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Recent advances in the synthesis of indolizine and its derivatives by radical cyclization/cross-coupling

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What this work says

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

inferredcites →https://doi.org/10.1002/adsc.201600506openalex-snapshot
Decarboxylative (4+1) Oxidative Annulation of Malonate Monoesters with 2‐Vinylpyridine Derivatives
inferredcites →https://doi.org/10.1002/adsc.202000103openalex-snapshot
Iodine Mediated Base‐Controlled Regio‐Selective Annulation of 2‐(Pyridin‐2‐yl)acetate Derivatives with Acrylic Esters for the Synthesis of Indolizines
inferredcites →https://doi.org/10.1002/ajoc.202100013openalex-snapshot
Recent Developments in the Cyclization of Alkynes and Nitrogen Compounds for the Synthesis of Indole Derivatives
inferredcites →https://doi.org/10.1002/ange.200900014openalex-snapshot
Organosulfur Chemistry in Asymmetric Synthesis .Herausgegeben von T. Toru und C. Bolm.
inferredcites →https://doi.org/10.1002/ange.201207410openalex-snapshot
Sustainable Synthesis of Diverse Privileged Heterocycles by Palladium‐Catalyzed Aerobic Oxidative Isocyanide Insertion
inferredcites →https://doi.org/10.1002/anie.201506868openalex-snapshot
External‐Photocatalyst‐Free Visible‐Light‐Mediated Synthesis of Indolizines
inferredcites →https://doi.org/10.1002/anie.202013089openalex-snapshot
Heterocyclization Reagents for Rapid Assembly of N‐Fused Heteroarenes from Alkenes
inferredcites →https://doi.org/10.1002/ejoc.201901803openalex-snapshot
One‐Pot Synthesis of Indolizines Using TBHP as the Methylene Source Under Metal‐Free Condition
inferredcites →https://doi.org/10.1002/ejoc.202000162openalex-snapshot
Photocatalytic Synthesis of 3‐Sulfanyl‐ and 1,3‐Bis(sulfanyl)indolizines Mediated by Visible Light
inferredcites →https://doi.org/10.1002/slct.201804056openalex-snapshot
Mn(OAc) 3 ‐Mediated Regioselective C‐H Phosphonylation of Indolizines with H ‐Phosphonates
inferredcites →https://doi.org/10.1002/slct.202100045openalex-snapshot
Synthesis of Indolizines by Dimerization of N‐ Propargylated Pyrroles via Allene Intermediates
inferredcites →https://doi.org/10.1007/s00044-014-0940-1openalex-snapshot
Indolizine: a biologically active moiety
inferredcites →https://doi.org/10.1016/j.ejmech.2010.02.056openalex-snapshot
Synthesis and antiproliferative activity of indolizine derivatives incorporating a cyclopropylcarbonyl group against Hep-G2 cancer cell line
inferredcites →https://doi.org/10.1016/j.ejmech.2011.02.066openalex-snapshot
Amberlite–IRA-402 (OH) ion exchange resin mediated synthesis of indolizines, pyrrolo [1,2-a] quinolines and isoquinolines: Antibacterial and antifungal evaluation of the products
inferredcites →https://doi.org/10.1016/j.tet.2014.07.085openalex-snapshot
Silver-mediated C–H bond functionalization: one-pot to construct substituted indolizines from 2-alkylazaarenes with alkynes
inferredcites →https://doi.org/10.1016/j.tet.2016.10.052openalex-snapshot
Pyridyl-indolizine derivatives as DNA binders and pH-sensitive fluorescent dyes
inferredcites →https://doi.org/10.1016/j.tetlet.2016.01.082openalex-snapshot
Metal-free synthesis of indolizines through oxidative C C and C N bond formations of C (sp 3 ) H bonds
inferredcites →https://doi.org/10.1016/j.tetlet.2016.05.083openalex-snapshot
Iodine-catalyzed [3+2] cyclization of 2-pyridylesters and chalcones: metal-free approach for the synthesis of substituted indolizines
inferredcites →https://doi.org/10.1016/j.theochem.2008.01.004openalex-snapshot
TD-DFT investigation on the electronic spectra of novel N-methylmaleimides linked with indolizine ring system
inferredcites →https://doi.org/10.1021/acs.accounts.7b00148openalex-snapshot
Iodine(III) Reagents in Radical Chemistry
inferredcites →https://doi.org/10.1021/acs.accounts.8b00267openalex-snapshot
Photocatalytic Activation of Less Reactive Bonds and Their Functionalization via Hydrogen-Evolution Cross-Couplings
inferredcites →https://doi.org/10.1021/acs.accounts.9b00472openalex-snapshot
Chemistry with Electrochemically Generated N-Centered Radicals
inferredcites →https://doi.org/10.1021/acs.chemrev.0c00030openalex-snapshot
Visible Light-Driven Radical-Mediated C–C Bond Cleavage/Functionalization in Organic Synthesis
inferredcites →https://doi.org/10.1021/acs.joc.0c01253openalex-snapshot
Synthesis of Pyrrolo[2,1,5- cd ]indolizine Rings via Visible-Light-Induced Intermolecular [3+2] Cycloaddition of Indolizines and Alkynes
inferredcites →https://doi.org/10.1021/acs.joc.1c00747openalex-snapshot
Radical and Ionic Reactions of Indolizin-1-ols: Synthesis of 3-Arylsulfanyl-, 3-(Tropon-2-yl)- and 3-(Tropolon-5-ylazo)-1-hydroxyindolizines from 3,3-Difluorocyclopropenes
inferredcites →https://doi.org/10.1021/acs.joc.1c00873openalex-snapshot
Oxidation Potential-Guided Electrochemical Radical–Radical Cross-Coupling Approaches to 3-Sulfonylated Imidazopyridines and Indolizines
inferredcites →https://doi.org/10.1021/acs.joc.6b02455openalex-snapshot
CuBr-Catalyzed Aerobic Decarboxylative Cycloaddition for the Synthesis of Indolizines under Solvent-Free Conditions
inferredcites →https://doi.org/10.1021/acs.joc.6b02928openalex-snapshot
General C–H Arylation Strategy for the Synthesis of Tunable Visible Light-Emitting Benzo[a]imidazo[2,1,5-c,d]indolizine Fluorophores
inferredcites →https://doi.org/10.1021/acs.orglett.0c01094openalex-snapshot
Visible-Light-Induced Regioselective Dicarbonylation of Indolizines with Oxoaldehydes via Direct C–H Functionalization
inferredcites →https://doi.org/10.1021/acs.orglett.1c02575openalex-snapshot
Mechanochemical Synthesis of 1,2-Diketoindolizine Derivatives from Indolizines and Epoxides Using Piezoelectric Materials
inferredcites →https://doi.org/10.1021/acs.orglett.5b01334openalex-snapshot
Indolizine Synthesis via Oxidative Cross-Coupling/Cyclization of Alkenes and 2-(Pyridin-2-yl)acetate Derivatives
inferredcites →https://doi.org/10.1021/acs.orglett.8b01168openalex-snapshot
Transition-Metal-Free Regioselective Cross-Coupling: Controlled Synthesis of Mono- or Dithiolation Indolizines
inferredcites →https://doi.org/10.1021/ja301196xopenalex-snapshot
Enantioselective Synthesis of Dihydropyrazoles by Formal [4+1] Cycloaddition of in Situ-Derived Azoalkenes and Sulfur Ylides
inferredcites →https://doi.org/10.1021/ja402274gopenalex-snapshot
A Coupling of Benzamides and Donor/Acceptor Diazo Compounds To Form γ-Lactams via Rh(III)-Catalyzed C–H Activation
inferredcites →https://doi.org/10.1021/ja900046zopenalex-snapshot
Ruthenium-Catalyzed Carbonylation at Ortho C−H Bonds in Aromatic Amides Leading to Phthalimides: C−H Bond Activation Utilizing a Bidentate System
inferredcites →https://doi.org/10.1021/jm2013997openalex-snapshot
Update on the Development of Antagonists of Chemoattractant Receptor-Homologous Molecule Expressed on Th2 Cells (CRTH2). From Lead Optimization to Clinical Proof-of-Concept in Asthma and Allergic Rhinitis
inferredcites →https://doi.org/10.1021/jo501626bopenalex-snapshot
Copper(II)-Catalyzed Indolizines Formation Followed by Dehydrogenative Functionalization Cascade to Synthesize 1-Bromoindolizines
inferredcites →https://doi.org/10.1039/c2jm14904dopenalex-snapshot
Multifunctional electron-transporting indolizine derivatives for highly efficient blue fluorescence, orange phosphorescence host and two-color based white OLEDs
inferredcites →https://doi.org/10.1039/c3ob41408fopenalex-snapshot
Synthesis of substituted nitroolefins: a copper catalyzed nitrodecarboxylation of unsaturated carboxylic acids
inferredcites →https://doi.org/10.1039/c5cc01825kopenalex-snapshot
Tuning radical reactivity using iodine in oxidative C(sp 3 )–H/C(sp)–H cross-coupling: an easy way toward the synthesis of furans and indolizines
inferredcites →https://doi.org/10.1039/c5ra01234aopenalex-snapshot
An I 2 -catalyzed oxidative cyclization for the synthesis of indolizines from aromatic/aliphatic olefins and α-picoline derivatives
inferredcites →https://doi.org/10.1039/c6ob00985aopenalex-snapshot
Recent advances in the synthesis of indolizines and their π-expanded analogues
inferredcites →https://doi.org/10.1039/c6ob01902aopenalex-snapshot
Synthesis of substituted indolizines via radical oxidative decarboxylative annulation of 2-(pyridin-2-yl)acetate derivatives with α,β-unsaturated carboxylic acids
inferredcites →https://doi.org/10.1039/c8cs00947copenalex-snapshot
Catalytic cascade reactions by radical relay
inferredcites →https://doi.org/10.1039/c9cc04730aopenalex-snapshot
Synthesis of a crystallochromic indolizine dye by a base- and catalyst-free photochemical route
inferredcites →https://doi.org/10.1039/c9gc01766fopenalex-snapshot
A visible-light-induced intermolecular [3 + 2] alkenylation–cyclization strategy: metal-free construction of pyrrolo[2,1,5- cd ]indolizine rings
inferredcites →https://doi.org/10.1039/d0qo01453bopenalex-snapshot
Recent advances in cascade radical cyclization of radical acceptors for the synthesis of carbo- and heterocycles
inferredcites →https://doi.org/10.1039/d0ra09198gopenalex-snapshot
Prescribed drugs containing nitrogen heterocycles: an overview
inferredcites →https://doi.org/10.1039/d1qo00550bopenalex-snapshot
Indolizine synthesis via radical cyclization and demethylation of sulfoxonium ylides and 2-(pyridin-2-yl)acetate derivatives

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.4676491openalex-extracted
Synthesis of Novel Π-Extended 2,5-Disubstituted Indolizines and Their Photophysical Properties
inferred← citeshttps://doi.org/10.2139/ssrn.4761082openalex-extracted
I2-Catalyzed Cascade Annulation of 2-(Pyridin-2-Yl)Acetate Derivatives with N,N-Dimethylenamine Ketones: Site-Selective Synthesis of Functionalized Indolizines
inferred← citeshttps://doi.org/10.1002/adsc.202300634openalex-snapshot
Cu(II)‐Catalyzed [3+2]‐Annulation of 2‐Pyridinyl‐substituted p ‐Quinone Methides with Enaminones: Access to Functionalized Indolizine Derivatives
inferred← citeshttps://doi.org/10.1002/adsc.202300812openalex-snapshot
Recent Advances in Visible‐Light‐Driven C−S Bond Formation
inferred← citeshttps://doi.org/10.1002/ajoc.202200569openalex-snapshot
AgOTf/Et3N Cooperative Catalysis Enabled One‐Pot Access to α‐(Indolizinylethyl)‐Substituted N‐Sulfonyl Ketimines via an Imino‐Alkyne Cyclization
inferred← citeshttps://doi.org/10.1002/cjoc.202400798openalex-snapshot
Recent Advances in the Development of Indolizine Scaffolds: Synthetic Methodology and Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/cssc.202401114openalex-snapshot
C−H Functionalization of Heteroarenes via Electron Donor‐Acceptor Complex Photoactivation
inferred← citeshttps://doi.org/10.1002/cssc.70642openalex-snapshot
Mechanochemical Tandem Reactions: A Sustainable and Direct Route to 1,2‐Di‐Functional Indolizines via In Situ Baylis–Hillman Reaction, Cyclocondensation, Electrophilic C–H Chalcogenocyanation
inferred← citeshttps://doi.org/10.1002/ejoc.202200261openalex-snapshot
Visible Light‐Promoted, Photocatalyst‐Free C(sp2)−H Bond Functionalization of Indolizines via EDA Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.202400013openalex-snapshot
Synthesis and Photochemical Characterization of Indolizine Fluorophores Obtained by a Multicomponent Palladium Iodide−Catalyzed Oxidative Aminocarbonylation Approach
inferred← citeshttps://doi.org/10.1002/slct.202202420openalex-snapshot
Dinitro Anacardic Acid Copper(II) Complex—A Bio‐based Catalyst for Room Temperature Synthesis of Indolizine
inferred← citeshttps://doi.org/10.1002/slct.73631openalex-snapshot
Di‐ tert‐ Butyl Peroxide: An Effective Oxidizing Agent for Oxidative Transformations in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/tcr.202400135openalex-snapshot
Recent Advances on the Construction of Functionalized Indolizine and Imidazo[1,2‐ a ]pyridine Derivatives
inferred← citeshttps://doi.org/10.1007/s11224-023-02193-1openalex-snapshot
Unveiling [3 + 2] cycloaddition reactions of pyridinium bis(methoxycarbonyl)methylides and pyridinium dicyanomethylides with cyclooctyne for indolizine synthesis from the molecular electron density theory perspective
inferred← citeshttps://doi.org/10.1016/b978-0-443-18939-5.00012-3openalex-snapshot
Six-membered ring systems: pyridines and benzo derivatives
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.113310openalex-snapshot
Cobalt-catalyzed highly enantioselective radical alkylation of indolizines with styrenes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111332openalex-snapshot
Fast and efficient one-pot ultrasound-mediated synthesis of solid state (full color tunable) fluorescent indolizine derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.117908openalex-snapshot
Recent developments in the synthesis of indolizines and their derivatives as compounds of interest in medicinal chemistry: a review
inferred← citeshttps://doi.org/10.1016/j.fuel.2025.136932openalex-snapshot
Multiscale study on supercritical water gasification of agricultural films plastics: from experimental performance to molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138980openalex-snapshot
Synthesis of novel π-extended 2,5-disubstituted indolizines and their absorption and fluorescence properties
inferred← citeshttps://doi.org/10.1016/j.scp.2025.102059openalex-snapshot
Synthesis of indolizines via Pd-catalyzed selective ring recasting of oxazolidines with deesterification of methyl acrylates
inferred← citeshttps://doi.org/10.1016/j.tet.2023.133787openalex-snapshot
Recent advances in the synthesis of N-fused heterocycles from N-aroylmethylpyrrole-2-carboxaldehyde derivatives via annulative functionalization strategies
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134015openalex-snapshot
I2−catalyzed cascade annulation of 2-(pyridin−2−yl)acetate derivatives with ,−dimethylenamine ketones: Site-selective synthesis of functionalized indolizines
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135178openalex-snapshot
Synthesis of 1,3-diaryl-5,6-dihydropyrrolo[2,1-a] isoquinolines via copper-promoted reaction of tetrahydroisoquinolines with α,β-unsaturated ketones under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2026.135249openalex-snapshot
Copper-catalyzed synthesis of 2,2,2-trifluoroethylated indolizines via [4 + 1] annulation of pyridinium 1,4-zwitterionic thiolates with 2-bromo-3,3,3-trifluoropropene
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01219openalex-snapshot
Synthesis of Ester-Substituted Indolizines from 2-Propargyloxypyridines and 1,3-Dicarbonyls
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00447openalex-snapshot
Copper-Catalyzed Formal [4 + 1] Annulation toward Diverse Trifunctionalized Indolizines from Pyridinium 1,4-Zwitterionic Thiolates and Diazos
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02024openalex-snapshot
Ag(I)-Mediated Annulation of 2-(2-Enynyl)pyridines and Propargyl Amines to Access 1-(2H-Pyrrol-3-yl)indolizines
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02459openalex-snapshot
Switchable Synthesis of Spirodihydroindolizines and Indolizines from Aurones and Pyridin-2-yl Active Methylene Compounds
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02522openalex-snapshot
Thermodynamic Controlled Regioselective C1-Functionalization of Indolizines with 3-Hydroxyisoindolinones via Brønsted Acid Catalyzed aza-Friedel–Crafts Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02879openalex-snapshot
Pyridinium Ylide-Mediated Diastereoselective Synthesis of Spirocyclopropanyl-pyrazolones via Cascade Michael/Substitution Reaction
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00064openalex-snapshot
Controlled and Site-Selective C–H/N–H Alkenylation, Dialkenylation, and Dehydrogenative β-Alkenylation of Various N-Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01006openalex-snapshot
Domino Approach to Heterocycles-Based Unsymmetrical Triarylmethanes through Heteroannulation of 2-(2-Enynyl)-pyridines with Enaminones
inferred← citeshttps://doi.org/10.1021/acs.joc.4c02385openalex-snapshot
Base-Promoted Regioselective Annulation of Pyridinium Ylides and Bromoalkynes for the Chemodivergent Synthesis of Indolizines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00026openalex-snapshot
Synthesis of Highly Functionalized Indolizines via NIS-Promoted Spiroannulation/Ring-Opening Aromatization of Alkylidene Oxindoles with 2-(Pyridin-2-yl)acetate Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00319openalex-snapshot
Bichromophoric Ruthenium Complexes for Photocatalyzed Late-Stage Synthesis of Trifluoromethylated Indolizines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00435openalex-snapshot
Dearomative Ring-Opening of N-Fused Heteroarenes: Access to Tetrasubstituted Alkenes and Ketimines
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00060openalex-snapshot
Assembly of 3-Acylaminoindolizines through Domino Reaction of 4-Alkylidene Oxazolones with 2-(Pyridin-2-yl)acetates
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00867openalex-snapshot
Iodine-Mediated Controlled and Odorless Mono- and Dithiolation of Indolizines with Sodium Sulfinates
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02905openalex-snapshot
B2pin2-Mediated Cascade Cyclization/Aromatization Reaction: Facial Access to Functionalized Indolizines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00177openalex-snapshot
Synthesis of Indolizines via Tf 2 O-Mediated Cascade Reaction of Pyridyl-enaminones with Thiophenols/Thioalcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01295openalex-snapshot
Reusable Supported Pyridine-Mediated Cascade Synthesis of trans-2,3-Dihydroindoles via In Situ-Generated N-Ylide
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02079openalex-snapshot
Access to SCF3-Substituted Indolizines via a Photocatalytic Late-Stage Functionalization Protocol
inferred← citeshttps://doi.org/10.1021/acsorginorgau.5c00110openalex-snapshot
C–C Bond Formation via Direct Functionalization of Indolizines with a Bichromophoric Ruthenium Photocatalyst
inferred← citeshttps://doi.org/10.1038/s42004-023-00828-2openalex-snapshot
A recyclable stereoauxiliary aminocatalyzed strategy for one-pot synthesis of indolizine-2-carbaldehydes
inferred← citeshttps://doi.org/10.1039/d2cc04395eopenalex-snapshot
Pd( ii )-catalyzed annulation of terminal alkynes with 2-pyridinyl-substituted p -quinone methides: direct access to indolizines
inferred← citeshttps://doi.org/10.1039/d2ob01400aopenalex-snapshot
Rh( ii )-catalyzed synthesis of 5 H -isochromeno[3,4- b ]indolizines from 4-diazoisochroman-3-imines and pyridines
inferred← citeshttps://doi.org/10.1039/d2ob01846bopenalex-snapshot
Transition metal-free annulative vinylene transfer via the 1,3-dipolar reaction of N -ylides: access to benzo-fused indolizines
inferred← citeshttps://doi.org/10.1039/d3gc03552bopenalex-snapshot
Weak-coordination-auxiliary aminocatalysis enables directed [3 + 2] cyclization for 2-acylindolizines
inferred← citeshttps://doi.org/10.1039/d3ob00346aopenalex-snapshot
One-pot organocatalyzed synthesis of tricyclic indolizines
inferred← citeshttps://doi.org/10.1039/d3ob00804eopenalex-snapshot
A reusable polymer anchored pyridine mediated formal [4 + 1] annulation reaction for the diastereoselective synthesis of 2,3-dihydrobenzofurans
inferred← citeshttps://doi.org/10.1039/d3ra03395copenalex-snapshot
Discovery of indolizine lactones as anticancer agents and their optimization through late-stage functionalization
inferred← citeshttps://doi.org/10.1039/d4cc00810copenalex-snapshot
One-pot C–N/C–C bond formation and oxidation of donor–acceptor cyclopropanes with tetrahydroisoquinolines: access to benzo-fused indolizines
inferred← citeshttps://doi.org/10.1039/d4qo00035hopenalex-snapshot
Regioselective electrochemical cascade C–H sulfonylation–bromination of indolizines to access difunctionalized indolizines
inferred← citeshttps://doi.org/10.1039/d4qo00580eopenalex-snapshot
Gold-catalyzed intermolecular tandem cyclization/[4 + 3] cycloaddition of 2-(1-alkynyl)-cyclopropyl pyridines with nitrones: an efficient strategy for the synthesis of [1,2]oxazepino[5,4- a ] indolizines
inferred← citeshttps://doi.org/10.1039/d4qo02082kopenalex-snapshot
Advances in the synthesis of indolizines and their π-expanded analogues: update 2016–2024
inferred← citeshttps://doi.org/10.1039/d5cc05424aopenalex-snapshot
Greening indolizine chemistry: advances in electro-/photochemical direct C–H functionalization
inferred← citeshttps://doi.org/10.1055/a-1934-1189openalex-snapshot
Use of Polymer-Supported 4-(N,N-Dimethylamino)pyridine in a Formal Conjugate Addition/Elimination Mediated by an N-Ylide Generated In Situ for the Construction of Highly Functionalized Itaconimides/Alkenes
inferred← citeshttps://doi.org/10.1055/a-2039-1728openalex-snapshot
Recent Advances in Electrochemical Cascade Cyclization Reactions
inferred← citeshttps://doi.org/10.1055/a-2262-9575openalex-snapshot
Transition-Metal-Catalyzed C–H Activation Reactions for the Creation and Modification of Organic Fluorophores
inferred← citeshttps://doi.org/10.1515/gps-2023-0046openalex-snapshot
Green “one-pot” fluorescent bis-indolizine synthesis with whole-cell plant biocatalysis
inferred← citeshttps://doi.org/10.71267/mencom.7789openalex-snapshot
Synthesis of 3-acylindolizines based on β-nitro-substituted benzochromenes and carbonyl-stabilized pyridinium ylides
inferred← citeshttps://doi.org/10.71267/mencom.8160openalex-snapshot
Synthesis of indolizines via the A3-coupling reaction catalyzed by Cu-Salphen-Zr metal-organic framework
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