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Recent advances in the chemistry of organic thiocyanates

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What this work says

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

inferredcites →https://doi.org/10.1002/1521-3765(20020703)8:13<2910::aid-chem2910>3.0.co;2-ropenalex-snapshot
Easy Access to Phosphonothioates
inferredcites →https://doi.org/10.1002/anie.200250621openalex-snapshot
Insertion of Thiocyanogen into a PC Bond and Subsequent Formation of Polysulfide Derivatives
inferredcites →https://doi.org/10.1002/anie.201500899openalex-snapshot
Synthesis of Difluoromethyl Thioethers from Difluoromethyl Trimethylsilane and Organothiocyanates Generated In Situ
inferredcites →https://doi.org/10.1002/aoc.3230openalex-snapshot
Synthesis of diaryl thioethers from aryl halides and potassium thiocyanate
inferredcites →https://doi.org/10.1002/chem.201003657openalex-snapshot
Difunctionalisation of Arenes and Heteroarenes by Directed Metallation and Sulfoxide–Magnesium Exchange
inferredcites →https://doi.org/10.1002/chem.201406171openalex-snapshot
General and Practical Formation of Thiocyanates from Thiols
inferredcites →https://doi.org/10.1002/ejoc.200400502openalex-snapshot
Facile Ring‐Expansion Substitution Reactions of 1,3‐Dithiolanes and 1,3‐Dithianes Initiated by Electrophilic Reagents to Produce Monohalo‐, ‐cyano‐, ‐azido‐ and ‐thiocyanato‐1,4‐dithiins and ‐1,4‐dithiepins
inferredcites →https://doi.org/10.1002/ejoc.201403279openalex-snapshot
Practical Access to Aromatic Thiocyanates by CuCN‐Mediated Direct Aerobic Oxidative Cyanation of Thiophenols and Diaryl Disulfides
inferredcites →https://doi.org/10.1002/hlca.201300075openalex-snapshot
Copper‐Catalyzed One‐Pot Synthesis of N‐Sulfonylalkanimidoyl Thiocyanates from Sulfonyl Azides, Alkynes, and KSCN
inferredcites →https://doi.org/10.1016/j.jfluchem.2014.09.026openalex-snapshot
A new synthesis of trifluoromethyl sulfides utilizing thiocyanates and fluoroform
inferredcites →https://doi.org/10.1016/j.tet.2005.03.138openalex-snapshot
2-Cyanopyridazin-3(2H)-ones: effective and chemoselective electrophilic cyanating agents
inferredcites →https://doi.org/10.1016/j.tet.2006.03.030openalex-snapshot
Preparation of thiocyanates and isothiocyanates from alcohols, thiols, trimethylsilyl-, and tetrahydropyranyl ethers using triphenylphosphine/2,3-dichloro-5,6-dicyanobenzoquinone (DDQ)/n-Bu4NSCN system
inferredcites →https://doi.org/10.1016/j.tetasy.2006.06.032openalex-snapshot
Creation of quarternary stereocentres via [3,3]-sigmatropic rearrangement of allylic thiocyanates. A synthetic approach to (+)-myriocin
inferredcites →https://doi.org/10.1016/s0040-4020(02)00026-1openalex-snapshot
Asymmetric induction in a new domino reaction of [3,3]-sigmatropic rearrangement of allylic thiocyanates and intramolecular heterocyclisation
inferredcites →https://doi.org/10.1016/s0040-4020(99)00386-5openalex-snapshot
The chemistry of thiocyanic esters
inferredcites →https://doi.org/10.1016/s0040-4039(02)00421-5openalex-snapshot
Efficient conversion of thiols to thiocyanates by in situ generated Ph3P(SCN)2
inferredcites →https://doi.org/10.1016/s0957-4166(03)00316-1openalex-snapshot
Synthesis of chiral, nonracemic α-sulfanylphosphonates and derivatives
inferredcites →https://doi.org/10.1021/acs.orglett.5b00494openalex-snapshot
Activation of Aryl Thiocyanates Followed by Aryne Insertion: Access to 1,2-Thiobenzonitriles
inferredcites →https://doi.org/10.1021/acs.orglett.5b00754openalex-snapshot
Transition-Metal-Free Tandem Radical Thiocyanooxygenation of Olefinic Amides: A New Route to SCN-Containing Heterocycles
inferredcites →https://doi.org/10.1021/acs.orglett.5b01677openalex-snapshot
Copper-Catalyzed Intermolecular Trifluoromethylazidation and Trifluoromethylthiocyanation of Allenes: Efficient Access to CF 3 -Containing Allyl Azides and Thiocyanates
inferredcites →https://doi.org/10.1021/ja512880gopenalex-snapshot
Peptide/Protein Stapling and Unstapling: Introduction of s -Tetrazine, Photochemical Release, and Regeneration of the Peptide/Protein
inferredcites →https://doi.org/10.1021/jacs.5b05287openalex-snapshot
Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents
inferredcites →https://doi.org/10.1021/jo010635wopenalex-snapshot
Preparation of 5-Substituted 1 H -Tetrazoles from Nitriles in Water
inferredcites →https://doi.org/10.1021/jo035050bopenalex-snapshot
Scope of Ru(II)-Catalyzed Synthesis of Pyridines from Alkynes and Nitriles
inferredcites →https://doi.org/10.1021/jo061114hopenalex-snapshot
Revisiting Nucleophilic Substitution Reactions: Microwave-Assisted Synthesis of Azides, Thiocyanates, and Sulfones in an Aqueous Medium
inferredcites →https://doi.org/10.1021/jo300250xopenalex-snapshot
Concise Approach to Benzisothiazol-3(2H)-one via Copper-Catalyzed Tandem Reaction of o-Bromobenzamide and Potassium Thiocyanate in Water
inferredcites →https://doi.org/10.1021/jo5015799openalex-snapshot
A Visible-Light-Promoted Aerobic Metal-Free C-3 Thiocyanation of Indoles
inferredcites →https://doi.org/10.1021/ol010220xopenalex-snapshot
An Intramolecular [2 + 3] Cycloaddition Route to Fused 5-Heterosubstituted Tetrazoles
inferredcites →https://doi.org/10.1021/ol061741topenalex-snapshot
Palladium-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids and Benzylthiocyanate. A Cyanide-Free Cyanation of Boronic Acids
inferredcites →https://doi.org/10.1021/ol070159hopenalex-snapshot
An Efficient and General Approach to β-Functionalized Ketones
inferredcites →https://doi.org/10.1021/ol102784copenalex-snapshot
An Efficient Copper-Catalyzed Carbon−Sulfur Bond Formation Protocol in Water
inferredcites →https://doi.org/10.1021/ol901561jopenalex-snapshot
Acyl-isothiocyanates as Efficient Thiocyanate Transfer Reagents
inferredcites →https://doi.org/10.1021/om0600442openalex-snapshot
A Highly Regioselective Cyanothiolation of Alkynes via Oxidative Addition of Thiocyanates to Tetrakis(triphenylphosphine)palladium(0) Catalyst
inferredcites →https://doi.org/10.1039/b900137aopenalex-snapshot
Simple and quick preparation of α-thiocyanate ketones in hydroalcoholic media. Access to 5-aryl-2-imino-1,3-oxathiolanes
inferredcites →https://doi.org/10.1039/c4cc04578eopenalex-snapshot
Copper-catalyzed cyanation of disulfides by azobisisobutyronitrile leading to thiocyanates
inferredcites →https://doi.org/10.1039/c4ob01655fopenalex-snapshot
Oxidative nucleophilic strategy for synthesis of thiocyanates and trifluoromethyl sulfides from thiols
inferredcites →https://doi.org/10.1039/c4ra03592eopenalex-snapshot
Microwave-assisted synthesis of asymmetric disulfides
inferredcites →https://doi.org/10.1039/c5cc00875aopenalex-snapshot
Transition-metal-free cross-coupling of thioethers with aryl(cyano)iodonium triflates: a facile and efficient method for the one-pot synthesis of thiocyanates
inferredcites →https://doi.org/10.1055/s-2004-829150openalex-snapshot
Ferric(III) Chloride-Promoted Efficient Thiocyanation of Arylalkenes: A Facile Synthesis of Dithiocyanates
inferredcites →https://doi.org/10.1055/s-2008-1072517openalex-snapshot
Iron(III) Chloride as Mild and Efficient Reagent for the α-Thiocyanation of Ketones: An Expedient Synthesis of α-Oxo Thiocyanates
inferredcites →https://doi.org/10.1070/mc2006v016n05abeh002403openalex-snapshot
Catalytic thiocyanation of aryldiazonium salts in the presence of copper salts
inferredcites →https://doi.org/10.1155/2013/561649openalex-snapshot
Al‐MCM‐41: An Efficient and Recyclable Heterogeneous Catalyst for the Synthesis of β‐Hydroxy Thiocyanates in Water

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.4057421openalex-extracted
An Efficient Synthesis of 4-Thiocyanato Anilines Using Benzyltrimethylammonium Dichloroiodate and Ammonium Thiocyanate in Dmso:H2o
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz16655openalex-snapshot
thiocyanation
inferred← citeshttps://doi.org/10.1002/9783527834242.chf0017openalex-snapshot
Pd‐Catalyzed CChalcogen Bond Formation (CS, CSe) by CH Bond Activation
inferred← citeshttps://doi.org/10.1002/adsc.201800968openalex-snapshot
Synthesis of α‐Trifluoromethylthiolated and α‐Thiocyanated Ketones Using Umpoled Enolates
inferred← citeshttps://doi.org/10.1002/adsc.201801138openalex-snapshot
Direct Oxidative Disulfenylation/Cyclization of 2′‐Hydroxyacetophenones with Thiophenols for the Synthesis of 2,2‐Dithio‐Benzofuran‐3(2 H )‐Ones
inferred← citeshttps://doi.org/10.1002/adsc.201801232openalex-snapshot
Potassium Persulfate‐Mediated Thiocyanation of 2H‐Indazole under Iron‐Catalysis
inferred← citeshttps://doi.org/10.1002/adsc.201900156openalex-snapshot
Electrochemical ipso‐Thiocyanation of Arylboron Compounds
inferred← citeshttps://doi.org/10.1002/adsc.201901014openalex-snapshot
Ruthenium‐Catalyzed Highly Regioselective Azide‐Internal Thiocyanatoalkyne Cycloaddition under Mild Conditions: Experimental and Theoretical Studies
inferred← citeshttps://doi.org/10.1002/adsc.201901104openalex-snapshot
Copper‐Catalyzed Domino Cyclization/Thiocyanation of Unactivated Olefins: Access to SCN‐Containing Pyrazolines
inferred← citeshttps://doi.org/10.1002/adsc.202000458openalex-snapshot
Modern Synthetic Approaches to Phosphorus‐Sulfur Bond Formation in Organophosphorus Compounds
inferred← citeshttps://doi.org/10.1002/adsc.202000754openalex-snapshot
Copper‐Catalyzed Remote Direct Thiocyanation of Alkyl C(sp3)−H Bonds
inferred← citeshttps://doi.org/10.1002/adsc.202100469openalex-snapshot
Catalyst‐Free Decarbonylative Trifluoromethylthiolation Enabled by Electron Donor‐Acceptor Complex Photoactivation
inferred← citeshttps://doi.org/10.1002/adsc.202300008openalex-snapshot
Synthesis of Aryl Thiocyanates and Aryl Selenocyanates via Visible‐Light Activation of Arylazo Sulfones
inferred← citeshttps://doi.org/10.1002/adsc.202300224openalex-snapshot
Electrochemical Oxidative Carbon‐atom Multifunctionalization and N‐Cyanation of Imine: Synthesis of (Z)‐N′‐Cyano‐N‐carbamimidothioate
inferred← citeshttps://doi.org/10.1002/adsc.202300255openalex-snapshot
Electrosynthesis of Thiocyanated/Iodinated/Brominated Pyrazol‐5‐amines and Thiocyanated Enamines via C(sp2)−H Functionalization
inferred← citeshttps://doi.org/10.1002/adsc.202301229openalex-snapshot
Direct Synthesis of (E)‐β‐(Thiocyanato)vinyl Sulfones by 1,2‐Difunctionalization of Alkynes with Sulfinic Acids and Potassium Thiocyanate
inferred← citeshttps://doi.org/10.1002/adsc.202400153openalex-snapshot
Self‐ or Acridinium‐Catalyzed Electrophotosynthesis of Thiocyanato Heterocycles from Activated Alkenes
inferred← citeshttps://doi.org/10.1002/adsc.202400714openalex-snapshot
Domino Doyle‐Kirmse/Claisen‐Thioimidate Rearrangements: Access to 2‐Aminobuta‐1,3‐diene Derivatives of Benzazole‐2‐thiones
inferred← citeshttps://doi.org/10.1002/adsc.202401373openalex-snapshot
Visible‐Light‐Induced Acyl and Thiocyano Pyridylation of Alkenes with Aldehyde and NH4SCN
inferred← citeshttps://doi.org/10.1002/adsc.202500277openalex-snapshot
Photocatalytic Selective 1,2‐Thiocyanato‐Imination of Alkenes
inferred← citeshttps://doi.org/10.1002/adsc.70509openalex-snapshot
Visible‐Light‐Induced Thiocyanation of Unactivated Alkenes with N ‐Thiocyanatosaccharin via Remote Quinoxalinone Migration under Catalyst Free Conditions
inferred← citeshttps://doi.org/10.1002/ajoc.202100649openalex-snapshot
Organocatalyzed Asymmetric Tandem Intramolecular oxa‐Michael Addition/Electrophilic Thiocyanation: Synthesis of Chiral α‐Thiocyanato Flavanones
inferred← citeshttps://doi.org/10.1002/ajoc.202200007openalex-snapshot
Me3SiCl‐Catalyzed Electrophilic Thiocyanation/Cyclization of Alkynylbenzoates to Synthesize 4‐Thiocyanatoisocourmarins
inferred← citeshttps://doi.org/10.1002/ajoc.202200274openalex-snapshot
DMSO as C1 Source under Metal‐ and Oxidant‐free Conditions: NH 4 SCN‐mediated Synthesis of Quinazolinone and Dihydroquinazolin‐4(1H)‐one Derivatives
inferred← citeshttps://doi.org/10.1002/ajoc.202200595openalex-snapshot
Electrophilic Oxythio/selenocyanation of o‐Alkenyl Benzoic Acids: Divergent Synthesis of Thio/selenocyanated Isobenzofuranones and Isocoumarins
inferred← citeshttps://doi.org/10.1002/ajoc.202300290openalex-snapshot
Visible‐Light‐Induced Synthesis of Thioethers through Three‐Component Reactions of α‐Diazoesters, Thiols, and Cyclic Ethers
inferred← citeshttps://doi.org/10.1002/ajoc.202300495openalex-snapshot
Lewis Base Catalyzed C−S Bond Formation Through Methyl C(sp3)‐H Thiocyanation of Indoles
inferred← citeshttps://doi.org/10.1002/ajoc.70385openalex-snapshot
Modular Synthesis of Fully Substituted 5‐Thioureido‐Triazoles via Transition‐Metal‐Free KO t Bu‐Catalyzed Three‐Component Reaction
inferred← citeshttps://doi.org/10.1002/ajoc.70390openalex-snapshot
Recent Advances for the Synthesis of 4 H ‐3,1‐Benzoxazines via Annulation of Olefinic Amides
inferred← citeshttps://doi.org/10.1002/ajoc.70466openalex-snapshot
The Electrophilic Thiocyanation/Cyclization Reaction of Allenic Acids: One‐Step Preparation of Thiocyanated 2(5H)‐furanones
inferred← citeshttps://doi.org/10.1002/ajoc.70487openalex-snapshot
Light‐Induced Three‐Component Synthesis of Sulfur‐Containing Compounds: A Concise Overview
inferred← citeshttps://doi.org/10.1002/ajoc.70535openalex-snapshot
Iron‐Catalyzed Thiocyanation of Heterocycles and Aromatics Utilizing a Combination of NH 3 ·H 2 O and CS 2
inferred← citeshttps://doi.org/10.1002/ange.201805348openalex-snapshot
A General Synthesis of Phosphorus‐ and Arsenic‐Containing Analogues of the Thio‐ and Seleno‐cyanate Anions
inferred← citeshttps://doi.org/10.1002/ange.201813356openalex-snapshot
Dual Photoredox/Copper Catalysis for the Remote C(sp3)−H Functionalization of Alcohols and Alkyl Halides by N‐Alkoxypyridinium Salts
inferred← citeshttps://doi.org/10.1002/ange.202010889openalex-snapshot
Selective Synthesis of Non‐Aromatic Five‐Membered Sulfur Heterocycles from Alkynes by using a Proton Acid/N‐Chlorophthalimide System
inferred← citeshttps://doi.org/10.1002/ange.202014518openalex-snapshot
Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202210509openalex-snapshot
Sulfenofunctionalization of Chiral α‐Trifluoromethyl Allylboronic Acids: Asymmetric Synthesis of SCF3, SCF2R, SCN and SAr Compounds
inferred← citeshttps://doi.org/10.1002/ange.202309684openalex-snapshot
Photoredox‐Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts
inferred← citeshttps://doi.org/10.1002/anie.201805348openalex-snapshot
A General Synthesis of Phosphorus‐ and Arsenic‐Containing Analogues of the Thio‐ and Seleno‐cyanate Anions
inferred← citeshttps://doi.org/10.1002/anie.201813356openalex-snapshot
Dual Photoredox/Copper Catalysis for the Remote C(sp 3 )−H Functionalization of Alcohols and Alkyl Halides by N ‐Alkoxypyridinium Salts
inferred← citeshttps://doi.org/10.1002/anie.202010889openalex-snapshot
Selective Synthesis of Non‐Aromatic Five‐Membered Sulfur Heterocycles from Alkynes by using a Proton Acid/N‐Chlorophthalimide System
inferred← citeshttps://doi.org/10.1002/anie.202014518openalex-snapshot
Selective 1,2‐Aminoisothiocyanation of 1,3‐Dienes Under Visible‐Light Photoredox Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202210509openalex-snapshot
Sulfenofunctionalization of Chiral α‐Trifluoromethyl Allylboronic Acids: Asymmetric Synthesis of SCF3, SCF2R, SCN and SAr Compounds
inferred← citeshttps://doi.org/10.1002/anie.202309684openalex-snapshot
Photoredox‐Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts
inferred← citeshttps://doi.org/10.1002/asia.202200256openalex-snapshot
Phosphoric Acid Catalyzed Electrophilic Thiocyanation of Indoles: Access to SCN‐Containing Aryl‐Indole Compounds
inferred← citeshttps://doi.org/10.1002/asia.202200802openalex-snapshot
Electrophilic Thiocyanation of Tryptamine Derivatives: Divergent Synthesis of SCN‐Containing Indole Compounds
inferred← citeshttps://doi.org/10.1002/asia.202300321openalex-snapshot
The “Weak” C−H⋅⋅⋅S Interaction Drives Enantioselectivity in Cinchona Alkaloid Complex Catalyzed Thiocyanation
inferred← citeshttps://doi.org/10.1002/asia.202300997openalex-snapshot
The Role of Aromatic Alcohol Additives on Asymmetric Organocatalysis Reactions: Insights from Theory
inferred← citeshttps://doi.org/10.1002/asia.202500241openalex-snapshot
Copper‐Catalyzed 1,5‐Trifluoromethyl‐thio(seleno)cyanation of 5‐Hexenenitriles with an Intramolecular Cyano Migration
inferred← citeshttps://doi.org/10.1002/asia.202500423openalex-snapshot
Aryl Thiocyanate as an Organic ‘CN’ Source: Access to Thiocyano‐Thioesters from Cyclic Thioacetals
inferred← citeshttps://doi.org/10.1002/cbdv.71358openalex-snapshot
Antidiabetic and Cytotoxicity Studies of Novel Quinazolinone–1,3,4‐Thiadiazole Molecular Hybrids
inferred← citeshttps://doi.org/10.1002/cctc.201600785openalex-snapshot
Nitrogen Dioxide Catalyzed Oxidative Thiocyanation of Arenes with Ambient Air as the Terminal Oxidant
inferred← citeshttps://doi.org/10.1002/chem.202001815openalex-snapshot
Electrophilic Chlorine from Chlorosulfonium Salts: A Highly Chemoselective Reduction of Sulfoxides
inferred← citeshttps://doi.org/10.1002/chem.202003521openalex-snapshot
Pd‐Catalyzed Directed Thiocyanation Reaction by C−H Bond Activation
inferred← citeshttps://doi.org/10.1002/chem.202004974openalex-snapshot
Design and Use of Electrophilic Thiocyanating and Selenocyanating Reagents: An Interesting Trend for the Construction of SCN‐ and SeCN‐Containing Compounds
inferred← citeshttps://doi.org/10.1002/chem.202203306openalex-snapshot
Synthesis of 3‐Thiocyanobenzothiophene via Difunctionalization of Active Alkyne Promoted by Electrochemical‐Oxidation
inferred← citeshttps://doi.org/10.1002/chem.202300611openalex-snapshot
Deciphering the Differences in Ambident Reactivity between the Cyanate, Thiocyanate Ions, and their P‐ and As‐Containing Analogues
inferred← citeshttps://doi.org/10.1002/chem.202400453openalex-snapshot
Organophotocatalytic Remote Thiocyanation Reaction via Ring‐Opening Functionalization of Cycloalkanols
inferred← citeshttps://doi.org/10.1002/chem.202403990openalex-snapshot
Base‐Free Synthesis of S‐Alkyl Isothioureas Through Ring‐Opening Reaction of Sulfonium Salts with Isothiocyanates and Amines
inferred← citeshttps://doi.org/10.1002/chin.201613251openalex-snapshot
ChemInform Abstract: Recent Advances in the Chemistry of Organic Thiocyanates
inferred← citeshttps://doi.org/10.1002/cjoc.201600344openalex-snapshot
Catalytic Thiourea Promoted Electrophilic Thiocyanation of Indoles and Aromatic Amines with NCS/NH4SCN
inferred← citeshttps://doi.org/10.1002/cjoc.202300188openalex-snapshot
Thianthrene Radical Cation as a Transient SET Mediator: Photoinduced Thiocyanation and Selenocyanation of Arylthianthrenium Salts†
inferred← citeshttps://doi.org/10.1002/cjoc.70097openalex-snapshot
Electrochemical C3 ‐Thiocyanation of Quinolines
inferred← citeshttps://doi.org/10.1002/cjoc.70170openalex-snapshot
Electrochemical Selective C(sp 3 )–S/C(sp 2 )–S Bond Cleavage of Heteroaryl Alkyl Sulfides
inferred← citeshttps://doi.org/10.1002/cmdc.201800320openalex-snapshot
Synthesis, Computational Docking Study, and Biological Evaluation of a Library of Heterocyclic Curcuminoids with Remarkable Antitumor Activity
inferred← citeshttps://doi.org/10.1002/cphc.201900899openalex-snapshot
Theoretical Investigation of Cyano‐Chalcogen Dimers and Their Importance in Molecular Recognition
inferred← citeshttps://doi.org/10.1002/cptc.202200335openalex-snapshot
Photoredox‐Catalyzed Thiocyanative Cyclization of Biaryl Ynones to Thiocyanated Spiro[5.5]trienones: An External‐Oxidant‐ and Transition‐Metal‐Free Approach
inferred← citeshttps://doi.org/10.1002/cssc.70642openalex-snapshot
Mechanochemical Tandem Reactions: A Sustainable and Direct Route to 1,2‐Di‐Functional Indolizines via In Situ Baylis–Hillman Reaction, Cyclocondensation, Electrophilic C–H Chalcogenocyanation
inferred← citeshttps://doi.org/10.1002/ejoc.201600485openalex-snapshot
Highly Efficient and Practical Thiocyanation of Imidazopyridines Using an N ‐Chlorosuccinimide/NaSCN Combination
inferred← citeshttps://doi.org/10.1002/ejoc.201700819openalex-snapshot
Thiocyanation of N,N‐Dialkylhydrazonoyl Bromides: An Entry to Sulfur‐Containing 1,2,4‐Triazole Derivatives
inferred← citeshttps://doi.org/10.1002/ejoc.201701722openalex-snapshot
Synthesis of Triazolium Inner Salts by Thiocyanation of Aldehyde‐Derived Hydrazones
inferred← citeshttps://doi.org/10.1002/ejoc.201800833openalex-snapshot
Metal‐Free Synthesis of 3‐Thiocyanatobenzothiophenes by Eosin Y Photoredox‐Catalyzed Cascade Radical Annulation of 2‐Alkynylthioanisoles
inferred← citeshttps://doi.org/10.1002/ejoc.201900343openalex-snapshot
Copper‐Catalyzed Regioselective Direct C–H Thiolation and Thiocyanation of Uracils
inferred← citeshttps://doi.org/10.1002/ejoc.201900390openalex-snapshot
Electrooxidative C–H Functionalization of Heteroarenes. Thiocyanation of Pyrazolo[1,5‐a]pyrimidines
inferred← citeshttps://doi.org/10.1002/ejoc.201900749openalex-snapshot
C4‐Selective Synthesis of Vinyl Thiocyanates and Selenocyanates Through 3,4‐Dihalo‐2(5H)‐furanones
inferred← citeshttps://doi.org/10.1002/ejoc.202100517openalex-snapshot
Recent Progress in the Synthesis of Heterocycles through Base Metal‐Catalyzed Acceptorless Dehydrogenative and Borrowing Hydrogen Approach
inferred← citeshttps://doi.org/10.1002/ejoc.202101031openalex-snapshot
Temperature‐Controlled Chemoselective Synthesis of Thiosulfonates and Thiocyanates: Novel Reactivity of KXCN (X=S, Se) towards Organosulfonyl Chlorides
inferred← citeshttps://doi.org/10.1002/ejoc.202101255openalex-snapshot
N‐Thiocyanato‐2,10‐camphorsultam Derivatives: Design and Applications of Original Electrophilic Thiocyanating Reagents
inferred← citeshttps://doi.org/10.1002/ejoc.202200359openalex-snapshot
Dithiocyanation of Alkynes with N‐Thiocyanato‐dibenzenesulfonimide and Ammonium Thiocyanate
inferred← citeshttps://doi.org/10.1002/ejoc.202201233openalex-snapshot
Iodine‐Mediated Three‐Component Strategy to Synthesize 2‐Aminothiazoles from β‐Diketones/β‐ketoesters, Arylamines and Ammonium Thiocyanate
inferred← citeshttps://doi.org/10.1002/ejoc.202201278openalex-snapshot
One‐Pot Synthesis of 4‐Thiocyanato‐1 H ‐pyrazoles through Electrochemical Multicomponent Thiocyanation under Metal‐ and Oxidant‐Free Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202300665openalex-snapshot
Photoinduced Regioselective Chalcogenation and Thiocyanation of 4H‐Pyrido[1,2‐a] pyrimidin‐4‐ones Under Benign Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202300733openalex-snapshot
Synthesis of Alkynyl Sulfides: Alkynyl Trifluoromethyl Sulfides and Thiocyanates
inferred← citeshttps://doi.org/10.1002/ejoc.202300868openalex-snapshot
Radical Thiocyano(Selenocyano)trifluoromethylations of Alkenes on Water
inferred← citeshttps://doi.org/10.1002/ejoc.202300969openalex-snapshot
Dibenzoylperoxide‐Mediated Oxidative α‐Thio/Seleno‐Cyanation of β‐Ketoesters and Oxindoles
inferred← citeshttps://doi.org/10.1002/ejoc.202301205openalex-snapshot
C‐Centered radical intermediates for C(sp3)‐H bonds functionalization: An emerging approach towards alkyl thiocyanates
inferred← citeshttps://doi.org/10.1002/ejoc.202500393openalex-snapshot
Copper/Bis(imine)‐Catalyzed Fluoroalkylative Thiocyanation of Unactivated Alkenes
inferred← citeshttps://doi.org/10.1002/ejoc.202500518openalex-snapshot
Molecular Iodine‐Mediated Functionalization of α‐Carbonyl Sulfoxonium Ylides with Thiocyanates, Xanthates, and Dithiocarbamates
inferred← citeshttps://doi.org/10.1002/ejoc.202500895openalex-snapshot
Electrochemically Promoted Aminothiocyanation of Unactivated Alkenes for the Synthesis of Thiocyanated Pyrrolidines
inferred← citeshttps://doi.org/10.1002/elan.201700821openalex-snapshot
Sensitive Amperometric Determination of Thiocyanates at Ionic Liquid Nanohybrid Kaolinite Modified Glassy Carbon Electrode
inferred← citeshttps://doi.org/10.1002/hlca.202300132openalex-snapshot
Immobilized Rose Bengal as Photocatalyst for Metal‐Free Thiocyanation of Azaheterocycles under Continuous Flow Conditions
inferred← citeshttps://doi.org/10.1002/jhet.70217openalex-snapshot
N ‐Bromosuccinimide ( NBS ) in Heterocyclic Ring Construction: A Decade of Advances
inferred← citeshttps://doi.org/10.1002/open.202400139openalex-snapshot
Green Synthesis of Diphenyl‐Substituted Alcohols Via Radical Coupling of Aromatic Alcohols Under Transition‐Metal‐Free Conditions
inferred← citeshttps://doi.org/10.1002/slct.202203719openalex-snapshot
Fe(III)‐Mediated para ‐Selective Nucleophilic Thiocyanation and Oxidation Reactions, Access to Thiocyanated Amidophenols and Amidoquinones
inferred← citeshttps://doi.org/10.1002/slct.202301018openalex-snapshot
N ‐Chlorosuccinimide Mediated Direct C−H Thiocyanation of 1‐Aryl‐5‐pyrazolones at Room Temperature
inferred← citeshttps://doi.org/10.1002/slct.202302849openalex-snapshot
Microwave‐Assisted Metal‐Free C(sp 2 )−H Thiocyanation of Aromatic Amines
inferred← citeshttps://doi.org/10.1002/slct.202303465openalex-snapshot
Regioselective C(sp 2 )3−H thiocyanation of substituted 4 H ‐pyrido[1,2‐ a ]pyrimidin‐4‐ones and its derivatizations
inferred← citeshttps://doi.org/10.1002/slct.202303845openalex-snapshot
Iodine and DMSO as Surrogate of Hazardous Metal and Non‐Metal Reagents in Organic Synthesis
inferred← citeshttps://doi.org/10.1002/slct.202502075openalex-snapshot
Recent Advances in the Electrochemical Cascade Cyclization of Thiocyanates for the Construction of Heterocyclic Compounds
inferred← citeshttps://doi.org/10.1002/slct.74518openalex-snapshot
Aerobic Trans ‐Iodothiocyanation of Internal Alkynes With CHI 3 /NH 4 SCN
inferred← citeshttps://doi.org/10.1002/tcr.202300312openalex-snapshot
Recent Advancement on the Indirect or Combined Alternative Thiocyanate Sources for the Construction of S−CN Bonds
inferred← citeshttps://doi.org/10.1002/zaac.202500075openalex-snapshot
NaSC2H: A First Crystalline Compound with a −SC2H Anion, an Isolobal Variant of Ubiquitous −SCN
inferred← citeshttps://doi.org/10.1007/s10562-020-03414-6openalex-snapshot
Visible-Light-Mediated Decarboxylative Thiocyanation of Cinnamic acids: An Efficient Photocatalytic Approach to the Synthesis of (E)-Vinyl Thiocyanates
inferred← citeshttps://doi.org/10.1007/s10593-021-02938-yopenalex-snapshot
NaSCN–(NH4)2Ce(NO3)6 system in heterocycle thiocyanation: synthesis of novel highly potent broad-spectrum fungicides for crop protection
inferred← citeshttps://doi.org/10.1007/s11030-026-11513-6openalex-snapshot
Cu-catalyzed deaminative thiocyanation of anilines via nitrate reduction
inferred← citeshttps://doi.org/10.1007/s11144-017-1276-xopenalex-snapshot
Magnetic hydroxyapatite-immobilized 1,4-diazabicyclo [2.2.2] octane as a highly efficient and eco-friendly nanocatalyst for the promotion of nucleophilic substitution reactions of benzyl halides under green conditions
inferred← citeshttps://doi.org/10.1007/s11164-024-05375-6openalex-snapshot
1,3-Dithiocyanatoacetone: improved synthesis, detailed structural studies and in silico docking studies
inferred← citeshttps://doi.org/10.1007/s11172-019-2681-2openalex-snapshot
“Metal-free” electrooxidative C—H thiocyanation of arenes
inferred← citeshttps://doi.org/10.1007/s12039-017-1412-1openalex-snapshot
A sustainable process for gram-scale synthesis of stereoselective aryl substituted (E)-2-thiocyanatoacrylic acids
inferred← citeshttps://doi.org/10.1007/s12039-021-01897-3openalex-snapshot
KSCN and K2CO3 mediated one-pot synthesis of cyclopropanyl coumarin derivatives
inferred← citeshttps://doi.org/10.1007/s13659-024-00456-wopenalex-snapshot
Chemically engineered essential oils prepared through thiocyanation under solvent-free conditions: chemical and bioactivity alteration
inferred← citeshttps://doi.org/10.1007/s13738-026-03381-6openalex-snapshot
From mortars to mills: mechanochemistry as a tool for efficient organic transformations
inferred← citeshttps://doi.org/10.1007/s41061-018-0197-0openalex-snapshot
Sulfur Radicals and Their Application
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00122-8openalex-snapshot
Reduction of S O and SO2 to S, S–X to S–H, and P O to P
inferred← citeshttps://doi.org/10.1016/bs.aihch.2018.02.003openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XVI, 2016
inferred← citeshttps://doi.org/10.1016/j.aca.2018.10.040openalex-snapshot
Ultrasensitive and recyclable superstructure of Au SiO2@Ag wire for surface-enhanced Raman scattering detection of thiocyanate in urine and human serum
inferred← citeshttps://doi.org/10.1016/j.anifeedsci.2019.114338openalex-snapshot
Review of Moringa oleifera as forage meal (leaves plus stems) intended for the feeding of non-ruminant animals
inferred← citeshttps://doi.org/10.1016/j.apcatb.2018.01.065openalex-snapshot
Photocatalytic cyanation of carbon nitride scaffolds: Tuning band structure and enhancing the performance in green light driven C S bond formation
inferred← citeshttps://doi.org/10.1016/j.bbagen.2019.01.001openalex-snapshot
Covalent inhibition of histone deacetylase 8 by 3,4-dihydro-2H-pyrimido[1,2-c][1,3]benzothiazin-6-imine
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.109107openalex-snapshot
Additive-free synthesis of S-substituted isothioureas via visible-light-induced four-component reaction of α-diazoesters, aryl isothiocyanates, amines and cyclic ethers
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110784openalex-snapshot
An update on the advances in chromone and the derivatives synthesis based on the key chromone annulation of o-hydroxyaryl enaminones
inferred← citeshttps://doi.org/10.1016/j.cdc.2025.101183openalex-snapshot
Crystal structure of 3-methyl-2,6-diphenyl-1-(2-thiocyanatoacetyl)piperidin-4-one: A combined experimental and theoretical study
inferred← citeshttps://doi.org/10.1016/j.crci.2016.12.007openalex-snapshot
Comparative study on the reactivity of propargyl and alkynyl sulfides in palladium-catalyzed domino reactions
inferred← citeshttps://doi.org/10.1016/j.electacta.2024.145517openalex-snapshot
Electrochemical synthesis of isothiocyanogen and its reactivity in thiocyanation reactions
inferred← citeshttps://doi.org/10.1016/j.gresc.2021.12.003openalex-snapshot
Synthesis of 3-thiocyanated chromones via TCCA/NH4SCN-mediated cyclization/thiocyanation of alkynyl aryl ketones
inferred← citeshttps://doi.org/10.1016/j.jcis.2025.138580openalex-snapshot
Multilevel supramolecular assemblies achieving cascaded enhancement of superoxide anion radical generation for visible-light-driven thiocyanation of anilines
inferred← citeshttps://doi.org/10.1016/j.mcat.2025.115210openalex-snapshot
Electrochemical C H Thiocyanation/Halogenation of 4-Arylthioazol-2-ones
inferred← citeshttps://doi.org/10.1016/j.mencom.2023.01.037openalex-snapshot
Efficient thiocyanation of phenols and anilines in the CeBr3 / H2O2 system
inferred← citeshttps://doi.org/10.1016/j.mencom.2023.06.016openalex-snapshot
Visible light-induced thiocyanation of gem-difluorinated phosphonium salts
inferred← citeshttps://doi.org/10.1016/j.mineng.2020.106689openalex-snapshot
A review of thiocyanate gold leaching – Chemistry, thermodynamics, kinetics and processing
inferred← citeshttps://doi.org/10.1016/j.mineng.2023.108074openalex-snapshot
A review of environmentally friendly gold lixiviants: Fundamentals, applications, and commonalities
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131751openalex-snapshot
Synthesis and cytotoxic activity of 1,2,3-triazoles derived from 2,3-seco-dihydrobetulin via a click chemistry approach
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139322openalex-snapshot
Sonochemical thiocyanation of pyrrolo[1,2-a]quinoxalines: Identification of potential inhibitors of SIRT1
inferred← citeshttps://doi.org/10.1016/j.poly.2019.114132openalex-snapshot
Silver-based monomer and coordination polymer with organic thiocyanate ligand: Structural, computational and antiproliferative activity study
inferred← citeshttps://doi.org/10.1016/j.tet.2018.04.023openalex-snapshot
Aerobic intramolecular aminothiocyanation of unactivated alkenes promoted by in situ generated iodine thiocyanate
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.053openalex-snapshot
Metal-free visible-light-promoted thiocyanation/cyclization cascade for the synthesis of thiocyanato-containing isoquinolinediones
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130763openalex-snapshot
Visible-light-mediated selective thiocyanation/ipso-cyclization/oxidation cascade for the synthesis of thiocyanato-containing azaspirotrienediones
inferred← citeshttps://doi.org/10.1016/j.tet.2022.133233openalex-snapshot
A efficient, metal-free and sustainable synthesis, C-S linked by simple C-H thiocyanation of 4-aminocoumarin or 4-(N-aryl)aminocoumarin derivativess
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134645openalex-snapshot
Electrophilic thiocyanation of aromatic, heteroaromatic and aliphatic compounds: A novel perspective on recent advances
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134756openalex-snapshot
Transition metal-free direct C(sp2)-H thiocyanation of 2-iminothiazolines at room temperature
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.028openalex-snapshot
Visible-light-induced aerobic thiocyanation of indoles using reusable TiO2/MoS2 nanocomposite photocatalyst
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.10.059openalex-snapshot
Synthesis of sterically hindered allyl thiocyanates: kinetic and DFT studies of their rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.06.025openalex-snapshot
Stereoselective electrochemical thioalkylation of glycine in Ni(II) coordination environment
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.03.070openalex-snapshot
Metal-free and efficient approach to 4-thiocyanated 2H-chromenes via TFA-mediated cascade cyclization of 2-propynolphenols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.153253openalex-snapshot
Visible-light enabled C4-thiocyanation of pyrazoles by graphite-phase carbon nitride (g-C3N4)
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153809openalex-snapshot
An efficient synthesis of 4-Thiocyanato anilines using benzyltrimethylammonium dichloroiodate and ammonium thiocyanate in DMSO:H2O
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153875openalex-snapshot
An electrophilic thiocyanation/ipso-cyclization leading to spirocyclohexadienones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153929openalex-snapshot
Efficient thiocyanation of aromatic compounds using NH4SCN, DMSO and H2SO4
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154090openalex-snapshot
Convenient thiocyanation of indoles in CeBr3/H2O2 system
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154341openalex-snapshot
Electrochemical oxythiocyanation of ortho-olefinic amides: Access to diverse thiocyanated benzoxazines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154534openalex-snapshot
Me3SiCl-catalyzed tandem thiocyanation/cyclization of tryptamine and tryptophol derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155819openalex-snapshot
Photoinduced regioselective C H thiocyanation and selenocyanation of arylamines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.155986openalex-snapshot
Recent advances in potassium persulfate (K2S2O8)-mediated C C, C–heteroatom, and heteroatom–heteroatom bond formations
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156247openalex-snapshot
Electrochemical C3-thiocyanation or selenocyanation of 2H-indazoles under transition-metal-catalyst- and oxidant-free conditions
inferred← citeshttps://doi.org/10.1016/j.tifs.2026.105625openalex-snapshot
Microorganisms achieve the transformation of sulforaphane through active the synergistic action of myrosinase-like enzyme systems and transport networks
inferred← citeshttps://doi.org/10.1021/acs.accounts.6c00314openalex-snapshot
Advanced Oxidation Processes for Precious Metal Recycling
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c01041openalex-snapshot
Historical and Recent Developments in the Chemistry of Cyanate Congeners
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c11728openalex-snapshot
Characterization of Myrosinase-Mediated Glucosinolate Degradation Pathways in Lactiplantibacillus plantarum ZUST49
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.4c02174openalex-snapshot
Potent and Selective Human 5-HT2B Serotonin Receptor Antagonists: 4′-Cyano-(N)-methanocarba-adenosines by Synthetic Serendipity
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01035openalex-snapshot
Temperature-Controlled Chalcogenation and Chalcogenocyanation of Imidazopyridines in Water under Transition Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01738openalex-snapshot
Hydrogen Peroxide-Mediated Rapid Room Temperature Metal-Free C(sp2)-H Thiocyanation of Amino Pyrazoles, Amino Uracils, and Enamines
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02780openalex-snapshot
Atom-Economical Thiocyanation-Amination of Alkynes with N-Thiocyanato-Dibenzenesulfonimide
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01350openalex-snapshot
Visible-Light-Mediated Difunctionalization of Alkynes: Synthesis of β-Substituted Vinylsulfones Using O- and S-Centered Nucleophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01993openalex-snapshot
Electrophilic Thiocyanato Reagent Assisted Oxa-Michael/Thiocyanation of α,β-Unsaturated Ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02431openalex-snapshot
α-Selective C(sp 3 )–H Thio/Selenocyanation of Ketones with Elemental Chalcogen
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00059openalex-snapshot
Visible-Light-Promoted Intramolecular C–O Bond Formation via C sp 3 – H Functionalization: A Straightforward Synthetic Route to Biorelevant Dihydrofuro[3,2- c ]chromenone Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00918openalex-snapshot
Cascade Reaction of Tertiary Enaminones, KSCN, and Anilines: Temperature-Controlled Synthesis of 2-Aminothiazoles and 2-Iminothiazoline
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00995openalex-snapshot
Direct Cyanation of Thiophenols or Thiols to Access Thiocyanates under Electrochemical Conditions
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00454openalex-snapshot
Regioselective C–H Thiocyanation of Arenes by Iron(III) Chloride Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02102openalex-snapshot
Organophotocatalyzed Mono- and Bis-Alkyl/Difluoroalkylative Thio/Selenocyanation of Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02896openalex-snapshot
Visible-Light-Promoted Aerobic α-Thiocyanation of Carbonyl Compounds with Ammonium Thiocyanate
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00215openalex-snapshot
Redox Relay-Induced C–S Radical Cross-Coupling Strategy: Application in Nontraditional Site-Selective Thiocyanation of Quinoxalinones
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00612openalex-snapshot
Highly Selective C–N and C–S Dual Functionalization of 1,3-Dicarbonyl Derivatives Using TBHP as an Oxidant
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00707openalex-snapshot
Electrochemical Oxidative 1,2-Dithiocyanation: Access to Functionalized Alkenes and Alkynes
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00077openalex-snapshot
Access to Methylidene-Azaspiro[4.5]decatrienones via Radical-Promoted Domino Thio-Functionalization/Dearomative Ipso-Annulation
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00493openalex-snapshot
Photo-Thiocyanoamination of π- and σ-Bonds: Reagent Development and Synthetic Applications
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00167openalex-snapshot
Pd(II)-Catalyzed ortho- Acylation of Aryl C–H Bond Using─SCN as a Weak Directing Group
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00648openalex-snapshot
Electrochemical Thiocyanation Utilizing Ammonium Carbamodithioate or NH 3 ·H 2 O and CS 2 : A Protocol for Synthesizing Thiocyanated Heterocycles and Aromatics
inferred← citeshttps://doi.org/10.1021/acs.joc.6c00948openalex-snapshot
Ring-Opening Thiocyanation Reaction of Sulfonium Salts with Elemental Sulfur and TMSCN
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01118openalex-snapshot
Radical-Mediated Tandem Functional Group Transfer, Desulfonylation, and Cyclization Reactions: Synthesis of Oxindoles
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01742openalex-snapshot
Visible-Light-Induced Phosphonium Salt Catalysis for Site-Selective Aromatic C–H Halogenation and Chalcogenation
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00836openalex-snapshot
Copper-Catalyzed Cyanation of N -Tosylhydrazones with Thiocyanate Salt as the “CN” Source
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01122openalex-snapshot
Copper-Catalyzed Aerobic Oxidative Regioselective Thiocyanation of Aromatics and Heteroaromatics
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02700openalex-snapshot
Palladium-Catalyzed Site-Selective sp 3 C–H Bond Thiocyanation of 2-Aminofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02850openalex-snapshot
N -Thiocyanatosaccharin: A “Sweet” Electrophilic Thiocyanation Reagent and the Synthetic Applications
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02929openalex-snapshot
Phosphinoyl Radical-Initiated 1,2-Bifunctional Thiocyanodiphenylphosphinoylation of Alkenes
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00887openalex-snapshot
Direct Photocatalytic S–H Bond Cyanation with Green “CN” Source
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02235openalex-snapshot
Metal-Free Oxidative Thioesterification of Methyl Ketones with Thiols/Disulfides for the Synthesis of α-Ketothioesters
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02981openalex-snapshot
Visible Light-Induced Thiocyanation of Enaminone C–H Bond to Access Polyfunctionalized Alkenes and Thiocyano Chromones
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00545openalex-snapshot
Perylenequinonoid-Catalyzed [4 + 1] and [4 + 2] Annulations of Azoalkenes: Photocatalytic Access to 1,2,3-Thiadiazole/1,4,5,6-Tetrahydropyridazine Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00782openalex-snapshot
Organocatalyzed Asymmetric α-Thiocyanation of Oxindoles: Synthesis of Chiral Tertiary 3-Thiocyanatoxindoles
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00965openalex-snapshot
Fluorium-Initiated Dealkylative Cyanation of Thioethers to Thiocyanates
inferred← citeshttps://doi.org/10.1021/acs.joc.9b03275openalex-snapshot
Lewis Base/Brønsted Acid Cocatalysis for Thiocyanation of Amides and Thioamides
inferred← citeshttps://doi.org/10.1021/acs.jpcb.1c06775openalex-snapshot
Population Dynamics of Stretching Excitations of p-Azido-phenylalanine Incorporated in Calmodulin–Peptide Complexes
inferred← citeshttps://doi.org/10.1021/acs.langmuir.4c03647openalex-snapshot
Carbazole and Triazine-Based D–A Covalent Organic Framework for Visible Light-Mediated Photocatalytic C–H Activation of Imidazopyridine and Indole
inferred← citeshttps://doi.org/10.1021/acs.macromol.1c00190openalex-snapshot
Porphyrin-Based Conjugated Microporous Polymer Tubes: Template-Free Synthesis and A Photocatalyst for Visible-Light-Driven Thiocyanation of Anilines
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02308openalex-snapshot
Copper-Catalyzed Thiolation of Terminal Alkynes Employing Thiocyanate as the Sulfur Source Leading to Enaminone-Based Alkynyl Sulfides under Ambient Conditions
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c00460openalex-snapshot
Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02896openalex-snapshot
Photoinduced Synthesis of Thiocyanates through Hydrogen Atom Transfer and One-Pot Derivatization to Isothiocyanates
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c03396openalex-snapshot
Highly Diastereoselective Preparation of Tertiary Alkyl Thiocyanates en Route to Thiols by Stereoinvertive Nucleophilic Substitution at Nonclassical Carbocations
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