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First Total Synthesis of Hinckdentine A
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Nukleophile Reaktionen an 2‐Phenylindolenin‐3‐onen
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Nitration in the thiazole series
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3H‐Indol‐3‐ols by a novel ring contraction
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Synthesis of polyfunctional indoles and related heterocycles mediated by cesium and potassium bases
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Hinckdentine-a: A novel alkaloid from the marine bryozoan hincksinoflustra denticulata
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Efficient modified von Niementowski synthesis of novel derivatives of 5a,14b,15-triazabenzo[a]indeno[1,2-c]anthracen-5-one from indolo[1,2-c]quinazoline
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Base-induced intramolecular cyclisation of -azidophenyl -alkyl ketones. A new synthesis of 2,2-dialkylindoxyls
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Dimethyldioxirane oxidation of indole derivatives. Formation of novel indole-2,3-epoxides and a versatile synthetic route to indolinones and indolines
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The Structure of the So-called 11-Hydroxytetrahydrocarbazolenine1
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REARRANGEMENTS AND REVISIONS IN THE TETRAHYDROCARBAZOLE SERIES
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Synthesis of 8-Desbromohinckdentine A1
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Total Synthesis of the Duocarmycins
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Alkenyl and Aryl BoronatesMild Nucleophiles for the Stereoselective Formation of Functionalized N-Heterocycles
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Chemistry of Indolo[1,2-c]quinazoline: An Approach to the Marine Alkaloid Hinckdentine A
inferredcites →https://doi.org/10.1021/jo020715fopenalex-snapshot
Study of the Addition of Grignard Reagents to 2-Aryl-3H-indol-3-ones1
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Palladium-Catalyzed Arylation and Heteroarylation of Azolopyrimidines
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Synthesis and Absolute Structure of Manzacidin B
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1,2-Nucleophilic addition on 2-phenyl-3H-indol-3-one and 2-phenyl-3-phenylimino-3H-indole and their corresponding 1-oxides. An attempt to synthesize water-soluble aminoxyls. Crystal structure of 3-ethoxycarbonyl-2,3,3a,4-tetrahydro-2,4-dioxo-3a-phenylisoxazolo[2,3-a]indole
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Competition between single electron transfer and nucleophilic attack. Part 2. Reaction of 2-phenyl-3H-indol-3-one with Grignard reagents
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Ring-chain tautomerism and some reactions of 2-hydroxyindoline derivatives.
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Versatile Synthesis of 2,2-Disubstituted Indolinones via Protected Indolones Generated by One-Pot Multi-oxidation of 2-Substituted Indoles
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Asymmetric Alkylation of 2-Monosubstituted Indolin-3-ones
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The Reaction of Indolyl Grignard and Related Organometallic Reagents with 2-Phenylsulphonylbuta-1,3-diene and 2,3-Diphenylsulphonylbuta-1,3-diene
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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1,3,2-Dioxaborolane, 4,4,5,5-Tetramethyl-2-(2-propen-1-yl)
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Bryozoa, Phoronida, and Brachiopoda
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One‐Pot Asymmetric Oxidative Dearomatization of 2‐Substituted Indoles by Merging Transition Metal Catalysis with Organocatalysis to Access C2‐Tetrasubstituted Indolin‐3‐Ones
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PPh3‐Mediated Wittig‐Like/Mannich Tandem Reactions of 2‐Alkynylnitrobenzenes with Ketones for the Synthesis of 2,2‐Disubstituted Indolin‐3‐Ones
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Recent Advances in Stetter Reaction and Related Chemistry: An update
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Organocatalyst‐Controlled Divergent Asymmetric Aza‐Friedel‐Crafts Reactions of Indol‐3‐ones with 1‐ and 2‐Naphthols
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Total Synthesis of (−)‐Isatisine A
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Brønsted Acid Catalyzed Asymmetric Hydroamination of Alkenes: Synthesis of Pyrrolidines Bearing a Tetrasubstituted Carbon Stereocenter
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Nickel‐Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Afford Indolines
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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
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Concurrent Asymmetric Reactions Combining Photocatalysis and Enzyme Catalysis: Direct Enantioselective Synthesis of 2,2‐Disubstituted Indol‐3‐ones from 2‐Arylindoles
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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.201101621openalex-snapshot
Total Synthesis of (−)‐Isatisine A
inferred← citeshttps://doi.org/10.1002/anie.201501762openalex-snapshot
Brønsted Acid Catalyzed Asymmetric Hydroamination of Alkenes: Synthesis of Pyrrolidines Bearing a Tetrasubstituted Carbon Stereocenter
inferred← citeshttps://doi.org/10.1002/anie.201707134openalex-snapshot
Nickel‐Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Afford Indolines
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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
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Concurrent Asymmetric Reactions Combining Photocatalysis and Enzyme Catalysis: Direct Enantioselective Synthesis of 2,2‐Disubstituted Indol‐3‐ones from 2‐Arylindoles
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B(C6F5)3/Chiral Phosphoric Acid Catalyzed Ketimine–Ene Reaction of 2‐Aryl‐3H‐indol‐3‐ones and α‐Methylstyrenes
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Organocatalytic Asymmetric Cascade Aerobic Oxidation and Semipinacol Rearrangement Reaction: A Visible Light‐Induced Approach to Access Chiral 2,2‐Disubstituted Indolin‐3‐ones
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A Brønsted Acid Catalyzed Cascade Reaction for the Conversion of Indoles to α‐(3‐Indolyl) Ketones by Using 2‐Benzyloxy Aldehydes
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Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines
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inferred← citeshttps://doi.org/10.1002/chin.200920183openalex-snapshot
ChemInform Abstract: First Total Synthesis of Hinckdentine A (VI).
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Electrochemical Synthesis of (Aza)indolines via Dehydrogenative [3+2] Annulation: Application to Total Synthesis of (±)‐Hinckdentine A
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Synthesis of Polycyclic Indolines by Utilizing a Reduction/Cyclization Cascade Reaction
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Asymmetric Proline‐Catalyzed Addition of Aldehydes to 3H‐Indol‐3‐ones: Enantioselective Synthesis of 2,3‐Dihydro‐1H‐indol‐3‐ones with Quaternary Stereogenic Centers
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Efficient Domino Approach to Polysubstituted 2‐Hydroxyindole‐3,4‐(2H,5H)‐diones
inferred← citeshttps://doi.org/10.1002/jhet.4939openalex-snapshot
Synthesis of Terminal Alkenylindolines via Rhodium‐Catalyzed Direct CH Alkenylation With Alkenyl Borates
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
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Recent Advances on the C2-Functionalization of Indole via Umpolung
inferred← citeshttps://doi.org/10.1016/b978-0-08-096805-6.00006-1openalex-snapshot
Five-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-818655-8.00032-9openalex-snapshot
Bicyclic 5-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 0:1
inferred← citeshttps://doi.org/10.1016/b978-0-323-89812-6.00016-xopenalex-snapshot
Seven-membered rings
inferred← citeshttps://doi.org/10.1016/b978-0-323-95652-9.00012-0openalex-snapshot
Synthesis of azocines
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.11.001openalex-snapshot
Synthesis of pyrimidine-containing alkaloids
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2014.02.017openalex-snapshot
Palladium catalyzed direct C-2 arylation of indoles
inferred← citeshttps://doi.org/10.1016/j.tet.2009.12.028openalex-snapshot
Preparation of 2,2-disubstituted 1,2-dihydro-3H-indol-3-ones via oxidation of 2-substituted indoles and Mannich-type reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.062openalex-snapshot
Iodine/CuI-mediated alkyne–carbonyl metathesis reaction: synthesis of 1-aryl-1,2-dihydrochromeno[2,3-b]azepine-3,6-dione
inferred← citeshttps://doi.org/10.1016/j.tet.2015.06.065openalex-snapshot
Transition-metal free highly selective aerobic oxidation of hindered 2-alkylindoles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.159openalex-snapshot
Synthesis of 2-hydroxy-3-indolinones and 3-hydroxy-2-indolinones by anionic cyclization, in situ oxidation and rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.04.061openalex-snapshot
Synthesis of 3-substituted 8,9-didehydroazepino[4,5-b]indolines via ring expansion reaction of pyrroloindolines
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Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination–cyclization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152880openalex-snapshot
Reinventing the wheel for enabling the synthesis of hinckdentine A
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B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
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inferred← citeshttps://doi.org/10.1016/s0959-6380(11)22006-3openalex-snapshot
Five-Membered Ring Systems
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Palladium-Catalyzed Amination/Dearomatization Reaction of Indoles and Benzofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01308openalex-snapshot
One-Pot Tandem Assembly of Amides, Amines, and Ketones: Synthesis of C4-Quaternary 3,4- and 1,4-Dihydroquinazolines
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Dieckmann Condensation of Ugi N-Acylamino Amide Product: Facile Access to Functionalized 2,2-Disubstituted Indolin-3-ones
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Pd-Catalyzed Asymmetric Allylation Reaction of 2-Aryl-3H-indol-3-ones with Allyltrimethylsilane
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.5c01284openalex-snapshot
Stereoselective Synthesis of Spirocyclic Indolin-3-ones through a Gold(I)-Catalyzed Cascade Cyclization of Azido-alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02924openalex-snapshot
Trials into Triumphs: The Emergence of a Concise Total Synthesis of Hinckdentine A
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01993openalex-snapshot
The Cs2CO3–Catalyzed Reaction of 2-Oxindoles with Enones for the Preparation of Indolin-3-Ones and Their Further Transformation
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.orglett.1c00323openalex-snapshot
Total Synthesis of Hinckdentine A
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00837openalex-snapshot
Ru-Catalyzed Redox-Neutral Cleavage of the N–O Bond in Isoxazolidines: Isatogens to Pseudoindoxyls via a One-Pot [3 + 2]-Cycloaddition/N–O Cleavage
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.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.8b00332openalex-snapshot
Double “Open and Shut” Transformation of γ-Carbolines Triggered by Ammonium Salts: One-Pot Synthesis of Multiheterocyclic Compounds
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/acscatal.8b02651openalex-snapshot
Carbene-Catalyzed Enantioselective Addition of Benzylic Carbon to Unsaturated Acyl Azolium for Rapid Synthesis of Pyrrolo[3,2- c ]quinolines
inferred← citeshttps://doi.org/10.1021/cs5015496openalex-snapshot
Enantioselective Formation of 3-Substituted Indolinoazepines via Organocatalyzed Conjugate Addition of Indoloazepines to Propargyl Aldehyde
inferred← citeshttps://doi.org/10.1021/jacs.0c04760openalex-snapshot
Discovery and Total Synthesis of a Bis(cyclotryptamine) Alkaloid Bearing the Elusive Piperidinoindoline Scaffold
inferred← citeshttps://doi.org/10.1021/jacs.1c01100openalex-snapshot
Taming Radical Pairs in the Crystalline Solid State: Discovery and Total Synthesis of Psychotriadine
inferred← citeshttps://doi.org/10.1021/jacs.3c03611openalex-snapshot
Rapid Access to 2,2-Disubstituted Indolines via Dearomative Indolic-Claisen Rearrangement: Concise, Enantioselective Total Synthesis of (+)-Hinckdentine A
inferred← citeshttps://doi.org/10.1021/jacs.5c18159openalex-snapshot
Catalytic Asymmetric Synthesis of 3-Hydroxyindolenines Using Achiral Oxaziridines
inferred← citeshttps://doi.org/10.1021/jacs.6b04077openalex-snapshot
A Dual-Catalytic Strategy To Direct Asymmetric Radical Aminotrifluoromethylation of Alkenes
inferred← citeshttps://doi.org/10.1021/jacs.6b10237openalex-snapshot
Enantioselective Total Synthesis of (+)-Hinckdentine A via a Catalytic Dearomatization Approach
inferred← citeshttps://doi.org/10.1021/jacsau.2c00048openalex-snapshot
Total Synthesis of (+)-Hinckdentine A: Harnessing Noncovalent Interactions for Organocatalytic Bromination
inferred← citeshttps://doi.org/10.1021/jo201951sopenalex-snapshot
Synthesis and Biological Activity of Kalkitoxin and its Analogues
inferred← citeshttps://doi.org/10.1021/jo4020358openalex-snapshot
Total Synthesis, Stereochemical Assignment, and Biological Activity of All Known (−)-Trigonoliimines
inferred← citeshttps://doi.org/10.1021/jo501282hopenalex-snapshot
Rh(II)/Brønsted Acid Cocatalyzed Intramolecular Trapping of Ammonium Ylides with Enones: Diastereoselective Synthesis of 2,2,3-Trisubstituted Indolines
inferred← citeshttps://doi.org/10.1021/ol101178uopenalex-snapshot
Nitrophenylacetonitriles as Versatile Nucleophiles in Enantioselective Organocatalytic Conjugate Additions
inferred← citeshttps://doi.org/10.1021/ol202475ropenalex-snapshot
An Approach to the Hexacyclic Skeleton of Trigonoliimines
inferred← citeshttps://doi.org/10.1021/ol5033865openalex-snapshot
Asymmetric Total Synthesis of (−)-Leuconoxine via Chiral Phosphoric Acid Catalyzed Desymmetrization of a Prochiral Diester
inferred← citeshttps://doi.org/10.1039/c005345gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c2cc34539kopenalex-snapshot
A cascade reaction of azolopyrimidines. Synthesis of unusual indole and azaindole derivatives
inferred← citeshttps://doi.org/10.1039/c3cc41348aopenalex-snapshot
Synthesis of pseudo-indoxyl derivatives via sequential Cu-catalyzed SNAr and Smalley cyclization
inferred← citeshttps://doi.org/10.1039/c4cc03565hopenalex-snapshot
Flexible and practical synthesis of 3-oxyindoles through gold-catalyzed intermolecular oxidation of o-ethynylanilines
inferred← citeshttps://doi.org/10.1039/c6ra19741hopenalex-snapshot
Metal-free regioselective construction of indolin-3-ones via hypervalent iodine oxidation of N-substituted indoles
inferred← citeshttps://doi.org/10.1039/c7cc03754fopenalex-snapshot
Facile access to 2,2-disubstituted indolin-3-ones via a cascade Fischer indolization/Claisen rearrangement reaction
inferred← citeshttps://doi.org/10.1039/c7nj02246hopenalex-snapshot
Facile oxidative cyclization to access C2-quaternary 2-hydroxy-indolin-3-ones: synthetic studies towards matemone
inferred← citeshttps://doi.org/10.1039/c7ob00715aopenalex-snapshot
FeCl 3 catalysed 7-membered ring formation in a single pot: a new route to indole-fused oxepines/azepines and their cytotoxic activity
inferred← citeshttps://doi.org/10.1039/c8cc05125aopenalex-snapshot
Chiral phosphoric acid-catalyzed direct asymmetric mannich reaction of cyclic C -acylimines with simple ketones: facile access to C2-quaternary indolin-3-ones
inferred← citeshttps://doi.org/10.1039/c8cc09949aopenalex-snapshot
Unified enantioselective total syntheses of (−)-scholarisine G, (+)-melodinine E, (−)-leuconoxine and (−)-mersicarpine
inferred← citeshttps://doi.org/10.1039/c8np00047fopenalex-snapshot
Non-monoterpenoid azepinoindole alkaloids
inferred← citeshttps://doi.org/10.1039/c8ob02683aopenalex-snapshot
Intramolecular trapping of ammonium ylides with N -benzoylbenzotriazoles in aqueous medium: direct access to the pseudoindoxyl scaffold
inferred← citeshttps://doi.org/10.1039/c8ra04807jopenalex-snapshot
Palladium-catalyzed direct C(sp 3 )–H arylation of indole-3-ones with aryl halides: a novel and efficient method for the synthesis of nucleophilic 2-monoarylated indole-3-ones
inferred← citeshttps://doi.org/10.1039/c9cc02956gopenalex-snapshot
Direct oxidative dearomatization of indoles: access to structurally diverse 2,2-disubstituted indolin-3-ones
inferred← citeshttps://doi.org/10.1039/d0ob00818dopenalex-snapshot
Palladium-catalyzed asymmetric dearomative cyclization in natural product synthesis
inferred← citeshttps://doi.org/10.1039/d0sc00001aopenalex-snapshot
Desymmetrization of unactivated bis-alkenes via chiral Brønsted acid-catalysed hydroamination
inferred← citeshttps://doi.org/10.1039/d2nj05797bopenalex-snapshot
Recent synthetic journey on pyrrole-fused compounds
inferred← citeshttps://doi.org/10.1039/d2ob01063aopenalex-snapshot
Dearomative oxyphosphorylation of indoles enables facile access to 2,2-disubstituted indolin-3-ones
inferred← citeshttps://doi.org/10.1039/d2qo00048bopenalex-snapshot
Synthesis of 2-monosubstituted indolin-3-ones by cine -substitution of 3-azido-2-methoxyindolines
inferred← citeshttps://doi.org/10.1039/d3qo00233kopenalex-snapshot
Enantioselective total syntheses of (−)-cephalotaxine and (−)-amathaspiramide F through a key Ir/Cu dual catalysis
inferred← citeshttps://doi.org/10.1039/d4qo00481gopenalex-snapshot
Diverting the Mannich reaction to access 2,2-disubstituted indolin-3-ones by merging 1,2-aryl migration and copper-catalyzed aerobic oxidation
inferred← citeshttps://doi.org/10.1039/d6nj01151aopenalex-snapshot
PPh 3 -Mediated synthesis of multifunctional indolin-3-one derivatives from 2-(ethynyl)nitrobenzenes and aryl ketones
inferred← citeshttps://doi.org/10.1055/sos-sd-236-00280openalex-snapshot
14 Electrochemistry in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1107/s1600536811045302openalex-snapshot
2-Hydroxy-2-methyl-1-phenylindolin-3-one
inferred← citeshttps://doi.org/10.1248/cpb.c25-00355openalex-snapshot
Catalytic Synthesis of Azepinoindoles from Ynamides Containing Indolyl Moieties via Ruthenium–Vinylidene Species
inferred← citeshttps://doi.org/10.2174/0122133461270888231128050236openalex-snapshot
Organic Electrosynthesis: A Promising Green Tool in Solving Key Steps for the Total Synthesis of Complex Natural Products
inferred← citeshttps://doi.org/10.3390/molecules25020419openalex-snapshot
Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones
inferred← citeshttps://doi.org/10.3987/com-10-s(e)127openalex-snapshot
Oxidative Coupling of Indoles with 3-Oxindoles
inferred← citeshttps://doi.org/10.4155/fmc-2018-0012openalex-snapshot
Review of Bioactive Secondary Metabolites from Marine Bryozoans in the Progress of New Drugs Discovery
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.73.821openalex-snapshot
Synthetic Development of 2,2-Disubstituted Indolin-3-ones Using Mannich-type Reactions and Its Application to Natural Product Synthesis
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.75.1115openalex-snapshot
Synthetic Studies on Heteropolycyclic Natural Products: Strategies via Novel Reactions and Reactivities
inferred← citeshttps://doi.org/10.59761/rcr5195openalex-snapshot
The Stetter reaction: modern methodologies and useful applications in total synthesis of natural products and drugs
inferred← citeshttps://doi.org/10.6023/cjoc202408037openalex-snapshot
Total Syntheses of Marine-Derived Polyhalogenated Natural Products
inferred← citeshttps://doi.org/10.70675/68d2886ezd2c3z465fzb777zd5ef1db3b782openalex-snapshot
Oxydation électrochimique de fonctions 1,3-dicarbonylées pour la synthèse de squelettes de diterpénoïdes de type abiétanes aromatiques par bicyclisation et de γ-lactones par couplage avec des styrènes
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