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Aryl(trimethylsilyl)selenides as Reagents for the Synthesis of Mono- and Diselenoesters

https://doi.org/10.1021/om200768m

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What this work says

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

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A facile synthesis of potassium selenocarboxylates and their oxidation with XeF2 to diacyl diselenides: An X-ray structural analysis of di(4-methoxybenzoyl) diselenide

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Enantioselective Total Synthesis of the Nonisoprenoid Sesquiterpene (−)-Kumausallene

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Poly(p-phenylenephosphaalkene): A π-Conjugated Macromolecule Containing PC Bonds in the Main Chain

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Synthetic Metal‐Containing Polymers

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Carbon Monoxide/Water as a Reducing Agent: Formation of Selane from Selenium

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Synthesis and Characterization of O‐Triorganosilyl Selenocarboxylates

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Acyl carbamoyl selenides and related sulfur isologues: synthesis and x‐ray structural analyses

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Steroids and sex hormones. Part 262. The radical induced stannane reduction of selenoesters and selenocarbonates: A new method for the degradation of carboxylic acids to nor‐alkanes and for desoxygenation of alcohols to alkanes

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Synthesis and Characterization of trans‐PdII Trimethylsilylchalcogenolates

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Thio-, Seleno-, and Telluro-Carboxylic Acid Esters

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Neutral and Cationic Macromolecules based on Iron Sandwich Complexes

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Co2(CO)8-mediated and -catalyzed carbonylation of diaryl diselenides and ditellurides to seleno and telluro esters

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Synthèse de ferrocènes hétérodisubstitués à ancrage soufre ou sélénium via un précurseur original Fe(C5H4ELi)2,2THF (E S, Se). Nouvelle préparation des ferrocènes 1,1′-dithiol et -disélénol

inferredcites →https://doi.org/10.1016/0022-328x(89)80090-7openalex-snapshot

Acylderivate der ferrocenchalkogenole Fe(C5H5)(C5H4EH) und Fe(C5H4EH)2 (E = S, Se, Te)

inferredcites →https://doi.org/10.1016/0022-328x(89)87352-8openalex-snapshot

A new route to seleno and telluro esters by Co2(CO)8-mediated and -catalyzed carbonylation of diaryl diselenides and ditellurides with carbon monoxide

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Soluble, rigid-rod polyimides having phenyl substituted pyromellitic diimide units via Pd-catalysed polycondensation

inferredcites →https://doi.org/10.1016/0040-4039(94)02162-5openalex-snapshot

Stereoselective synthesis of cis-2,5-disubstituted tetrahydrofuran-3-ones via an acyl radical cyclization

inferredcites →https://doi.org/10.1016/0040-4039(95)00320-copenalex-snapshot

Methylenations of heteroatom-substituted carbonyls with dimethyl titanocene

inferredcites →https://doi.org/10.1016/j.jorganchem.2004.06.054openalex-snapshot

Synthesis, reactivity, electrochemical and crystallographic studies of diferrocenoyl diselenide and ferrocenoyl selenides

inferredcites →https://doi.org/10.1016/s0022-328x(00)00738-5openalex-snapshot

Electrochemical and NMR spectroscopic studies of selenium- and tellurium-substituted ferrocenes I: ferrocenyl alkyl chalcogenides [Fe(η-C5H5)(η-C5H4ER)]

inferredcites →https://doi.org/10.1016/s0040-4020(01)96721-3openalex-snapshot

Dimethylaluminum methaneselenolate—a useful reagent for the preparation of selenoesters. A new friedel-crafts acylation procedure promoted by Cu(I)

inferredcites →https://doi.org/10.1016/s0040-4039(00)00960-6openalex-snapshot

Indium(I) bromide-mediated bromocyanomethylation of carbonyl compounds

inferredcites →https://doi.org/10.1016/s0040-4039(00)87580-2openalex-snapshot

Homologation of selenoesters to (phenylseleno)- or (methylseleno)methyl ketones with diazomethane

inferredcites →https://doi.org/10.1016/s0040-4039(00)88340-9openalex-snapshot

Selenoesters in organic synthesis. 1. A novel synthesis of ketones.

inferredcites →https://doi.org/10.1016/s0040-4039(00)88341-0openalex-snapshot

Selenoesters in organic synthesis. 2. Synthesis of α,β -unsaturated ketones.

inferredcites →https://doi.org/10.1016/s0040-4039(02)00048-5openalex-snapshot

Synthesis of selenol esters: palladium-catalyzed coupling of phenyl tributylstannyl selenide with aryl iodides and carbon monoxide

inferredcites →https://doi.org/10.1021/ic980815xopenalex-snapshot

First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester

inferredcites →https://doi.org/10.1021/ja00026a013openalex-snapshot

Palladium-catalyzed addition and carbonylative addition of diaryl disulfides and diselenides to terminal acetylenes

inferredcites →https://doi.org/10.1021/ja000530vopenalex-snapshot

The First Example of Ammonium Selenothioates: Isolation and Characterization

inferredcites →https://doi.org/10.1021/ja001213ropenalex-snapshot

Isolable, Stable Diselenocarboxylate and Selenothiocarboxylate Salts: Syntheses, Structures, and Reactivities of 2-(1,3-Dimethylimidazolidinio)diselenocarboxylate and 2-(1,3-Dimethylimidazolidinio)selenothiocarboxylate

inferredcites →https://doi.org/10.1021/ja00181a033openalex-snapshot

New tandem radical cyclizations directed toward the synthesis of crinipellin A

inferredcites →https://doi.org/10.1021/ja00187a057openalex-snapshot

Cyclizations of ene radicals. Imidoyl radicals as intermediates in the synthesis of heterocyclic compounds

inferredcites →https://doi.org/10.1021/ja00522a079openalex-snapshot

Copper(I) promoted acylation reactions. A transition metal mediated version of the Friedel-Crafts reaction

inferredcites →https://doi.org/10.1021/ja026110iopenalex-snapshot

The First Ammonium Aromatic Diselenoates: Stable Heavy Congeners of Aromatic Carboxylic Acid Salts

inferredcites →https://doi.org/10.1021/ja060816lopenalex-snapshot

Phosphorus Copies of PPV: π-Conjugated Polymers and Molecules Composed of Alternating Phenylene and Phosphaalkene Moieties

inferredcites →https://doi.org/10.1021/ja993120jopenalex-snapshot

An Unusual Planar Diacyl Ditelluride (2-MeOC6H4COTe)2: The Origin of Its Planarity

inferredcites →https://doi.org/10.1021/jo00003a047openalex-snapshot

A practical and efficient method for the synthesis of .beta.-lactones

inferredcites →https://doi.org/10.1021/jo00012a006openalex-snapshot

Synthesis utilizing reducing ability of carbon monoxide: a new method for selective synthesis of diorgano selenides and diselenides using selenium-carbon monoxide-water reaction system

inferredcites →https://doi.org/10.1021/jo00031a021openalex-snapshot

Acyl radicals: intermolecular and intramolecular alkene addition reactions

inferredcites →https://doi.org/10.1021/jo00098a053openalex-snapshot

Synthesis of Thiol, Selenol, and Tellurol Esters from Aldehydes by the Reaction with iBu2AlYR (Y = S, Se, Te)

inferredcites →https://doi.org/10.1021/jo00206a017openalex-snapshot

Synthesis and multinuclear magnetic resonance study of para-substituted phenyl selenobenzoates

inferredcites →https://doi.org/10.1021/jo00249a053openalex-snapshot

Acyl radicals: functionalized free radicals for intramolecular cyclization reactions

inferredcites →https://doi.org/10.1021/jo00269a001openalex-snapshot

Phenyl selenoesters as effective precursors of acyl radicals for use in intermolecular alkene addition reactions

inferredcites →https://doi.org/10.1021/jo00393a015openalex-snapshot

Mild reductions of oxides of the Group 6a elements sulfur, selenium, and tellurium with (phenylseleno)trimethylsilane

inferredcites →https://doi.org/10.1021/jo00400a070openalex-snapshot

Aryl selenocyanates and aryl thiocyanates: reagents for the preparation of activated esters

inferredcites →https://doi.org/10.1021/jo00407a053openalex-snapshot

Dimethylaluminum methylselenolate: a remarkable reagent for the preparation of active acyl-transfer agents

inferredcites →https://doi.org/10.1021/jo01289a018openalex-snapshot

Substitution reactions of thallous thiophenoxide and thallous phenyl selenide with halogen-bearing substrates

inferredcites →https://doi.org/10.1021/jo026894iopenalex-snapshot

Phenyl Tributylstannyl Selenide as a Promising Reagent for Introducion of the Phenylseleno Group

inferredcites →https://doi.org/10.1021/jo0493727openalex-snapshot

Indium(I) Iodide-Promoted Cleavage of Diaryl Diselenides and Disulfides and Subsequent Condensation with Alkyl or Acyl Halides. One-Pot Efficient Synthesis of Diorganyl Selenides, Sulfides, Selenoesters, and Thioesters

inferredcites →https://doi.org/10.1021/jo051266xopenalex-snapshot

Employment of Palladium Pincer-Complexes in Phenylselenylation of Organohalides

inferredcites →https://doi.org/10.1021/jo960175kopenalex-snapshot

Stereoselective Construction of Cyclic Ethers via Intramolecular Acyl Radical Cyclizations: A Practical Solution to Decarbonylation

inferredcites →https://doi.org/10.1021/jo960349yopenalex-snapshot

Group Transfer Carbonylations: Photoinduced Alkylative Carbonylation of Alkenes Accompanied by Phenylselenenyl Transfer

inferredcites →https://doi.org/10.1021/jo961578nopenalex-snapshot

Tetrahydrofuran Derivatives from Epoxides via Group Transfer Cyclization or Reductive Radical Cyclization of Organotellurium and Organoselenium Intermediates

inferredcites →https://doi.org/10.1021/jo972144aopenalex-snapshot

Protecting Groups for Organoselenium Compounds

inferredcites →https://doi.org/10.1021/jo980710bopenalex-snapshot

Palladium-Mediated Reactions of Chloroformates with Phenylselenotris(trimethylsilyl)silane and Aryltellurotris(trimethylsilyl)silane: Improved Procedure for the Preparation of (Phenylseleno)- and (Aryltelluro)formates

inferredcites →https://doi.org/10.1021/jo991970bopenalex-snapshot

Stereoselective Synthesis of Cyclic Ethers Using Vinylogous Sulfonates as Radical Acceptors: Effect of E/Z Geometry and Temperature on Diastereoselectivity

inferredcites →https://doi.org/10.1021/ol016127qopenalex-snapshot

Construction of Tetrahydrofuran-3-ones from Readily Available Organochalcogen Precursors via Radical Carbonylation/Reductive Cyclization

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Indium(I) Iodide-Mediated Cleavage of Diphenyl Diselenide. An Efficient One-Pot Procedure for the Synthesis of Unsymmetrical Diorganyl Selenides

inferredcites →https://doi.org/10.1021/ol0354223openalex-snapshot

The Pt-Catalyzed Carboselenation of Alkynes by Selenoesters

inferredcites →https://doi.org/10.1021/ol051588nopenalex-snapshot

Rhodium-Catalyzed Reductive Coupling of Disulfides and Diselenides with Alkyl Halides, Using Hydrogen as a Reducing Agent

inferredcites →https://doi.org/10.1021/om00060a005openalex-snapshot

Palladium-catalyzed chemo- and site-selective reduction of (Z)-1,3-bis(arylseleno)-2-alken-1-ones with tributylstannane

inferredcites →https://doi.org/10.1021/om049721nopenalex-snapshot

Biphenylene-4,4‘-diselenolate as a Molecular Bridge: Preparation and Characterization of [PdCl(PnBu3)2Se-C6H4-C6H4-Se-PdCl(PnBu3)2]

inferredcites →https://doi.org/10.1021/om990589eopenalex-snapshot

Synthesis of Thiol, Selenol, and Tellurol Esters by the Reaction of Organochalcogeno Mercurials with Acid Chlorides

inferredcites →https://doi.org/10.1023/a:1013913816069openalex-snapshot

Tributylstannyl Aryl Selenides as Efficient Arylselenating Agents in the Synthesis of Seleno Esters

inferredcites →https://doi.org/10.1039/b010023oopenalex-snapshot

1,1′-Bis(trimethylsilylseleno)ferrocene in cluster synthesis: a redox active surface on a copper–selenide core

inferredcites →https://doi.org/10.1039/c39870000820openalex-snapshot

Evidence for the 1,3-silyl shift equilibrium between the CO- and CTe-bonded isomers of a stable trimethylsilyl tellurocarboxylate

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A Novel Method of Synthesis of 2-Methylthio-1,3-oxazoles

inferredcites →https://doi.org/10.1080/00397910008087155openalex-snapshot

Cleavage of Se-Se Bond by Sm/cat. CoCl2System: A Novel Method for the Synthesis of Selenoesters

inferredcites →https://doi.org/10.1080/00397919208021636openalex-snapshot

Mild Transformation of Telluro and Seleno Esters into Carboxylic Acid and Esters

inferredcites →https://doi.org/10.1080/00397919308009767openalex-snapshot

Reductive Cleavage of Se-Se and Te-Te Bond by Samarium Diiodide: Synthesis of Selenoesters, Telluroesters, Unsymmetrical Alkylphenyl Selenides and Tellurides

inferredcites →https://doi.org/10.1080/00397919908085925openalex-snapshot

Reductive Cleavage of the Se-Se Bond by the Sm/CrCl3System: A Novel One-Pot Method for the Synthesis of Selenoesters

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Water Accelerated Sm/TMSCl Reductive Cleavage of the Se-Se Bond: Synthesis of Selenoesters and Selenoformates

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A short history of SHELX

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METHODS IN SELENIUM CHEMISTRY IV. SYNTHETIC APPROACHES TO POLYDISELENIDES*

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Phenylene-1,4- and biphenylene-4,4′-diselenolate bridged complexes of gold(I)

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A FACILE PREPARATION OF TELLUROL ESTERS FROM PHENYLTELLUROTRIMETHYLSILANE AND ACYL CHLORIDES

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A Convenient One-pot Synthesis of Unsymmetrical Selenium Compounds Using Bis(trimethylsilyl) Selenide

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Facile Synthesis of Optically Active anti-α,β-Dihydroxy Ester Derivatives

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Isolation of Crystalline Potassium Alkanecarboselenoates

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/chem.201400185openalex-snapshot

New Polydentate Trimethylsilyl Chalcogenide Reagents for the Assembly of Polyferrocenyl Architectures

inferred← citeshttps://doi.org/10.1002/ejic.201800361openalex-snapshot

Formation of Multinuclear s‐Block Metal Systems by Enhancement of the Coordination Properties of 1,2,3‐Triazole

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Synthesis of Chloro‐Substituted β‐Ketiminate Palladium Complexes, Spectral and Thermal Investigation of their Structures

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Selenoesters of All Oxidation States☆

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Functions Containing Three Chalcogens (and No Halogens)

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Aryl ferrocenylmethylesters: Synthesis, solid-state structure and electrochemical investigations

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Preparation and characterization of new chiral ferrocenyl selenides

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inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.03.053openalex-snapshot

Ferrocenyl thiocarboxylates: Synthesis, solid-state structure and electrochemical investigations

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From ferrocenyl selenoesters to diferrocenyl methanols

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123170openalex-snapshot

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Tethered Polynuclear Copper–Chalcogenolate Assemblies Enabled via NHC Ligation

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The Chemistry of Selenosilanes: A Topic Overview

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