Works matching DE "PICTET-Spengler reaction"
Results: 83
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
Synthesis of Tetrahydroisoquinoline-Alkaloid Analogs with a Diphenyloxide Fragment.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 5, p. 903, doi. 10.1007/s10600-022-03825-4
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- Article
Furan Analog of the Alkaloid Dubiamine Based on 5-Hydroxymethylfurfurol.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 1, p. 185, doi. 10.1007/s10600-022-03630-z
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- Article
Synthesis of Hydroxyethyl Derivatives of 1-Aryltetrahydroisoquinoline Alkaloids.
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- Chemistry of Natural Compounds, 2014, v. 49, n. 6, p. 1095, doi. 10.1007/s10600-014-0828-9
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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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- 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
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
Tailored SnO<sub>2</sub>@MWCNTs efficient and recyclable nano-catalyst for selective synthesis of 4, 5-dihydropyrrolo [1, 2-a] quinoxalines via Pictet–Spengler reaction.
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- Research on Chemical Intermediates, 2022, v. 48, n. 12, p. 4901, doi. 10.1007/s11164-022-04852-0
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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
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
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
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
Tricycles by a New Ugi Variation and Pictet-Spengler Reaction in One Pot.
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- Chemistry - A European Journal, 2013, v. 19, n. 25, p. 8048, doi. 10.1002/chem.201300962
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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
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
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
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
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
Synthesis of Thieno[3,2- e][1,4]diazepin-2-ones: Application of an Uncatalysed Pictet-Spengler Reaction.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 32, p. 7146, doi. 10.1002/ejoc.201500943
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- Article
Synthetic Studies toward Actinorhodin and γ-Actinorhodin by using a Homo-coupling Strategy: Synthesis of Hemiactinorhodin and Hemi-γ-actinorhodin.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 22, p. 4931, doi. 10.1002/ejoc.201500510
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- Article
Diastereodivergent Pictet-Spengler Cyclization of Bicyclic N-Acyliminium Ions: Controlling a Quaternary Stereocenter.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 6, p. 1273, doi. 10.1002/ejoc.201403469
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- Article
First Practical and Efficient Synthesis of 3-Phosphorylated β-Carboline Derivatives Using the Pictet-Spengler Reaction.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 5, p. 1084, doi. 10.1002/ejoc.201403418
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- Article
One-Pot α-Amidosulfone-Mediated Variation of the Pictet-Spengler Tetrahydroisoquinoline Synthesis, Suitable for Amide-Type Substrates.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 26, p. 5720, doi. 10.1002/ejoc.201402487
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- Article
Microwave-Assisted Synthesis of Tetrahydro-β-carbolines and β-Carbolines.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 8, p. 1653, doi. 10.1002/ejoc.201301580
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- Article
Chemoenzymatic Synthesis of Enantiomerically Pure syn-Configured 1-Aryl-3-methylisochroman Derivatives.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 1, p. 111, doi. 10.1002/ejoc.201301429
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- Article
Asymmetric Synthesis of (R)‐1‐Alkyl‐Substituted Tetrahydro‐ß‐carbolines Catalyzed by Strictosidine Synthases.
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- Angewandte Chemie, 2018, v. 130, n. 33, p. 10843, doi. 10.1002/ange.201803372
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- Article
Construction of Chiral Tetrahydro-β-Carbolines: Asymmetric Pictet-Spengler Reaction of Indolyl Dihydropyridines.
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- Angewandte Chemie, 2017, v. 129, n. 26, p. 7548, doi. 10.1002/ange.201703178
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- Article
Pictet-Spengler Synthesis of Quinoline-Fused Porphyrins and Phenanthroline-Fused Diporphyrins.
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- Angewandte Chemie, 2016, v. 128, n. 42, p. 13232, doi. 10.1002/ange.201606293
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- Article
New approaches towards the synthesis of 1,2,3,4-tetrahydro isoquinoline-3-phosphonic acid (TicP).
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- Amino Acids, 2021, v. 53, n. 3, p. 451, doi. 10.1007/s00726-021-02962-4
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- Article
Chemical tags for site-specific fluorescent labeling of biomolecules.
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- Amino Acids, 2016, v. 48, n. 6, p. 1357, doi. 10.1007/s00726-016-2204-5
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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
Formal Synthesis of the Human Rhinovirus 3 C Protease Inhibitor (−)-Thysanone.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 6, p. 560, doi. 10.1002/ajoc.201500070
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- Article
Heterogeneous Catalysts in Pictet-Spengler-Type Reactions.
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/125302
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- Article
A divergent approach to the synthesis of the yohimbinoid alkaloids venenatine and alstovenine.
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- Nature Chemistry, 2013, v. 5, n. 2, p. 126, doi. 10.1038/nchem.1528
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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
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
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
Organocatalytic Cascade Reactions for the Diversification of Thiopyrano‐Piperidone Fused Rings Utilizing Trienamine Activation.
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- Chemistry - A European Journal, 2021, v. 27, n. 2, p. 618, doi. 10.1002/chem.202004553
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- Article
Asymmetric Biocatalytic Synthesis of 1‐Aryltetrahydro‐β‐carbolines Enabled by "Substrate Walking".
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- Chemistry - A European Journal, 2020, v. 26, n. 69, p. 16281, doi. 10.1002/chem.202004449
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- Article
Total Syntheses of (−)‐Secologanin, (−)‐5‐Carboxystrictosidine, and (−)‐Rubenine.
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- Chemistry - A European Journal, 2019, v. 25, n. 38, p. 8996, doi. 10.1002/chem.201902073
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- Article
Ultrasound Assisted Pictet-Spengler Synthesis of Tetrahydro-β-Carboline Derivatives.
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- 2016
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- Other