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Three New Indole Alkaloids from Trigonostemon lii

https://doi.org/10.1021/ol100715x
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Structural studies of vinblastine alkaloids by exciton coupled circular dichroism
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Site-directed PEGylation of trichosanthin retained its anti-HIV activity with reduced potency in vitro
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New phenanthrenes from Trigonostemon lii Y.T. Chang
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Lotthanongine, an unprecedented flavonoidal indole alkaloid from the roots of Thai medicinal plant, Trigonostemon reidioides
inferredcites →https://doi.org/10.1021/ja994074qopenalex-snapshot
Structure and Stereochemistry of Rediocide A, A Highly Modified Daphnane from Trigonostemon reidioides Exhibiting Potent Insecticidal Activity
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Calculation of Optical Rotation Using Density Functional Theory
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Hartree−Fock and Density Functional Theory ab Initio Calculation of Optical Rotation Using GIAOs: Basis Set Dependence
inferredcites →https://doi.org/10.1021/np070502ropenalex-snapshot
Determination of the Absolute Configurations of Natural Products Using TDDFT Optical Rotation Calculations: The Iridoid Oruwacin
inferredcites →https://doi.org/10.1021/np50071a002openalex-snapshot
Structure of Trigonostemone, a New Phenanthrenone from the Thai Plant Trigonostemon reidioides
inferredcites →https://doi.org/10.1021/np800256xopenalex-snapshot
Antimicrobial Diterpenes from Trigonostemon chinensis
inferredcites →https://doi.org/10.1021/ol901506xopenalex-snapshot
Trigochilides A and B, Two Highly Modified Daphnane-Type Diterpenoids from Trigonostemon chinensis
inferredcites →https://doi.org/10.1021/ol9025638openalex-snapshot
Highly Functionalized Daphnane Diterpenoids from Trigonostemon thyrsoideum
inferredcites →https://doi.org/10.1055/s-0029-1185505openalex-snapshot
Carboline Alkaloids fromTrigonostemon lii
inferredcites →https://doi.org/10.1248/cpb.53.1321openalex-snapshot
A New Cytotoxic Daphnane Diterpenoid, Rediocide G, from Trigonostemon reidioides
inferredcites →https://doi.org/10.1248/cpb.53.241openalex-snapshot
Acaricidal Daphnane Diterpenoids from Trigonostemon reidioides (KURZ) CRAIB roots

What points at this work

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

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Novel γ-lactone derivatives from Trigonostemon heterophyllus with their potential antiproliferative activities
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Novel tetrahydrofuran derivatives from Trigonostemon howii with their potential anti-HIV-1 activities
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β-Carboline alkaloids from the leaves of Trigonostemon lii Y.T. Chang
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Trigoxyphins H and I: Two new daphnane diterpenoids from Trigonostemon xyphophylloides
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Five new degraded diterpenoids from Trigonostemon xyphophylloides
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Antiviral chlorinated daphnane diterpenoid orthoesters from the bark and wood of Trigonostemon cherrieri
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Daphnane diterpenoids from the stems of Trigonostemon lii and their anti-HIV-1 activity
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Anti-HIV active daphnane diterpenoids from Trigonostemon thyrsoideum
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Globostelletins J–S, isomalabaricanes with unusual cyclopentane sidechains from the marine sponge Rhabdastrella globostellata
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3,4-seco-Diterpenoids from Trigonostemon flavidus
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BINOL-phosphoric acid catalyzed asymmetric Mannich addition of β-ketoesters to indolenines generated in situ by DDQ
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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
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Trigonoines A and B, two novel alkaloids from the leaves of Trigonostemon lii
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A biomimetic synthesis of the skeleton of trigonoliimine C
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Catharoseumine, a new monoterpenoid indole alkaloid possessing a peroxy bridge from Catharanthus roseus
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Reductive Heck coupling: an efficient approach toward the iboga alkaloids. Synthesis of ibogamine, epiibogamine and iboga analogs
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Mekongenines A and B, two new alkaloids from Bousigonia mekongensis
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A modified approach to the skeleton of trigonoliimines A and B
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Trigoxyphins O–T, six new heterodimers from Trigonostemon xyphophylloides
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B(C6F5)3-catalyzed regio- and stereoselective cyanation of isatogens and their derivatives
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Regio- and Stereoselective [3 + 2] cycloaddition of Isatogens with functionalized alkenes and its application to the synthesis of Halichrome A
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Regioselective Synthesis of Indole-Fused Seven-Membered N-Heterocycles via Photoredox-Catalyzed Intramolecular Cyclization
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Quinazoline-Derived Azomethine Imines as Substrates To Access Polycyclic Compounds
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General Approach To Construct Azepino[2,3-b:4,5-b′]diindoles, Azocino[2,3-b:4,5-b′]diindoles, and Azonino[2,3-b:4,5-b′]diindoles via Rh(II)-Catalyzed Reactions of 3-Diazoindolin-2-imines with 3-(Bromoalkyl)indoles
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Copper(0)/PPh3-Mediated Bisheteroannulations of o-Nitroalkynes with Methylketoximes Accessing Pyrazo-Fused Pseudoindoxyls
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Visible-Light Photocatalytic Tri- and Difluoroalkylation Cyclizations: Access to a Series of Indole[2,1- a ]isoquinoline Derivatives in Continuous Flow
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Dearomative Arylcyanation of Indoles via C–CN Bond Activation Enabled by Ni/Lewis Acid Cooperative Catalysis
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Copper-Catalyzed, N-Directed Distal C(sp3)–H Functionalization toward Azepanes
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inferred← citeshttps://doi.org/10.1021/acs.orglett.3c02009openalex-snapshot
Electron Donor–Acceptor Complex Induced Fused Indoles with Hypervalent Iodine(III) Reagents
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Synthesis of Complex Tetracyclic Fused Scaffolds Enabled by (3 + 2) Cycloaddition
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.6b02460openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b02798openalex-snapshot
Synthesis of the Azepinobisindole Alkaloid Iheyamine A Enabled by a Cross-Mannich Reaction
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.8b00330openalex-snapshot
Dehydrative Mannich-Type Reaction for the Synthesis of Azepinobisindole Alkaloid Iheyamine A
inferred← citeshttps://doi.org/10.1021/acscatal.5c02364openalex-snapshot
Programmable Divergence in Conia-ene and Hydroarylation Pathways for Collective Synthesis of Skeletally Diverse Alkaloid-like Scaffolds
inferred← citeshttps://doi.org/10.1021/acsomega.6c00954openalex-snapshot
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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/ja203960bopenalex-snapshot
Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine
inferred← citeshttps://doi.org/10.1021/ja204597kopenalex-snapshot
Concise Total Synthesis and Stereochemical Revision of all (−)-Trigonoliimines
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.6b02678openalex-snapshot
Enantioselective Synthesis of Indole-Annulated Medium-Sized Rings
inferred← citeshttps://doi.org/10.1021/jo101727ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo4020358openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np1006444openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np200231uopenalex-snapshot
Daphnane-Type Diterpenoids from Trigonostemon howii
inferred← citeshttps://doi.org/10.1021/np3001128openalex-snapshot
Trigoflavidols A–C, Degraded Diterpenoids with Antimicrobial Activity, from Trigonostemon flavidus
inferred← citeshttps://doi.org/10.1021/np3006315openalex-snapshot
Trigohowilols A–G, Degraded Diterpenoids from the Stems of Trigonostemon howii
inferred← citeshttps://doi.org/10.1021/np4005823openalex-snapshot
Angustifonines A and B, Cytotoxic Bisindole Alkaloids from Bousigonia angustifolia
inferred← citeshttps://doi.org/10.1021/ol202475ropenalex-snapshot
An Approach to the Hexacyclic Skeleton of Trigonoliimines
inferred← citeshttps://doi.org/10.1021/ol2030907openalex-snapshot
Trigocherrin A, the First Natural Chlorinated Daphnane Diterpene Orthoester from Trigonostemon cherrieri
inferred← citeshttps://doi.org/10.1021/ol300249yopenalex-snapshot
A Concise Total Synthesis of (±)-Trigonoliimine B
inferred← citeshttps://doi.org/10.1021/ol3008149openalex-snapshot
Aphanamixoid A, a Potent Defensive Limonoid, with a New Carbon Skeleton from Aphanamixis polystachya
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/ol3034065openalex-snapshot
Myriberine A, a New Alkaloid with an Unprecedented Heteropentacyclic Skeleton from Myrioneuron faberi
inferred← citeshttps://doi.org/10.1021/ol4002619openalex-snapshot
Two New Types of Bisindole Alkaloid from Trigonostemon lutescens
inferred← citeshttps://doi.org/10.1021/ol501856vopenalex-snapshot
Peganumine A, a β-Carboline Dimer with a New Octacyclic Scaffold from Peganum harmala
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/c4ra07985jopenalex-snapshot
Pegaharmalines A and B, two novel β-carboline alkaloids with unprecedented carbon skeletons from Peganum harmala
inferred← citeshttps://doi.org/10.1039/c5cs00721fopenalex-snapshot
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Formal [3 + 2] cycloaddition of α-unsubstituted isocyanoacetates and methyleneindolinones: enantioselective synthesis of spirooxindoles
inferred← citeshttps://doi.org/10.1039/c8cc03804jopenalex-snapshot
Substrate-controlled divergent synthesis of polycyclic indoloazepines and indolodiazepines via 1,5-hydride shift/7-cyclization cascades
inferred← citeshttps://doi.org/10.1039/c8np00047fopenalex-snapshot
Non-monoterpenoid azepinoindole alkaloids
inferred← citeshttps://doi.org/10.1039/c8qo00205copenalex-snapshot
Palladium-catalyzed asymmetric dearomative alkenylation of indoles through a reductive-Heck reaction
inferred← citeshttps://doi.org/10.1039/c9ra04741gopenalex-snapshot
Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles
inferred← citeshttps://doi.org/10.1039/d0cc00435aopenalex-snapshot
Palladium-catalyzed α-arylation of indolin-3-ones
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/d2cc01134dopenalex-snapshot
A new type of δ-vinylvalerolactone for palladium-catalyzed cycloaddition: synthesis of nine-membered heterocycles
inferred← citeshttps://doi.org/10.1039/d2ob00397jopenalex-snapshot
Direct, four-step synthetic pathway to iheyamine A and several analogues
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/d4ob00766bopenalex-snapshot
Recent advances in oxidative dearomatization involving C–H bonds for constructing value-added oxindoles
inferred← citeshttps://doi.org/10.1039/d4ob01736fopenalex-snapshot
Catalyst-free coupling of peroxypyrroloindolenines with amines to afford stable peroxyindolenines
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/10.1055/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/10.1055/a-2626-0265openalex-snapshot
A Straightforward Access to Specific Bisindole Systems Related to Fascaplysin Alkaloids
inferred← citeshttps://doi.org/10.1080/10406638.2020.1737828openalex-snapshot
Preparation and Characterization of Nano-coc-OSO3H as a Novel Nanocatalyst for the One-Pot Synthesis of Spirooxindoles
inferred← citeshttps://doi.org/10.1080/10406638.2020.1871039openalex-snapshot
Ionic Liquid as Green and Recyclable Solvent for the Synthesis of Pyrazinoquinazolines: Study of Antioxidant Activity
inferred← citeshttps://doi.org/10.1080/14786419.2015.1009066openalex-snapshot
Three new phenanthrenone constituents fromTrigonostemonlii
inferred← citeshttps://doi.org/10.1080/14786419.2015.1032281openalex-snapshot
Isolation of a new carboline alkaloid from Trigonostemon lii
inferred← citeshttps://doi.org/10.1080/14786419.2018.1462184openalex-snapshot
Structurally diverse diterpenoids from Trigonostemon howii
inferred← citeshttps://doi.org/10.1093/nsr/nwx028openalex-snapshot
Recent progress in organocatalytic asymmetric total syntheses of complex indole alkaloids
inferred← citeshttps://doi.org/10.1248/cpb.c25-00202openalex-snapshot
Efficient Synthesis of 8-Membered Fused Indoles via Intramolecular Friedel–Crafts Reaction of N-(2,2-Dimethoxyethyl)sulfonamides
inferred← citeshttps://doi.org/10.13005/ojc/350231openalex-snapshot
Synthesis and Anticancer Activity Evaluation of Azepinobisindoles; the Isomeric Iheyamine A Derivatives
inferred← citeshttps://doi.org/10.2174/0113852728294270240425093501openalex-snapshot
Alternative Reactions to Friedel-crafts Acylation on Highly Activated Substrates
inferred← citeshttps://doi.org/10.2174/1568026621666211012111901openalex-snapshot
Therapeutic Potential of Indole Derivatives as Anti-HIV Agents: A Mini-review
inferred← citeshttps://doi.org/10.3390/molecules19033617openalex-snapshot
Trigocherrierin A, a Potent Inhibitor of Chikungunya Virus Replication
inferred← citeshttps://doi.org/10.3390/molecules26082297openalex-snapshot
Plant-Based Indole Alkaloids: A Comprehensive Overview from a Pharmacological Perspective
inferred← citeshttps://doi.org/10.3390/molecules26144274openalex-snapshot
Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
inferred← citeshttps://doi.org/10.3390/molecules27031078openalex-snapshot
Voacanga globosa Spirobisindole Alkaloids Exert Antiviral Activity in HIV Latently Infected Cell Lines by Targeting the NF-κB Cascade: In Vitro and In Silico Investigations
inferred← citeshttps://doi.org/10.3762/bjoc.22.90openalex-snapshot
Discovery of sugarnitriles A and B, and structural reassignment of SF-2140, from a sugarcane endophytic actinomycete Amycolatopsis sp. JS-O27
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