Works matching DE "PYRROLIDINE synthesis"
Results: 190
Dipolarophile‐Steered Formal Stereodivergent Synthesis of 2,5‐cis/trans‐Pyrrolidines Based on Asymmetric 1,3‐Dipolar Cycloaddition of Imino Lactones.
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- Chemistry - A European Journal, 2023, v. 29, n. 66, p. 1, doi. 10.1002/chem.202302609
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Catalytic Enantioselective [3+2] Cycloaddition of N‐Metalated Azomethine Ylides.
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- Chemistry - A European Journal, 2023, v. 29, n. 28, p. 1, doi. 10.1002/chem.202300296
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Synthesis of 3‐Borylated Pyrrolidines by 1,3‐Dipolar Cycloaddition of Alkenyl Boronates and Azomethine Ylide.
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- Chemistry - A European Journal, 2022, v. 28, n. 54, p. 1, doi. 10.1002/chem.202202117
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- Article
Carbene Formation or Reduction of the Diazo Functional Group? An Unexpected Solvent‐Dependent Reactivity of Cyclic Diazo Imides.
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- Angewandte Chemie, 2023, v. 135, n. 40, p. 1, doi. 10.1002/ange.202309184
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Picolinamides and Iodoalkynes Enable Palladium‐Catalyzed syn‐Aminoalkynylation of Di‐ and Trisubstituted Alkenes to Give Pyrrolidines.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202204535
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Asymmetric Ruthenium‐Catalyzed Hydroalkylation of Racemic Allylic Alcohols for the Synthesis of Chiral Amino Acid Derivatives.
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- Angewandte Chemie, 2022, v. 134, n. 26, p. 1, doi. 10.1002/ange.202203244
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Combination of Pseudo‐Natural Product Design and Formal Natural Product Ring Distortion Yields Stereochemically and Biologically Diverse Pseudo‐Sesquiterpenoid Alkaloids.
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- Angewandte Chemie, 2021, v. 133, n. 39, p. 21554, doi. 10.1002/ange.202106654
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Synthesis of Indanones and Spiroindanones by Diastereoselective Annulation Based on a Hydrogen Autotransfer Strategy.
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- Angewandte Chemie, 2021, v. 133, n. 10, p. 5333, doi. 10.1002/ange.202013792
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p‐Substituted Tris(2‐pyridylmethyl)amines as Ligands for Highly Active ATRP Catalysts: Facile Synthesis and Characterization.
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- Angewandte Chemie, 2020, v. 132, n. 35, p. 15020, doi. 10.1002/ange.202004724
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Huisgen's 1,3‐Dipolar Cycloadditions to Fulvenes Proceed via Ambimodal [6+4]/[4+2] Transition States.
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- Angewandte Chemie, 2020, v. 132, n. 30, p. 12512, doi. 10.1002/ange.202005265
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Generation and Reactivity of Amidyl Radicals: Manganese‐Mediated Atom‐Transfer Reaction.
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- Angewandte Chemie, 2020, v. 132, n. 11, p. 4458, doi. 10.1002/ange.201913042
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Ligand‐Controlled Regiodivergent Hydroalkylation of Pyrrolines.
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- Angewandte Chemie, 2019, v. 131, n. 51, p. 18690, doi. 10.1002/ange.201912629
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- Article
Diastereodivergent Asymmetric 1,3‐Dipolar Cycloaddition of Azomethine Ylides and β‐Fluoroalkyl Vinylsulfones: Low Copper(II) Catalyst Loading and Theoretical Studies.
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- Angewandte Chemie, 2019, v. 131, n. 46, p. 16790, doi. 10.1002/ange.201908227
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The Dual‐Stereocontrol Mechanism: Heteroselective Polymerization of rac‐Lactide and Syndioselective Polymerization of meso‐Lactide by Chiral Aluminum Salan Catalysts.
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- Angewandte Chemie, 2019, v. 131, n. 41, p. 14821, doi. 10.1002/ange.201906848
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Manipulation of Spiroindolenine Intermediates for Enantioselective Synthesis of 3‐(Indol‐3‐yl)‐Pyrrolidines.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1170, doi. 10.1002/ange.201812344
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Formation Reaction and Chemical Structure of a Novel Supramolecular Triad Based on Cobalt(II) 5,10,15,20-(Tetra-4-Tert-Butylphenyl)-21Н,23Н-Porphyrin and 1-Methyl-2-(Pyridin-4′-Yl)- 3,4-Fullero[60]Pyrrolidine.
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- Journal of Structural Chemistry, 2018, v. 59, n. 3, p. 711, doi. 10.1134/S0022476618030320
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- Article
A Room-Temperature Processable PDI-Based Electron-Transporting Layer for Enhanced Performance in PDI-Based Non-Fullerene Solar Cells.
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- Advanced Materials Interfaces, 2016, v. 3, n. 18, p. n/a, doi. 10.1002/admi.201600476
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Synthesis and biological evaluation of pyrrolidine-based T-type calcium channel inhibitors for the treatment of neuropathic pain.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1460, doi. 10.1080/14756366.2018.1513926
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- Article
Supported Tris-Triazole Ligands for Batch and Continuous-Flow Copper-Catalyzed Huisgen 1,3-Dipolar Cycloaddition Reactions.
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- Catalysts (2073-4344), 2020, v. 10, n. 4, p. 434, doi. 10.3390/catal10040434
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Synergistic Palladium-Phosphoric Acid Catalysis in (3 + 2) Cycloaddition Reactions between Vinylcyclopropanes and Imines.
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- Catalysts (2073-4344), 2020, v. 10, n. 2, p. 150, doi. 10.3390/catal10020150
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Recent Developments on 1,3-Dipolar Cycloaddition Reactions by Catalysis in Green Solvents.
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- Catalysts (2073-4344), 2020, v. 10, n. 1, p. 65, doi. 10.3390/catal10010065
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Endo-Selective Construction of Spiro-[butyrolactone-pyrrolidine] via Ag(I)/CAAA-Amidphos-Catalyzed 1,3-Dipolar Cycloaddition between Azomethine Ylides and α-Methylene-γ-Butyrolactone.
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- Catalysts (2073-4344), 2020, v. 10, n. 1, p. 28, doi. 10.3390/catal10010028
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Synthesis of heteroleptic pyrrolide/bipyridyl complexes of ruthenium(II).
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- Canadian Journal of Chemistry, 2012, v. 90, n. 8, p. 693, doi. 10.1139/v2012-045
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- Article
Synthesis of Some Novel Isoxazolidine Derivatives via 1,3-Dipolar Cycloaddition and Their Biological Evaluation.
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- Gazi University Journal of Science, 2019, v. 32, n. 1, p. 78
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Asymmetric synthesis of aryl‐substituted pyrrolidines by using CFAM ligand–AgOAc chiral system via 1,3‐dipolar cycloaddition reaction.
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- Chirality, 2023, v. 35, n. 7, p. 435, doi. 10.1002/chir.23557
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Efficient preparation of (R)‐2‐(2,5‐difluorophenyl)pyrrolidine via a recycle process of resolution.
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- Chirality, 2021, v. 33, n. 12, p. 931, doi. 10.1002/chir.23366
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Synthesis of pyrrolizidines and indolizidines by multicomponent 1,3-dipolar cycloaddition of azomethine ylides.
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- Pure & Applied Chemistry, 2019, v. 91, n. 4, p. 575, doi. 10.1515/pac-2018-0710
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Site-, enantio- and stereo-selectivities of the 1,3-dipolar cycloaddition reactions of oxanorbornadiene with C,N-disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2020, v. 139, n. 1, p. 1, doi. 10.1007/s00214-019-2529-8
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Synthesis, spectral characterization, crystal structures of lanthanide(III) pyrrolidine dithiocarbamate complexes and their catalytic activity.
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- Journal of Coordination Chemistry, 2015, v. 68, n. 12, p. 2167, doi. 10.1080/00958972.2015.1037299
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Synthetic Studies of Alkaloids Containing Pyrrolidine and Piperidine Structural Motifs.
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- 2015
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- Other
RECENT ADVANCES IN THE SYNTHESIS OF SPECIALIZED HETEROCYCLIC MOLECULES BY 1, 3-DIPOLAR CYCLOADDITION REACTION: A STUDY BASED ON GREENER PROTOCOLS.
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- Rasayan Journal of Chemistry, 2019, v. 12, n. 4, p. 2183, doi. 10.31788/RJC.2019.1245480
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SYNTHESIS OF PYRROLIDINES AND TETRAHYDROPYRIMIDINES VIA ONE-POT AND THREE COMPONENT CASCADE COUPLING STRATEGY IN WATER.
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- Rasayan Journal of Chemistry, 2017, v. 10, n. 1, p. 6, doi. 10.7324/RJC.2017.1011545
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Novel nucleoside analogs tethered on (3 R,4 R)-4-(hydroxymethyl)pyrrolidin-3-ol.
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- Journal of the Iranian Chemical Society, 2015, v. 12, n. 4, p. 655, doi. 10.1007/s13738-014-0524-5
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Synthesis of a pyrrolidine derivative of a carvotacetone and monoterpenes for anti-methicillin-resistant Staphylococcus aureus and anti-cryptococcal properties.
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- Natural Product Research, 2022, v. 36, n. 9, p. 2321, doi. 10.1080/14786419.2020.1833201
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Copper‐Catalyzed Intramolecular Radical Amination of Tertiary C(sp<sup>3</sup>)−H Bonds to Access α‐Quaternary Pyrrolidines.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 7, p. 1, doi. 10.1002/ajoc.202300220
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- Article
The Asymmetric Construction α‐CF<sub>2</sub>H Pyrrolidine via 1,3‐Dipolar Cycloaddition of N‐2,2‐Difluoroethylthioisatin Ketoimines with Meldrum's Acid Derived Electron‐Deficient Olefins.
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- Asian Journal of Organic Chemistry, 2023, v. 12, n. 6, p. 1, doi. 10.1002/ajoc.202300184
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Chiral Trifluoromethylated Pyrrolidines via Cu–Catalyzed Asymmetric 1,3‐Dipolar Cycloaddition.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 10, p. 1567, doi. 10.1002/ajoc.202000295
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- Article
Synthesis of Highly Enantioenriched Bis‐spirooxindole Pyrrolizidine/Pyrrolidines through Asymmetric [3+2] Cycloaddition Reaction.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 5, p. 822, doi. 10.1002/ajoc.202000056
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- Article
Cationic Iron(III) Salt as an Initiator for Radical Cation‐induced [4+2] Cycloaddition.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 3, p. 395, doi. 10.1002/ajoc.201900749
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Chemoselective Kumada‐Type Iron Catalysis with Alkyl Grignard Reagents: Reductive Cyclization and Cyclomethylation.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 9, p. 1648, doi. 10.1002/ajoc.201900359
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- Article
Desymmetrization‐Initiated Stereocontrolled Synthesis of (−)‐Kaitocephalin.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 9, p. 1687, doi. 10.1002/ajoc.201900103
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- Article
Rhodium‐Catalyzed [5+1]‐Cycloaddition Reactions to Spiro‐Benzo[e][1,3]Oxazineindoline Imines.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 8, p. 1385, doi. 10.1002/ajoc.201900274
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A Redox Auxiliary Strategy for Pyrrolidine Synthesis via Photocatalytic [3+2] Cycloaddition.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 7, p. 978, doi. 10.1002/ajoc.201900113
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- Article
Asymmetric 1,3‐Dipolar Cycloaddition Reactions of Enones by Primary Amine Catalysis.
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- Asian Journal of Organic Chemistry, 2019, v. 8, n. 7, p. 1049, doi. 10.1002/ajoc.201900013
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- Article
Iminosugar-Phosphines as Organocatalysts in the [3 + 2] Cycloaddition of Allenoates and N -Tosylimines.
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- Catalysts (2073-4344), 2022, v. 12, n. 8, p. 876, doi. 10.3390/catal12080876
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MgSiO<sub>3</sub> nanoparticle‐catalyzed 1,3‐dipolar cycloaddition reactions in the synthesis of novel spiroindane‐1,3‐diones derived from substituted chalcones.
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- Journal of the Chinese Chemical Society, 2019, v. 66, n. 12, p. 1708, doi. 10.1002/jccs.201800445
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1,3‐Dipolar Cycloaddition of 3‐Chromonyl‐Substituted Glycine Imino Esters with Arylidenes and in situ Diastereodivergent via Retrocycloaddition.
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- Chemistry - An Asian Journal, 2023, v. 18, n. 10, p. 1, doi. 10.1002/asia.202300215
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- Article
Synthesis of Nitrone‐derived Pyrrolidine Scaffolds and Their Combinatorial Libraries to Develop Selective α‐l‐Rhamnosidase Inhibitors.
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- Chemistry - An Asian Journal, 2022, v. 17, n. 14, p. 1, doi. 10.1002/asia.202200172
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- Article
Regioselective Photochemical Cycloaddition Reactions of Diolefinic Ligands in Coordination Polymers.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 20, p. 3635, doi. 10.1002/asia.201900646
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- Article
Alkene–Azide 1,3‐Dipolar Cycloaddition as a Trigger for Ultrashort Peptide Hydrogel Dissolution.
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- Chemistry - An Asian Journal, 2019, v. 14, n. 8, p. 1143, doi. 10.1002/asia.201801184
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- Article