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Zinc-Mediated Conversion of β-Keto Esters to γ-Keto Esters
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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C‐Acylation under Virtually Neutral Conditions
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Deprotonierung und diastereoselektive Alkylierung von Cyclopropancarbonsäure‐methylestern
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Heterocyclen durch Diensynthese, IV1) 3‐Hydroxypyrrole aus Diels‐Alder‐Addukten von Nitrosoverbindungen
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Synthese von 2‐siloxysubstituierten Cyclopropancarbonsäure‐methylestern
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Deprotonierung und diastereoselektive Alkylierung von 2‐siloxysubstituierten Cyclopropancarbonsäure‐methylestern
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Donor-acceptor-substituted cyclopropanes: Versatile building blocks in organic synthesis
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Investigation of complex networks of spin-spin coupling by two-dimensional NMR
inferredcites →https://doi.org/10.1016/0040-4020(68)89007-6openalex-snapshot
Synthesis of cyclopropanes by the reaction of olefins with dialkylzinc and methylene iodide
inferredcites →https://doi.org/10.1016/0040-4020(89)80035-3openalex-snapshot
Novel free radical ring-expansion reactions
inferredcites →https://doi.org/10.1016/s0040-4039(01)82791-xopenalex-snapshot
A novel route to cyclopropanes from olefins
inferredcites →https://doi.org/10.1016/s0040-4039(01)91751-4openalex-snapshot
A specific insertion of carbenes into carbon-carbon bonds
inferredcites →https://doi.org/10.1016/s0040-4039(01)93322-2openalex-snapshot
Free radical ring-expansion leading to novel six- and seven-membered heterocycles
inferredcites →https://doi.org/10.1016/s0040-4039(01)93745-1openalex-snapshot
-methylation of phenols with ethyl(iodomethyl)zinc
inferredcites →https://doi.org/10.1021/ja00218a020openalex-snapshot
1,2-Migrations in free radicals related to coenzyme B12-dependent rearrangements
inferredcites →https://doi.org/10.1021/ja00245a069openalex-snapshot
A new tributyltin hydride-based rearrangement of bromomethyl .beta.-keto esters. A synthetically useful ring expansion to .gamma.-keto esters
inferredcites →https://doi.org/10.1021/ja00255a071openalex-snapshot
Free radical ring expansion by three and four carbons
inferredcites →https://doi.org/10.1021/ja00811a023openalex-snapshot
Alkylation of dianions of .beta.-keto esters
inferredcites →https://doi.org/10.1021/ja951171kopenalex-snapshot
Spectroscopic Characterization of (Iodomethyl)zinc Reagents Involved in Stereoselective Reactions: Spectroscopic Evidence That IZnCH2I Is Not Zn(CH2I)2 + ZnI2 in the Presence of an Ether
inferredcites →https://doi.org/10.1021/jo00008a043openalex-snapshot
Synthesis of 1,4-keto esters and 1,4-diketones via palladium-catalyzed acylation of siloxycyclopropanes. Synthetic and mechanistic studies
inferredcites →https://doi.org/10.1021/jo00149a033openalex-snapshot
Methyl 5-triphenylphosphoranylidenelevulinate: a reagent for homologation of aldehydes to E-.delta.-ene-.gamma.-keto esters
inferredcites →https://doi.org/10.1021/jo00202a017openalex-snapshot
2-Siloxy-substituted methyl cyclopropanecarboxylates as building blocks in synthesis: efficient one-pot conversion to .gamma.-butyrolactones
inferredcites →https://doi.org/10.1021/jo00275a006openalex-snapshot
A selective method for the direct conversion of aldehydes into .beta.-keto esters with ethyl diazoacetate catalyzed by tin(II) chloride
inferredcites →https://doi.org/10.1021/jo00339a033openalex-snapshot
Metalloaldimines. 4. Reaction of lithium aldimines with carbonyl compounds and with activated alkyl halides
inferredcites →https://doi.org/10.1021/jo00342a002openalex-snapshot
Reactions of propargyl alcohols with amide acetals
inferredcites →https://doi.org/10.1080/00304948909356218openalex-snapshot
PREPARATION AND REACTIONS OF 4-OXOCARBONYL COMPOUNDS. A REVIEW
inferredcites →https://doi.org/10.1080/00397918408075721openalex-snapshot
Conversion of 1,3-Dicarbonyls to 1,4-Dicarbonyls
inferredcites →https://doi.org/10.1080/00397918508063863openalex-snapshot
The Double Simmons-Smith ReactionsVIASilatropies
inferredcites →https://doi.org/10.1246/bcsj.62.3537openalex-snapshot
A Convenient Reductive Removal of Benzylic Hydroxyl and Trimethylsilyloxyl Groups with Me3SiCl–NaI–MeCN Reagent
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Preparation and Applications of Functionalized Organozinc Compounds
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Formation of γ‐Keto Esters From β‐Keto Esters: Methyl 5,5‐Dimethyl‐4‐Oxohexanoate
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Discussion Addendum for: Formation of γ‐Keto Esters from β‐Keto Esters: Methyl 5,5‐dimethyl‐4‐oxohexanoate
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Cyclopropanation Mediated by Zinc Organometallics
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Preparation of Difunctional Compounds
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Formation of Nitriles, Carboxylic Acids, and Derivatives by Carbonyl Homologation and Degradation
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Homologation Reactions Based on Zinc Carbenoids and Related Reagents
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Zinc‐Catalyzed Organic Synthesis: CC, CN, CO Bond Formation Reactions
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Catalyst‐Dependent Chemoselective Formal Insertion of Diazo Compounds into C−C or C−H Bonds of 1,3‐Dicarbonyl Compounds
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Catalyst‐Dependent Chemoselective Formal Insertion of Diazo Compounds into C−C or C−H Bonds of 1,3‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1002/chin.199802046openalex-snapshot
ChemInform Abstract: Zinc‐Mediated Conversion of β‐Keto Esters to γ‐Keto Esters.
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Microwave‐Assisted Paal–Knorr Reaction – Three‐Step Regiocontrolled Synthesis of Polysubstituted Furans, Pyrroles and Thiophenes
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Towards the Total Synthesis of Vibsanin E, 15‐O‐Methylcyclovibsanin B,3‐Hydroxyvibsanin E, Furanovibsanin A, and 3‐O‐Methylfuranovibsanin A
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Formation of Five‐Membered Cyclic Orthoesters from Tribromides with Participation of a Neighboring Carbonyl Group
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Modern Developments in the Chemistry of Homoenolates
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Intermolecular Stetter Reactions on Morita‐Baylis‐Hillman Adducts: an Approach to Highly Functionalized 1,4‐Dicarbonyl Compounds
inferred← citeshttps://doi.org/10.1016/b978-0-12-386540-3.00017-4openalex-snapshot
The Story Behind the Total Synthesis of Vibsanin E and 5-epi-Vibsanin E
inferred← citeshttps://doi.org/10.1016/j.isci.2018.09.006openalex-snapshot
Silver-Catalyzed Regio- and Stereoselective Formal Carbene Insertion into Unstrained C−C σ-Bonds of 1,3-Dicarbonyls
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Carbene insertion reactions for the construction of C C and C − heteroatom bonds using surface modified Silica microspheres as catalysts
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A stable Copper-Modified silica microsphere catalyst for the synthesis of N-substituted carbazoles and organosilanes
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Tandem chain extension–iodomethylation reactions: formation of α-functionalized γ-keto carbonyls
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Tandem chain extension–Mannich reaction: an approach to β-proline derivatives
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Total syntheses via cyclopropanols
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Tandem homologation-acylation chemistry: Single and double homologation
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An unexpected Lewis acids-catalyzed tandem ring-opening rearrangement of vinylcyclopropane ketone with aryl aldehyde
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Expansion to Seven-Membered Rings
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Zinc carbenoid-mediated chain extension of β-keto amides
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Sp3 organozinc carbenoid homologation in organic synthesis
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Chain extension of amino acid skeletons: preparation of ketomethylene isosteres
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Organozinc mediated reactions
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Synthesis of cyclopropanols via cyclopropanation of zinc enolates
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The Journey of Schinortriterpenoid Total Syntheses
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Selective Carbon–Carbon Bond Cleavage of Cyclopropanols
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Spirocyclizations Involving Oxonium Ylides Derived from Cyclic α-Diazocarbonyl Compounds: An Entry into 6-Oxa-2-azaspiro[4.5]decane Scaffold
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Photochemical Synthesis of 1,4-Dicarbonyl Bifluorene Compounds via Oxidative Radical Coupling Using TEMPO as the Oxygen Atom Donor
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Copper-Catalyzed Three-Component Reactions of α-Ketoaldehyde, 1,3-Dicarbonyl Compound, and Organic Boronic Acid in Water: A Route to 1,4-Diketones
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Total Synthesis of the Labdane Diterpenes Galanal A and B from Geraniol
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Rh(II)-Catalyzed Spirocyclization of α-Diazo Homophthalimides with Cyclic Ethers
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Desulfonylative Methenylation of β-Keto Sulfones
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Asymmetric Total Synthesis of Pre-schisanartanin C
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Zinc-Mediated Chain Extension of β-Keto Phosphonates
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Zinc-Mediated Ring-Expansion and Chain-Extension Reactions of β-Keto Esters
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Zinc-Mediated Chain Extension Reaction of 1,3-Diketones to 1,4-Diketones and Diastereoselective Synthesis oftrans-1,2-Disubstituted Cyclopropanols
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A Mechanistic Investigation into the Zinc Carbenoid-Mediated Homologation Reaction by DFT Methods: Is a Classical Donor−Acceptor Cyclopropane Intermediate Involved?
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Zinc-Mediated C−C Bond Sigmatropic Rearrangement: A New and Efficient Methodology for the Synthesis of β-Diketones
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Formation of γ-Lactones through CAN-Mediated Oxidative Cleavage of Hemiketals
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Stereoselective Formation of a Functionalized Dipeptide Isostere by Zinc Carbenoid-Mediated Chain Extension
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Tandem Chain Extension−Aldol Reaction: Syn Selectivity with a Zinc Enolate
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Regioselective Ring Opening and Isomerization Reactions of 3,4-Epoxyesters Catalyzed by Boron Trifluoride
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Main group organometallics in organic synthesis
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Chapter 3. Organometallic chemistry . Part (ii) Stoichiometric methods
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26.12 Product Class 12: Seven-Membered and Larger-Ring Cyclic Ketones
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Efficient Synthesis of γ‐Keto Esters from Enamines and EDA
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FORMATION OF b-KETO ESTERS FROM b-KETO ESTERS: METHYL 5,5-DIMETHYL-4-OXOHEXANOATE
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Asymmetric Synthesis of a Potent hNK-1 Receptor Antagonist
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