On the public citation graph

Regioselective synthesis of enantiopure 1,2- and 1,3-dispirooxindoles along with a DFT study

https://doi.org/10.1039/d2ob02311c
0 signed · 68 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/1521-3773(20000915)39:18<3168::aid-anie3168>3.0.co;2-uopenalex-snapshot
Multicomponent Reactions with Isocyanides
inferredcites →https://doi.org/10.1002/adsc.201801732openalex-snapshot
Pd‐Catalyzed Diastereoselective Intramolecular Amide α‐C−H Arylation in Sterically Hindered Monospirooxindole Motifs
inferredcites →https://doi.org/10.1002/adsc.202000942openalex-snapshot
Dienolate‐Mediated, Regioselective C2‐Polarity Reversal of Chromone‐Based Reactants and Their Application in Nucleophilic Strategies
inferredcites →https://doi.org/10.1002/ajoc.202000056openalex-snapshot
Synthesis of Highly Enantioenriched Bis‐spirooxindole Pyrrolizidine/Pyrrolidines through Asymmetric [3+2] Cycloaddition Reaction
inferredcites →https://doi.org/10.1002/ange.200605005openalex-snapshot
Modulating the Reactivity of α‐Isocyanoacetates: Multicomponent Synthesis of 5‐Methoxyoxazoles and Furopyrrolones
inferredcites →https://doi.org/10.1002/anie.201706629openalex-snapshot
Construction of Quaternary Stereogenic Centers in the Total Synthesis of Natural Products
inferredcites →https://doi.org/10.1002/ejoc.200390167openalex-snapshot
Recent Developments in the Isonitrile‐Based Multicomponent Synthesis of Heterocycles
inferredcites →https://doi.org/10.1002/ejoc.200901438openalex-snapshot
A Marriage of Convenience: Combining the Power of Isocyanide‐Based Multicomponent Reactions with the Versatility of (Hetero)norbornene Chemistry
inferredcites →https://doi.org/10.1002/jhet.685openalex-snapshot
An efficient multicomponent and stereoselective synthesis of new spiro[indeno[1,2‐b]quinoxaline‐11,2′‐pyrrolidine] derivatives
inferredcites →https://doi.org/10.1002/poc.3710openalex-snapshot
Steric interactions controlling thesyndiastereofacial selectivity in the [3 + 2] cycloaddition reaction between acetonitrile oxide and 7-oxanorborn-5-en-2-ones: A molecular electron density theory study
inferredcites →https://doi.org/10.1007/s00706-011-0518-2openalex-snapshot
A regioselective and diastereoselective synthesis of new spiro-isoxazolidines via 1,3-dipolar cycloaddition of stable isatin ketonitrone and various dipolarophiles
inferredcites →https://doi.org/10.1016/b978-0-444-63462-7.00008-7openalex-snapshot
Recent Developments on the Synthesis and Applications of Natural Products-Inspired Spirooxindole Frameworks
inferredcites →https://doi.org/10.1016/j.bmc.2016.07.032openalex-snapshot
Origins of regioselectivity in 1,3-dipolar cycloadditions of nitrile oxides with alkynylboronates
inferredcites →https://doi.org/10.1016/j.bmcl.2010.09.108openalex-snapshot
Substituted spiro [2.3′] oxindolespiro [3.2″]-5,6-dimethoxy-indane-1″-one-pyrrolidine analogue as inhibitors of acetylcholinesterase
inferredcites →https://doi.org/10.1016/j.bmcl.2013.01.023openalex-snapshot
Facile one-pot synthesis of novel dispirooxindole-pyrrolidine derivatives and their antimicrobial and anticancer activity against A549 human lung adenocarcinoma cancer cell line
inferredcites →https://doi.org/10.1016/j.bmcl.2020.127410openalex-snapshot
Study on antitumor activities of the chrysin-chromene-spirooxindole on Lewis lung carcinoma C57BL/6 mice in vivo
inferredcites →https://doi.org/10.1016/j.cclet.2019.06.015openalex-snapshot
Highly efficient enantioselective synthesis of bispiro[benzofuran-oxindole/benzofuran-chromanone]s through organocatalytic inter-/intramolecular Michael cycloaddition
inferredcites →https://doi.org/10.1016/j.ejmech.2008.03.013openalex-snapshot
Regioselective synthesis of dispiro[1H-indene-2,3′-pyrrolidine-2′,3″-[3H]indole]-1,2″(1″H)-diones of potential anti-tumor properties
inferredcites →https://doi.org/10.1016/j.ejmech.2009.09.044openalex-snapshot
Novel three-component domino reactions of ketones, isatin and amino acids: Synthesis and discovery of antimycobacterial activity of highly functionalised novel dispiropyrrolidines
inferredcites →https://doi.org/10.1016/j.tet.2005.03.088openalex-snapshot
A regioselective synthesis of dispiro[oxindole-cyclohexanone]pyrrolidines and dispiro[oxindole-hexahydroindazole]pyrrolidines by sequential 1,3-dipolar cycloaddition and annulation through a microwave induced solvent-free approach
inferredcites →https://doi.org/10.1016/j.tet.2014.08.005openalex-snapshot
Recent advances in the synthesis of biologically active spirooxindoles
inferredcites →https://doi.org/10.1016/j.tetasy.2015.08.013openalex-snapshot
Asymmetric synthesis approach of enantiomerically pure spiro-indenoquinoxaline pyrrolidines and spiro-indenoquinoxaline pyrrolizidines
inferredcites →https://doi.org/10.1016/j.tetlet.2005.06.114openalex-snapshot
Synthesis of spirooxindoles via asymmetric 1,3-dipolar cycloaddition
inferredcites →https://doi.org/10.1016/j.tetlet.2012.07.066openalex-snapshot
Synthesis of new enantiomerically pure spirooxindolopyrrolizidines via a three-component asymmetric 1,3-dipolar cycloaddition reaction of azomethine ylides derived from isatin
inferredcites →https://doi.org/10.1016/j.tetlet.2013.07.126openalex-snapshot
Cu-mediated 1,3-dipolar cycloaddition of azomethine ylides with dipolarophiles: a faster access to spirooxindoles of potential pharmacological interest
inferredcites →https://doi.org/10.1016/j.tetlet.2013.11.097openalex-snapshot
An efficient, one-pot, three-component procedure for the synthesis of chiral spirooxindolopyrrolizidines via catalytic highly enantioselective 1,3-dipolar cycloaddition
inferredcites →https://doi.org/10.1016/j.tetlet.2018.07.051openalex-snapshot
Dipolar cycloaddition based multi-component reaction: Synthesis of spiro tethered acenaphthylene–indolizine–pyridinone hybrids
inferredcites →https://doi.org/10.1016/s0040-4039(03)00698-1openalex-snapshot
A simple method removing 2-oxazolidinone and 2-hydroxyethylamine auxiliaries in methoxide–carbonate systems for synthesis of planar-chiral nicotinate
inferredcites →https://doi.org/10.1021/acs.joc.5b00708openalex-snapshot
Diastereo- and Enantioselective Construction of 3,3′-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions
inferredcites →https://doi.org/10.1021/acs.joc.7b00153openalex-snapshot
β-Functionalization of Indolin-2-one-Derived Aliphatic Acids for the Divergent Synthesis of Spirooxindole γ-Butyrolactones
inferredcites →https://doi.org/10.1021/acs.joc.8b00035openalex-snapshot
Diastereoselective Construction of Indole-Bridged Chroman Spirooxindoles through a TfOH-Catalyzed Michael Addition-Inspired Cascade Reaction
inferredcites →https://doi.org/10.1021/acs.joc.8b00632openalex-snapshot
Organocatalytic Asymmetric Synthesis of 3,3′-Pyrrolidinyl-bispirooxindoles via Michael/ N -Hemiketalization Cascade Reaction between 3-Aminooxindoles and Isatin-Derived β,γ-Unsaturated α-Keto Esters
inferredcites →https://doi.org/10.1021/acs.joc.9b00645openalex-snapshot
Access to Chiral 2,5-Pyrrolidinyl Dispirooxindoles via Dinuclear Zinc-Catalyzed Asymmetric Cascade Reactions
inferredcites →https://doi.org/10.1021/ar700111aopenalex-snapshot
Density Functionals with Broad Applicability in Chemistry
inferredcites →https://doi.org/10.1021/cc900157wopenalex-snapshot
Use of Cyclohexylisocyanide and Methyl 2-Isocyanoacetate as Convertible Isocyanides for Microwave-Assisted Fluorous Synthesis of 1,4-Benzodiazepine-2,5-dione Library
inferredcites →https://doi.org/10.1021/cr0505728openalex-snapshot
Recent Developments in Isocyanide Based Multicomponent Reactions in Applied Chemistry
inferredcites →https://doi.org/10.1021/cr970324eopenalex-snapshot
Asymmetric 1,3-Dipolar Cycloaddition Reactions
inferredcites →https://doi.org/10.1021/ja064157oopenalex-snapshot
CO2 Incorporation Reaction Using Arynes: Straightforward Access to Benzoxazinone
inferredcites →https://doi.org/10.1021/jm100410fopenalex-snapshot
Spirotetrahydro β-Carbolines (Spiroindolones): A New Class of Potent and Orally Efficacious Compounds for the Treatment of Malaria
inferredcites →https://doi.org/10.1021/jm800271copenalex-snapshot
Asymmetric Synthesis of 2,3-Dihydro-2-arylquinazolin-4-ones: Methodology and Application to a Potent Fluorescent Tubulin Inhibitor with Anticancer Activity
inferredcites →https://doi.org/10.1021/jm800545kopenalex-snapshot
Discovery of Antimycobacterial Spiro-piperidin-4-ones: An Atom Economic, Stereoselective Synthesis, and Biological Intervention
inferredcites →https://doi.org/10.1021/jo0345603openalex-snapshot
The Role of Steric and Electronic Interactions in the Stereocontrol of the Asymmetric 1,3-Dipolar Reactions of 5-Ethoxy-3-p-(S)-tolylsulfinylfuran-2(5H)-ones with Diazoalkanes: Theoretical Calculations and Experimental Evidences
inferredcites →https://doi.org/10.1021/jo4017259openalex-snapshot
Synthesis of Pyrrolo(spiro-[2.3′]-oxindole)-spiro-[4.3″]-oxindole via 1,3-Dipolar Cycloaddition of Azomethine Ylides with 3-Acetonylideneoxindole
inferredcites →https://doi.org/10.1021/jo7016235openalex-snapshot
New Light on an Old Story: Facile and Efficient Synthesis of 1,3-Diaryl-5-spirohexahydro- pyrimidines via a Six-Molecule, Three-Component Mannich-Type Reaction
inferredcites →https://doi.org/10.1021/jp207563hopenalex-snapshot
Computational Methods To Calculate Accurate Activation and Reaction Energies of 1,3-Dipolar Cycloadditions of 24 1,3-Dipoles
inferredcites →https://doi.org/10.1021/ol100513yopenalex-snapshot
Enantioselective Formal Synthesis of Eurylene: Synthesis of the cis- and trans-THF Fragments Using Oxidative Cyclization
inferredcites →https://doi.org/10.1021/ol501547popenalex-snapshot
Lewis Acid Catalyzed Unprecedented [3 + 2] Cycloaddition Yields 3,3′-Pyrrolidinyldispirooxindoles Containing Four Contiguous Chiral Stereocenters with Two Contiguous Quaternary Spirostereocenters
inferredcites →https://doi.org/10.1021/op049768kopenalex-snapshot
A Practical Large-Scale Synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol via Asymmetric 1,3-Dipolar Cycloaddition
inferredcites →https://doi.org/10.1039/c4cc04381bopenalex-snapshot
Recent advances in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides
inferredcites →https://doi.org/10.1039/c5ob00774gopenalex-snapshot
A cinchona alkaloid catalyzed enantioselective sulfa-Michael/aldol cascade reaction of isoindigos: construction of chiral bispirooxindole tetrahydrothiophenes with vicinal quaternary spirocenters
inferredcites →https://doi.org/10.1039/c6ob02187eopenalex-snapshot
Catalytic enantioselective cascade Michael/cyclization reaction of 3-isothiocyanato oxindoles with exocyclic α,β-unsaturated ketones en route to 3,2′-pyrrolidinyl bispirooxindoles
inferredcites →https://doi.org/10.1039/c6ob02254eopenalex-snapshot
A DBU-catalyzed Michael–Pinner–isomerization cascade reaction of 3-hydroxyoxindoles with isatylidene malononitriles: access to highly functionalized bispirooxindoles containing a fully substituted dihydrofuran motif
inferredcites →https://doi.org/10.1039/c6qo00723fopenalex-snapshot
Asymmetric synthesis of trifluoromethyl-substituted 3,3′-pyrrolidinyl-dispirooxindoles through organocatalytic 1,3-dipolar cycloaddition reactions
inferredcites →https://doi.org/10.1039/c7cc05813fopenalex-snapshot
Metal-free diastereoselective construction of bridged ketal spirooxindoles via a Michael addition-inspired sequence
inferredcites →https://doi.org/10.1039/c7sc05138gopenalex-snapshot
The self-disproportionation of enantiomers (SDE): a menace or an opportunity?
inferredcites →https://doi.org/10.1039/c8cc02364fopenalex-snapshot
Catalytic asymmetric synthesis of spirooxindoles: recent developments
inferredcites →https://doi.org/10.1039/c8ob00306hopenalex-snapshot
Construction of bridged cyclic N , O -ketal spirooxindoles through a Michael addition/ N , O -ketalization sequence
inferredcites →https://doi.org/10.1039/c8ob01493kopenalex-snapshot
Diastereoselective construction of pyrrolo[2,1- a ]isoquinoline-based bispirooxindoles through a three-component [3 + 2] cycloaddition
inferredcites →https://doi.org/10.1039/c9cc07114hopenalex-snapshot
An unexpected cascade reaction of 3-hydroxyoxindoles with coumarin-3-carboxylates to construct 2,3-dihydrobenzofuran spirooxindoles
inferredcites →https://doi.org/10.1039/c9ob01197hopenalex-snapshot
Organocatalytic synthesis of enantiopure spiro acenaphthyl-pyrrolizidine/pyrrolidines: justifying the regioselectivity based on a distortion/interaction model
inferredcites →https://doi.org/10.1039/d0qo01085eopenalex-snapshot
Stereoselective synthesis and applications of spirocyclic oxindoles
inferredcites →https://doi.org/10.1080/00397910802374091openalex-snapshot
TiO2-Mediated, One-Pot, Four-Component 1,3-Dipolar Cycloaddition Reaction: A Facile Synthesis of Dispiro-pyrrolidine Ring Systems
inferredcites →https://doi.org/10.3390/molecules21060748openalex-snapshot
Applications of the Conceptual Density Functional Theory Indices to Organic Chemistry Reactivity
inferredcites →https://doi.org/10.3390/molecules26133994openalex-snapshot
A Call for a Change in Policy Regarding the Necessity for SDE Tests to Validate the Veracity of the Outcome of Enantioselective Syntheses, the Inherent Chiral State of Natural Products, and Other Cases Involving Enantioenriched Samples

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.4658095openalex-extracted
Dft Study on the Effect of Chloroxime Indole Compounds with Different Substituents on the Mechanism of 1,3-Dipolar Cycloaddition Reaction
inferred← citeshttps://doi.org/10.1038/s41557-025-02041-1openalex-snapshot
Collective asymmetric synthesis of the Strychnos alkaloids via thiophene S,S-dioxide cycloadditions
inferred← citeshttps://doi.org/10.1039/d3ra05587fopenalex-snapshot
Elucidating anticancer drugs release from UiO-66 as a carrier through the computational approaches
inferred← citeshttps://doi.org/10.1039/d5qo01408eopenalex-snapshot
Origin of chemo- and stereoselectivity in NHC-catalyzed asymmetric intermolecular cycloadditions of hydrazone and isatin
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.