Advances in the Synthesis of Benzo‐Fused Spiro Nitrogen Heterocycles: New Approaches and Modification of Old Strategies
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Title
Advances in the Synthesis of Benzo‐Fused Spiro Nitrogen Heterocycles: New Approaches and Modification of Old Strategies
Authors
Keywords
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Journal
HELVETICA CHIMICA ACTA
Volume 103, Issue 12, Pages -
Publisher
Wiley
Online
2020-11-26
DOI
10.1002/hlca.202000137
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- Synthesis of spiro[isoindole-1,5’-isoxazolidin]-3(2H)-ones as potential inhibitors of the MDM2-p53 interaction
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- Design and optimization of (3-aryl-1 H -indazol-6-yl)spiro[cyclopropane-1,3′-indolin]-2′-ones as potent PLK4 inhibitors with oral antitumor efficacy
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- Highly diastereoselective entry into chiral spirooxindole-based 4-methyleneazetidines via formal [2+2] annulation reaction
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- Highly Stereoselective [3+2] Cycloadditions of Chiral Palladium-ContainingN1-1,3-Dipoles: A Divergent Approach to Enantioenriched Spirooxindoles
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- A Convenient 1,3-Dipolar Cycloaddition Reaction for the Synthesis of Spirooxindoles and Some Other Spirocompounds Containing the 1,3,4-Oxadiazole Moiety
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- Anti-inflammatory Activity of Two New Indole Alkaloids from the Stems ofNauclea officinalis
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- Novel and one-pot Synthesis of Tetrahydropyrrolo[1,2-a ]-2-Methylbenzothiazole-3-Spiro-1′ -Cyclohexa-2′ ,5′ -Dien-4′ -one-4,5-Dicarboxylate Derivatives via a Three Component Reaction
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- Synthesis and biological evaluation of new spirooxindoles with embedded pharmacophores
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- DABCO-catalyzed unusual [4 + 2] cycloaddition reaction: non-substituted allenoate acts as a four-carbon synthon and facile synthesis of spirooxindoles
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- Stereoselective Synthesis of Alkylidene Phthalides
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- Preparation and Reactions of Indoleninyl Halides: Scaffolds for the Synthesis of Spirocyclic Indole Derivatives
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- Synthesis of new substituted acetamide derivatives of 6′,7′-dimethoxy-2′,3′-dihydro-1′H-spiro[isoquinoline-1,4′-cyclopentane]-1′-carboxamide
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- Recyclization of 5′-acetyl-2′-amino-6′-methyl-2-oxo-1,2-dihydrospiro[indole-3,4′-pyran]-3′-carbonitrile in reactions with some nitrogen binucleophiles
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- Efficient Synthesis of Spirooxindole-Fused 3-Thiazoline Derivatives by a One-Pot Asinger-Type Reaction
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- Palladium-Catalyzed Nitration of Arenes by 1,2,3-Triazole-Directed C–H Activation
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- Regioselective Michael Addition of Anthrone to Methyleneindolinones
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- Rh2(OAc)4 catalyzed highly diastereoselective synthesis of 2,4,5-triaryl-1,3-oxazolidines and spirooxindolyl oxazolidines
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- Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: synthesis of trihalomethylated spiro[indoline-3,2′-pyrrolidin]-2-ones and spiro[indoline-3,3′-pyrrolizin]-2-ones
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- A highly stereoselective, catalytic four-component synthesis of dispiroindolo-pyrrolidines/-imidazolidines via azomethine ylides
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- Highly efficient synthesis of enantioenriched fully-substituted spirocyclohexane oxindoles via a Michael-Michael-aldol cascade reaction
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- NHC-Catalyzed Enantioselective Dearomatizing Hydroacylation of Benzofurans and Benzothiophenes for the Synthesis of Spirocycles
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- Stereodivergent Synthesis of N-Heterocycles by Catalyst-Controlled, Activity-Directed Tandem Annulation of Diazo Compounds with Amino Alkynes
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- Sulfamic acid promoted one-pot three-component synthesis and cytotoxic evaluation of spirooxindoles
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- Stability enhancement of fluorophores for lighting up practical application in bioimaging
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- Furan's Gambit: Electrophile-Attack-Triggered Sacrifice of Furan Rings for the Intramolecular Construction of Azaheterocycles
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- Cottoquinazolines E and F fromNeosartorya fischeriNRRL 181
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- An Efficient Synthesis of Spiro-oxindole Derivatives by Three-Component Reactions in Water
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- Synthesis of spiro[indoline-3,4′-pyrano[2,3-c]pyrazole] and spiro[indoline-3,4′-pyrano[2,3-c]chromene] derivatives using silica-bonded ionic liquids as a recyclable catalyst in aqueous medium
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- New efficient fused-ring spiro[benzoanthracene-fluorene] dopant materials for blue fluorescent organic light-emitting diodes
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- Diverse synthesis of natural product inspired fused and spiro-heterocyclic scaffolds via ring distortion and ring construction strategies
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- Construction of dispirocyclohexanes via amine-catalyzed [2 + 2 + 2] annulations of Morita–Baylis–Hillman acetates with exocyclic alkenes
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- Facile synthesis of spirooxindole-pyrazolines and spirobenzofuranone-pyrazolines and their fungicidal activity
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- Convenient synthesis of functionalized spiro[indoline-3,2′-pyrrolizines] or spiro[indoline-3,3′-pyrrolidines] via multicomponent reactions
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- One-pot three components synthesis of novel 2-iminoquinazolines and 2-imino spiro[indoline-quinazoline/pyrimidine]ones catalyzed by sodium fluoride
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- Synthesis of new spiro compounds proceeding from 11H-Indeno[1,2-b]quinoxalin-2-one
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- Synthesis of 2-propanol derivatives of N-methyl-6′,7′-dimethoxy-2′,3′-dihydro-1′H-spiro[cyclopentan-1,4′-isoquinoline]-1′-carboxamide
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- Rhodamine-chloronicotinaldehyde-based “OFF–ON” chemosensor for the colorimetric and fluorescent determination of Al3+ ions
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- Recent Advances in Organocatalytic Cascade Reactions toward the Formation of Quaternary Stereocenters
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- Diastereoselective synthesis of spirooxindole derivatives via biocatalytic domino reaction
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- Polar [3+2] cycloaddition of isatin-3-imines with electrophilically activated heteroaromatic N-ylides: Synthesis of spirocyclic imidazo[1,2-a]pyridine and isoquinoline derivatives
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- Organocatalytic Asymmetric Vinylogous Michael Addition of 3-(2-Oxoindolin-3-ylidene)butanoates to Nitroalkenes Catalyzed by a Bifunctional Cinchona-Based Squaramide
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- Diverse Applications of Nitrones for the Synthesis of Heterocyclic Compounds
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- Oxidation reactions of azines: XIII. Synthesis, molecular structure, and oxidation reactions of 3-methyl-3,3′,4,4′,5,6-hexahydro-1′H,2H-spiro[benzo[f]isoquinoline-1,2′-naphthalen]-1′-one
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- Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis
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- Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3′-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions
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- Metal Complex Catalysis in the Synthesis of Spirocarbocycles
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- Four-Membered Ring-Containing Spirocycles: Synthetic Strategies and Opportunities
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- Iodine-Catalyzed Synthesis of Spiro[1,3,4-benzotriazepine-2,3′-indole]-2′,5(1H,1′H)-diones under Mild Conditions
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- The Discovery of Polo-Like Kinase 4 Inhibitors: Identification of (1R,2S)-2-(3-((E)-4-(((cis)-2,6-Dimethylmorpholino)methyl)styryl)-1H-indazol-6-yl)-5′-methoxyspiro[cyclopropane-1,3′-indolin]-2′-one (CFI-400945) as a Potent, Orally Active Antitumor Agent
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- The Discovery of Polo-Like Kinase 4 Inhibitors: Design and Optimization of Spiro[cyclopropane-1,3′[3H]indol]-2′(1′H)-ones as Orally Bioavailable Antitumor Agents
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- Silver-Catalyzed Tandem Hydroamination/Hydroarylation of 1-(2-Allylamino)phenyl-4-hydroxy-but-2-yn-1-ones to 1′-Allylspiro[indene-1,2′-indolin]-3′-ones
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- The Concise Synthesis of Spiro-Cyclopropane Compounds via the Dearomatization of Indole Derivatives
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- Biochemical and pharmacological characterization of isatin and its derivatives: from structure to activity
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- Synthesis of 4′-[3-methyl-5-thioxo-1H-1,2,4-triazol-4(5H)-yl]-2′,5′-diphenyl-2′,4′-dihydro spiro[indolin-3,3′[1,2,4]triazol]-2-one derivatives
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- Preparation, photochromism, and complex formation with metal ions of pyrazolylazomethine derivative of spirooxazine
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- Synthesis of 1′-substituted 4′,4′-dimethyl-6′-methoxy-4′H-spiro[cyclohexane-1,3′-isoquinolines]
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- Design, Synthesis, and Optimization of Balanced Dual NK1/NK3 Receptor Antagonists
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- Highly efficient [3 + 2] reaction of 3-vinylindoles with 3-indolylmethanols by Brønsted-acid catalysis
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- Phosphine-Catalyzed Rauhut-Currier Domino Reaction: A Facile Strategy for the Construction of Carbocyclic Spirooxindoles Skeletons
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- One-Pot, Three-Component Synthesis of Novel Spiro[3H-indole-3,2′-thiazolidine]-2,4′(1H)-diones in an Ionic Liquid as a Reusable Reaction Media
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- Synthesis of Monospiro-2-amino-4H-pyran Derivatives Catalyzed by Propane-1-sulfonic Acid-Modified Magnetic Hydroxyapatite Nanoparticles
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- One-Pot Synthesis of Dispiro[oxindole-3,3′-pyrrolidines] by Three-Component [3+2] Cycloadditions ofin situ-Generated Azomethine Ylides with 3-Benzylidene-2,3-dihydro-1H-indol-2-ones
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- One-Pot, Four-Component Synthesis of Novel Spiro[indeno[2,1-b]quinoxaline-11,4′-pyran]-2′-amines
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- Microwave-assisted Aqueous Multicomponent Reaction: Facile Synthesis of Polyfunctionalized Indoline-spiro Fused Pyran Derivatives
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- Distinct mechanisms for spiro-carbon formation reveal biosynthetic pathway crosstalk
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- Synthetic bacteriochlorins with integral spiro-piperidine motifs
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- Synthesis and Antimicrobial and Antifungal Activity of Carbamate-Functionized Spiro Compounds
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- New synthesis of nitro-substituted 3,1-benzoxazines
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- Spiro heterocyclization of 4,5-diaroyl-1H-pyrrole-2,3-diones with heterocyclic enamine
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- An organocatalytic Michael-aldol cascade: formal [3+2] annulation to construct enantioenriched spirocyclic oxindole derivatives
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- Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks
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- Fast, solvent-free and hydrogen-bonding-mediated asymmetric Michael addition in a ball mill
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- Diketopiperazine Alkaloids Produced by the Endophytic Fungus Aspergillus fumigatus from the Stem of Erythrophloeum fordiiOliv.
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- Enantioselective Halocyclization Using Reagents Tailored for Chiral Anion Phase-Transfer Catalysis
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- Facile Synthesis of Dispirooxindole-Fused Heterocycles via Domino 1,4-Dipolar Addition and Diels–Alder Reaction of in Situ Generated Huisgen 1,4-Dipoles
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- Phenyliodine Bis(trifluoroacetate)-Mediated Oxidative C–C Bond Formation: Synthesis of 3-Hydroxy-2-oxindoles and Spirooxindoles from Anilides
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- Two directions in spiroheterocyclization of 1H-pyrrole-2,3-diones upon the action of 3-arylamino-1H-inden-1-ones
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- A new ligand system based on 7′-hydroxy-3-methyl-8′-formyl-3,4-dihydro-2H-1,3-benzoxazine-2-spiro-2(H)-chromene Ferrocenoylhydrazone
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- Synthesis of spiroindoline phytoalexin (S)-(−)-spirobrassinin and its unnatural (R)-(+)-enantiomer
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- Diastereoselective synthesis of 3,3-disubstituted oxindoles from atropisomeric N-aryl oxindole derivatives
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- Aromatic Rings in Chemical and Biological Recognition: Energetics and Structures
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- Asymmetric Binary-Acid Catalysis with InBr3 in the Inverse-Electron-Demanding Hetero-Diels-Alder Reaction of Mono- and Bis-Substituted Cyclopentadienes: Remote Fluoro-Effect on Stereocontrol
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- Diversity-Oriented Synthesis of Novel 2′-Aminospiro[11H-indeno[1,2-b]quinoxaline-11,4′-[4H]pyran] Derivatives via a One-Pot Four-Component Reaction
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- Efficient and Chemoselective Methods for the Synthesis of Some Isobenzofuran and Spiro[isobenzofuran-1,2′-pyrrole] Derivatives
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- A New Four-Component Reaction for the Synthesis of Spiro[4H-indeno[1,2-b]pyridine-4,3′-[3H]indoles]
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- Organic Reaction in Water: A Highly Efficient and Environmentally Friendly Synthesis of Spiro Compounds Catalyzed by L-Proline
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- A Novel, One-Pot Four-Component Route to 2′-Thioxo-2′,3′-dihydrospiro[indole-3,6′-[1,3]thiazin]-2-one Derivatives
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- An efficient synthesis of fluorescent spiro[benzopyrazoloquinoline-indoline]triones and spiro[acenaphthylenebenzopyrazoloquinoline]triones
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- Diastereoselective synthesis of spiro derivatives of 3-substituted 2,3,4,4a,5,6-hexahydro-1H-benzo[c]quinolizines
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- Synthesis of new spiro compounds containing a carbamate group
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- Synthesis of 3-pyrrol-3′-yloxindoles with a carbamate function
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- L-proline-catalyzed 1,3-dipolar cycloaddition of some Schiff bases to methyl 4-[1-oxo-2-(2-oxo-2,3-dihydro-1H-indol-3-ylidene)ethyl]phenylcarbamate
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- Three-component synthesis of spiro compounds with a carbamate functionality
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- Total Synthesis of the Polycyclic Fungal Metabolite (±)-Communesin F
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- An Organocatalytic [3+2] Cyclisation Strategy for the Highly Enantioselective Synthesis of Spirooxindoles
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- Two Novel Sesquiterpenoids from the Roots of Ferula ferulaeoides (Steud.) Korov.
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- Efficient and Convenient Polyethylene Glycol (PEG)-Mediated Synthesis of Spiro-oxindoles
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- Discovery of (7R)-14-Cyclohexyl-7-{[2-(dimethylamino)ethyl](methyl) amino}-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylic Acid (MK-3281), a Potent and Orally Bioavailable Finger-Loop Inhibitor of the Hepatitis C Virus NS5B Polymerase
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- Pd-Catalyzed Assembly of Spirooxindole Natural Products: A Short Synthesis of Horsfiline
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- Synthesis of a Highly Luminescent Three-Dimensional Pyrene Dye Based on the Spirobifluorene Skeleton
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- First C−H Activation Route to Oxindoles using Copper Catalysis
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- Palladium-Catalyzed Carbo-Heterofunctionalization of Alkenes for the Synthesis of Oxindoles and Spirooxindoles
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- Investigation of complexation of functionalized 1,3-benzoxazinone spiropyrans with metal ions
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- Synthesis of 4′H-spiro[adamantane-2,3′-isoquinoline] derivatives
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- Five-membered 2,3-dioxo heterocycles: LXX. Spiro heterocyclization of 1H-pyrrole-2,3-diones by the action of 1,5-binucleophiles. Crystalline and molecular structure of ethyl 1′-benzyl-7-methoxy-3,3-dimethyl-1,2′-dioxo-5′-phenyl-1′,2,2′,3,4,10-hexahydro-1H-spiro[acridine-9,3′-pyrrole]-4′-carboxylate
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- Some condensations of methyl 4-acetylphenylcarbamate
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- Synthetic aspects of the oxidative amidation of phenols
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- Generation ofN-(tert-Butoxycarbonyl)indole-2,3-quinodimethane and Its [4+2]-Type Cycloaddition
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- Palladium-Catalyzed Highly Diastereoselective Oxidative Cascade Cyclization Reactions
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- Synthesis of fused 2′-amino-3′-R-spiro-[indole-3,4′-pyran]-2(1H)-ones
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- An Expedient Strategy for the Synthesis of Tryptamines and Other Heterocycles
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- Spiro Skeletons: A Class of Privileged Structure for Chiral Ligand Design
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- Mn(III)-based radical addition reactions of 2-nitroindole with activated CH compounds
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