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A Concise Total Synthesis of (±)-Trigonoliimine B

https://doi.org/10.1021/ol300249y
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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/anie.197407891openalex-snapshot
α‐Metalated Isocyanides in Organic Synthesis. New synthetic methods (6)
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Recent Applications of α‐Metalated Isocyanides in Organic Synthesis
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Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
inferredcites →https://doi.org/10.1002/anie.200461864openalex-snapshot
Short, Enantioselective Total Synthesis of Stephacidin A
inferredcites →https://doi.org/10.1002/anie.200601278openalex-snapshot
2‐Thioindoles as Precursors to Spiro‐Fused Indolines: Synthesis of (±)‐Dehaloperophoramidine
inferredcites →https://doi.org/10.1002/anie.200700612openalex-snapshot
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.200800599openalex-snapshot
Synthesis of Diastereomers of Complestatin and Chloropeptin I: Substrate‐Dependent Atropstereoselectivity of the Intramolecular Suzuki–Miyaura Reaction
inferredcites →https://doi.org/10.1002/anie.200801735openalex-snapshot
It All Began with an Error: The Nomofungin/Communesin Story
inferredcites →https://doi.org/10.1002/anie.200806086openalex-snapshot
Redox Economy in Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.200904588openalex-snapshot
Total Synthesis of (+)‐Haplophytine
inferredcites →https://doi.org/10.1002/anie.200906797openalex-snapshot
Total Synthesis of Complestatin (Chloropeptin II)
inferredcites →https://doi.org/10.1002/anie.200906818openalex-snapshot
Total Synthesis of the Polycyclic Fungal Metabolite (±)‐Communesin F
inferredcites →https://doi.org/10.1002/anie.201103145openalex-snapshot
Total Synthesis of (+)‐Gliocladin C Enabled by Visible‐Light Photoredox Catalysis
inferredcites →https://doi.org/10.1002/chem.201002098openalex-snapshot
Exploiting the Divergent Reactivity of α‐Isocyanoacetate: Multicomponent Synthesis of 5‐Alkoxyoxazoles and Related Heterocycles
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Biomimetic Approach to Communesin B (a.k.a. Nomofungin).
inferredcites →https://doi.org/10.1002/ejoc.200390167openalex-snapshot
Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles
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Application of Task-specific Ionic Liquids for Intensified Separations
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
inferredcites →https://doi.org/10.1016/j.tetlet.2010.05.075openalex-snapshot
Amidation of esters assisted by Mg(OCH3)2 or CaCl2
inferredcites →https://doi.org/10.1016/j.tetlet.2011.08.087openalex-snapshot
A biomimetic synthesis of the skeleton of trigonoliimine C
inferredcites →https://doi.org/10.1016/s0040-4039(02)02790-9openalex-snapshot
Biomimetic approach to communesin B (a.k.a. nomofungin)
inferredcites →https://doi.org/10.1021/cr800296popenalex-snapshot
Natural Product Synthesis Using Multicomponent Reaction Strategies
inferredcites →https://doi.org/10.1021/cr900411fopenalex-snapshot
Isocyanoacetate Derivatives: Synthesis, Reactivity, and Application
inferredcites →https://doi.org/10.1021/cr950027eopenalex-snapshot
Domino Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/ja00547a015openalex-snapshot
1-(Arylthio)cyclopropanecarboxaldehydes. Conjunctive reagents for secoalkylation
inferredcites →https://doi.org/10.1021/ja049569gopenalex-snapshot
Total Synthesis of (±)-Perophoramidine
inferredcites →https://doi.org/10.1021/ja061660sopenalex-snapshot
Enantioselective Total Synthesis of Avrainvillamide and the Stephacidins
inferredcites →https://doi.org/10.1021/ja075100kopenalex-snapshot
Total Synthesis of (+)-Suaveolindole: Establishment of Its Absolute Configuration
inferredcites →https://doi.org/10.1021/ja075705gopenalex-snapshot
Total Synthesis of (±)-Communesin F
inferredcites →https://doi.org/10.1021/ja1009458openalex-snapshot
Scalable Total Syntheses of N -Linked Tryptamine Dimers by Direct Indole−Aniline Coupling: Psychotrimine and Kapakahines B and F
inferredcites →https://doi.org/10.1021/ja106739gopenalex-snapshot
Total Synthesis and Absolute Stereochemical Assignment of (−)-Communesin F
inferredcites →https://doi.org/10.1021/ja203960bopenalex-snapshot
Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine
inferredcites →https://doi.org/10.1021/ja204597kopenalex-snapshot
Concise Total Synthesis and Stereochemical Revision of all (−)-Trigonoliimines
inferredcites →https://doi.org/10.1021/jo061471sopenalex-snapshot
Palladium-Catalyzed, Modular Synthesis of Highly Functionalized Indoles and Tryptophans by Direct Annulation of Substituted o-Haloanilines and Aldehydes
inferredcites →https://doi.org/10.1021/jo9012755openalex-snapshot
Efficient Total Synthesis of (−)-cis-Clavicipitic Acid
inferredcites →https://doi.org/10.1021/jo970278iopenalex-snapshot
Syntheses of Indoles via a Palladium-Catalyzed Annulation between Iodoanilines and Ketones
inferredcites →https://doi.org/10.1021/ma100011xopenalex-snapshot
N-Vinyltriazoles: A New Functional Monomer Family through Click Chemistry
inferredcites →https://doi.org/10.1021/ol070889popenalex-snapshot
Synthesis of DEFG Ring of Complestatin and Chloropeptin I: Highly Atropdiastereoselective Macrocyclization by Intramolecular Suzuki-Miyaura Reaction
inferredcites →https://doi.org/10.1021/ol100715xopenalex-snapshot
Three New Indole Alkaloids from Trigonostemon lii
inferredcites →https://doi.org/10.1021/ol202475ropenalex-snapshot
An Approach to the Hexacyclic Skeleton of Trigonoliimines
inferredcites →https://doi.org/10.1038/160197a0openalex-snapshot
Effect of Bending on Selenium Rectifier Disks
inferredcites →https://doi.org/10.1038/460197aopenalex-snapshot
Synthesis at the molecular frontier
inferredcites →https://doi.org/10.1038/nchem.216openalex-snapshot
Protecting-group-free synthesis as an opportunity for invention
inferredcites →https://doi.org/10.1039/b705909bopenalex-snapshot
Recent advances in biomimetic natural product synthesis
inferredcites →https://doi.org/10.1039/b819925fopenalex-snapshot
Biogenetically inspired syntheses of alkaloid natural products
inferredcites →https://doi.org/10.1055/s-2006-950311openalex-snapshot
Protecting-Group-Free Synthesis
inferredcites →https://doi.org/10.1055/s-2008-1078411openalex-snapshot
Synthesis of the Central Tryptophan-Leucine Residue of Celogentin C
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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B(C6f5)3-Catalyzed Regio- and Stereoselective Cyanation of Isatogens and Their Derivatives
inferred← citeshttps://doi.org/10.1002/9781118754085.ch14openalex-snapshot
Anthranilic Acid–Tryptophan Alkaloids
inferred← citeshttps://doi.org/10.1002/9783527828166.ch10openalex-snapshot
Synthesis of Some Heterocyclic Compounds Using Named Reactions
inferred← citeshttps://doi.org/10.1002/adsc.202101498openalex-snapshot
One‐Pot Asymmetric Oxidative Dearomatization of 2‐Substituted Indoles by Merging Transition Metal Catalysis with Organocatalysis to Access C2‐Tetrasubstituted Indolin‐3‐Ones
inferred← citeshttps://doi.org/10.1002/ajoc.202300513openalex-snapshot
Recent Progress Toward Total Syntheses of Iheyamines A and B
inferred← citeshttps://doi.org/10.1002/ange.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/ange.201310929openalex-snapshot
Total Synthesis of (±)‐Aspidophylline A
inferred← citeshttps://doi.org/10.1002/ange.201405842openalex-snapshot
Phosphoric Acid Catalyzed Desymmetrization of Bicyclic Bislactones Bearing an All‐Carbon Stereogenic Center: Total Syntheses of (−)‐Rhazinilam and (−)‐Leucomidine B
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.201310929openalex-snapshot
Total Synthesis of (±)‐Aspidophylline A
inferred← citeshttps://doi.org/10.1002/anie.201405842openalex-snapshot
Phosphoric Acid Catalyzed Desymmetrization of Bicyclic Bislactones Bearing an All‐Carbon Stereogenic Center: Total Syntheses of (−)‐Rhazinilam and (−)‐Leucomidine B
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/cjoc.202100419openalex-snapshot
Bischler‐Napieralski Cyclization: A Versatile Reaction towards Functional Aza‐PAHs and Their Conjugated Polymers†
inferred← citeshttps://doi.org/10.1007/978-3-030-50865-4_15openalex-snapshot
Bischler–Napieralski Reaction
inferred← citeshttps://doi.org/10.1007/978-3-031-52850-7_15openalex-snapshot
Bischler–Napieralski-Reaktion
inferred← citeshttps://doi.org/10.1007/978-3-031-84798-1_21openalex-snapshot
Bischler–Napieralski Reaction
inferred← citeshttps://doi.org/10.1007/978-3-319-03979-4_27openalex-snapshot
Bischler–Napieralski reaction
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.11.001openalex-snapshot
Synthesis of pyrimidine-containing alkaloids
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104058openalex-snapshot
Four new sucrose diesters of substituted truxinic acids from Trigonostemon honbaensis with their anoctamin-1 inhibitory activity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.06.047openalex-snapshot
Regioselective assembly of 3,4-dihydroisoquinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.033openalex-snapshot
A modified approach to the skeleton of trigonoliimines A and B
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/10.1021/acs.joc.0c01308openalex-snapshot
One-Pot Tandem Assembly of Amides, Amines, and Ketones: Synthesis of C4-Quaternary 3,4- and 1,4-Dihydroquinazolines
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/ja509329xopenalex-snapshot
Unified Strategy to Monoterpene Indole Alkaloids: Total Syntheses of (±)-Goniomitine, (±)-1,2-Dehydroaspidospermidine, (±)-Aspidospermidine, (±)-Vincadifformine, and (±)-Kopsihainanine A
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/ol303344dopenalex-snapshot
Rapid Total Synthesis of (±)Trigonoliimine A via a Strecker/Houben–Hoesch Sequence
inferred← citeshttps://doi.org/10.1021/ol500447ropenalex-snapshot
Three-Component Povarov Reaction–Heteroannulation with Arynes: Synthesis of 5,6-Dihydroindolo[1,2-a]quinolines
inferred← citeshttps://doi.org/10.1021/op300108wopenalex-snapshot
Sulfolane: A Versatile Dipolar Aprotic Solvent
inferred← citeshttps://doi.org/10.1039/c3cc45512bopenalex-snapshot
A modular total synthesis of (±)-trigonoliimine C
inferred← citeshttps://doi.org/10.1039/c3cc46361copenalex-snapshot
Heteroannulation of arynes with N-aryl-α-aminoketones for the synthesis of unsymmetrical N-aryl-2,3-disubstituted indoles: an aryne twist of Bischler–Möhlau indole synthesis
inferred← citeshttps://doi.org/10.1039/c4qo00161copenalex-snapshot
Recent studies on the chemical constituents of Trigonostemon plants
inferred← citeshttps://doi.org/10.1039/c5cc08105jopenalex-snapshot
Catalytic asymmetric conjugate addition of isocyanoacetate to (Z)-3-substituted-2-(4-pyridyl)-acrylonitrile, a reactive class of Michael acceptor
inferred← citeshttps://doi.org/10.1039/c5np00032gopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c5ob01880copenalex-snapshot
Catalytic enantioselective addition of isocyanoacetate to 3-methyl-4-nitro-5-styrylisoxazoles under phase transfer catalysis conditions
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/c7qo00490gopenalex-snapshot
Multifunctional odorless isocyano(triphenylphosphoranylidene)-acetates: synthesis and direct one-pot four-component Ugi/Wittig cyclization to multisubstituted oxazoles
inferred← citeshttps://doi.org/10.1039/c8np00047fopenalex-snapshot
Non-monoterpenoid azepinoindole alkaloids
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/d2ob00397jopenalex-snapshot
Direct, four-step synthetic pathway to iheyamine A and several analogues
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Synthesis of 2-monosubstituted indolin-3-ones by cine -substitution of 3-azido-2-methoxyindolines
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Asymmetric synthesis of chaetogline A: expedient preparation of the indolizino[8,7- b ]indole template and optical properties in a push–pull configuration
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New Truxinic and Truxillic Acid Sucrose Diesters From the Leaves of Trigonostemon honbaensis
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Catalytic Synthesis of Azepinoindoles from Ynamides Containing Indolyl Moieties via Ruthenium–Vinylidene Species
inferred← citeshttps://doi.org/10.3390/molecules26144274openalex-snapshot
Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
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A Mild Bischler–Napieralski-Type Cyclization of Trichloromethyl Carbamates for the Synthesis of β-Carbolinones
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