On the public citation graph

Rapid Access to 2,2-Disubstituted Indolines via Dearomative Indolic-Claisen Rearrangement: Concise, Enantioselective Total Synthesis of (+)-Hinckdentine A

0 signed · 124 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/(sici)1521-3773(19980817)37:15<1986::aid-anie1986>3.0.co;2-zopenalex-snapshot

Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method

inferredcites →https://doi.org/10.1002/9783527610549.ch3openalex-snapshot

Aliphatic and Aromatic Claisen Rearrangement

inferredcites →https://doi.org/10.1002/adsc.200600495openalex-snapshot

Asymmetric Friedel–Crafts Alkylations of Indoles with Ethyl Glyoxylate Catalyzed by (S)‐BINOL‐Titanium(IV) Complex: Direct Access to Enantiomerically Enriched 3‐Indolyl(hydroxy)acetates

inferredcites →https://doi.org/10.1002/anie.201107417openalex-snapshot

Asymmetric Synthesis of Allenyl Oxindoles and Spirooxindoles by a Catalytic Enantioselective Saucy–Marbet Claisen Rearrangement

inferredcites →https://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

inferredcites →https://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

inferredcites →https://doi.org/10.1002/cber.19711040624openalex-snapshot

Über die Alkylierung von Indoxyl‐carbonsäure‐(2)‐estern und über die Claisen‐Umlagerung der Allyloxyindole

inferredcites →https://doi.org/10.1002/chem.201003591openalex-snapshot

Steering Reaction Pathways: From Benzyl Claisen Rearrangements to Powerful Ionic Shifts

inferredcites →https://doi.org/10.1002/cjoc.201800301openalex-snapshot

Electrochemical Synthesis of (Aza)indolines via Dehydrogenative [3+2] Annulation: Application to Total Synthesis of (±)‐Hinckdentine A

inferredcites →https://doi.org/10.1002/ejoc.201000599openalex-snapshot

Application of Selective Palladium‐Mediated Functionalization of the Pyrido[3′,2′:4,5]pyrrolo[1,2‐c]pyrimidine Heterocyclic System for the Total Synthesis of Variolin B and Deoxyvariolin B

inferredcites →https://doi.org/10.1002/hlca.19640470835openalex-snapshot

C LAISEN 'sche Umlagerungen bei Allyl‐ und Benzylalkoholen mit Hilfe von Acetalen des N, N‐Dimethylacetamids. Vorläufige Mitteilung

inferredcites →https://doi.org/10.1002/hlca.19690520418openalex-snapshot

C LAISEN 'sche Umlagerungen bei Allyl‐ und Benzylalkoholen mit 1‐Dimethylamino‐1‐methoxy‐äthen

inferredcites →https://doi.org/10.1002/hlca.19780610836openalex-snapshot

A New Type of Claisen Rearrangement Involving 1,3‐Dipolar Intermediates. Preliminary communication

inferredcites →https://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

inferredcites →https://doi.org/10.1002/jlac.19616410102openalex-snapshot

Über Säureamidacetale, Harnstoffacetale und Lactamacetale

inferredcites →https://doi.org/10.1007/s11172-007-0053-9openalex-snapshot

A study of the Claisen—Eschenmoser reaction for hydroxymethylbenzofurans and-indoles

inferredcites →https://doi.org/10.1016/0040-4039(96)01690-5openalex-snapshot

A short route to “reverse-prenylated” pyrrolo[2,3-b]indolesvia tandem olefination and claisen rearrangement of 2-(3,3-dimethylallyloxy)indol-3-ones: First total synthesis of flustramine C

inferredcites →https://doi.org/10.1016/j.tet.2004.02.015openalex-snapshot

Total syntheses of (−)-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate

inferredcites →https://doi.org/10.1016/j.tetlet.2004.09.148openalex-snapshot

Radical dearomatising spirocyclisations onto the C-2 position of benzofuran and indole

inferredcites →https://doi.org/10.1016/j.tetlet.2013.06.079openalex-snapshot

Assembly of indolo[1,2-c]quinazolines using ZnBr2-promoted domino hydroamination–cyclization

inferredcites →https://doi.org/10.1016/j.tetlet.2021.152880openalex-snapshot

Reinventing the wheel for enabling the synthesis of hinckdentine A

inferredcites →https://doi.org/10.1016/s0040-4039(00)75392-5openalex-snapshot

Synthèse d'amides β alléniques par transposition des adduits formés lors de la réaction des alcools propargyliques sur les ynamines.

inferredcites →https://doi.org/10.1016/s0040-4039(00)76120-xopenalex-snapshot

Rearrangement de Claisen et elimination, au cours de l'addition des ynamines sur les alcools et les amines allyliques.

inferredcites →https://doi.org/10.1016/s0040-4039(00)81519-1openalex-snapshot

(+) Melonine and NB-oxy melonine, a new indoline skeleton

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)01364-8openalex-snapshot

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

inferredcites →https://doi.org/10.1016/s0040-4039(02)01168-1openalex-snapshot

[1,3] Sigmatropic rearrangement of ketene silyl acetals derived from benzyl α-substituted propanoates

inferredcites →https://doi.org/10.1016/s0040-4039(99)00855-2openalex-snapshot

Enantiodivergent synthesis of both enantiomeric forms of substituted paraconic acids starting from d-mannitol as a chiral pool

inferredcites →https://doi.org/10.1016/s1099-4831(08)00201-0openalex-snapshot

Chapter 1 Alkaloids of Kopsia

inferredcites →https://doi.org/10.1016/s1099-4831(09)06708-xopenalex-snapshot

The alkaloids Chemistry and Biology

inferredcites →https://doi.org/10.1016/s1876-0813(08)60118-9openalex-snapshot

Chapter 6 The Eburnamine-Vincamine Alkaloids

inferredcites →https://doi.org/10.1021/acs.chemrev.5b00400openalex-snapshot

Use of Bromine and Bromo-Organic Compounds in Organic Synthesis

inferredcites →https://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

inferredcites →https://doi.org/10.1021/acs.orglett.1c00323openalex-snapshot

Total Synthesis of Hinckdentine A

inferredcites →https://doi.org/10.1021/acs.orglett.1c02055openalex-snapshot

Structure Reassignment of Melonine and Quantum-Chemical Calculations-Based Assessment of Biosynthetic Scenarios Leading to Its Revised and Original Structures

inferredcites →https://doi.org/10.1021/acs.orglett.2c01381openalex-snapshot

Diastereoselective Indole-Dearomative Cope Rearrangements by Compounding Minor Driving Forces

inferredcites →https://doi.org/10.1021/acs.orglett.8b04120openalex-snapshot

Direct C4-Benzylation of Indoles via Tandem Benzyl Claisen/Cope Rearrangements

inferredcites →https://doi.org/10.1021/acscatal.0c02377openalex-snapshot

Catalytic Reductive Functionalization of Tertiary Amides using Vaska’s Complex: Synthesis of Complex Tertiary Amine Building Blocks and Natural Products

inferredcites →https://doi.org/10.1021/cr020703uopenalex-snapshot

Claisen Rearrangement over the Past Nine Decades

inferredcites →https://doi.org/10.1021/ja00252a056openalex-snapshot

Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications

inferredcites →https://doi.org/10.1021/ja00259a075openalex-snapshot

A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses

inferredcites →https://doi.org/10.1021/ja00426a033openalex-snapshot

The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation

inferredcites →https://doi.org/10.1021/ja00483a051openalex-snapshot

Regiospecific synthesis of substituted arenes. [3,3]Sigmatropic rearrangement of benzyl vinyl ethers

inferredcites →https://doi.org/10.1021/ja00706a074openalex-snapshot

Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene

inferredcites →https://doi.org/10.1021/ja00771a062openalex-snapshot

Claisen rearrangement of allyl esters

inferredcites →https://doi.org/10.1021/ja01062a049openalex-snapshot

The Formation of 2,4-Dimethoxy-6-methylphenylacetone from 3,5-Dimethoxybenzyl isopropenyl Ether. A New Variant of the Claisen Rearrangement

inferredcites →https://doi.org/10.1021/ja021380mopenalex-snapshot

Synthesis of 8-Desbromohinckdentine A1

inferredcites →https://doi.org/10.1021/ja4095473openalex-snapshot

Brønsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement Mediated by an Arene CH–O Interaction

inferredcites →https://doi.org/10.1021/ja807026zopenalex-snapshot

Catalytic Enantioselective Meerwein−Eschenmoser Claisen Rearrangement: Asymmetric Synthesis of Allyl Oxindoles

inferredcites →https://doi.org/10.1021/jacs.1c00283openalex-snapshot

Catalyst-Controlled Regiodivergence in Rearrangements of Indole-Based Onium Ylides

inferredcites →https://doi.org/10.1021/jacs.1c10279openalex-snapshot

Asymmetric Total Syntheses of Schizozygane Alkaloids

inferredcites →https://doi.org/10.1021/jacs.6b10237openalex-snapshot

Enantioselective Total Synthesis of (+)-Hinckdentine A via a Catalytic Dearomatization Approach

inferredcites →https://doi.org/10.1021/jacsau.2c00048openalex-snapshot

Total Synthesis of (+)-Hinckdentine A: Harnessing Noncovalent Interactions for Organocatalytic Bromination

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/jo00154a023openalex-snapshot

Reactions of haloketenes with allyl ethers and thioethers: a new type of Claisen rearrangement

inferredcites →https://doi.org/10.1021/jo00352a001openalex-snapshot

Synthesis via sigmatropic rearrangements. 10. Synthesis of 2,3-disubstituted indoles via Claisen ortho ester rearrangement. An approach for the synthesis of vindorosine

inferredcites →https://doi.org/10.1021/jo026582fopenalex-snapshot

Sulfur Ylide-Initiated Thio-Claisen Rearrangements. The Synthesis of Highly Substituted Indolines

inferredcites →https://doi.org/10.1021/jo040289topenalex-snapshot

Synthesis of Diversely Functionalized Hexahydropyrrolo[2,3-b]indoles Using Domino Reactions, Olefination, Isomerization and Claisen Rearrangement Followed by Reductive Cyclization

inferredcites →https://doi.org/10.1021/jo302039nopenalex-snapshot

Copper(II)- and Palladium(II)-Catalyzed Enantioselective Claisen Rearrangement of Allyloxy- and Propargyloxy-Indoles to Quaternary Oxindoles and Spirocyclic Lactones

inferredcites →https://doi.org/10.1021/jo302210topenalex-snapshot

Mechanistic Insight into the Formal [1,3]-Migration in the Thermal Claisen Rearrangement

inferredcites →https://doi.org/10.1021/jo4020358openalex-snapshot

Total Synthesis, Stereochemical Assignment, and Biological Activity of All Known (−)-Trigonoliimines

inferredcites →https://doi.org/10.1021/jo901425zopenalex-snapshot

Highly Efficient Asymmetric Synthesis of 3-Indolyl(hydroxy)acetates via Friedel−Crafts Alkylation of Indoles

inferredcites →https://doi.org/10.1021/jo9023107openalex-snapshot

Total Syntheses of (−)-Fructigenine A and (−)-5-N-Acetylardeemin

inferredcites →https://doi.org/10.1021/ol030061copenalex-snapshot

Highly Stereoselective Saucy−Marbet Rearrangement Using Chiral Ynamides. Synthesis of Highly Substituted Chiral Homoallenyl Alcohols

inferredcites →https://doi.org/10.1021/ol061552aopenalex-snapshot

Enantioselective Friedel−Crafts Reaction of Indoles with Carbonyl Compounds Catalyzed by Bifunctional Cinchona Alkaloids

inferredcites →https://doi.org/10.1021/ol102931nopenalex-snapshot

Vinyl Diazophosphonates as Precursors to Quaternary Substituted Indolines and Cyclopentenes

inferredcites →https://doi.org/10.1021/ol300584mopenalex-snapshot

Efficient Construction of Fused Indolines with a 2-Quaternary Center via an Intramolecular Heck Reaction with a Low Catalyst Loading

inferredcites →https://doi.org/10.1021/ol3016435openalex-snapshot

Copper-Catalyzed Sequential Ullmann N-Arylation and Aerobic Oxidative C–H Amination: A Convenient Route to Indolo[1,2-c]quinazoline Derivatives

inferredcites →https://doi.org/10.1021/ol802394nopenalex-snapshot

First Total Synthesis of Hinckdentine A

inferredcites →https://doi.org/10.1021/ol9904085openalex-snapshot

Intramolecular Diels−Alder Cyclizations of (E)-1-Nitro-1,7,9-decatrienes: Synthesis of the AB Ring System of Norzoanthamine

inferredcites →https://doi.org/10.1039/b512485aopenalex-snapshot

Enantioselective total synthesis of (−)-flustramines A, B and (−)-flustramides A, B via domino olefination/isomerization/Claisen rearrangement sequence

inferredcites →https://doi.org/10.1039/b714881jopenalex-snapshot

The [1, 3] O-to-C rearrangement: opportunities for stereoselective synthesis

inferredcites →https://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

inferredcites →https://doi.org/10.1039/c1cc00049gopenalex-snapshot

Quaternary centres bearing nitrogen (α-tertiary amines) as products of molecular rearrangements

inferredcites →https://doi.org/10.1039/c1ob06212copenalex-snapshot

Decarboxylative Claisen rearrangement reactions: synthesis and reactivity of alkylidene-substituted indolines

inferredcites →https://doi.org/10.1039/c2cc34539kopenalex-snapshot

A cascade reaction of azolopyrimidines. Synthesis of unusual indole and azaindole derivatives

inferredcites →https://doi.org/10.1039/c39830000919openalex-snapshot

1,4-Stereoselection by sequential aldol addition–Claisen rearrangement. Stereostructure of the C 30 diol from Messel shale kerogen

inferredcites →https://doi.org/10.1039/c3ra41644eopenalex-snapshot

General and efficient copper-catalyzed aerobic oxidative synthesis of N-fused heterocycles using amino acids as the nitrogen source

inferredcites →https://doi.org/10.1039/c5np00096copenalex-snapshot

Synthetic approaches towards alkaloids bearing α-tertiary amines

inferredcites →https://doi.org/10.1039/p19960000729openalex-snapshot

Synthesis of 2-allyl-2,3-dihydro-1H-indol-3-ones using in situ Claisen rearrangement of 2,3-dihydro-1H-indol-3-ones with allyl alcohols

inferredcites →https://doi.org/10.1039/qr9682200391openalex-snapshot

Molecular rearrangements related to the Claisen rearrangement

inferredcites →https://doi.org/10.1055/s-0030-1260773openalex-snapshot

Proline-Catalyzed Enantioselective Synthesis of Aza-Quaternary Carbon Derivatives

inferredcites →https://doi.org/10.1055/s-0036-1589529openalex-snapshot

Claisen Rearrangements of Benzyl Vinyl Ethers and Heterobenzyl Vinyl Ethers

inferredcites →https://doi.org/10.1055/s-2005-918448openalex-snapshot

Heteroaromatic Decarboxylative Claisen Rearrangement Reactions

inferredcites →https://doi.org/10.1080/00397911.2014.956367openalex-snapshot

Rapid and Total Bromination of Aromatic Compounds Using TsNBr2 Without Any Catalyst

inferredcites →https://doi.org/10.3762/bjoc.14.218openalex-snapshot

Synthesis of indolo[1,2-c]quinazolines from 2-alkynylaniline derivatives through Pd-catalyzed indole formation/cyclization with N,N-dimethylformamide dimethyl acetal

inferredcites →https://doi.org/10.3987/com-93-s21openalex-snapshot

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.

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/adsc.70295openalex-snapshot

Synthesis of 1,3‐Oxazole‐Substituted 2‐Naphthols and Phenols From Their Corresponding Ethers via Claisen Rearrangement

inferred← citeshttps://doi.org/10.1002/ange.202314308openalex-snapshot

Enantioselective Total Synthesis of (+)‐Incargranine A Enabled by Bifunctional Iminophosphorane and Iridium Catalysis

inferred← citeshttps://doi.org/10.1002/ange.202408195openalex-snapshot

Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis

inferred← citeshttps://doi.org/10.1002/ange.202413557openalex-snapshot

Stereoselective Vinylic C−H Addition via Metallaphotoredox Migration

inferred← citeshttps://doi.org/10.1002/ange.7232106openalex-snapshot

Dearomative [3,3]‐Claisen Rearrangement of 2‐Indolyl Alcohols: An Efficient and General Protocol for Synthesizing 3,3‐Disubstituted Indolines and Related Indole Alkaloids

inferred← citeshttps://doi.org/10.1002/ange.8101956openalex-snapshot

Total Synthesis of (+)‐Melonine and (+)‐ N 4 ‐Oxy Melonine Enabled by an Intramolecular Alkene Diamination Reaction

inferred← citeshttps://doi.org/10.1002/anie.202314308openalex-snapshot

Enantioselective Total Synthesis of (+)‐Incargranine A Enabled by Bifunctional Iminophosphorane and Iridium Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202408195openalex-snapshot

Chromium‐ and Metal‐Reductant‐Free Asymmetric Nozaki–Hiyama–Kishi (NHK) Reaction Enabled by Metallaphotoredox Catalysis

inferred← citeshttps://doi.org/10.1002/anie.202413557openalex-snapshot

Stereoselective Vinylic C−H Addition via Metallaphotoredox Migration

inferred← citeshttps://doi.org/10.1002/anie.7232106openalex-snapshot

Dearomative [3,3]‐Claisen Rearrangement of 2‐Indolyl Alcohols: An Efficient and General Protocol for Synthesizing 3,3‐Disubstituted Indolines and Related Indole Alkaloids

inferred← citeshttps://doi.org/10.1002/anie.8101956openalex-snapshot

Total Synthesis of (+)‐Melonine and (+)‐ N 4 ‐Oxy Melonine Enabled by an Intramolecular Alkene Diamination Reaction

inferred← citeshttps://doi.org/10.1002/chem.202302963openalex-snapshot

On Demand Synthesis of C3−N1’ Bisindoles by a Formal Umpolung Strategy: First Total Synthesis of (±)‐Rivularin A

inferred← citeshttps://doi.org/10.1002/ejoc.202400983openalex-snapshot

Recent Advances in Sustainable Total Synthesis and Chiral Pool Strategies with Emphasis on (−)‐Sclareol in Natural Products Synthesis

inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00122-3openalex-snapshot

One or More =CH, =CC, and/or C=C Bond(s) Formed by Rearrangement

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.4c02508openalex-snapshot

Synthesis of Carboxylic Acids Containing α-All-Carbon Quaternary Centers from Diazo Compounds and Trialkylboranes

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.orglett.4c04500openalex-snapshot

Site-Selective Electrophilic Trifluoromethylthiolation for the Synthesis of C5- or C7-SCF3-Substituted Indolines

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04851openalex-snapshot

Total Synthesis of Melonine

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03639openalex-snapshot

Synchronized Aromaticity Enables Syntheses of 2,4-Cyclohexadienones via [3 + 2]/[3,3]-Cascade Reaction

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03771openalex-snapshot

Asymmetric Synthesis of the Pentacyclic Framework of Kopsia Alkaloids

inferred← citeshttps://doi.org/10.1021/acscatal.4c01584openalex-snapshot

Organocatalytic Highly Enantioselective Formal [1,3] Sigmatropic Rearrangement of Indole Alkyl Ethers and Mechanistic Insight

inferred← citeshttps://doi.org/10.1021/acscatal.4c05762openalex-snapshot

Direct Synthesis of N-Fused Indoles Enabled by Copper-Catalyzed Aerobic Oxygenative Rearrangement

inferred← citeshttps://doi.org/10.1021/jacs.3c08714openalex-snapshot

Enantioselective Total Syntheses of (−)-Caulamidine D and (−)-Isocaulamidine D and Their Absolute Configuration Reassignment

inferred← citeshttps://doi.org/10.1021/jacs.5c11779openalex-snapshot

Asymmetric Total Synthesis of (−)-Psychotriadine Featuring [3,3]-Rearrangement and Stereo-Controllable Ring-Contraction

inferred← citeshttps://doi.org/10.1021/jacs.5c18159openalex-snapshot

Catalytic Asymmetric Synthesis of 3-Hydroxyindolenines Using Achiral Oxaziridines

inferred← citeshttps://doi.org/10.1038/s41557-025-02022-4openalex-snapshot

The catalytic enantioselective [1,2]-Wittig rearrangement cascade of allylic ethers

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/d5cc00612kopenalex-snapshot

Asymmetric synthesis of quinolinone-based polycyclic indoles through [1,3]-rearrangement/cyclization reaction

inferred← citeshttps://doi.org/10.1039/d5cc01615kopenalex-snapshot

MHAT-enabled cascade radical annulation to access N -fused indoles and pyrroles

inferred← citeshttps://doi.org/10.1039/d6ob01177bopenalex-snapshot

Indole dearomative [3,3]-Claisen rearrangement: access to indole alkaloids with C2/C3 quaternary stereocenters

inferred← citeshttps://doi.org/10.1055/s-0042-1752912openalex-snapshot

Synthesis of (+)-Hinckdentine A

inferred← citeshttps://doi.org/10.12677/jocr.2024.121001openalex-snapshot

Study of Aromatics Dearomatization by Claisen Rearrangement

inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-fz2fzopenalex-snapshot

The Catalytic Enantioselective [1,2]-Wittig Rearrangement of Allylic Ethers

inferred← citeshttps://doi.org/10.6023/cjoc202408037openalex-snapshot

Total Syntheses of Marine-Derived Polyhalogenated Natural Products

inferred← citeshttps://doi.org/10.6023/cjoc202510018openalex-snapshot

Ruthenium(II)-Catalyzed C7—H Monofluoroalkenylation of Indolines with gem -Difluorostyrenes

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.