Using Flow Microreactors, file dd9e0c6a-d48d-1e9c-e053-3a05fe0a45ef
|
1
|
|
Continuous flow synthesis of heterocycles: A recent update on the flow synthesis of indoles, file dd9e0c6a-efd3-1e9c-e053-3a05fe0a45ef
|
1
|
|
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
|
|
Synthesis of Biaryls Having a Piperidylmethyl Group Based on Space Integration of Lithiation, Borylation, and Suzuki–Miyaura Coupling, file dd9e0c6b-0ab4-1e9c-e053-3a05fe0a45ef
|
1
|
|
Straightforward Tactics and Enabling Technologies as useful tools for Fluoroalkylations, file df16cb67-ceac-49b5-b23e-30b5196eb45d
|
1
|
| Totale |
1.456 |