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Selenium and Tellurium Electrophiles in Organic Synthesis

https://doi.org/10.1515/psr-2017-0131

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inferredcites →https://doi.org/10.1002/(sici)1099-0690(199811)1998:11<2275::aid-ejoc2275>3.0.co;2-oopenalex-snapshot

Asymmetric Selenohydroxylation of Alkenes with Camphorselenenyl Sulfate

inferredcites →https://doi.org/10.1002/1521-3765(20020301)8:5<1125::aid-chem1125>3.0.co;2-iopenalex-snapshot

New and Efficient Chiral Selenium Electrophiles

inferredcites →https://doi.org/10.1002/adsc.200900095openalex-snapshot

Iron‐Catalyzed Ligand‐Free Carbon‐Selenium (or Tellurium) Coupling of Arylboronic Acids with Diselenides and Ditellurides

inferredcites →https://doi.org/10.1002/adsc.201100587openalex-snapshot

Copper‐Mediated One‐Pot Transformation of 2‐ N ‐Sulfonyl‐ aminoaryl Diselenides into Benzo[ b ][1,4]selenazines

inferredcites →https://doi.org/10.1002/adsc.201401159openalex-snapshot

Synthesis of Chalcogenophenes via Cyclization of 1,3‐Diynes Promoted by Iron(III) Chloride and Dialkyl Dichalcogenides

inferredcites →https://doi.org/10.1002/adsc.201501096openalex-snapshot

Cover Picture: Why Does Industry Not Use Immobilized Transition Metal Complexes as Catalysts? (Adv. Synth. Catal. 1/2016)

inferredcites →https://doi.org/10.1002/adsc.201600759openalex-snapshot

Iron‐Promoted Tandem Cyclization of 1,3‐Diynyl Chalcogen Derivatives with Diorganyl Dichalcogenides for the Synthesis of Benzo[b]furan‐Fused Selenophenes

inferredcites →https://doi.org/10.1002/adsc.201600855openalex-snapshot

A Transition‐Metal‐Free and Base‐Mediated Carbene Insertion into Sulfur‐Sulfur and Selenium‐Selenium Bonds: An Easy Access to Thio‐ and Selenoacetals

inferredcites →https://doi.org/10.1002/adsc.201700166openalex-snapshot

Copper‐Catalyzed Carbon‐Nitrogen/Carbon‐Selenium Bonds Formation: Synthesis of 2‐(Organochalcogenyl)‐indolizines

inferredcites →https://doi.org/10.1002/ajoc.201500192openalex-snapshot

Efficient Palladium‐Catalyzed Direct C−H Phenylselenylation of (Hetero)Arenes in Water

inferredcites →https://doi.org/10.1002/anie.199517261openalex-snapshot

Asymmetric Reaction of Arylalkenes with Diselenides

inferredcites →https://doi.org/10.1002/anie.200806148openalex-snapshot

Fast Synthesis of Benzofluorenes by Selenium‐Mediated Carbocyclizations

inferredcites →https://doi.org/10.1002/asia.201300882openalex-snapshot

Copper‐Catalyzed CH Bond Direct Chalcogenation of Aromatic Compounds Leading to Diaryl Sulfides, Selenides, and Diselenides by Using Elemental Sulfur and Selenium as Chalcogen Sources Under Oxidative Conditions

inferredcites →https://doi.org/10.1002/chem.19970031123openalex-snapshot

Asymmetric Addition Reactions with Optimized Selenium Electrophiles

inferredcites →https://doi.org/10.1002/chem.201600800openalex-snapshot

Regioselective, Solvent‐ and Metal‐Free Chalcogenation of Imidazo[1,2‐ a ]pyridines by Employing I 2 /DMSO as the Catalytic Oxidation System

inferredcites →https://doi.org/10.1002/chin.200238074openalex-snapshot

Synthesis of Cross‐Conjugated Geminal Enediynes via Palladium‐Catalyzed Cross‐Coupling Reaction of Ketene Butyltelluroacetals.

inferredcites →https://doi.org/10.1002/ejoc.200400686openalex-snapshot

Conjugated Additions of Selenium Containing Enolates to Enones – Enantioselective Synthesis of δ‐Oxo‐α‐Seleno Esters and Their Facile Transformations

inferredcites →https://doi.org/10.1002/ejoc.200600044openalex-snapshot

Syntheses and Reactions of New Optically Active Terpene Dialkyl Diselenides

inferredcites →https://doi.org/10.1002/ejoc.201000308openalex-snapshot

Diselenide‐ and Disulfide‐Mediated Synthesis of Isocoumarins

inferredcites →https://doi.org/10.1002/ejoc.201000514openalex-snapshot

Synthesis of New Sulfoxide‐Containing Diselenides and Unexpected Cyclization Reactions to 2,3‐Dihydro‐1,4‐benzoselenothiine 1‐Oxides

inferredcites →https://doi.org/10.1002/ejoc.201500766openalex-snapshot

Synthesis of 3‐Organoseleno‐Substituted Quinolines through Cyclization of 2‐Aminophenylprop‐1‐yn‐3‐ols Promoted by Iron(III) Chloride with Diorganyl Diselenides

inferredcites →https://doi.org/10.1002/ejoc.201600351openalex-snapshot

A One‐Pot Access to Benzo[b][1,4]selenazines from 2‐Aminoaryl Diselenides

inferredcites →https://doi.org/10.1002/hlca.19960790718openalex-snapshot

Chiral Diselenides from Benzylamines: Catalysts in the Diethylzinc Addition to Aldehydes

inferredcites →https://doi.org/10.1002/poc.610010308openalex-snapshot

Synthesis of optically active 2,2′‐diselenocyanato‐1,1′‐binaphthyl and its molecular structure. Hypervalent nature of divalent selenium atom in crystal state

inferredcites →https://doi.org/10.1007/3-540-48171-0_8openalex-snapshot

Selenoxide Elimination and [2,3]Sigmatropic Rearrangement

inferredcites →https://doi.org/10.1007/s11172-012-0013-xopenalex-snapshot

Cycloaddition of 2-pyridinetellurenyl chloride to alkenes

inferredcites →https://doi.org/10.1007/s11172-013-0139-5openalex-snapshot

Polar cycloaddition of 2-pyridinetellurium trichloride to multiple bonds

inferredcites →https://doi.org/10.1016/0014-5793(73)80755-0openalex-snapshot

Glutathione peroxidase: A selenoenzyme

inferredcites →https://doi.org/10.1016/0022-328x(95)05763-fopenalex-snapshot

Palladium-catalyzed cross-coupling reactions between organic tellurides and alkenes

inferredcites →https://doi.org/10.1016/0040-4039(95)00139-4openalex-snapshot

A new stereoselective synthesis of chiral tetrahydrothiopyrans and their corresponding sulfoxides

inferredcites →https://doi.org/10.1016/0040-4039(95)00976-jopenalex-snapshot

Asymmetric methoxyselenenylation of olefins using an optically active diaryl diselenide derived from d-mannitol

inferredcites →https://doi.org/10.1016/j.bmc.2017.03.013openalex-snapshot

Evaluation of selenide, diselenide and selenoheterocycle derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors

inferredcites →https://doi.org/10.1016/j.cclet.2015.05.029openalex-snapshot

Potassium bromide or sodium chloride catalyzed acetoxyselenenylation of alkenes with diselenides and mCPBA

inferredcites →https://doi.org/10.1016/j.cclet.2017.06.023openalex-snapshot

Iodine-mediated regioselective hydroxyselenenylation of alkenes: Facile access to β -hydroxy selenides

inferredcites →https://doi.org/10.1016/j.jorganchem.2009.06.009openalex-snapshot

The reaction of selenium dichloride with divinyl sulfide

inferredcites →https://doi.org/10.1016/j.jorganchem.2015.09.040openalex-snapshot

Palladium(II)-catalyzed switchable mono-/diselenylation of arenes controlled by solvent effects

inferredcites →https://doi.org/10.1016/j.tet.2006.03.090openalex-snapshot

Ultrasound-assisted synthesis of Z and E stilbenes by Suzuki cross-coupling reactions of organotellurides with potassium organotrifluoroborate salts

inferredcites →https://doi.org/10.1016/j.tet.2012.08.034openalex-snapshot

Selenenylations of alkenes with styrene nucleophiles

inferredcites →https://doi.org/10.1016/j.tet.2013.04.124openalex-snapshot

Copper-catalyzed C–Se coupling of diphenyl diselenide with arylboronic acids at room temperature

inferredcites →https://doi.org/10.1016/j.tetlet.2004.11.160openalex-snapshot

Synthesis of 1,3-enynes via Suzuki-type reaction of vinylic tellurides and potassium alkynyltrifluoroborate salts

inferredcites →https://doi.org/10.1016/j.tetlet.2005.03.073openalex-snapshot

Convenient route to dialkyl diselenides from alkyl tosylates. Synthesis of di(cis-myrtanyl) diselenide

inferredcites →https://doi.org/10.1016/j.tetlet.2006.05.088openalex-snapshot

Palladium-catalyzed cross-coupling of vinylic tellurides and potassium vinyltrifluoroborate salt: synthesis of 1,3-dienes

inferredcites →https://doi.org/10.1016/j.tetlet.2006.08.068openalex-snapshot

N-Phenylselenosaccharin (NPSSac): a new electrophilic selenium-containing reagent

inferredcites →https://doi.org/10.1016/j.tetlet.2006.09.024openalex-snapshot

Selenium-catalyzed iodohydrin formation from alkenes

inferredcites →https://doi.org/10.1016/j.tetlet.2008.05.129openalex-snapshot

Chemoselective cross-coupling Suzuki–Miyaura reaction of (Z)-(2-chlorovinyl)tellurides and potassium aryltrifluoroborate salts

inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.164openalex-snapshot

Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid

inferredcites →https://doi.org/10.1016/j.tetlet.2009.03.078openalex-snapshot

Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides

inferredcites →https://doi.org/10.1016/j.tetlet.2009.09.052openalex-snapshot

CuO nanoparticles: an efficient and recyclable catalyst for cross-coupling reactions of organic diselenides with aryl boronic acids

inferredcites →https://doi.org/10.1016/j.tetlet.2011.06.025openalex-snapshot

Negishi cross-coupling of organotellurium compounds: synthesis of biaryls, aryl-, and diaryl acetylenes

inferredcites →https://doi.org/10.1016/s0040-4020(01)96722-5openalex-snapshot

N-phenylselenophthalimide (NPSP)

inferredcites →https://doi.org/10.1016/s0040-4020(01)96781-xopenalex-snapshot

Phenylselenenyl chloride in acetonitrile-water

inferredcites →https://doi.org/10.1016/s0040-4020(96)01166-0openalex-snapshot

Design of optically active selenium reagents having a chiral tertiary amino group and their application to asymmetric inter- and intramolecular oxyselenenylations

inferredcites →https://doi.org/10.1016/s0040-4020(98)01133-8openalex-snapshot

Asymmetric electrophilic methoxyselenenylations and cyclizations with 3-camphorseleno derivatives

inferredcites →https://doi.org/10.1016/s0040-4039(00)00358-0openalex-snapshot

Efficient asymmetric selenomethoxylation and selenohydroxylation of alkenes with a new sulfur containing chiral diselenide

inferredcites →https://doi.org/10.1016/s0040-4039(00)76844-4openalex-snapshot

Synthesis of chiral diferrocenyl diselenides and their application to asymmetric reactions

inferredcites →https://doi.org/10.1016/s0040-4039(00)78554-6openalex-snapshot

A highly selective asymmetric methoxyselenylation of alkenes with a chiral ferrocenylselenium reagent

inferredcites →https://doi.org/10.1016/s0040-4039(00)96489-xopenalex-snapshot

Cyclization of olefinic alcohol by benzeneselenenyl triflate

inferredcites →https://doi.org/10.1016/s0040-4039(00)99480-2openalex-snapshot

The reaction of diphenyl diselenide with peroxydisulphate ions in methanol a convenient procedure to effect the methoxyselenenylation of alkenes

inferredcites →https://doi.org/10.1016/s0040-4039(03)00098-4openalex-snapshot

Sonogashira cross-coupling reaction of organotellurium dichlorides with terminal alkynes

inferredcites →https://doi.org/10.1016/s0040-4039(97)01030-7openalex-snapshot

2,6-Bis[(2S)-tetrahydrofuran-2-yl]phenyl diselenide: An effective reagent for asymmetric electrophilic addition reactions to olefins

inferredcites →https://doi.org/10.1016/s0040-4039(98)00252-4openalex-snapshot

Asymmetric selenomethoxylation of alkenes with camphorselenenyl sulfate

inferredcites →https://doi.org/10.1016/s0040-4039(98)01141-1openalex-snapshot

Asymmetric arene-alkene cyclizations mediated by a chiral organoselenium reagent

inferredcites →https://doi.org/10.1016/s0040-4039(99)00773-xopenalex-snapshot

Coupling of Z-vinylic tellurides with alkynes catalysed by : synthesis of Z-enynes and Z-enediynes

inferredcites →https://doi.org/10.1016/s0040-4039(99)02087-0openalex-snapshot

Palladium-catalyzed cross-coupling reactions of dimethyl- and diethylzinc with unsaturated organotellurium compounds

inferredcites →https://doi.org/10.1016/s0957-4166(00)00469-9openalex-snapshot

New nitrogen containing chiral diselenides: synthesis and asymmetric addition reactions to olefins

inferredcites →https://doi.org/10.1016/s0957-4166(98)00031-7openalex-snapshot

Catalytic asymmetric oxyselenenylation–elimination reactions using chiral selenium compounds

inferredcites →https://doi.org/10.1016/s0957-4166(98)00380-2openalex-snapshot

Synthesis of a new chiral nitrogen containing diselenide as a precursor for selenium electrophiles

inferredcites →https://doi.org/10.1021/acs.joc.5b01448openalex-snapshot

Iron-Catalyzed Cyclization of Alkynols with Diorganyl Diselenides: Synthesis of 2,5-Dihydrofuran, 3,6-Dihydro-2H-pyran, and 2,5-Dihydro-1H-pyrrole Organoselanyl Derivatives

inferredcites →https://doi.org/10.1021/acs.joc.6b02108openalex-snapshot

Silver-Catalyzed Synthesis of Diaryl Selenides by Reaction of Diaryl Diselenides with Aryl Boronic Acids

inferredcites →https://doi.org/10.1021/acs.joc.7b00050openalex-snapshot

Sequential Carbon–Carbon/Carbon–Selenium Bond Formation Mediated by Iron(III) Chloride and Diorganyl Diselenides: Synthesis and Reactivity of 2-Organoselenyl-Naphthalenes

inferredcites →https://doi.org/10.1021/acs.joc.7b02368openalex-snapshot

Synthesis of Allahabadolactone A

inferredcites →https://doi.org/10.1021/acs.orglett.5b00213openalex-snapshot

Organoselenium-Catalyzed, Hydroxy-Controlled Regio- and Stereoselective Amination of Terminal Alkenes: Efficient Synthesis of 3-Amino Allylic Alcohols

inferredcites →https://doi.org/10.1021/acs.orglett.5b01156openalex-snapshot

Selenium-Catalyzed Oxidative C(sp2)–H Amination of Alkenes Exemplified in the Expedient Synthesis of (Aza-)Indoles

inferredcites →https://doi.org/10.1021/acs.orglett.5b02511openalex-snapshot

Copper-Mediated Remote C–H Bond Chalcogenation of Quinolines on the C5 Position

inferredcites →https://doi.org/10.1021/acs.orglett.6b01130openalex-snapshot

Oxidative Allylic Esterification of Alkenes by Cooperative Selenium-Catalysis Using Air as the Sole Oxidant

inferredcites →https://doi.org/10.1021/acs.orglett.6b01420openalex-snapshot

Copper-Catalyzed 8-Aminoquinoline-Directed Selenylation of Arene and Heteroarene C–H Bonds

inferredcites →https://doi.org/10.1021/acs.orglett.6b03735openalex-snapshot

Transition-Metal-Free Selective Oxidative C(sp 3 )–S/Se Coupling of Oxindoles, Tetralone, and Arylacetamides: Synthesis of Unsymmetrical Organochalcogenides

inferredcites →https://doi.org/10.1021/ar50133a004openalex-snapshot

Functional group manipulation using organoselenium reagents

inferredcites →https://doi.org/10.1021/ja00507a069openalex-snapshot

N-Phenylselenophthalimide (N-PSP) and N-phenylselenosuccinimide (N-PSS). Two versatile carriers of the phenylseleno group. Oxyselenation of olefins and a selenium-based macrolide synthesis

inferredcites →https://doi.org/10.1021/ja00789a055openalex-snapshot

Mild procedure for the conversion of epoxides to allylic alcohols. First organoselenium reagent

inferredcites →https://doi.org/10.1021/jo00066a010openalex-snapshot

Asymmetric selenomethoxylation of olefins involving a chiral C2 symmetrical electrophilic organoselenium reagent

inferredcites →https://doi.org/10.1021/jo00108a038openalex-snapshot

1,3-Diselenetanes and 1,3-Dithietanes Derived from Camphor. Formation, Structure, Stereochemistry, and Oxidation to Selenoxide and Sulfoxide Products

inferredcites →https://doi.org/10.1021/jo00118a031openalex-snapshot

Synthesis of [R,S;R,S]- and [S,R;S,R]-Bis[2-[1-(dimethylamino)ethyl]ferrocenyl] Diselenides and Their Application to Asymmetric Selenoxide Elimination and [2,3]Sigmatropic Rearrangement

inferredcites →https://doi.org/10.1021/jo00119a055openalex-snapshot

Asymmetric Ring Closure Reactions Mediated by a Chiral C2 Symmetrical Organoselenium Reagent

inferredcites →https://doi.org/10.1021/jo00289a010openalex-snapshot

Ring-closure reactions initiated by the peroxydisulfate ion oxidation of diphenyl diselenide

inferredcites →https://doi.org/10.1021/jo01337a046openalex-snapshot

Selenium-catalyzed nonradical chlorination of olefins with N-chlorosuccinimide

inferredcites →https://doi.org/10.1021/jo016061copenalex-snapshot

Asymmetric Methoxyselenenylations and Cyclizations with 3-Camphorseleno Electrophiles Containing Oxime Substituents at C-2. Formation of an Unusual Oxaselenazole from an Oxime-Substituted Selenenyl Bromide

inferredcites →https://doi.org/10.1021/jo048460oopenalex-snapshot

Selenium-Catalyzed Halolactonization: Nucleophilic Activation of Electrophilic Halogenating Reagents

inferredcites →https://doi.org/10.1021/jo052061ropenalex-snapshot

Suzuki−Miyaura Cross-Coupling Reactions of Aryl Tellurides with Potassium Aryltrifluoroborate Salts

inferredcites →https://doi.org/10.1021/jo060760dopenalex-snapshot

Solid-Phase Selenium-Catalyzed Selective Allylic Chlorination of Polyprenoids: Facile Syntheses of Biologically Active Terpenoids

inferredcites →https://doi.org/10.1021/jo062131+openalex-snapshot

Convenient Synthesis of Unsymmetrical Organochalcogenides Using Organoboronic Acids with Dichalcogenides via Cleavage of the S−S, Se−Se, or Te−Te Bond by a Copper Catalyst

inferredcites →https://doi.org/10.1021/jo301486copenalex-snapshot

Isoselenazolones as Catalysts for the Activation of Bromine: Bromolactonization of Alkenoic Acids and Oxidation of Alcohols

inferredcites →https://doi.org/10.1021/jo502621aopenalex-snapshot

Catalytic Chalcogenylation under Greener Conditions: A Solvent-Free Sulfur- and Seleno-functionalization of Olefins via I2/DMSO Oxidant System

inferredcites →https://doi.org/10.1021/jo951919hopenalex-snapshot

Practical Synthesis of (R,R)- and (S,S)-Bis[2,6-bis(1-ethoxyethyl)phenyl] Diselenide

inferredcites →https://doi.org/10.1021/jo970982zopenalex-snapshot

Asymmetric Methoxyselenenylation of Alkenes with Chiral Ferrocenylselenium Reagents

inferredcites →https://doi.org/10.1021/ol000187zopenalex-snapshot

New Chiral Auxiliaries for Highly Stereoselective Asymmetric Methoxyselenenylations

inferredcites →https://doi.org/10.1021/ol036525oopenalex-snapshot

Selective Selenocatalytic Allylic Chlorination

inferredcites →https://doi.org/10.1021/ol071223yopenalex-snapshot

Catalytic Use of Selenium Electrophiles in Cyclizations

inferredcites →https://doi.org/10.1021/ol100274eopenalex-snapshot

Selenium-Mediated Synthesis of Biaryls through Rearrangement

inferredcites →https://doi.org/10.1021/ol202800kopenalex-snapshot

Selenium-Catalyzed Regioselective Cyclization of Unsaturated Carboxylic Acids Using Hypervalent Iodine Oxidants

inferredcites →https://doi.org/10.1039/a806707dopenalex-snapshot

Asymmetric methoxyselenenylations with camphor-based selenium electrophiles

inferredcites →https://doi.org/10.1039/a909819dopenalex-snapshot

Bis[2-(2-pyridyl)phenyl] diselenide, a more effective catalyst for oxidation of alcohols to carbonyl compounds

inferredcites →https://doi.org/10.1039/b003237iopenalex-snapshot

A novel ferrocenyl diselenide for the catalytic asymmetric aryl transfer to aldehydes

inferredcites →https://doi.org/10.1039/b004645kopenalex-snapshot

Cr(salen) catalysed asymmetric ring opening reactions of epoxides in room temperature ionic liquids

inferredcites →https://doi.org/10.1039/b914533hopenalex-snapshot

Lewis acid InBr3-catalyzed arylation of diorgano diselenides and ditellurides with arylboronic acids

inferredcites →https://doi.org/10.1039/c1gc15725fopenalex-snapshot

Synthesis of diaryl selenides using electrophilic selenium species and nucleophilic boron reagents in ionic liquids

inferredcites →https://doi.org/10.1039/c2gc16427bopenalex-snapshot

Glycerol as a recyclable solvent for copper-catalyzed cross-coupling reactions of diaryl diselenides with aryl boronic acids

inferredcites →https://doi.org/10.1039/c39880001283openalex-snapshot

Synthesis of selenium-containing binaphthyls and their application to the asymmetric ring-opening of cyclohexene oxide

inferredcites →https://doi.org/10.1039/c39900000129openalex-snapshot

Double differentiation in asymmetric methoxyselenenylation of trans-β-methylstyrene

inferredcites →https://doi.org/10.1039/c39940000515openalex-snapshot

Unexpected formation of 1,3-diselenetanes from the reaction of camphor enolate with selenium

inferredcites →https://doi.org/10.1039/c39950001641openalex-snapshot

Asymmetric intramolecular selenoetherification and selenolactonization using an optically active diaryl diselenide derived from D-mannitol

inferredcites →https://doi.org/10.1039/c39950002321openalex-snapshot

Highly selective asymmetric intramolecular selenocyclisation

inferredcites →https://doi.org/10.1039/c5qo00179jopenalex-snapshot

Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination

inferredcites →https://doi.org/10.1039/c6nj00487copenalex-snapshot

New diphenyl diselenides o-substituted by an O(S,Se)-caranyl skeleton – synthesis and application in asymmetric reactions

inferredcites →https://doi.org/10.1039/c7gc02803bopenalex-snapshot

Visible-light-mediated aerobic selenation of (hetero)arenes with diselenides

inferredcites →https://doi.org/10.1039/cc9960002567openalex-snapshot

Asymmetric cyclization of unsaturated alcohols and carboxylic acids with camphor-based selenium electrophiles

inferredcites →https://doi.org/10.1055/s-1995-4978openalex-snapshot

Regioselective Phenylselenenylation at the 5-Position of Pyrimidine Nucleosides Mediated by Manganese(III) Acetate

inferredcites →https://doi.org/10.1055/s-1997-1210openalex-snapshot

Vinylic Selenides and Tellurides - Preparation, Reactivity and Synthetic Applications

inferredcites →https://doi.org/10.1055/s-1998-2011openalex-snapshot

Stereoselective Isoquinoline Alkaloid Synthesis with New Diselenides

inferredcites →https://doi.org/10.1055/s-2002-31922openalex-snapshot

Synthesis of Cross-Conjugated Geminal Enediynes via Palladium Catalyzed Cross-Coupling Reaction of Ketene Butyltelluroacetals

inferredcites →https://doi.org/10.1055/s-2008-1078507openalex-snapshot

Ultrasound-Assisted Synthesis of Functionalized 1,3-Enynes by Palladium-Catalyzed Cross-Coupling Reaction of α-Styrylbutyltelluride with Alkynyltrifluoroborate Salts

inferredcites →https://doi.org/10.1080/00397911.2017.1364766openalex-snapshot

Ammonium iodide-mediated regioselective chalcogenation of chromones with diaryl disulfides and diselenides

inferredcites →https://doi.org/10.1080/00397919808007007openalex-snapshot

Iodosobenzene Diacetate and Diphenyl Diselenide: An Electrophilic Selenenylating Agent of Double Bonds

inferredcites →https://doi.org/10.1080/10426500590907282openalex-snapshot

Synthesis of a Selenium-Substituted Diselenide

inferredcites →https://doi.org/10.1080/10426500902930167openalex-snapshot

Synthesis of Chiral Acetals by Asymmetric Selenenylations

inferredcites →https://doi.org/10.1080/10426509208045843openalex-snapshot

Asymmetric Trans-Addition Reactions Using Chiral Selenobinaphthyls

inferredcites →https://doi.org/10.1080/10426509808042615openalex-snapshot

Chiral Diferrocenyl Dichalcogenides in Asymmetric Synthesis

inferredcites →https://doi.org/10.1246/bcsj.64.416openalex-snapshot

Oxidative Cleavage of Diselenide by m-Nitrobenzenesulfonyl Peroxide. Novel Method for the Electrophilic Benzeneselenenylations of Olefins and Aromatic Rings

inferredcites →https://doi.org/10.1246/cl.1987.849openalex-snapshot

Stereoselective Selenolactonization by Superelectrophilic Benzeneselenenyl Triflate

inferredcites →https://doi.org/10.1246/cl.1988.1895openalex-snapshot

Asymmetric Trans-addition Reactions of a Chiral Selenobinaphthyl with Prochiral Olefins. The Case of Methoxyselenenylation

inferredcites →https://doi.org/10.1246/cl.1990.1123openalex-snapshot

Hydrochlorination of Acryloylureas Using Titanium Tetrachloride and 2-Propanol

inferredcites →https://doi.org/10.1246/cl.1992.1123openalex-snapshot

Asymmetric Oxyselenenylation of Olefins Using Optically Active Selenobinaphthyls and d-Menthol as a Nucleophile

inferredcites →https://doi.org/10.1246/cl.1999.245openalex-snapshot

Highly Diastereoselective Reduction of Chiral (Ferrocenylseleno)methyl Aryl and Alkyl Ketones

inferredcites →https://doi.org/10.3390/ecsoc-16-01013openalex-snapshot

New Chiral Electrophilic Selenium Reagents: Synthesis and Structural Investigation

inferredcites →https://doi.org/10.3390/molecules200610866openalex-snapshot

Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement

inferredcites →https://doi.org/10.3998/ark.5550190.p009.756openalex-snapshot

Reactivity of dipinanyl diselenides functionalized at C-10-position with -CH2O(Se)Ph, -OH and -OCPh3 substituents

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.4765835openalex-extracted

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inferred← citeshttps://doi.org/10.1016/j.ica.2021.120272openalex-snapshot

Cu(II) and Ag(I) complexes of the pyrazole-derived diorganoselenide (pzCH2CH2)2Se. Synthesis, solid state structure and solution behavior

inferred← citeshttps://doi.org/10.1021/acs.joc.3c01577openalex-snapshot

Palladium-Catalyzed Direct Selanylation of Chalcogenophenes and Arenes Assisted by 2-(Methylthio)amide

inferred← citeshttps://doi.org/10.1021/acscatal.4c01660openalex-snapshot

Cyclopropenium Sulfide as Lewis Base Catalyst for Chemoselective and Regioselective Electrophilic Selenylation of Phenols

inferred← citeshttps://doi.org/10.1021/acsomega.2c00323openalex-snapshot

Selective Synthesis of Bis-Heterocycles via Mono- and Di-Selenylation of Pyrazoles and Other Heteroarenes

inferred← citeshttps://doi.org/10.1038/s41598-023-44152-0openalex-snapshot

A novel method for extracting metals from asteroids using non-aqueous deep eutectic solvents

inferred← citeshttps://doi.org/10.1039/c9qo01497gopenalex-snapshot

Chelation-assisted transition metal-catalysed C–H chalcogenylations

inferred← citeshttps://doi.org/10.1039/d6nj01095dopenalex-snapshot

Efficient one-pot synthesis of 2-(sulfanylselanylmethyl)-1,3-thiaselenoles using 2-bromomethyl-1,3-thiaselenole

inferred← citeshttps://doi.org/10.1080/17568919.2024.2435254openalex-snapshot

Organoselenium compounds beyond antioxidants

inferred← citeshttps://doi.org/10.3762/bjoc.16.47openalex-snapshot

Regio- and stereoselective synthesis of new ensembles of diversely functionalized 1,3-thiaselenol-2-ylmethyl selenides by a double rearrangement reaction

inferred← citeshttps://doi.org/10.59761/rcr5143openalex-snapshot

Metal complexes with selenium-based ligands in organic synthesis

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