On the public citation graph

Synthesis of 8-Desbromohinckdentine A1

https://doi.org/10.1021/ja021380m
0 signed · 188 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/chin.198626145openalex-snapshot
ChemInform Abstract: Reaction of Aryl Grignard Reagents with Hexahalobenzenes: Novel Arenes via a Multiple Aryne Sequence.
inferredcites →https://doi.org/10.1002/jhet.5570070316openalex-snapshot
3H‐Indol‐3‐ols by a novel ring contraction
inferredcites →https://doi.org/10.1002/jhet.5570330615openalex-snapshot
The beckmann rearrangement of cyclohex‐2‐enone oximes. Synthesis of 4,5‐diphenyl‐2,3,4,5‐tetrahydro‐1H‐azepin‐2‐one
inferredcites →https://doi.org/10.1016/s0040-4039(00)74372-3openalex-snapshot
Regiocontrol synthesis of β-trimetylsilyloxy carbonyl compounds through an aldol-grignard elaboration sequence.
inferredcites →https://doi.org/10.1016/s0040-4039(00)78643-6openalex-snapshot
The selective reduction of αβ-olefinic amides
inferredcites →https://doi.org/10.1016/s0040-4039(00)93853-xopenalex-snapshot
3,3-Ethylenedioxybutylmagnesiumbromide - a nucleophilic 3-ketobutyl equivalent
inferredcites →https://doi.org/10.1016/s0040-4039(00)96781-9openalex-snapshot
Hinckdentine-a: A novel alkaloid from the marine bryozoan hincksinoflustra denticulata
inferredcites →https://doi.org/10.1016/s0040-4039(01)00559-7openalex-snapshot
Synthesis of N-arylated oxazolidinones via a palladium catalyzed cross coupling reaction. Application to the synthesis of the antibacterial agent Dup-721
inferredcites →https://doi.org/10.1016/s0040-4039(97)01465-2openalex-snapshot
An Ammonia Equivalent for the Palladium-Catalyzed Amination of Aryl Halides and Triflates
inferredcites →https://doi.org/10.1021/ja00063a082openalex-snapshot
1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive
inferredcites →https://doi.org/10.1021/ja004176copenalex-snapshot
On the Regiospecificity of Vanadium Bromoperoxidase
inferredcites →https://doi.org/10.1021/ja01149a079openalex-snapshot
The Course and Kinetics of the Acid-Base-Catalyzed Rearrangements of 11-Hydroxytetrahydrocarbazolenine 1
inferredcites →https://doi.org/10.1021/ja973524gopenalex-snapshot
Palladium-Catalyzed C−N(sp2) Bond Formation: N-Arylation of Aromatic and Unsaturated Nitrogen and the Reductive Elimination Chemistry of Palladium Azolyl and Methyleneamido Complexes
inferredcites →https://doi.org/10.1021/jo000604lopenalex-snapshot
Variable Strategy toward Carbasugars and Relatives. 1. Stereocontrolled Synthesis of Pseudo-β- d -gulopyranose, Pseudo-β- d -xylofuranose, (Pseudo-β- d -gulopyranosyl)amine, and (Pseudo-β- d -xylofuranosyl)amine
inferredcites →https://doi.org/10.1021/jo00101a043openalex-snapshot
Chemistry of Indolo[1,2-c]quinazoline: An Approach to the Marine Alkaloid Hinckdentine A
inferredcites →https://doi.org/10.1021/jo00317a027openalex-snapshot
Nucleophilic annulations of aromatics. Novel route to benzo-fused ring systems via oxazoline activation
inferredcites →https://doi.org/10.1021/jo00350a018openalex-snapshot
Reaction of aryl Grignard reagents with hexahalobenzenes: novel arenes via multiple aryne sequence
inferredcites →https://doi.org/10.1021/jo01270a097openalex-snapshot
Stereochemistry. XXXIV. Nitro compounds. 7. Chemistry of 3-oxo-2-phenylindolenine
inferredcites →https://doi.org/10.1039/jr9560001319openalex-snapshot
268. The action of acyl cyanides on 2- and 1 : 2-substituted indoles. Part II. Derivatives of 2-o-aminophenylindole
inferredcites →https://doi.org/10.1039/p19730001653openalex-snapshot
A synthesis of (–)-(R)-trans-β-(1,2,3-trimethylcyclopent-2-enyl)acrylic acid
inferredcites →https://doi.org/10.1039/p19810002912openalex-snapshot
Selective reduction of αβ-olefinic amides and lactams by magnesium and methanol
inferredcites →https://doi.org/10.1039/p19830002417openalex-snapshot
Indole β-nucleophilic substitution. Part 7. β-Halogenation of indoles. Attempted intramolecular β-nucleophilic substitution of α-arylindoles
inferredcites →https://doi.org/10.1039/p19960002417openalex-snapshot
Palladium-catalysed hydrostannylations of 1-bromoalkynes. A practical synthesis of (E)-1-stannylalk-1-enes
inferredcites →https://doi.org/10.1039/p29790000233openalex-snapshot
Competition between single electron transfer and nucleophilic attack. Part 2. Reaction of 2-phenyl-3H-indol-3-one with Grignard reagents
inferredcites →https://doi.org/10.1039/p29910000233openalex-snapshot
Synthesis and structure of tricarbonylchromium mono-, bis- and tris-complexes of 10-methyltribenzotriquinacene
inferredcites →https://doi.org/10.1080/00397919008052825openalex-snapshot
An Improved Synthesis of 2-(β-Bromoethyl)-2-methyl-1,3-dioxolane, a Useful Methyl Vinyl Ketone Equivalent
inferredcites →https://doi.org/10.1080/00397919508011457openalex-snapshot
Facile Synthesis of 2-Aryl-3H-indol-3-onesviaSinglet Oxygenation of 2-Arylindoles
inferredcites →https://doi.org/10.1246/bcsj.67.1918openalex-snapshot
Halogenation Using N -Halogenocompounds. II. Acid Catalyzed Bromination of Aromatic Compounds with 1,3-Dibromo-5,5-dimethylhydantoin
inferredcites →https://doi.org/10.3987/rev-95-sr1openalex-snapshot
Indoloquinazolines: A Century in Review

What points at this work

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/10.1002/9781118695692.ch2openalex-snapshot
Fischer Indole Synthesis
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod022openalex-snapshot
Bryozoa, Phoronida, and Brachiopoda
inferred← citeshttps://doi.org/10.1002/9783527687800.ch6openalex-snapshot
Electrophilic Formation of Aromatic C–N Bonds
inferred← citeshttps://doi.org/10.1002/adsc.201200430openalex-snapshot
Cesium Carbonate‐Promoted Hydroamidation of Alkynes: Enamides, Indoles and the Effect of Iron(III) Chloride
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.201900551openalex-snapshot
3‐Aminoindole Synthesis from 2‐Nitrochalcones and Ammonia or Primary Amines
inferred← citeshttps://doi.org/10.1002/adsc.202000449openalex-snapshot
Iridium‐Catalyzed Oxidative Annulation of 2‐Arylindoles with Benzoquinone Leading to Indolo[1,2‐f]phenanthridin‐6‐ols
inferred← citeshttps://doi.org/10.1002/adsc.202000957openalex-snapshot
Silver‐Catalyzed Three‐Component Coupling Reaction of Amines, 2‐Isocyanobenzaldehydes, and 2,2,2‐Trifluorodiazoethane and Synthesis of Trifluoromethyl‐Substituted Indolo[1,2‐ c ]quinazolines
inferred← citeshttps://doi.org/10.1002/adsc.202001079openalex-snapshot
Recent Developments in Photo‐Catalyzed/Promoted Synthesis of Indoles and Their Functionalization: Reactions and Mechanisms
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/adsc.202200323openalex-snapshot
PPh3‐Mediated Wittig‐Like/Mannich Tandem Reactions of 2‐Alkynylnitrobenzenes with Ketones for the Synthesis of 2,2‐Disubstituted Indolin‐3‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.202401463openalex-snapshot
Synthesis of 2‐Aminoquinazolines through I2‐Catalyzed Cyclization of 2‐Aminoaryl Ketone Oximes and Isocyanides
inferred← citeshttps://doi.org/10.1002/ajoc.202300204openalex-snapshot
Organocatalyst‐Controlled Divergent Asymmetric Aza‐Friedel‐Crafts Reactions of Indol‐3‐ones with 1‐ and 2‐Naphthols
inferred← citeshttps://doi.org/10.1002/ange.201505173openalex-snapshot
An Indoxyl‐Based Strategy for the Synthesis of Indolines and Indolenines
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.201811085openalex-snapshot
Concurrent Asymmetric Reactions Combining Photocatalysis and Enzyme Catalysis: Direct Enantioselective Synthesis of 2,2‐Disubstituted Indol‐3‐ones from 2‐Arylindoles
inferred← citeshttps://doi.org/10.1002/ange.201904805openalex-snapshot
Pd/PC‐Phos‐Catalyzed Enantioselective Intermolecular Denitrogenative Cyclization of Benzotriazoles with Allenes and N‐Allenamides
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/anie.201505173openalex-snapshot
An Indoxyl‐Based Strategy for the Synthesis of Indolines and Indolenines
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.201811085openalex-snapshot
Concurrent Asymmetric Reactions Combining Photocatalysis and Enzyme Catalysis: Direct Enantioselective Synthesis of 2,2‐Disubstituted Indol‐3‐ones from 2‐Arylindoles
inferred← citeshttps://doi.org/10.1002/anie.201904805openalex-snapshot
Pd/PC‐Phos‐Catalyzed Enantioselective Intermolecular Denitrogenative Cyclization of Benzotriazoles with Allenes and N‐Allenamides
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/aoc.6871openalex-snapshot
Synthesis of benzo[4,5]imidazo[1,2‐a]indolo[1,2‐c]quinazolines from 2‐(2‐bromoaryl)indoles and 2‐methoxybenzimidazoles under recyclable magnetic MOF‐199 catalysis
inferred← citeshttps://doi.org/10.1002/asia.201402394openalex-snapshot
Wurster’s Blue‐type Cation Radicals Framed in a 5,10‐Dihydrobenzo[a]indolo[2,3‐c]carbazole (BIC) Skeleton: Dual Electrochromism with Drastic Changes in UV/Vis/NIR and Fluorescence
inferred← citeshttps://doi.org/10.1002/asia.201601067openalex-snapshot
Pd‐Catalyzed Cyclocarbonylation of 2‐(2‐Bromoaryl)indoles with CO as a C1 Source: Selective Access to 6 H‐Isoindolo[2,1‐a]indol‐6‐ones and Indeno[1,2‐b]indol‐10(5 H)‐ones
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/bkcs.11545openalex-snapshot
Copper‐catalyzed CN Coupling and Cyclization of 2‐(2‐Bromophenyl)‐1H‐indoles with Primary Amides Leading to Indolo[1,2‐c]quinazolines
inferred← citeshttps://doi.org/10.1002/chem.201100144openalex-snapshot
Facile Creation of 2‐Substituted Indolin‐3‐ones by Using Primary–Secondary Diamine Catalysts
inferred← citeshttps://doi.org/10.1002/chem.201404017openalex-snapshot
C‐2 Selective Arylation of Indoles with Heterogeneous Nanopalladium and Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1002/chem.201601573openalex-snapshot
Organocatalytic Enantioselective Aza‐Friedel–Crafts Reaction of Cyclic Ketimines with Pyrroles using Imidazolinephosphoric Acid Catalysts
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.201903144openalex-snapshot
Access to Enantioenriched Spiro‐ ϵ ‐Lactam Oxindoles by an N‐Heterocyclic Carbene‐Catalyzed [4+3] Annulation of Flexible Oxotryptamines with Enals
inferred← citeshttps://doi.org/10.1002/chem.202201113openalex-snapshot
Indole Editing Enabled by HFIP‐Mediated Ring‐Switch Reactions of 3‐Amino‐2‐Hydroxyindolines
inferred← citeshttps://doi.org/10.1002/chem.202402974openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/cjoc.201800301openalex-snapshot
Electrochemical Synthesis of (Aza)indolines via Dehydrogenative [3+2] Annulation: Application to Total Synthesis of (±)‐Hinckdentine A
inferred← citeshttps://doi.org/10.1002/ejoc.201200953openalex-snapshot
Copper‐Catalyzed Cascade Synthesis of 1H‐Indolo[1,2‐c]quinazoline Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201700085openalex-snapshot
Phosphoric Acid Catalyzed 1,2‐Rearrangements of 3‐Hydroxyindolenines to Indoxyls and 2‐Oxindoles: Reagent‐Controlled Regioselectivity Enabled by Dual Activation
inferred← citeshttps://doi.org/10.1002/ejoc.202000238openalex-snapshot
Copper‐Catalyzed Synthesis of Trinuclear N‐Fused Hybrid Scaffolds by Double C( sp 2 )–N Bond Formation between 2‐(2‐Bromoaryl)indoles and 2‐Aminoazoles
inferred← citeshttps://doi.org/10.1002/ejoc.202200479openalex-snapshot
Copper‐Catalyzed Synthesis of 5‐Arylindolo[1,2‐c]quinazolin‐6(5H)‐ones from 2‐(2‐Bromoaryl)indoles and Aryl Isocyanates under Microwave Irradiation
inferred← citeshttps://doi.org/10.1002/ejoc.202300689openalex-snapshot
Synthesis of Alkaloids and Compounds Containing the 3,4‐Benzomorphan Scaffold
inferred← citeshttps://doi.org/10.1002/ejoc.202401037openalex-snapshot
A Green Synthetic Approach to Construct C2‐Quaternary Indolin‐3‐Ones at Room Temperature via Regioselective Oxidative Dearomatization of Indoles
inferred← citeshttps://doi.org/10.1002/hlca.201200498openalex-snapshot
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
inferred← citeshttps://doi.org/10.1007/s11030-022-10378-9openalex-snapshot
Synthesis and in vitro evaluation of antitumor activity of spiro[indolo[2,1-b]quinazoline-pyrano[2,3-d]pyrimidine] and spiro[indolo[2,1-b]quinazoline-pyrido[2,3-d]pyrimidine] derivatives by using 2D and 3D cell culture models
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/10.1016/b978-0-08-097742-3.00321-9openalex-snapshot
3.16 The Semipinacol Rearrangements
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00028-4openalex-snapshot
The Semipinacol Rearrangements
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00303-5openalex-snapshot
Pyrroles and their Benzo Derivatives: Synthesis
inferred← citeshttps://doi.org/10.1016/j.bmc.2009.06.067openalex-snapshot
Aerobic oxidation of indolomorphinan without the 4,5-epoxy bridge and subsequent rearrangement of the oxidation product to spiroindolinonyl-C-normorphinan derivative
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.12.015openalex-snapshot
I2/TBHP/cyclohexanone a novel catalyst system for the oxidative dearomatization of indoles to indolin-3-ones at room temperature under solvent-free condition
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.108902openalex-snapshot
Recent advances in electrocatalytic generation of indole-derived radical cations and their applications in organic synthesis
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.molcatb.2013.01.024openalex-snapshot
Saccharomyces cerevisiae catalyzed one pot synthesis of isoindolo[2,1-a]quinazoline performed under ultrasonication
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131759openalex-snapshot
Synthesis and in vitro anticancer activity evaluation of spiro[indolo[2,1-b]quinazoline-pyrano[2,3-c]pyrazole] via sequential four-component reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2004.11.069openalex-snapshot
The consecutive [2+2] cycloaddition-ring expansion route to diastereomeric 1,4-diazepin-5-ones from imino-ketenimines. Alternative intramolecular transamidation of β-lactams
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.tet.2016.05.054openalex-snapshot
One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.01.063openalex-snapshot
A post-Ugi carbonylation/intramolecular amidation approach toward the synthesis of macrolactams
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
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.06.079openalex-snapshot
Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination–cyclization
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.06.102openalex-snapshot
Photocatalytic aerobic oxidation/semipinacol rearrangement sequence: a concise route to the core of pseudoindoxyl alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.069openalex-snapshot
Acid-mediated aryl migration reaction of C-3 aryl substituted pyrrolidinoindolines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152880openalex-snapshot
Reinventing the wheel for enabling the synthesis of hinckdentine A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153987openalex-snapshot
In(OTf)3 catalyzed regioselective acyloin rearrangement of 1-acyl-1-indanols
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(05)80048-0openalex-snapshot
Chapter 5.2 Five-membered ring systems: Pyrroles and benzo derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00774openalex-snapshot
Construction of Bridged Carbocycles and Heterocycles via Rh(III)-Catalyzed C–H Alkylation/Michael Addition of 2-Arylindoles with Quinone Monoacetals
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.1c01485openalex-snapshot
Synthesis of Hydroxysuccinimide Substituted Indolin-3-ones via One-Pot Cascade Reaction of o-Alkynylnitrobenzenes with Maleimides under Au(III)–Cu(II) Relay/Synergetic Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.1c03120openalex-snapshot
Indoles Oxidative Ring-Opening/Cyclization Cascade with the 1,2-Diaminoarenes: Direct Synthesis of 2-Aryl-3-(2-aminoaryl)quinoxalines
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00408openalex-snapshot
Construction of C2-Quaternary-indol-3-ones via RhIII-Catalyzed [3+2] Spirocyclization from Indole Ketones and Nitroolefins
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.5b02076openalex-snapshot
Regioselective Synthesis of Indolo[1,2- c ]quinazolines and 11 H -Indolo[3,2- c ]quinolines via Copper-Catalyzed Cascade Reactions of 2-(2-Bromoaryl)-1 H -indoles with Aldehydes and Aqueous Ammonia
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02086openalex-snapshot
Synthesis of Benzofuro- and Indolo[3,2- b ]indoles via Palladium-Catalyzed Double N -Arylation and Their Physical Properties
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.joc.8b00231openalex-snapshot
Solvent-Dependent Copper-Catalyzed Indolyl C3-Oxygenation and N1-Cyclization Reactions: Selective Synthesis of 3H-Indol-3-ones and Indolo[1,2-c]quinazolines
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01887openalex-snapshot
Synthesis of 1H-Pyrrol-3(2H)-ones via Three-Component Reactions of 2,3-Diketo Esters, Amines, and Ketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01626openalex-snapshot
Catalytic Asymmetric Acyloin Rearrangements of α-Ketols, α-Hydroxy Aldehydes, and α-Iminols by N,N′-Dioxide–Metal Complexes
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.0c04214openalex-snapshot
α-Iminol Rearrangement Triggered by Pd-Catalyzed C–H Addition to Nitriles Sequences: Synthesis of Functionalized α-Amino Cyclopentanones
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.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.6b00689openalex-snapshot
Rhodium(III)-Catalyzed Cascade Cyclization/Electrophilic Amidation for the Synthesis of 3-Amidoindoles and 3-Amidofurans
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01545openalex-snapshot
Nitrogen-Atom Insertion of Indolyl Phosphonium Salts through C–P and C–C Bond Functionalization
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.7b01397openalex-snapshot
Syntheses of Tetrahydrobenzoazepinoindoles and Dihydrobenzodiazepinoindoles via Ring-Opening Cyclization of Activated Aziridines with 2-(2-Bromophenyl)-1 H -indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01575openalex-snapshot
Asymmetric Robinson Annulation of 3-Indolinone-2-carboxylates with Cyclohexenone: Access to Chiral Bridged Tricyclic Hydrocarbazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01492openalex-snapshot
Rhodium-Catalyzed Formal C–O Insertion in Carbene/Alkyne Metathesis Reactions: Synthesis of 3-Substituted 3H-Indol-3-ols
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.9b02615openalex-snapshot
Rh(III)-Catalyzed C–H Amidation of 2-Arylindoles with Dioxazolones: A Route to Indolo[1,2- c ]quinazolines
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03768openalex-snapshot
Rh(III)-Catalyzed Tandem Acylmethylation/Nitroso Migration/Cyclization of N-Nitrosoanilines with Sulfoxonium Ylides in One Pot: Approach to 3-Nitrosoindoles
inferred← citeshttps://doi.org/10.1021/acsomega.7b00693openalex-snapshot
Synthesis of Benzo[4,5]imidazo[1,2- c ]pyrimidin-1-amines and Their Analogs via Copper-Catalyzed C–N Coupling and Cyclization
inferred← citeshttps://doi.org/10.1021/cr0505270openalex-snapshot
Practical Methodologies for the Synthesis of Indoles
inferred← citeshttps://doi.org/10.1021/cr200055gopenalex-snapshot
Semipinacol Rearrangement in Natural Product Synthesis
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/ja203960bopenalex-snapshot
Total Synthesis of (±)-Trigonoliimine C via Oxidative Rearrangement of an Unsymmetrical Bis-Tryptamine
inferred← citeshttps://doi.org/10.1021/ja5065685openalex-snapshot
Catalytic Asymmetric α-Iminol Rearrangement: New Chiral Platforms
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.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/jo0358168openalex-snapshot
Reaction of Bromomethylazoles and Tosylmethyl Isocyanide. A Novel Heterocyclization Method for the Synthesis of the Core of Marine Alkaloids Variolins and Related Azolopyrimidines
inferred← citeshttps://doi.org/10.1021/jo048898oopenalex-snapshot
Pyrrolodiazines. 6. Palladium-Catalyzed Arylation, Heteroarylation, and Amination of 3,4-Dihydropyrrolo[1,2-a]pyrazines
inferred← citeshttps://doi.org/10.1021/jo051848eopenalex-snapshot
Palladium-Catalyzed Arylation and Heteroarylation of Azolopyrimidines
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/ol0364071openalex-snapshot
Nucleophilic Addition to Electron-Rich Heteroaromatics: Dearomatizing Anionic Cyclizations of Pyrrolecarboxamides
inferred← citeshttps://doi.org/10.1021/ol048638topenalex-snapshot
Synthesis of Diazepinones via Intramolecular Transamidation
inferred← citeshttps://doi.org/10.1021/ol802394nopenalex-snapshot
First Total Synthesis of Hinckdentine A
inferred← citeshttps://doi.org/10.1039/b110074mopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/b316241aopenalex-snapshot
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c0cc03197fopenalex-snapshot
Synthesis of 6-trifluoromethylindolo[1,2-c]quinazolines and related heterocycles using N-(2-iodophenyl)trifluoroacetimidoyl chlorides as starting material via C–H bond functionalization
inferred← citeshttps://doi.org/10.1039/c2cc34053dopenalex-snapshot
Enantioselective aza-Henry reactions of cyclic α-carbonyl ketimines under bifunctional catalysis
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/c6cc05378eopenalex-snapshot
Highly fluorescent 1,2-dihydropyrimido[1,6-α]indole: an efficient metal free synthesis and photophysical study
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/c7qo00129kopenalex-snapshot
Asymmetric amination of 2-substituted indolin-3-ones catalyzed by natural cinchona alkaloids
inferred← citeshttps://doi.org/10.1039/c7ra10716aopenalex-snapshot
Fischer indole synthesis applied to the total synthesis of natural products
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/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/c9cc09178eopenalex-snapshot
Highly enantioselective electrosynthesis of C2-quaternary indolin-3-ones
inferred← citeshttps://doi.org/10.1039/c9ob02090jopenalex-snapshot
Thiamine hydrochloride as a recyclable organocatalyst for the synthesis of bis(indolyl)methanes, tris(indolyl)methanes, 3,3-di(indol-3-yl)indolin-2-ones and biscoumarins
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/d0cy01820aopenalex-snapshot
Recent advances in Wacker oxidation: from conventional to modern variants and applications
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/d1gc02849aopenalex-snapshot
An iron( iii )-catalyzed dehydrogenative cross-coupling reaction of indoles with benzylamines to prepare 3-aminoindole derivatives
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/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/d3qo00233kopenalex-snapshot
Enantioselective total syntheses of (−)-cephalotaxine and (−)-amathaspiramide F through a key Ir/Cu dual catalysis
inferred← citeshttps://doi.org/10.1039/d3ra03641copenalex-snapshot
An efficient method to access spiro pseudoindoxyl ketones: evaluation of indoxyl and their N -benzylated derivatives for inhibition of the activity of monoamine oxidases
inferred← citeshttps://doi.org/10.1039/d4ob01091dopenalex-snapshot
Mechanochemical deprotection of t -butoxycarbonyl (Boc) group using basic alumina
inferred← citeshttps://doi.org/10.1055/a-1337-5504openalex-snapshot
Nickel-Catalyzed C–F/N–H Annulation of 2-(2-Fluoroaryl) N-Heteroaromatic Compounds with Alkynes: Activation of C–F Bonds
inferred← citeshttps://doi.org/10.1080/00397910903043017openalex-snapshot
Synthesis of Indolo[1,2-b]indazole Derivatives via Copper(I)-Catalyzed Intramolecular Amination Reaction
inferred← citeshttps://doi.org/10.1080/00397911.2020.1836564openalex-snapshot
Ru-catalyzed oxidative dearomatization-hydroxylation of N-Boc indoles
inferred← citeshttps://doi.org/10.1080/00397911.2020.1859542openalex-snapshot
Ru-catalyzed oxidative dearomatization-alkoxylation of N-Boc indoles
inferred← citeshttps://doi.org/10.1107/s1600536807011166openalex-snapshot
5,7-Diacetyl-13-benzyl-7,8-dihydro-5H,8aH,13H-diindolo[2,3-c;2,3-d]pyrimidin-8-yl acetate, the result of an intramolecular cycloaddition between anN-benzylindole and a 1,2,4,5-tetrazine
inferred← citeshttps://doi.org/10.1139/cjc-2019-0288openalex-snapshot
Ru-catalyzed oxidation and C–C bond formation of indoles for the synthesis of 2-indolyl indolin-3-ones under mild reaction conditions
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/10.21577/1984-6835.20220018openalex-snapshot
Indole: a Versatile and Promising Heterocycle for the Discovery of Novel Antibacterial and Antifungal Agents
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/10.3762/bjoc.8.208openalex-snapshot
Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene
inferred← citeshttps://doi.org/10.3987/com-06-s(k)39openalex-snapshot
Versatile Synthesis of 2,2-Disubstituted Indolinones via Protected Indolones Generated by One-Pot Multi-oxidation of 2-Substituted Indoles
inferred← citeshttps://doi.org/10.3987/com-07-s(u)42openalex-snapshot
Asymmetric Alkylation of 2-Monosubstituted Indolin-3-ones
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/10.70675/28971a24z5bccz4759zaac8z999388a03d29openalex-snapshot
Synthèse et études physico-chimiques de dérivés d’indoles, indolinones et de 1,2 dihydrophosphètes
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.