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Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ange.200901039openalex-snapshot
Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes and m‐CPBA
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A Concise Total Synthesis of the Notoamides C and D
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Total Synthesis of Complex Cyclotryptamine Alkaloids: Stereocontrolled Construction of Quaternary Carbon Stereocenters
inferredcites →https://doi.org/10.1002/anie.200700705openalex-snapshot
Concise Total Synthesis of (−)‐Calycanthine, (+)‐Chimonanthine, and (+)‐Folicanthine
inferredcites →https://doi.org/10.1002/anie.200901039openalex-snapshot
Asymmetric Hydroxylative Phenol Dearomatization through In Situ Generation of Iodanes from Chiral Iodoarenes and m ‐CPBA
inferredcites →https://doi.org/10.1002/anie.200904588openalex-snapshot
Total Synthesis of (+)‐Haplophytine
inferredcites →https://doi.org/10.1016/0040-4039(95)00648-vopenalex-snapshot
Reactions of indole-3-acetic acid derivatives in trifluoroacetic acid
inferredcites →https://doi.org/10.1016/j.tet.2006.01.105openalex-snapshot
The structural and synthetic implications of the biosynthesis of the calycanthaceous alkaloids, the communesins, and nomofungin
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Cyclizations of unsymmetrical bis-1,2-(3-indolyl)ethanes: Synthesis of (−)-tjipanazole F1
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Chapter 4 Bisindole Alkaloids
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Paraherquamides, Brevianamides, and Asperparalines: Laboratory Synthesis and Biosynthesis. An Interim Report
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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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Total synthesis of (+)- and (-)-tryptoquivaline G by biomimetic double cyclization
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3a-Hydroperoxypyrroloindole from tryptophan. Isolation and transformation to formylkynurenine
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Stereospecific total synthesis of dl-austamide
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Oxidative Transformations of Indole Alkaloids. I. The Preparation of Oxindoles from Yohimbine; the Structures and Partial Syntheses of Mitraphylline, Rhyncophylline and Corynoxeine
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Biogenetically Inspired Approach to the Strychnos Alkaloids. Concise Syntheses of (±)-Akuammicine and (±)-Strychnine
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Addition Reactions and Wagner-Meerwein Rearrangements in the Indoxyl Series
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The Course and Kinetics of the Acid-Base-Catalyzed Rearrangements of 11-Hydroxytetrahydrocarbazolenine 1
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Synthesis of 8-Desbromohinckdentine A1
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A Short Synthetic Route to (+)-Austamide, (+)-Deoxyisoaustamide, and (+)-Hydratoaustamide from a Common Precursor by a Novel Palladium-Mediated Indole → Dihydroindoloazocine Cyclization
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Short, Enantioselective Total Synthesis of Okaramine N
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Enantioselective Total Syntheses of Welwitindolinone A and Fischerindoles I and G
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Nonenzymatic Oxidative Steps Accompanying Action of the Cytochrome P450 Enzymes StaP and RebP in the Biosynthesis of Staurosporine and Rebeccamycin
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Scalable Total Syntheses of N -Linked Tryptamine Dimers by Direct Indole−Aniline Coupling: Psychotrimine and Kapakahines B and F
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Chemoselective and Enantioselective Oxidation of Indoles Employing Aspartyl Peptide Catalysts
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A New Catalyst for a Pd Catalyzed Alder Ene Reaction. A Total Synthesis of (+)-Cassiol
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Molecular Rearrangements. VIII. The Equilibration of 3,3-Dimethyl-2-phenyl- and 2,3-Dimethyl-3-phenyl-3H-indoles1
inferredcites →https://doi.org/10.1021/jo020715fopenalex-snapshot
Study of the Addition of Grignard Reagents to 2-Aryl-3H-indol-3-ones1
inferredcites →https://doi.org/10.1021/jo062627ropenalex-snapshot
Oxidative Rearrangement of Indoles: A New Approach to the EFHG-Tetracyclic Core of Diazonamide A
inferredcites →https://doi.org/10.1021/ol0627348openalex-snapshot
Total Synthesis of Flustramine C via Dimethylallyl Rearrangement
inferredcites →https://doi.org/10.1021/ol100715xopenalex-snapshot
Three New Indole Alkaloids from Trigonostemon lii
inferredcites →https://doi.org/10.1021/ol702132vopenalex-snapshot
Concise, Stereoselective Approach to the Spirooxindole Ring System of Citrinadin A
inferredcites →https://doi.org/10.1021/ol8015176openalex-snapshot
Stereoselective Oxidative Rearrangement of 2-Aryl Tryptamine Derivatives
inferredcites →https://doi.org/10.1038/ja.2008.4openalex-snapshot
Chemical biology of natural indolocarbazole products: 30 years since the discovery of staurosporine
inferredcites →https://doi.org/10.1038/nchem.110openalex-snapshot
Asymmetric total syntheses of (+)- and (−)-versicolamide B and biosynthetic implications
inferredcites →https://doi.org/10.1039/b410180dopenalex-snapshot
A concise total synthesis of (+)-okaramine C
inferredcites →https://doi.org/10.1039/b819925fopenalex-snapshot
Biogenetically inspired syntheses of alkaloid natural products
inferredcites →https://doi.org/10.1039/c39770000025openalex-snapshot
2-Arylsulphonyl-3-phenyloxaziridines: a new class of stable oxaziridine derivatives
inferredcites →https://doi.org/10.1055/s-1996-4175openalex-snapshot
Palladium-Catalyzed Hydrogenolysis of Allylic and Propargylic Compounds with Various Hydrides
inferredcites →https://doi.org/10.1073/pnas.0702946104openalex-snapshot
Crystal structures and catalytic mechanism of cytochrome P450 StaP that produces the indolocarbazole skeleton
inferredcites →https://doi.org/10.1126/science.1170777openalex-snapshot
Total Synthesis of (+)-11,11'-Dideoxyverticillin A
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Anthranilic Acid–Tryptophan Alkaloids
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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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Domino Ring‐Opening Cyclization of Aziridines with Isatogens: A Stereoselective Synthetic Route to Fluorescent Tetrahydrooxadiazino[2,3‐ a ]indolones
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Ru(II)‐Catalyzed C3‐H Functionalization of Indoles With Isatogens
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Catalytic Enantioselective Michael Addition of α‐Aryl‐α‐Isocyanoacetates to Vinyl Selenone: Synthesis of α,α‐Disubstituted α‐Amino Acids and (+)‐ and (−)‐Trigonoliimine A
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Enantiospecific Total Synthesis of N‐Methylwelwitindolinone D Isonitrile
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Bioinspired Total Synthesis of Sespenine
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Nickel‐Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Afford Indolines
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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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Total Synthesis of (±)‐Baphicacanthcusine A Enabled by Sequential Ring Contractions
inferred← citeshttps://doi.org/10.1002/anie.201306663openalex-snapshot
Catalytic Enantioselective Michael Addition of α‐Aryl‐α‐Isocyanoacetates to Vinyl Selenone: Synthesis of α,α‐Disubstituted α‐Amino Acids and (+)‐ and (−)‐Trigonoliimine A
inferred← citeshttps://doi.org/10.1002/anie.201307464openalex-snapshot
Enantiospecific Total Synthesis of N ‐Methylwelwitindolinone D Isonitrile
inferred← citeshttps://doi.org/10.1002/anie.201404191openalex-snapshot
Bioinspired Total Synthesis of Sespenine
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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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.202409139openalex-snapshot
Total Synthesis of (±)‐Baphicacanthcusine A Enabled by Sequential Ring Contractions
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Cascade Oxidative Dearomatization/Semipinacol Rearrangement: An Approach to 2‐Spirocyclo‐3‐oxindole Derivatives
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Oxidative Asymmetric Aza‐Friedel–Crafts Alkylation of Indoles with 3‐Indolinone‐2‐carboxylates Catalyzed by a BINOL Phosphoric Acid and Promoted by DDQ
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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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Enantioselective Alkynylation of 2‐Aryl‐3H‐indol‐3‐ones via Cooperative Catalysis of Copper/Chiral Phosphoric Acid
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InCl3‐Mediated Addition of Indole to Isatogens: An Expeditious Synthesis of 13‐deoxy‐Isatisine A
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One‐Pot Aminoethylation of Indoles/Pyrroles with Alkynes and Sulfonyl Azides
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B(C6F5)3/CPA‐Catalyzed Aza‐Diels‐Alder Reaction of 3,3‐Difluoro‐2‐Aryl‐3H‐indoles and Unactivated Dienes
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Microwave Promoted Tandem Reaction of Free Primary Arylamines with Diazo Compounds Under Metal‐Free Condition in Water: Clean Synthesis of 2,2‐Disubstituted 3‐Oxindoles
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Phosphoric Acid Catalyzed 1,2‐Rearrangements of 3‐Hydroxyindolenines to Indoxyls and 2‐Oxindoles: Reagent‐Controlled Regioselectivity Enabled by Dual Activation
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B(C6F5)3‐Catalyzed Aza‐Friedel–Crafts Reaction of Indolizines with 2‐Aryl‐3H‐indol‐3‐ones
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Synthesis of Fluorine‐Containing C2‐Tetrasubstituted Indolin–3‐ones via Rapid Incorporation of Difluoroacetate Radical Into 2‐Aryl‐3H‐indol‐3‐ones
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Biindoles. A Synthetic Overview
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Vinylogous Mannich Cyclization for the Stereoselective Construction of trans ‐2‐Alkenyl‐3‐Aminophenyl‐Dihydrobenzofuran and ‐Dihydroindole Derivatives
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Further Alkaloids from the Leaves of Trigonostemon lii
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3.14 The Pinacol Rearrangement
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A biomimetic synthesis of the skeleton of trigonoliimine C
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A modified approach to the skeleton of trigonoliimines A and B
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A biomimetic synthesis of homofascaplysin C from ditryptophans
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In(OTf)3 catalyzed regioselective acyloin rearrangement of 1-acyl-1-indanols
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Iron-catalyzed dimerization of pyrrolo[2,1-a]isoquinolines and pyrrolo[1,2-a]quinolines
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Dehydrative Mannich-Type Reaction for the Synthesis of Azepinobisindole Alkaloid Iheyamine A
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Electrophilic Oxidation and [1,2]-Rearrangement of the Biindole Core of Birinapant
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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/cr400611nopenalex-snapshot
Advances in the Chemistry of Oxaziridines
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Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds
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Catalytic Asymmetric α-Iminol Rearrangement: New Chiral Platforms
inferred← citeshttps://doi.org/10.1021/jacs.6b07846openalex-snapshot
Enantioselective Synthesis of (+)-Peganumine A
inferred← citeshttps://doi.org/10.1021/jo3010028openalex-snapshot
Synthesis of Tryptamine Derivatives via a Direct, One-Pot Reductive Alkylation of Indoles
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/ol202475ropenalex-snapshot
An Approach to the Hexacyclic Skeleton of Trigonoliimines
inferred← citeshttps://doi.org/10.1021/ol300249yopenalex-snapshot
A Concise Total Synthesis of (±)-Trigonoliimine B
inferred← citeshttps://doi.org/10.1021/ol303344dopenalex-snapshot
Rapid Total Synthesis of (±)Trigonoliimine A via a Strecker/Houben–Hoesch Sequence
inferred← citeshttps://doi.org/10.1039/c2cs35116aopenalex-snapshot
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance
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/c3cc45512bopenalex-snapshot
A modular total synthesis of (±)-trigonoliimine C
inferred← citeshttps://doi.org/10.1039/c3np20118jopenalex-snapshot
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c4qo00161copenalex-snapshot
Recent studies on the chemical constituents of Trigonostemon plants
inferred← citeshttps://doi.org/10.1039/c5qo00416kopenalex-snapshot
A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces
inferred← citeshttps://doi.org/10.1039/c6ob01685eopenalex-snapshot
4,4′-Bismoschamine: biomimetic synthesis and evidence to support structural equivalency to montamine
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/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/c8np00047fopenalex-snapshot
Non-monoterpenoid azepinoindole alkaloids
inferred← citeshttps://doi.org/10.1039/c8ob00865eopenalex-snapshot
Cascade reactions of indigo with oxiranes and aziridines: efficient access to dihydropyrazinodiindoles and spiro-oxazocinodiindoles
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/c9ob02607jopenalex-snapshot
FeCl 3 mediated dimerization of dihydropyrrolo[2,1- a ]isoquinolines and chlorination of tetrasubstituted pyrroles
inferred← citeshttps://doi.org/10.1039/d0cc05432aopenalex-snapshot
Organocatalytic asymmetric synthesis of arylindolyl indolin-3-ones with both axial and central chirality
inferred← citeshttps://doi.org/10.1039/d0nj04588hopenalex-snapshot
One-pot synthesis of 3-hydroxy-2-oxindoles via acyloin rearrangements of 2-hydroxy-indolin-3-ones generated in situ from 2-alkynyl arylazides
inferred← citeshttps://doi.org/10.1039/d1ob01285aopenalex-snapshot
Total synthesis of the pseudoindoxyl class of natural products
inferred← citeshttps://doi.org/10.1039/d1sc03533aopenalex-snapshot
A general approach to 2,2-disubstituted indoxyls: total synthesis of brevianamide A and trigonoliimine C
inferred← citeshttps://doi.org/10.1039/d2ob02179jopenalex-snapshot
Chiral phosphoric acid-catalyzed enantioselective aza-Friedel–Crafts reaction of naphthols and electron-rich phenols with 2-aryl-3 H -indol-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/d2qo00271jopenalex-snapshot
Mn( iii )-Catalyzed cascade cyclization reaction of o -acyl aromatic isocyanides with boronic acids
inferred← citeshttps://doi.org/10.1039/d2qo02024fopenalex-snapshot
Visible-light-driven reductive dearomatization of N -arylformyl indoles in EDA complexes with a thiophenol via a HAT pathway
inferred← citeshttps://doi.org/10.1039/d3ob00064hopenalex-snapshot
Nitroarenes and nitroalkenes as potential amino sources for the synthesis of N-heterocycles
inferred← citeshttps://doi.org/10.1039/d3qo02085aopenalex-snapshot
Enantioselective construction of chiral gem -difluorinated C2-quaternary indoline via dual MgSO 4 –CPA-catalyzed asymmetric Mannich reactions
inferred← citeshttps://doi.org/10.1055/a-2020-8717openalex-snapshot
2,2-Disubstituted Indoxyls via Oxidative Dearomatization: Generalization to 2-Alkylindoles and Application to Alkaloid Synthesis
inferred← citeshttps://doi.org/10.1055/a-2069-3913openalex-snapshot
Total Syntheses of 2,2′-Biindolyl Alkaloids via Cyanide-Catalyzed Imino-Stetter Reaction
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/10.20952/jrks3113081openalex-snapshot
Computational investigation of Schiff bases from tryptamine as COX-2 inhibitors with potential anti-inflammatory activity
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2995436/v1openalex-snapshot
De novo construction of chiral 3‑oxindoles via organocatalyzed enantioselective ortho-Friedel-Crafts addition/novel [1,2]-ester migration
inferred← citeshttps://doi.org/10.2139/ssrn.4897840openalex-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/10.3987/com-14-13065openalex-snapshot
Hypervalent Iodine Mediated One-Pot C-H Functionalization at 2α- or 3α-Position of Indole Derivatives
inferred← citeshttps://doi.org/10.3987/com-18-s(f)30openalex-snapshot
Biomimetic Synthesis of Iheyamine A from Spirocyclic Oxindoles
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