Works matching DE "PICTET-Spengler reaction"
Results: 86
Asymmetric synthesis of tetrahydroisoquinolines by enzymatic Pictet-Spengler reaction.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 4, p. 701, doi. 10.1080/09168451.2014.890039
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- Article
Synthesis of Tetrahydro‐β‐carbolines by a Manganese‐Catalysed Oxidative Pictet–Spengler Reaction.
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- Chemistry - A European Journal, 2023, v. 29, n. 39, p. 1, doi. 10.1002/chem.202203758
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- Article
Pentafluorophenol (C<sub>6</sub>F<sub>5</sub>OH) Catalyzed Pictet‐Spengler Reaction: A Facile and Metal‐Free Approach Towards Tetrahydro‐β‐Carbolines.
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- Chemistry - A European Journal, 2023, v. 29, n. 27, p. 1, doi. 10.1002/chem.202203924
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- Article
Cover Feature: Total Syntheses of (+)‐Villocarine A, (−)‐Apogeissoschizine, and (+)‐Geissoschizine (Chem. Eur. J. 18/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 18, p. 1, doi. 10.1002/chem.202300534
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- Article
Total Syntheses of (+)‐Villocarine A, (−)‐Apogeissoschizine, and (+)‐Geissoschizine.
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- Chemistry - A European Journal, 2023, v. 29, n. 18, p. 1, doi. 10.1002/chem.202300179
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- Article
Hidden Heptacyclic Chiral N‐Acyl Iminium Ions: A New Entry to Enantioenriched Polycyclic Azepanes and Azocanes by Superacid‐Promoted Intramolecular Pictet‐Spengler Reaction.
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- Chemistry - A European Journal, 2022, v. 28, n. 25, p. 1, doi. 10.1002/chem.202200432
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- Article
Site‐ and Stereoselective Glycomodification of Biomolecules through Carbohydrate‐Promoted Pictet–Spengler Reaction.
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- Angewandte Chemie, 2024, v. 136, n. 16, p. 1, doi. 10.1002/ange.202401394
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- Article
Divergent Asymmetric Total Synthesis of (−)‐Voacafricines A and B.
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- Angewandte Chemie, 2023, v. 135, n. 16, p. 1, doi. 10.1002/ange.202301517
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- Article
Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202213831
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- Article
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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- Article
Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst.
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- Angewandte Chemie, 2022, v. 134, n. 19, p. 1, doi. 10.1002/ange.202201788
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- Article
Tunable and Cooperative Catalysis for Enantioselective Pictet‐Spengler Reaction with Varied Nitrogen‐Containing Heterocyclic Carboxaldehydes.
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- Angewandte Chemie, 2021, v. 133, n. 46, p. 24778, doi. 10.1002/ange.202109694
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- Article
Catalytic and Enantioselective Control of the C–N Stereogenic Axis via the Pictet–Spengler Reaction.
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- Angewandte Chemie, 2021, v. 133, n. 22, p. 12387, doi. 10.1002/ange.202100363
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- Article
Total Syntheses of (−)‐Strictosidine and Related Indole Alkaloid Glycosides.
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- Angewandte Chemie, 2020, v. 132, n. 32, p. 13516, doi. 10.1002/ange.202005748
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- Article
Green Synthesis of 1-Aryl-2,3,4,9-Tetrahydro-1H-B-Carbolines using Fe(Iii)-Montmorillonite and Study of their Antimicrobial Activity.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 4, p. 365, doi. 10.1007/s11094-020-02205-y
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- Article
Chemoenzymatic One-Pot Process for the Synthesis of Tetrahydroisoquinolines.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1389, doi. 10.3390/catal11111389
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- Article
Uncovering the Mechanism of Azepino‐Indole Skeleton Formation via Pictet–Spengler Reaction by Strictosidine Synthase: A Quantum Chemical Investigation.
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- ChemistryOpen, 2023, v. 12, n. 6, p. 1, doi. 10.1002/open.202300043
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- Article
A facile and efficient method for the synthesis of crystalline tetrahydro-β-carbolines via the Pictet-Spengler reaction in water.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-57911-0
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- Article
Chiral Spirocyclic Phosphoric Acids and Their Growing Applications.
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- Chinese Journal of Chemistry, 2021, v. 39, n. 4, p. 802, doi. 10.1002/cjoc.202000446
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- Article
Sequential one-pot five-component synthesis of tetrazole-based spirotetrahydro-β-carbolines.
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- Journal of the Iranian Chemical Society, 2017, v. 14, n. 5, p. 1131, doi. 10.1007/s13738-017-1063-7
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- Article
Brown Seaweed‐Derived Alginic Acid: An Efficient and Reusable Catalyst for Pictet‐Spengler Reaction to Access Tetrahydro‐β‐Carboline and Tetrahydroisoquinoline Frameworks.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 5, p. 1, doi. 10.1002/ajoc.202200129
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- Article
A New Series of Tungstophosphoric Acid-Polymeric Matrix Catalysts: Application in the Green Synthesis of 2-Benzazepines and Analogous Rings.
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- Catalysts (2073-4344), 2022, v. 12, n. 10, p. 1155, doi. 10.3390/catal12101155
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- Article
A Visible Light Photoredox Catalysed Radical Pictet-Spengler Reaction*.
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- Australian Journal of Chemistry, 2020, v. 73, n. 2/3, p. 189, doi. 10.1071/CH19423
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- Article
Diastereoselective Synthesis of Camptothecin‐like Scaffolds: Construction of a New Class of Pseudo‐natural Products.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 13, p. 1, doi. 10.1002/ejoc.202300080
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- Article
Stereodivergent Transformation of Azepino[3,4,5‐cd]indoles En Route to Nature‐Inspired Scaffolds.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 9, p. 1, doi. 10.1002/ejoc.202201354
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- Article
Singlet oxygen-mediated transformation of furans into aromatic nitrogen-containing polycycles in water.
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- ARKIVOC: Online Journal of Organic Chemistry, 2015, v. 2015, p. 154, doi. 10.3998/ark.5550190.p008.973
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- Article
First highly stereocontrolled synthesis of tetrahydro trans-β-carboline derivatives by exploiting the influence of a cyclic amide.
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- ARKIVOC: Online Journal of Organic Chemistry, 2013, p. 22
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- Article
Tetrahydroisoquinoline-Based Non-Peptidomimetic Plasmepsin Inhibitors.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 1, p. 60, doi. 10.1007/s10593-020-02623-6
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- Article
Computational mechanistic investigation of the kinetic resolution of α-methyl-phenylacetaldehyde by norcoclaurine synthase.
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- Communications Chemistry, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42004-024-01146-x
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- Article
Squaramide-Based Catalysts in Organic Synthesis (A Review).
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- Russian Journal of General Chemistry, 2022, v. 92, n. 3, p. 287, doi. 10.1134/S107036322203001X
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Cysteine Catalyzed Pictet-Spengler Reaction: a Convenient and Mild Method for Synthesis of Spiroindolones.
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- Catalysis Letters, 2024, v. 154, n. 8, p. 4586, doi. 10.1007/s10562-024-04698-8
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- Article
Total Synthesis of 12,13‐Dibenzyl‐banistenoside B and Analogs.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 19, p. 1, doi. 10.1002/ejoc.202200222
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- Article
Novel, Chiral, and Enantiopure C<sub>2</sub>‐Symmetric Thioureas Promote Asymmetric Protio‐Pictet‐Spengler Reactions by Anion‐Binding Catalysis.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 5, p. 825, doi. 10.1002/ejoc.202001501
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- Article
Metal‐Free Decarboxylative A<sup>3</sup>‐Coupling/Pictet–Spengler Cascade Accessing Polycyclic Scaffolds: Propiolic Acids Exceed Alkynes.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 11, p. 1695, doi. 10.1002/ejoc.202000007
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- Article
Efficient One-Pot Synthesis of Tetrahydronaphtho[2,1-f]isoquinolines by Using Domino Pictet--Spengler/Friedel--Crafts-Type Reactions.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 43, p. 6434, doi. 10.1002/ejoc.201701243
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- Article
Establishing Consensus Stereostructures for the Naphthoquinonopyrano-γ-lactone Natural Products (-)-Arizonin B1 and (-)-Arizonin C1 by Total Syntheses. Diastereocontrol of Oxa-Pictet-Spengler Cyclizations by Protective-Group Optimization.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 17, p. 2512, doi. 10.1002/ejoc.201700013
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- Article
Organocatalytic Enantioselective Synthesis of 6-Aryl-5,6- dihydrophenanthridines by a Modified Pictet–Spengler Reaction of Biphenyl-2-amines and Aromatic Aldehydes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 14, p. 1865, doi. 10.1002/ejoc.201700185
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- Article
Facile Entry to 3,4-Dihydro-1 H-pyrrolo[2,1- c][1,4]oxazines through the oxa-Pictet-Spengler Reaction.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 31, p. 5274, doi. 10.1002/ejoc.201600928
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- Article
Consecutive Pictet-Spengler Condensations toward Bioactive 8-Benzylprotoberberines: Highly Selective Total Syntheses of (+)-Javaberine A, (+)-Javaberine B, and (-)-Latifolian A.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 22, p. 3705, doi. 10.1002/ejoc.201600764
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- Article
First Synthesis of (R)- and (S)-1,2,3,4-Tetrahydroisoquinoline-3- phosphonic Acid (Tic<sup>P</sup>) Using a Pictet-Spengler Reaction.
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- European Journal of Organic Chemistry, 2016, p. 2711, doi. 10.1002/ejoc.201600313
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- Article
First Synthesis of ( R)- and ( S)-1,2,3,4-Tetrahydroisoquinoline-3-phosphonic Acid (Tic<sup>P</sup>) Using a Pictet-Spengler Reaction.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 15, p. 2711, doi. 10.1002/ejoc.201600313
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- Article
MCR Synthesis of Praziquantel Derivatives.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 4, p. 470, doi. 10.1111/j.1747-0285.2011.01288.x
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- Article
Engineering a norcoclaurine synthase for one-step synthesis of (S)-1-aryl-tetrahydroisoquinolines.
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- Bioresources & Bioprocessing, 2023, v. 10, n. 1, p. 1, doi. 10.1186/s40643-023-00637-4
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- Article
ID 234. Synthesis and Investigation for Anticancer and Antibacterial Activities of Novel N2,N9- Benzylated-β-carbolineum Bromate Derivatives.
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- Journal of Pharmacy & Bioallied Sciences, 2020, v. 12, p. 931
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- Article
Synthesis, Molecular Docking and Antiplasmodial Activities of New Tetrahydro-β-Carbolines.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 24, p. 13569, doi. 10.3390/ijms222413569
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- Article
Synthesis of 3-(2-Nitroalkyl)pyrroles from Sulfonylpyrroles and their Conversion to 6-Azaindole Derivatives.
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- Advanced Synthesis & Catalysis, 2013, v. 355, n. 16, p. 3285, doi. 10.1002/adsc.201300701
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- Article
Evaluation of the Local Anesthetic Activity, Acute Toxicity, and Structure–Toxicity Relationship in Series of Synthesized 1-Aryltetrahydroisoquinoline Alkaloid Derivatives In Vivo and In Silico.
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- Molecules, 2023, v. 28, n. 2, p. 477, doi. 10.3390/molecules28020477
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- Article
Editorial to the Special Issue "Total Synthesis of Natural Products: A Themed Issue Dedicated to Professor Dr. Dieter Schinzer for His 65th Birthday".
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- 2020
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- Editorial
Novel Polycondensed Partly Saturated β-Carbolines Including Ferrocene Derivatives: Synthesis, DFT-Supported Structural Analysis, Mechanism of Some Diastereoselective Transformations and a Preliminary Study of their In Vitro Antiproliferative Effects.
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- Molecules, 2020, v. 25, n. 7, p. 1599, doi. 10.3390/molecules25071599
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- Article
The Pictet-Spengler Reaction Updates Its Habits.
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- Molecules, 2020, v. 25, n. 2, p. 414, doi. 10.3390/molecules25020414
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- Article