Works about INDOLE alkaloids
Results: 882
Engineered biosynthesis of plant heteroyohimbine and corynantheine alkaloids in Saccharomyces cerevisiae.
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- Journal of Industrial Microbiology & Biotechnology, 2024, v. 51, p. 1, doi. 10.1093/jimb/kuad047
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Tribule terrestre.
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- Phytothérapie, 2024, v. 22, n. 6, p. 298, doi. 10.3166/phyto-2024-0435
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Indole alkaloids from endophytic fungus Robillarda sessilis and their antibacterial activity.
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- Natural Product Research, 2025, v. 39, n. 5, p. 1156, doi. 10.1080/14786419.2023.2297853
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Exploring the Therapeutic Potential of Mitragynine and Corynoxeine: Kratom-Derived Indole and Oxindole Alkaloids for Pain Management.
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- Pharmaceuticals (14248247), 2025, v. 18, n. 2, p. 222, doi. 10.3390/ph18020222
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What Happens Inside the Germinating Grain After Microbial Decontamination by Pulsed Electric Field? Data-Driven Multi-Omics Helps Find the Answer.
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- Molecules, 2025, v. 30, n. 4, p. 924, doi. 10.3390/molecules30040924
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不同菜用甘薯品种茎尖代谢产物鉴定及途径分析.
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- Journal of Agricultural Science & Technology (1008-0864), 2025, v. 27, n. 2, p. 62, doi. 10.13304/j.nykjdb.2024.0371
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A fungal prenyltransferase catalyzes the regular di-prenylation at positions 20 and 21 of paxilline.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 3, p. 448, doi. 10.1080/09168451.2014.882759
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Oligomerization of N-Tosylindole with Aluminum Chloride.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 3, p. 764, doi. 10.1271/bbb.68.764
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Indole C5‐Selective Bromination of Indolo[2,3‐a]quinolizidine Alkaloids via In Situ‐Generated Indoline Intermediate.
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- Chemistry - A European Journal, 2024, v. 30, n. 35, p. 1, doi. 10.1002/chem.202401153
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Modular Divergent Synthesis of Indole Alkaloid Derivatives by an Atypical Ugi Multicomponent Reaction.
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- Chemistry - A European Journal, 2024, v. 30, n. 29, p. 1, doi. 10.1002/chem.202400477
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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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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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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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Enantioselective Total Synthesis of (+)‐Eucophylline.
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- Chemistry - A European Journal, 2022, v. 28, n. 16, p. 1, doi. 10.1002/chem.202200088
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Asymmetric Total Synthesis of Alstrostine G Utilizing a Catalytic Asymmetric Desymmetrization Strategy.
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- Angewandte Chemie, 2024, v. 136, n. 34, p. 1, doi. 10.1002/ange.202407127
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Asymmetric 1,2‐Migration at Vicinal Tetrasubstituted Stereocenters Constructed from α‐Keto Imines.
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- Angewandte Chemie, 2024, v. 136, n. 30, p. 1, doi. 10.1002/ange.202405212
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A Cytochrome P450 Catalyzes Oxidative Coupling Formation of Insecticidal Dimeric Indole Piperazine Alkaloids.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202404000
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Asymmetric Synthesis of Arboduridine.
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- Angewandte Chemie, 2024, v. 136, n. 3, p. 1, doi. 10.1002/ange.202316016
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Synthetic Matching of Complex Monoterpene Indole Alkaloid Chemical Space.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202310222
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Intermolecular Formal Cycloaddition of Indoles with Bicyclo[1.1.0]butanes by Lewis Acid Catalysis.
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- Angewandte Chemie, 2023, v. 135, n. 48, p. 1, doi. 10.1002/ange.202308606
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BiBr<sub>3</sub>‐Mediated Intramolecular Aza‐Prins Cyclization of Aza‐Achmatowicz Rearrangement Products: Asymmetric Total Synthesis of Suaveoline and Sarpagine Alkaloids.
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- Angewandte Chemie, 2023, v. 135, n. 44, p. 1, doi. 10.1002/ange.202311671
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Enzymatic Benzofuranoindoline Formation in the Biosynthesis of the Strained Bridgehead Bicyclic Dipeptide (+)‐Azonazine A.
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- Angewandte Chemie, 2023, v. 135, n. 40, p. 1, doi. 10.1002/ange.202311266
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A Homo‐Mannich Reaction Strategy Enables Collective Access to Ibophyllidine, Aspidosperma, Kopsia, and Melodinus Alkaloids.
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- Angewandte Chemie, 2023, v. 135, n. 37, p. 1, doi. 10.1002/ange.202307286
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Frontispiz: Synthetic Modulation of an Unstable Dehydrosecodine‐type Intermediate and Its Encapsulation into a Confined Cavity Enable Its X‐ray Crystallographic Observation.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202383262
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Synthetic Modulation of an Unstable Dehydrosecodine‐type Intermediate and Its Encapsulation into a Confined Cavity Enable Its X‐ray Crystallographic Observation.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202305122
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Collective Total Synthesis of Mavacuran Alkaloids through Intermolecular 1,4‐Addition of an Organolithium Reagent**.
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- Angewandte Chemie, 2023, v. 135, n. 21, p. 1, doi. 10.1002/ange.202302461
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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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Development of a Non‐Directed Petasis‐Type Reaction by an Aromaticity‐Disrupting Strategy.
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- Angewandte Chemie, 2023, v. 135, n. 14, p. 1, doi. 10.1002/ange.202218921
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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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Enantioselective Total Synthesis of (−)‐Limaspermidine and (−)‐Kopsinine by a Nitroaryl Transfer Cascade Strategy.
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- Angewandte Chemie, 2022, v. 134, n. 42, p. 1, doi. 10.1002/ange.202210592
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Total Synthesis of (+)‐Alstonlarsine A.
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- Angewandte Chemie, 2022, v. 134, n. 39, p. 1, doi. 10.1002/ange.202210297
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Total Synthesis of Ophiorrhine A, G and Ophiorrhiside E Featuring a Bioinspired Intramolecular Diels–Alder Cycloaddition.
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- Angewandte Chemie, 2022, v. 134, n. 38, p. 1, doi. 10.1002/ange.202209135
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Chemical Investigations of Differentially Oxidized Polycylic Pyrroles from Bipolaris Fungi: Synthetic Entry Into the Bipolamine Alkaloids.
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- Angewandte Chemie, 2022, v. 134, n. 37, p. 1, doi. 10.1002/ange.202209457
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Allenamide‐Initiated Cascade [2+2+2] Annulation Enabling the Divergent Total Synthesis of (−)‐Deoxoapodine, (−)‐Kopsifoline D and (±)‐Melotenine A.
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- Angewandte Chemie, 2022, v. 134, n. 34, p. 1, doi. 10.1002/ange.202207360
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Divergent Total Synthesis of Four Kopsane Alkaloids: N‐Carbomethoxy‐10,22‐dioxokopsane, Epikopsanol‐10‐lactam, 10,22‐Dioxokopsane, and N‐Methylkopsanone.
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- Angewandte Chemie, 2022, v. 134, n. 17, p. 1, doi. 10.1002/ange.202201712
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Catalytic Asymmetric Alkynylation of 3,4‐Dihydro‐β‐carbolinium Ions Enables Collective Total Syntheses of Indole Alkaloids.
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- Angewandte Chemie, 2021, v. 133, n. 47, p. 25339, doi. 10.1002/ange.202112383
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Photo Click Reaction of Acylsilanes with Indoles.
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- Angewandte Chemie, 2021, v. 133, n. 34, p. 18753, doi. 10.1002/ange.202101689
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Total Synthesis of (−)‐Arborisidine.
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- Angewandte Chemie, 2021, v. 133, n. 23, p. 12842, doi. 10.1002/ange.202101161
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Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H.
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- Angewandte Chemie, 2021, v. 133, n. 22, p. 12500, doi. 10.1002/ange.202103580
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Total Synthesis of (+)‐Alsmaphorazine C and Formal Synthesis of (+)‐Strictamine: A Photo‐Fries Approach.
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- Angewandte Chemie, 2021, v. 133, n. 19, p. 10697, doi. 10.1002/ange.202101752
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Unprecedented Reactivity of γ‐Amino Cyclopentenone Enables Diversity‐Oriented Access to Functionalized Indoles and Indole‐Annulated Ring Structures.
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- Angewandte Chemie, 2021, v. 133, n. 16, p. 8890, doi. 10.1002/ange.202016015
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Concise Total Synthesis of Tronocarpine.
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- Angewandte Chemie, 2021, v. 133, n. 2, p. 645, doi. 10.1002/ange.202009966
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Total Synthesis of Kopsinitarine E.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22223, doi. 10.1002/ange.202011093
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Collective Total Synthesis of Aspidofractinine Alkaloids through the Development of a Bischler–Napieralski/Semipinacol Rearrangement Reaction.
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- Angewandte Chemie, 2020, v. 132, n. 49, p. 22138, doi. 10.1002/ange.202009238
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A Divergent Enantioselective Total Synthesis of Post‐Iboga Indole Alkaloids.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18890, doi. 10.1002/ange.202008242
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TiCl<sub>3</sub>‐Mediated Synthesis of 2,3,3‐Trisubstituted Indolenines: Total Synthesis of (+)‐1,2‐Dehydroaspidospermidine, (+)‐Condyfoline, and (−)‐Tubifoline.
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- Angewandte Chemie, 2020, v. 132, n. 33, p. 14094, doi. 10.1002/ange.202005380
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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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Enantioselective Total Synthesis of Cymoside through a Bioinspired Oxidative Cyclization of a Strictosidine Derivative.
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- Angewandte Chemie, 2020, v. 132, n. 4, p. 1543, doi. 10.1002/ange.201912812
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Guanitrypmycin Biosynthetic Pathways Imply Cytochrome P450 Mediated Regio‐ and Stereospecific Guaninyl‐Transfer Reactions.
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- Angewandte Chemie, 2019, v. 131, n. 33, p. 11658, doi. 10.1002/ange.201906891
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Bioinspired Oxidative Cyclization of the Geissoschizine Skeleton for Enantioselective Total Synthesis of Mavacuran Alkaloids.
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- Angewandte Chemie, 2019, v. 131, n. 29, p. 9966, doi. 10.1002/ange.201905227
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