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Isatisine A, a Novel Alkaloid with an Unprecedented Skeleton from Leaves of Isatis indigotica

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Outgoing claims: the papers this work cites, builds on, or argues with.

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In VitroImmunotoxicity and Cytotoxicity of Trichosanthin Against Human Normal Immunocytes and Leukemia-Lymphoma Cells

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4647549openalex-extracted
B(C6f5)3-Catalyzed Regio- and Stereoselective Cyanation of Isatogens and Their Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.201401070openalex-snapshot
N‐Heterocyclic Carbene‐Catalyzed Umpolung Formal [3+3] Cycloaddition of Enals with Isatogens: Access to Fused Indolin‐3‐ones with a Tetrasubstituted Carbon Stereocenter
inferred← citeshttps://doi.org/10.1002/adsc.201800345openalex-snapshot
Organocatalytic Asymmetric Transformations Involving the Cyclic Imine Moiety in Indole and Isoindole Related Heterocycles
inferred← citeshttps://doi.org/10.1002/adsc.201800414openalex-snapshot
Copper‐Catalyzed Radical Sulfonylation of N‐Propargylindoles with Concomitant 1,2‐Aryl Migration
inferred← citeshttps://doi.org/10.1002/adsc.201801227openalex-snapshot
A Brønsted Acid‐Catalyzed Michael Addition/Cyclization Sequence for the Diastereoselective Assembly of Chroman‐Bridged Polycyclic Isoindolinones
inferred← citeshttps://doi.org/10.1002/adsc.201901409openalex-snapshot
Synthesis of 1H‐Pyrrolo[1,2‐a]indoles via Lewis Acid‐Catalyzed Annulation of Propargylic Alcohols with 2‐Ethynylanilines
inferred← citeshttps://doi.org/10.1002/adsc.202100290openalex-snapshot
Synthesis of N‐Fused Indolines via Copper (II)‐Catalyzed Dearomatizing Cyclization of Indoles
inferred← citeshttps://doi.org/10.1002/adsc.202100842openalex-snapshot
One‐Pot Synthesis of Fused Indolin‐3‐Ones via a [3+3] Cycloaddition Reaction
inferred← citeshttps://doi.org/10.1002/adsc.202400475openalex-snapshot
Copper‐Catalyzed Radical‐Induced Annulation‐Halo(bi)cyanomethylation of Indole‐Tethered 1,6‐Enynes toward Pyrrolo[1,2‐a]indoles
inferred← citeshttps://doi.org/10.1002/adsc.70587openalex-snapshot
Chemoselective Synthesis of 2,2‐Disubstituted Indolin‐3‐Ones via Palladium‐Catalyzed Allylation of 3‐Hydroxyindoles
inferred← citeshttps://doi.org/10.1002/adsc.70625openalex-snapshot
Ru(II)‐Catalyzed C3‐H Functionalization of Indoles With Isatogens
inferred← citeshttps://doi.org/10.1002/adsc.70799openalex-snapshot
CS 2 Induced Annulation of 2‐Alkynyl Nitroarenes With Indoles: Construction of 2,2‐Disubstituted Indolin‐3‐ones
inferred← citeshttps://doi.org/10.1002/ajoc.201900604openalex-snapshot
Visible Light‐Mediated C2‐Quaternarization of N‐Alkyl Indoles through Oxidative Dearomatization using Ir(III) Catalyst
inferred← citeshttps://doi.org/10.1002/ajoc.202100068openalex-snapshot
Synthesis of 3H‐Pyrrolo‐(1,2‐a) Indole‐based Fluorophore Macrocycles and their Stable Cation Radicals
inferred← citeshttps://doi.org/10.1002/ajoc.202200112openalex-snapshot
Synthesis of Expanded Crowned Macrocycles Containing Two Pyrrolo[1,2‐a]indole Units
inferred← citeshttps://doi.org/10.1002/ajoc.202200403openalex-snapshot
Asymmetric Friedel−Crafts Alkylation of Indoles with α,β‐unsaturated Trifluoromethyl Ketones Using a Squaramide Organocatalyst
inferred← citeshttps://doi.org/10.1002/ajoc.202300101openalex-snapshot
Radical Cascade Cyclization of Alkene‐Tethered Compounds: Versatile Approach towards Ring‐Fused Polycyclic Structures
inferred← citeshttps://doi.org/10.1002/ajoc.202400612openalex-snapshot
Copper‐Catalyzed Synthesis of C‐2 Substituted Indolin‐3‐Ones and Indolin‐3‐One [4+2] Cycloadducts Through Azide‐Tethered Iodonium Ylides
inferred← citeshttps://doi.org/10.1002/ajoc.70284openalex-snapshot
Diastereoselective Three‐Component Annulation for the Synthesis of Sulfonylated Polycyclic Indolines
inferred← citeshttps://doi.org/10.1002/ange.200906632openalex-snapshot
Total Synthesis of (+)‐Isatisine A
inferred← citeshttps://doi.org/10.1002/ange.201101621openalex-snapshot
Total Synthesis of (−)‐Isatisine A
inferred← citeshttps://doi.org/10.1002/ange.201306181openalex-snapshot
Iron‐Catalyzed Oxidative CH/CH Cross‐Coupling: An Efficient Route to α‐Quaternary α‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201504697openalex-snapshot
Dual Catalysis for the Redox Annulation of Nitroalkynes with Indoles: Enantioselective Construction of Indolin‐3‐ones Bearing Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/ange.201800746openalex-snapshot
Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A
inferred← citeshttps://doi.org/10.1002/ange.201915226openalex-snapshot
B(C6F5)3/Chiral Phosphoric Acid Catalyzed Ketimine–Ene Reaction of 2‐Aryl‐3H‐indol‐3‐ones and α‐Methylstyrenes
inferred← citeshttps://doi.org/10.1002/ange.202007549openalex-snapshot
Visible‐Light Cascade Photooxygenation of Tetrahydrocarbazoles and Cyclohepta[b]indoles: Access to C,N‐Diacyliminium Ions
inferred← citeshttps://doi.org/10.1002/ange.202014796openalex-snapshot
Palladium‐Catalyzed Enantioselective Heteroarenyne Cycloisomerization Reaction
inferred← citeshttps://doi.org/10.1002/anie.200906632openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201101621openalex-snapshot
Total Synthesis of (−)‐Isatisine A
inferred← citeshttps://doi.org/10.1002/anie.201306181openalex-snapshot
Iron‐Catalyzed Oxidative CH/CH Cross‐Coupling: An Efficient Route to α‐Quaternary α‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/anie.201504697openalex-snapshot
Dual Catalysis for the Redox Annulation of Nitroalkynes with Indoles: Enantioselective Construction of Indolin‐3‐ones Bearing Quaternary Stereocenters
inferred← citeshttps://doi.org/10.1002/anie.201800746openalex-snapshot
Heteroannulation of Arynes with α‐Amino Imides: Synthesis of 2,2‐Disubstituted Indolin‐3‐ones and Application to the Enantioselective Total Synthesis of (+)‐Hinckdentine A
inferred← citeshttps://doi.org/10.1002/anie.201915226openalex-snapshot
B(C6F5)3/Chiral Phosphoric Acid Catalyzed Ketimine–Ene Reaction of 2‐Aryl‐3H‐indol‐3‐ones and α‐Methylstyrenes
inferred← citeshttps://doi.org/10.1002/anie.202007549openalex-snapshot
Visible‐Light Cascade Photooxygenation of Tetrahydrocarbazoles and Cyclohepta[b]indoles: Access to C,N‐Diacyliminium Ions
inferred← citeshttps://doi.org/10.1002/anie.202014796openalex-snapshot
Palladium‐Catalyzed Enantioselective Heteroarenyne Cycloisomerization Reaction
inferred← citeshttps://doi.org/10.1002/asia.201800300openalex-snapshot
Oxidative Asymmetric Aza‐Friedel–Crafts Alkylation of Indoles with 3‐Indolinone‐2‐carboxylates Catalyzed by a BINOL Phosphoric Acid and Promoted by DDQ
inferred← citeshttps://doi.org/10.1002/asia.201800446openalex-snapshot
Organocatalytic Asymmetric Cascade Aerobic Oxidation and Semipinacol Rearrangement Reaction: A Visible Light‐Induced Approach to Access Chiral 2,2‐Disubstituted Indolin‐3‐ones
inferred← citeshttps://doi.org/10.1002/asia.202100799openalex-snapshot
Crowned Macrocycles Containing Two Pyrrolo[1,2‐a] Indoles Created By Intramolecular Fusion
inferred← citeshttps://doi.org/10.1002/asia.202300526openalex-snapshot
Enantioselective Alkynylation of 2‐Aryl‐3H‐indol‐3‐ones via Cooperative Catalysis of Copper/Chiral Phosphoric Acid
inferred← citeshttps://doi.org/10.1002/chem.201103604openalex-snapshot
InCl3‐Mediated Addition of Indole to Isatogens: An Expeditious Synthesis of 13‐deoxy‐Isatisine A
inferred← citeshttps://doi.org/10.1002/chem.201800348openalex-snapshot
Access to 3‐Oxindoles from Allylic Alcohols and Indoles
inferred← citeshttps://doi.org/10.1002/chem.201805909openalex-snapshot
Development, Scope, and Applications of Titanium(III)‐Catalyzed Cyclizations to Aminated N‐Heterocycles
inferred← citeshttps://doi.org/10.1002/chem.202201047openalex-snapshot
Radical/Iminium Domino Strategy (RIDS) for Rapid Construction of Sterically Congested γ‐Lactam‐Based Multiheterocycles
inferred← citeshttps://doi.org/10.1002/chem.202203914openalex-snapshot
Asymmetric aza‐Friedel–Crafts Reaction of Cyclic Ketimines with 5‐Aminopyrazole Derivatives: Expedient Access to Pyrazole‐Based C2‐quaternary Indolin‐3‐Ones
inferred← citeshttps://doi.org/10.1002/chem.202401008openalex-snapshot
B(C6F5)3/CPA‐Catalyzed Aza‐Diels‐Alder Reaction of 3,3‐Difluoro‐2‐Aryl‐3H‐indoles and Unactivated Dienes
inferred← citeshttps://doi.org/10.1002/chin.200809218openalex-snapshot
ChemInform Abstract: Isatisine A (Ia), a Novel Alkaloid with an Unpresedented Skeleton from Leaves of Isatis indigotica.
inferred← citeshttps://doi.org/10.1002/cmdc.202500726openalex-snapshot
Hydrophosphinylation of α ‐Ketimino Esters to Access Unnatural Tetrasubstituted α ‐Phosphinyl α ‐Amino Acids: Cytotoxicity against Cancer Cells
inferred← citeshttps://doi.org/10.1002/cssc.201900438openalex-snapshot
Oxidative Coupling of 3‐Oxindoles with Indoles and Arenes
inferred← citeshttps://doi.org/10.1002/ejoc.201900626openalex-snapshot
Synthesis and Applications of 9H‐Pyrrolo[1,2‐a]indole and 9H‐Pyrrolo[1,2‐a]indol‐9‐one Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.202000243openalex-snapshot
Synthesis of N‐Fused Seven‐Membered Indoline‐3‐ones via a Palladium‐Catalyzed One‐Pot Insertion Reaction from 2‐Alkynyl Arylazides and Cyclic β‐Diketones
inferred← citeshttps://doi.org/10.1002/ejoc.202101191openalex-snapshot
Synthesis of Polycyclic Indolines by Utilizing a Reduction/Cyclization Cascade Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.202300661openalex-snapshot
B(C6F5)3‐Catalyzed Aza‐Friedel–Crafts Reaction of Indolizines with 2‐Aryl‐3H‐indol‐3‐ones
inferred← citeshttps://doi.org/10.1002/ejoc.202400447openalex-snapshot
Synthesis of Fluorine‐Containing C2‐Tetrasubstituted Indolin–3‐ones via Rapid Incorporation of Difluoroacetate Radical Into 2‐Aryl‐3H‐indol‐3‐ones
inferred← citeshttps://doi.org/10.1002/ejoc.202500494openalex-snapshot
Biindoles. A Synthetic Overview
inferred← citeshttps://doi.org/10.1002/jhet.3206openalex-snapshot
Palladium Catalyzed Tricyclohexylphosphine Ligand Associated Synthesis of N‐(2‐(pyridine‐4‐yl)‐1H‐pyrrolo[3,2‐c]‐pyridin‐6‐yl‐(substituted)‐sulfonamide Derivatives as Antiproliferative Agents
inferred← citeshttps://doi.org/10.1002/med.21707openalex-snapshot
Development of anti‐influenza agents from natural products
inferred← citeshttps://doi.org/10.1002/slct.201802476openalex-snapshot
Pd‐Catalyzed One‐Pot Two‐Step Synthesis of 2‐(1 H ‐indol‐3‐yl)‐2‐phenylindolin‐3‐ones from 2‐Alkynyl Arylazides and Indoles
inferred← citeshttps://doi.org/10.1002/slct.201804029openalex-snapshot
Reductive Heck Reaction: An Emerging Alternative in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/slct.202000631openalex-snapshot
Synthesis of γ ‐Spirolactams from Blaise Reaction Intermediates and 1,2‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/slct.202101130openalex-snapshot
Catalytic Function of Cu (I) and Cu (II) in Total Synthesis of Alkaloids
inferred← citeshttps://doi.org/10.1002/slct.202304835openalex-snapshot
Copper–Catalyzed Construction of the Indole Core: Recent Advancements
inferred← citeshttps://doi.org/10.1002/slct.202403372openalex-snapshot
Applications of the Cu(I)‐Catalyzed Aryl Amidation in Total Synthesis of Complex Molecules
inferred← citeshttps://doi.org/10.1007/978-3-030-83350-3_22-1openalex-snapshot
Traditional Crude Drugs Against Encephalitis Infection: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies
inferred← citeshttps://doi.org/10.1007/978-3-031-12199-9_22openalex-snapshot
Traditional Crude Drugs Against Encephalitis Infection: Ethnopharmacology, Chemistry, and Clinical and Preclinical Studies
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_11openalex-snapshot
Classification of Diverse Novel Alkaloids
inferred← citeshttps://doi.org/10.1007/978-981-99-7329-3_14openalex-snapshot
Biological Activities
inferred← citeshttps://doi.org/10.1007/s11030-022-10381-0openalex-snapshot
A Rh(II)-catalyzed highly stereoselective [3 + 2] annulation of vinyl diazoacetates with indole-2-carbaldehyde for the synthesis of indolyl dihydrofurans
inferred← citeshttps://doi.org/10.1007/s41061-020-0287-7openalex-snapshot
Recent Advances on the C2-Functionalization of Indole via Umpolung
inferred← citeshttps://doi.org/10.1007/s41981-023-00261-5openalex-snapshot
Continuous one-pot synthesis of new spiro-fused indoles from biobased building blocks using carbamoylation and imidation reactions under ultrasonic irradiation
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14960-1openalex-snapshot
Three Heterocyclic Rings Fused (5-5-5)
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00654-7openalex-snapshot
Chinese Traditional Medicine
inferred← citeshttps://doi.org/10.1016/j.apsb.2018.08.005openalex-snapshot
Sulfur-enriched alkaloids from the root of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.apsb.2019.09.001openalex-snapshot
Indole alkaloid glycosides with a 1′-(phenyl)ethyl unit from Isatis indigotica leaves
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103650openalex-snapshot
Four pairs of alkaloid enantiomers from Isatis indigotica Fortune Ex Land with neuroprotective effects against H2O2-induced SH-SY5Y cell injury
inferred← citeshttps://doi.org/10.1016/j.bse.2020.104163openalex-snapshot
Alkaloids from the leaves of Isatis indigotica fortune and their chemotaxonomic significance
inferred← citeshttps://doi.org/10.1016/j.cclet.2015.05.052openalex-snapshot
Antiviral enantiomers of a bisindole alkaloid with a new carbon skeleton from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.01.042openalex-snapshot
Antiviral stereoisomers of 3,5-bis(2-hydroxybut-3-en-1-yl)-1,2,4-thiadiazole from the roots of Isatis indigotica
inferred← citeshttps://doi.org/10.1016/j.cclet.2016.08.006openalex-snapshot
Two pairs of unusual scalemic enantiomers from Isatis indigotica leaves
inferred← citeshttps://doi.org/10.1016/j.cclet.2017.12.001openalex-snapshot
Isatindolignanoside A, a glucosidic indole-lignan conjugate from an aqueous extract of the Isatis indigotica roots
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112405openalex-snapshot
Recent advances on cyclization reaction of indole-tethered alkenes for the construction of polyheterocycles
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112071openalex-snapshot
Discovery, synthesis, and optimization of an N-alkoxy indolylacetamide against HIV-1 carrying NNRTI-resistant mutations from the Isatis indigotica root
inferred← citeshttps://doi.org/10.1016/j.fitote.2010.10.016openalex-snapshot
Novel indole C-glycosides from Isatis indigotica and their potential cytotoxic activity
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116279openalex-snapshot
Enantioselective carbene-catalyzed tandem reaction for the efficient synthesis of pyrroloindolone and pyrrolidine derivatives with four consecutive stereocenters
inferred← citeshttps://doi.org/10.1016/j.jep.2021.114648openalex-snapshot
Isatidis Radix and Isatidis Folium: A systematic review on ethnopharmacology, phytochemistry and pharmacology
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147603openalex-snapshot
Scaffold-Hopped Isaindigotone-Tetrahydroacridine Hybrids as Dual‑Active Compounds against Cancer and Fungal Pathogens
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.02.016openalex-snapshot
Alkaloids with neuroprotective effects from the leaves of Isatis indigotica collected in the Anhui Province, China
inferred← citeshttps://doi.org/10.1016/j.tet.2011.02.057openalex-snapshot
Pd(II)-SPRIX catalyzed enantioselective construction of pyrrolizines/pyrroloindoles employing molecular oxygen as the sole oxidant
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.026openalex-snapshot
The synthesis of the central tricyclic core of the isatisine A: harmonious orchestration of [metal]-catalyzed reactions in a sequence
inferred← citeshttps://doi.org/10.1016/j.tet.2014.09.028openalex-snapshot
Total synthesis of (−)-isatisine A via a biomimetic benzilic acid rearrangement
inferred← citeshttps://doi.org/10.1016/j.tet.2017.01.032openalex-snapshot
TEMPO-catalyzed oxidative dimerization and cyanation of indoles for the synthesis of 2-(1H-indol-3-yl)-3-oxoindoline-2-carbonitriles
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131433openalex-snapshot
Copper(II)-catalyzed decarboxylative cyclization for accessing biologically relevant 3-(2-furanyl) Indoles via 3-cyanoacetyl indoles and cinnamic acids
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133038openalex-snapshot
Facile three-component reactions for the synthesis of N-unsubstituted 1H-pyrrol-3(2H)-ones and base induced divergent N–H and C–C bond derivatizations
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133527openalex-snapshot
Potassium persulfate mediated oxidative dearomatization and C–H functionalization of indoles in water: Green and transition metal free approach for the synthesis of indolone derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134242openalex-snapshot
Photoredox-catalyzed self-dimerization and cross-addition as well as Zn(OTf)2-mediated nucleophile coupling: A novel route to structurally diverse 2,2-disubstituted indolin-3-ones
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134294openalex-snapshot
Visible light mediated decarboxylative difluoroalkylations of cyclic N-sulfonyl ketimines: Efficient synthesis of difluoroalkylated Cα-tetrasubstituted α-amino acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134487openalex-snapshot
BF3-catalyzed nucleophilic addition reaction of 1,2-diaminobenzenes with α-ketoesters: Access to cyclic α,α-disubstituted α-amino acid derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.03.134openalex-snapshot
Microwave-assisted facile synthesis of [a]-annelated pyrazolopyrroloindoles via intramolecular azomethine imine 1,3-dipolar cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.01.014openalex-snapshot
Synthesis of 2-arylindoles by Suzuki coupling reaction of 3-bromoindoles with hindered benzoboronic acids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151059openalex-snapshot
First total synthesis of rhuscholide A, glabralide B and denudalide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152370openalex-snapshot
Recent advances in the construction of isoindolo[2,1-a]indol/indolin-6-ones via C C cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154909openalex-snapshot
B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80008-6openalex-snapshot
Chapter 5.2 Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70010-8openalex-snapshot
Chapter 5.2: Five-membered ring systems: pyrroles and benzo analogs
inferred← citeshttps://doi.org/10.1016/s1875-5364(21)60093-6openalex-snapshot
Discovery of alkaloids from the leaves of Isatis indigotica Fortune with neuroprotective activity
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b06417openalex-snapshot
Prenylated Chromones from the Fruits of Artocarpus heterophyllus and Their Potential Anti-HIV-1 Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00475openalex-snapshot
Palladium-Catalyzed Amination/Dearomatization Reaction of Indoles and Benzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00817openalex-snapshot
Application of Cp2TiCl-Promoted Radical-Induced Cyclization: An Expeditious Access to [a]-Annelated Indoles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01478openalex-snapshot
Palladium-Catalyzed Asymmetric Intramolecular Dearomative Heck Annulation of Aryl Halides to Furnish Indolines
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02501openalex-snapshot
Dieckmann Condensation of Ugi N-Acylamino Amide Product: Facile Access to Functionalized 2,2-Disubstituted Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02546openalex-snapshot
Retro-Aza-Piancatelli Rearrangement Triggered Cascade Reaction of Methyl Furylacrylates with Anilines to Access Cyclopenta[b]pyrrolidinones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01209openalex-snapshot
Palladium-Catalyzed Intramolecular Heck Dearomative Alkenylation of Indoles with N-Tosylhydrazones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01593openalex-snapshot
Diastereoselective Access to Triazolo[1,2-a]indolines via a Bio-Inspired Oxidative Cyclization of NH-Indoles
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01713openalex-snapshot
Copper- and Visible-Light-Catalyzed Cascade Radical Cyclization of N-Propargylindoles with Cyclic Ethers
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01734openalex-snapshot
Electrochemical Oxidative Addition of Nucleophiles on 2-Arylindoles: Synthesis of C2-Heteroquaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02583openalex-snapshot
Total Syntheses of Iheyamines A and B
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02765openalex-snapshot
Organocatalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction of Cyclic Ketimine with α,β-Unsaturated γ-Butyrolactam
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02183openalex-snapshot
Visible-Light-Induced Cascade Cyclization of 1-Acryloyl-2-cyanoindole: Access of Difluoroalkylated Pyrrolo[1,2-a]indolediones
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02217openalex-snapshot
Metal-Free One-Pot Domino Synthesis of Oxazolidinethione Derivatives of Quaternary Amino Acids from α-Amino Esters and Aldehydes Using CS2
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02599openalex-snapshot
Pd-Catalyzed Asymmetric Allylation Reaction of 2-Aryl-3H-indol-3-ones with Allyltrimethylsilane
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02807openalex-snapshot
Enantioselective Synthesis of C2-Quaternary Indolin-3-ones by Pt-Catalyzed Alkynylation of 2-Aryl-3 H -indol-3-one with Alkynylsilanes
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00051openalex-snapshot
Total Synthesis of (+)-Isatisine A: Application of a Silicon-Directed Mukaiyama-Type [3 + 2]-Annulation
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01028openalex-snapshot
High Enantioselective and Unprecedented Diastereoselective Synthesis of C2-Quaternary Indolin-3-ones by CPA-Catalyzed Asymmetric Mannich Reaction of 3,3-Difluoro-2-aryl-3H-indoles with Cycloketones
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01202openalex-snapshot
AgSCN/(NH4)2S2O8-Promoted Cascade Cyclization of 1-(2-Ethynylphenyl)-1H-indoles and Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01421openalex-snapshot
Divergent Synthesis of Pyrrolizine- and Indolizine-Fused Heterocycles via Pd(II)-Catalyzed Cascade Transformation of Functionalized Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01463openalex-snapshot
Chemodivergent Synthesis of 1,3-Benzoxazines, Indolin-3-ols, and Indoles from the Designer Amides: Applications to the Synthesis of Phenanthridine Natural Products
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02006openalex-snapshot
Green C3-Aminomethylation of Indoles
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02186openalex-snapshot
Photoactive Catalytic EDA Complex-Mediated Synthesis of Difluorinated Polycyclic Indolines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02194openalex-snapshot
Regioselective Introduction of Indolin-3-one Moieties to Substituted Heteroaromatic Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02847openalex-snapshot
Direct Synthesis of 2-Alkynylindolin-3-ones via Copper-Catalyzed Reductive Alkynylation of 2-Arylisatogens
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01730openalex-snapshot
Enantioselective Model Synthesis and Progress toward the Putative Structure of Yuremamine
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02070openalex-snapshot
Organocatalyzed Asymmetric Michael Addition of 1-Acetylindolin-3-ones to β,γ-Unsaturated α-Ketoesters: An Access to Chiral Indolin-3-ones with Two Adjacent Tertiary Stereogenic Centers
inferred← citeshttps://doi.org/10.1021/acs.joc.7b03017openalex-snapshot
Sustainable Radical Cascades to Synthesize Difluoroalkylated Pyrrolo[1,2-a]indoles
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00222openalex-snapshot
Dual Catalytic Synthesis of Antiviral Compounds Based on Metallocarbene–Azide Cascade Chemistry
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00511openalex-snapshot
FeCl2-Catalyzed Decarboxylative Radical Alkylation/Cyclization of Cinnamamides: Access to Dihydroquinolinone and Pyrrolo[1,2-a]indole Analogues
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03090openalex-snapshot
Visible Light-Catalyzed Cascade Radical Cyclization of N-Propargylindoles with Acyl Chlorides for the Synthesis of 2-Acyl-9H-pyrrolo[1,2-a]indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01522openalex-snapshot
Fe-Catalyzed Sequential C(sp3)–H/N–H Annulation of 2-Methylindoles with Ethyl Trifluoropyruvate at Room Temperature: Construction of Pyrrolo[1,2-α]indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02166openalex-snapshot
Palladium-Catalyzed, Enantioselective (3 + 2)-Cycloannulation of β-Keto Esters with Alkylidene 2H-Indoles toward Complex Indole-Based Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02180openalex-snapshot
Copper(0)/PPh3-Mediated Bisheteroannulations of o-Nitroalkynes with Methylketoximes Accessing Pyrazo-Fused Pseudoindoxyls
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02323openalex-snapshot
Selective Synthesis of 2-Indolyl-3-oxoindolines or 2-(2-Aminophenyl)quinolines through Cu(II)- or Bi(III)-Catalyzed Tunable Dimerizations of 2-Alkynylanilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02760openalex-snapshot
The Different Faces of [Ru(bpy)3Cl2] and fac[Ir(ppy)3] Photocatalysts: Redox Potential Controlled Synthesis of Sulfonylated Fluorenes and Pyrroloindoles from Unactivated Olefins and Sulfonyl Chlorides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02836openalex-snapshot
Unconventional [2 + 3] Cyclization Involving [1,4]-Sulfonyl Transfer to Construct Polysubstituted Fluorazones as Inhibitors of Indoleamine 2,3-Dioxygenase 1
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03897openalex-snapshot
Pd-Catalyzed Asymmetric Dearomatization of Indoles via Decarbonylative Heck-Type Reaction of Thioesters
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00354openalex-snapshot
Cobalt-Catalyzed Dearomatization of Indoles via Transfer Hydrogenation To Afford Polycyclic Indolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00927openalex-snapshot
1-Acryloyl-2-cyanoindole: A Skeleton for Visible-Light-Induced Cascade Annulation
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02179openalex-snapshot
Ag(I)-Promoted, Diastereoselective Cyclo-isomerization of N-Alkynyl-7-azaindole-2-carbinols. Selective Synthesis of syn-1,2-Diarylpyrrolo[1,2-a]indol-3-ones and (Z)-8-Benzylideneoxazolo[3′,4′’:1,5]pyrrolo[2,3-b]pyridines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00075openalex-snapshot
Copper-Catalyzed Diastereo- and Enantioselective Decarboxylative [3 + 2] Cyclization of Alkyne-Substituted Cyclic Carbamates with Azlactones: Access to γ-Butyrolactams Bearing Two Vicinal Tetrasubstituted Carbon Stereocenters
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02009openalex-snapshot
Electron Donor–Acceptor Complex Induced Fused Indoles with Hypervalent Iodine(III) Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00957openalex-snapshot
Direct S0 → Tn Transition under Visible Light Irradiation Enabling Synthesis of a Pseudoindoxyl Scaffold
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01528openalex-snapshot
Iron-Catalyzed Oxidative Rearrangement of Cyclopropanone Hemiaminals: General Access to Pyrroloindolones from Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01720openalex-snapshot
Heteroannulation of Arynes with α-Bromodifluorohydroxamates: An Efficient and General Approach to Access 2,2-Difluoro Indoxyls
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02862openalex-snapshot
Dearomative Cyclization/Spirocyclization via Electrochemical Reductive Hydroarylation of Nonactivated Arenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03337openalex-snapshot
Palladium-Catalyzed Carbonylative Cyclization of 1-Alkynyl-2-iodo- d -glucal
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00615openalex-snapshot
Counter-Ion-Dependent Alkyne Iminium Ion Cyclization for Divergent Synthesis of N -Fused Indolylidine, Indole, and Indoline Derivatives Promoted by the Lewis/Bronsted Acid
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00712openalex-snapshot
Chiral Phosphoric Acid Catalyzed Asymmetric Mannich Reaction of 2-Aryl-3H-indol-3-ones with α-H Diazoacetates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c01661openalex-snapshot
Efficient Synthesis of Pseudoindoxyls from 2-Nitrobenzylidenemalonates and Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03180openalex-snapshot
Organophotoredox Cascade Cyclization for the Synthesis of Silyl/Fluoroalkylated Tetracyclic Pyrrolizidinediones
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00244openalex-snapshot
Oxidative Dearomatization of Indoles via Pd-Catalyzed C–H Oxygenation: An Entry to C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01711openalex-snapshot
Palladium-Catalyzed Intramolecular Dearomatization of Indoles via Decarboxylative Alkynyl Termination
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03473openalex-snapshot
Organocatalytic Enantioselective Amination of 2-Substituted Indolin-3-ones: A Strategy for the Synthesis of Chiral α-Hydrazino Esters
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03585openalex-snapshot
Construction of Chiral Tricyclic Indoles through a Rhodium-Catalyzed Asymmetric Arylation Protocol
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03636openalex-snapshot
Diamination/Oxidative Cross-Coupling/Bicyclization of Anilines and Methyl Ketones: Direct I2-Promoted Synthesis of 1,2-Fused Oxindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03713openalex-snapshot
Silver-Catalyzed Radical-Involved Cascade Cyclization of Diphenylphosphine with Cinnamamides: Access to 2-Phosphinoyl-3H-pyrrolo[1,2-a]indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01896openalex-snapshot
Organocatalytic Nucleophilic Aromatic Addition Enabling Asymmetric Dearomatization of Azoindoles with Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03276openalex-snapshot
Palladium-Catalyzed Tandem Dearomative Heck Reaction of N -Propiolyl Indoles or Pyrroles with Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00200openalex-snapshot
Gold/Copper-Co-catalyzed Tandem Reactions of 2-Alkynylanilines: A Synthetic Strategy for the C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02005openalex-snapshot
Cascade Radical Cyclization of N-Propargylindoles: Substituents Dictate Stereoselective Formation of N-Fused Indolines versus Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02680openalex-snapshot
Lewis Acid Mediated Cascade Friedel–Craft/Alkyne Indol-2-yl Cation Cyclization/Vinyl Cation Trapping for the Synthesis of N-Fused Indole Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b03213openalex-snapshot
Catalytic Asymmetric Mukaiyama–Mannich Reaction of Cyclic C-Acylimines with Difluoroenoxysilanes: Access to Difluoroalkylated Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01321openalex-snapshot
Total Synthesis of an Isatis indigotica-Derived Alkaloid Using a Biomimetic Thio-Diels–Alder Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01823openalex-snapshot
Asymmetric Synthesis of C2-Quaternary Indolin-3-ones Enabled by N-Heterocyclic Carbene Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01965openalex-snapshot
Organocatalytic Asymmetric Dearomative Oxyalkylation of Indoles Enables Access to C2-Quaternary Indolin-3-ones
inferred← citeshttps://doi.org/10.1021/acscatal.4c00560openalex-snapshot
Diastereo- and Enantioselective Dearomative Reductive Aryl-Fluoroalkenylation of Indoles by Nickel Catalysis
inferred← citeshttps://doi.org/10.1021/acsomega.8b02132openalex-snapshot
Organocatalytic Enantioselective Mannich Reaction: Direct Access to Chiral β-Amino Esters
inferred← citeshttps://doi.org/10.1021/ja304767mopenalex-snapshot
A Labeled Substrate Approach to Discovery of Biocatalytic Reactions: A Proof of Concept Transformation with N-Methylindole
inferred← citeshttps://doi.org/10.1021/jacs.5b01705openalex-snapshot
Enantioselective Arylative Dearomatization of Indoles via Pd-Catalyzed Intramolecular Reductive Heck Reactions
inferred← citeshttps://doi.org/10.1021/jacs.5c22595openalex-snapshot
An Amino-Acid-Derived Metal–Organic Framework with Large Pores for Unspecific Enantioseparation
inferred← citeshttps://doi.org/10.1021/jacs.9b07418openalex-snapshot
Cyclohexyl-Fused, Spirobiindane-Derived, Phosphine-Catalyzed Synthesis of Tricyclic γ-Lactams and Kinetic Resolution of γ-Substituted Allenoates
inferred← citeshttps://doi.org/10.1021/jacs.9b12493openalex-snapshot
Enantioselective Synthesis of Polycyclic γ-Lactams with Multiple Chiral Carbon Centers via Ni(0)-Catalyzed Asymmetric Carbonylative Cycloadditions without Stirring
inferred← citeshttps://doi.org/10.1021/jo101209yopenalex-snapshot
Total Synthesis of (+)-Isatisine A
inferred← citeshttps://doi.org/10.1021/jo301035hopenalex-snapshot
Oxidative Coupling of Indoles with Ethyl 2-(Disubstituted Amino)Acetates: An Approach to Achieve Indolylglycine Derivatives
inferred← citeshttps://doi.org/10.1021/jo302198vopenalex-snapshot
Total Synthesis of (−)-Isatisine A
inferred← citeshttps://doi.org/10.1021/jo402759vopenalex-snapshot
Stereoselective Synthesis of Indoline, Tetrahydroquinoline, and Tetrahydrobenzazepine Derivatives from o-Bromophenyl N-tert-Butylsulfinyl Aldimines
inferred← citeshttps://doi.org/10.1021/np3002833openalex-snapshot
Alkaloids from the Root of Isatis indigotica
inferred← citeshttps://doi.org/10.1021/ol100033sopenalex-snapshot
Synthesis of Polycyclic Nitrogen Heterocycles via Alkene Aminopalladation/Carbopalladation Cascade Reactions
inferred← citeshttps://doi.org/10.1021/ol102848wopenalex-snapshot
Total Synthesis of (+)-Isatisine A
inferred← citeshttps://doi.org/10.1021/ol201123bopenalex-snapshot
Cascade Intramolecular N-Arylation/Intermolecular Carboamination Reactions for the Construction of Tricyclic Heterocycles
inferred← citeshttps://doi.org/10.1021/ol202431xopenalex-snapshot
Diastereoselective Intramolecular Friedel–Crafts Cyclizations of Substituted Methyl 2-(1H-indole-1-carbonyl)acrylates: Efficient Access to Functionalized 1H-Pyrrolo[1,2-a]indoles
inferred← citeshttps://doi.org/10.1021/ol300379gopenalex-snapshot
Biomimetic Total Synthesis of (−)-Isatisine A
inferred← citeshttps://doi.org/10.1021/ol300584mopenalex-snapshot
Efficient Construction of Fused Indolines with a 2-Quaternary Center via an Intramolecular Heck Reaction with a Low Catalyst Loading
inferred← citeshttps://doi.org/10.1021/ol302660topenalex-snapshot
Enantiomers of an Indole Alkaloid Containing Unusual Dihydrothiopyran and 1,2,4-Thiadiazole Rings from the Root of Isatis indigotica
inferred← citeshttps://doi.org/10.1021/ol401709topenalex-snapshot
Total Synthesis of a Pyrroloindoloquinazoline Alkaloid
inferred← citeshttps://doi.org/10.1039/b820693gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c0ob00858copenalex-snapshot
Divergent Pd(ii) and Au(iii) mediated nitroalkynol cycloisomerizations
inferred← citeshttps://doi.org/10.1039/c1sc00190fopenalex-snapshot
Chiral phosphoric acid-catalysed Friedel–Crafts alkylation reaction of indoles with racemic spiro indolin-3-ones
inferred← citeshttps://doi.org/10.1039/c2ob26390dopenalex-snapshot
Metal-free catalyzed oxidative trimerization of indoles by using TEMPO in air: a biomimetic approach to 2-(1H-indol-3-yl)-2,3′-biindolin-3-ones
inferred← citeshttps://doi.org/10.1039/c3cc40617bopenalex-snapshot
Cu(OTf)2 catalysed [6+2] cycloaddition reaction for the synthesis of highly substituted pyrrolo[1,2-a]indoles: rapid construction of the yuremamine core
inferred← citeshttps://doi.org/10.1039/c3ob42283fopenalex-snapshot
Rhodium-catalyzed three-component reaction of 3-diazooxindoles with indoles and isatin-derived ketimines: a facile and versatile approach to functionalized 3,3′,3′′-trisindoles
inferred← citeshttps://doi.org/10.1039/c3ra45702hopenalex-snapshot
meta-Chloroperbenzoic acid (mCPBA): a versatile reagent in organic synthesis
inferred← citeshttps://doi.org/10.1039/c4nj02308kopenalex-snapshot
Efficient synthesis of some new antiproliferative N-fused indoles and isoquinolines via 1,3-dipolar cycloaddition reaction in an ionic liquid
inferred← citeshttps://doi.org/10.1039/c4ra10309bopenalex-snapshot
Total synthesis of cruciferane via epoxidation/tandem cyclization sequence
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