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Phenyl Tributylstannyl Selenide as a Promising Reagent for Introducion of the Phenylseleno Group
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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/hlca.19800630823openalex-snapshot
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
inferredcites →https://doi.org/10.1016/0040-4039(76)80133-5openalex-snapshot
Selective and direct activation of O-esters. Conversion of phenyl and 2,2,2-trifluoroethyl esters into acyl imidazolides
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/s0022-328x(00)00265-5openalex-snapshot
New approaches to the synthesis of unsymmetrical diaryl selenides
inferredcites →https://doi.org/10.1016/s0040-4039(00)60019-9openalex-snapshot
New mild methodology for the synthesis of α-phenylthio and α-phenylseleno ketones
inferredcites →https://doi.org/10.1016/s0040-4039(00)61224-8openalex-snapshot
Palladium catalyzed cross-coupling and tandem cyclization-coupling of α-halo(thio)ethers with organotins
inferredcites →https://doi.org/10.1016/s0040-4039(00)61557-5openalex-snapshot
N-(Phenylseleno)phthalimide: A useful reagent for the α-selenylation of ketones and aldehydes.
inferredcites →https://doi.org/10.1016/s0040-4039(00)85720-2openalex-snapshot
A convenient method for the synthesis of α-phenylselenenyl 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(00)97143-0openalex-snapshot
Radical reaction of acetonyltributylstannane with α- (phenylseleno) carbonyl compounds: a novel procedure for preparation of 1,4-dicarbonyl compounds.
inferredcites →https://doi.org/10.1016/s0040-4039(00)99102-0openalex-snapshot
Palladium - catalyzed reactions of trialkylstannyl phenyl sulfides with alkenyl bromides. A new diastereoselective synthesis of (E)-1-alkenyl phenyl sulfides
inferredcites →https://doi.org/10.1016/s0040-4039(01)83509-7openalex-snapshot
The generation of uncomplexed phenyl selenide anion and its applicability to SN2 - type ester cleavages
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/ja00852a019openalex-snapshot
Organoselenium chemistry. Conversion of ketones to enones by selenoxide syn elimination
inferredcites →https://doi.org/10.1021/ja9714999openalex-snapshot
Carbon−Oxygen Reductive-Elimination from Nickel(II) Oxametallacycles and Factors That Control Formation of Ether, Aldehyde, Alcohol, or Ester Products
inferredcites →https://doi.org/10.1021/jo00128a024openalex-snapshot
Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters
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/jo00210a040openalex-snapshot
Coupling reactions of .alpha.-halo esters with allyl- and acetonyltin reagents. An improved synthesis of .alpha.-acetonyl-.gamma.-butyrolactone
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/jo00895a030openalex-snapshot
Olefin synthesis. Rate enhancement of the elimination of alkyl aryl selenoxides by electron-withdrawing substituents
inferredcites →https://doi.org/10.1021/jo00928a042openalex-snapshot
Organoselenium chemistry. Conversion of cyclic ketones and .beta.-dicarbonyl compounds to enones
inferredcites →https://doi.org/10.1021/ol990233zopenalex-snapshot
New Synthetic Method of Diorganyl Selenides: Palladium-Catalyzed Reaction of PhSeSnBu 3 with Aryl and Alkyl Halides
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/10.1023/a:1013460213633openalex-snapshot
Tributyltin Aryl Selenides as Efficient Arylselenating Agents. Synthesis of Diaryl and Aryl Organyl Selenides
inferredcites →https://doi.org/10.1080/00397917908064184openalex-snapshot
The Rearrangement of 2-Carbomethoxy-2-Phenylselenocyclohexanone1
inferredcites →https://doi.org/10.1080/00397919208021636openalex-snapshot
Mild Transformation of Telluro and Seleno Esters into Carboxylic Acid and Esters
inferredcites →https://doi.org/10.1246/bcsj.65.2848openalex-snapshot
A Convenient Preparation of 2,4,6-Trisubstituted 1,3,5-Triselenanes by Treating Aldehydes or Their Acetals with 2,2,4,4,6,6-Hexamethyl-1,3,5-triselena-2,4,6-tristannacyclohexane in the Presence of BF3·OEt2 and AlCl3
inferredcites →https://doi.org/10.1246/cl.1998.159openalex-snapshot
Activation of Sn-Se Bond: Regioselective Ring Opening Reaction of Epoxides with Tributylstannyl Phenylselenolate in the Presence of a Lewis Acid
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.4651064openalex-extracted
A Visible-Light Mediated Selenization of Olefins Catalyzed By Dithiocarbamate Anion
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0706openalex-snapshot
Synthesis of Organoselenium Compounds
inferred← citeshttps://doi.org/10.1002/9783527633388.ch3openalex-snapshot
The Formation of Csp 2 S and Csp 2 Se Bonds by Substitution and Addition Reactions Catalyzed by Transition Metal Complexes
inferred← citeshttps://doi.org/10.1002/adsc.200404355openalex-snapshot
A Convenient Synthesis of β‐Phenylselenocarbonyl Compounds by In‐TMSCl Promoted Cleavage of Diphenyl Diselenide and Subsequent Michael Addition
inferred← citeshttps://doi.org/10.1002/cctc.201402867openalex-snapshot
Copper Nanoparticles Catalyzed Se(Te)Se(Te) Bond Activation: A Straightforward Route Towards Unsymmetrical Organochalcogenides from Boronic Acids
inferred← citeshttps://doi.org/10.1002/chem.202005430openalex-snapshot
Synthetic Approaches to Selenoesters
inferred← citeshttps://doi.org/10.1002/chin.200335145openalex-snapshot
Phenyl Tributylstannyl Selenide as a Promising Reagent for Introduction of the Phenylseleno Group.
inferred← citeshttps://doi.org/10.1002/ejoc.200400177openalex-snapshot
Synthesis of Substituted Se‐Phenyl Selenocarboxylates from Terminal Alkynes
inferred← citeshttps://doi.org/10.1002/ejoc.200801171openalex-snapshot
Recent Advances in Organoselenium Chemistry
inferred← citeshttps://doi.org/10.1002/ejoc.202401399openalex-snapshot
Photoinduced, Decarboxylative Coupling of α‐Keto Acids with Diselenides to Form Selenoesters
inferred← citeshttps://doi.org/10.1002/hc.21461openalex-snapshot
Dehydrogenative Sn–E (E = S, Se) bond formation catalyzed by an iron complex
inferred← citeshttps://doi.org/10.1002/hlca.200800378openalex-snapshot
β‐Cyclodextrin‐Promoted Addition of Benzeneselenol to Conjugated Alkenes in Water
inferred← citeshttps://doi.org/10.1007/s00706-014-1188-7openalex-snapshot
α-Organylchalcogenation of aldehydes and ketones with diorganyl dichalcogenides promoted by K3PO4
inferred← citeshttps://doi.org/10.1007/s00706-020-02565-xopenalex-snapshot
Green synthesis and antibacterial activity of chalcogenoesters
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00049-0openalex-snapshot
Ketones: Dialkyl Ketones
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.11363-0openalex-snapshot
Selenoesters of All Oxidation States☆
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00092-8openalex-snapshot
Alkyl Chalcogenides: Selenium- and Tellurium-Based Functional Groups
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.03.033openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2003
inferred← citeshttps://doi.org/10.1016/j.ccr.2005.07.001openalex-snapshot
Syntheses and applications of organostannanes bonded to elements of groups XIV, XV, and XVI
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.02.029openalex-snapshot
A series of Se-ferrocenyl thiophene carboselenoates – Synthesis, solid-state structure and electrochemistry
inferred← citeshttps://doi.org/10.1016/j.tet.2009.01.072openalex-snapshot
Indium-mediated cleavage of diphenyl diselenide and diphenyl disulfide: efficient one-pot synthesis of unsymmetrical diorganyl selenides, sulfides, and selenoesters
inferred← citeshttps://doi.org/10.1016/j.tet.2010.07.023openalex-snapshot
A new odorless one-pot synthesis of thioesters and selenoesters promoted by Rongalite®
inferred← citeshttps://doi.org/10.1016/j.tet.2011.04.018openalex-snapshot
Zn in ionic liquid: an efficient reaction media for the synthesis of diorganyl chalcogenides and chalcogenoesters
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130624openalex-snapshot
Iron(III)-catalyzed synthesis of selenoesters from α-amino carbonyl derivatives at room temperature
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133978openalex-snapshot
Aluminum-catalyzed direct conversion of lactones to selenolactones in the presence of elemental selenium and its application in the indium-catalyzed syntheses of dibenzyl selenides from benzyl acetates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.03.106openalex-snapshot
Palladium-catalyzed phenyl-selenylation with n-Bu3SnSePh in one-pot two-step reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.01.068openalex-snapshot
α-Phenylselenenylation of aldehydes and ketones with diphenyl diselenide mediated by KF/Al2O3
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.09.093openalex-snapshot
KF/Al2O3 and PEG-400 as a recyclable medium for the selective α-selenation of aldehydes and ketones. Preparation of potential antimicrobial agents
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.04.125openalex-snapshot
Palladium-catalyzed alkynylselenation of acetylenedicarboxylates leading to enyne selenides and application to synthesis of multisubstituted aryl selenides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.08.076openalex-snapshot
Ionic liquid: an efficient and reusable media for seleno- and thioester synthesis promoted by indium
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.05.003openalex-snapshot
Bimetallic system for the synthesis of diorganyl selenides and sulfides, chiral β-seleno amines, and seleno- and thioesters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151920openalex-snapshot
Direct synthesis of regioselective α-allyl α-selanyl ketones and selanyl tetra-hydrofurans
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153317openalex-snapshot
Synthesis of selenol esters via the reaction of acyl chlorides with diselenides in the presence of Zn dust catalyzed by CoCl2·6H2O
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02028openalex-snapshot
Metal-Free Three-Component Coupling Reaction of Ketones with Electron-rich Arenes and Selenium Dioxide for the Synthesis of α-Arylselanyl Ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00173openalex-snapshot
General, Mild, and Metal-Free Synthesis of Phenyl Selenoesters from Anhydrides and Their Use in Peptide Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02757openalex-snapshot
Umpolung Synthesis of Selenoesters and Telluroesters via the Photoinduced Coupling of Acylsilanes with Electrophilic Chalcogen Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00896openalex-snapshot
Expeditious and Chemoselective Synthesis of α-Aryl and α-Alkyl Selenomethylketones via Homologation Chemistry
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02544openalex-snapshot
Redox-Neutral Synthesis of Selenoesters by Oxyarylation of Selenoalkynes under Mild Conditions
inferred← citeshttps://doi.org/10.1021/acsomega.5c07396openalex-snapshot
A Green, Facile Method for Selective α-Bromination of Flavanones
inferred← citeshttps://doi.org/10.1021/cr100347kopenalex-snapshot
Transition-Metal-Catalyzed C−S, C−Se, and C−Te Bond Formation via Cross-Coupling and Atom-Economic Addition Reactions
inferred← citeshttps://doi.org/10.1021/jo051266xopenalex-snapshot
Employment of Palladium Pincer-Complexes in Phenylselenylation of Organohalides
inferred← citeshttps://doi.org/10.1021/om200768mopenalex-snapshot
Aryl(trimethylsilyl)selenides as Reagents for the Synthesis of Mono- and Diselenoesters
inferred← citeshttps://doi.org/10.1021/om501027sopenalex-snapshot
Computational Study on the C–Heteroatom Bond Formation via Stille Cross-Coupling Reaction: Differences between Organoheterostannanes Me3SnAsPh2vs Me3SnPPh2
inferred← citeshttps://doi.org/10.1039/bk9781839167386-00300openalex-snapshot
Nucleophilic Chalcogen-containing Reagents
inferred← citeshttps://doi.org/10.1039/c002648dopenalex-snapshot
Efficient synthesis of selenoesters from acyl chlorides mediated by CuO nanopowder in ionic liquid
inferred← citeshttps://doi.org/10.1039/c1gc16243hopenalex-snapshot
Synthesis of selenol esters from diorganyl diselenides and acyl chlorides under solvent-free conditions and microwave irradiation
inferred← citeshttps://doi.org/10.1039/c2gc16541dopenalex-snapshot
On water preparation of phenylselenoesters
inferred← citeshttps://doi.org/10.1039/c4ob01159gopenalex-snapshot
Syntheses of thiol and selenol esters by oxidative coupling reaction of aldehydes with RYYR (Y = S, Se) under metal-free conditions
inferred← citeshttps://doi.org/10.1039/c4ra07983copenalex-snapshot
Syntheses of selenoesters through C–H selenation of aldehydes with diselenides under metal-free and solvent-free conditions
inferred← citeshttps://doi.org/10.1039/d1gc00049gopenalex-snapshot
Visible-light-induced oxidative coupling of vinylarenes with diselenides leading to α-aryl and α-alkyl selenomethyl ketones
inferred← citeshttps://doi.org/10.1039/d6ob01411aopenalex-snapshot
Visible-light driven macrocyclization of peptides: from a vinyl to an α-selenoketone motif
inferred← citeshttps://doi.org/10.1080/00397911.2022.2085050openalex-snapshot
(Phenylseleno)acetic acid based precursor for the regiospecific synthesis of 1-phenylseleno-2-alkanones*
inferred← citeshttps://doi.org/10.1080/10426500802040349openalex-snapshot
Selenophilicity of Copper in Selenium-Carbon Bond Formation from Selenous Acid Using Cu(II)/Sn(II) Reagent
inferred← citeshttps://doi.org/10.1080/10426507.2010.540605openalex-snapshot
Investigation on the Se-Acylation withN-Acylbenzotriazoles
inferred← citeshttps://doi.org/10.1080/10426507.2015.1024790openalex-snapshot
Silicon-Assisted Synthesis and Functionalization of Sulfurated and Selenated Compounds
inferred← citeshttps://doi.org/10.1246/cl.2005.1348openalex-snapshot
A Novel Route to the Synthesis of α-Arylselenosubstituted Carbonyl Compounds and Nitriles
inferred← citeshttps://doi.org/10.3184/030823404323000549openalex-snapshot
Reductive Cleavage of the Se–Se Bond in the Presence of a Zn/AlCl 3 System: Synthesis of Selenol Esters
inferred← citeshttps://doi.org/10.3390/molecules14093367openalex-snapshot
Cesium Carbonate-Catalyzed α-Phenylchalcogenation of Carbonyl Compounds with Diphenyl Dichalcogenide
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.78.1066openalex-snapshot
Dancing with Sulfur: Simple Preparation and Properties ofThiacalix[n]thiophene Derivatives
inferred← citeshttps://doi.org/10.6023/cjoc202507026openalex-snapshot
Indium-Promoted Efficient Synthesis of Se -Aryl-2,2-dimethylbutaneselenoates
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