On the public citation graph
Adventures in Sulfur−Nitrogen Chemistry
0 signed · 357 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0040-4039(81)89008-9openalex-snapshot
Epoxidation of olefins by oxaziridines
inferredcites →https://doi.org/10.1016/j.tet.2004.03.094openalex-snapshot
Asymmetric synthesis of (+)-preussin from N-sulfinyl δ-amino β-ketoesters
inferredcites →https://doi.org/10.1016/j.tet.2004.06.071openalex-snapshot
Recent advances in asymmetric reactions using sulfinimines (N-sulfinyl imines)
inferredcites →https://doi.org/10.1016/j.tet.2005.03.122openalex-snapshot
Practical and highly stereoselective technology for preparation of enantiopure sulfoxides and sulfinamides utilizing activated and functionally differentiated N-sulfonyl-1,2,3-oxathiazolidine-2-oxide derivatives
inferredcites →https://doi.org/10.1016/s0040-4020(01)96713-4openalex-snapshot
Asymmetric oxidation of achiral selenides to optically active selenoxides
inferredcites →https://doi.org/10.1016/s0040-4039(00)73717-8openalex-snapshot
Asymmetric synthesis of sulfinimines: Chiral ammonia imine synthons
inferredcites →https://doi.org/10.1016/s0040-4039(00)80471-2openalex-snapshot
Stereo- and regioselective formation of silyl enol ethers via oxidation of vinyl anions
inferredcites →https://doi.org/10.1016/s0040-4039(00)88132-0openalex-snapshot
First synthesis of simple optically active selenoxides
inferredcites →https://doi.org/10.1016/s0040-4039(00)95605-3openalex-snapshot
The mechanism of hydroxylation of organometallic reagents by 2-sulfonyloxaziridines
inferredcites →https://doi.org/10.1016/s0040-4039(01)85053-xopenalex-snapshot
Synthesis of sulfenic acids: Flash vacuum pyrolysis of aryl and alkyl t-butyl sulfoxides
inferredcites →https://doi.org/10.1016/s0040-4039(01)85841-xopenalex-snapshot
2-Arenesulfonyl-3-aryloxaziridines: A new class of aprotic oxidizing agents (oxidation of organic sulfur compounds)
inferredcites →https://doi.org/10.1016/s0040-4039(01)92153-7openalex-snapshot
Peracid oxidation of trimethylsilyl enol ethers: A facile α-hydroxylation procedure
inferredcites →https://doi.org/10.1016/s0040-4039(98)02331-4openalex-snapshot
Asymmetric synthesis of aziridine 2-phosphonates and azirinyl phosphonates from enantiopure sulfinimines
inferredcites →https://doi.org/10.1016/s1874-5296(00)80020-0openalex-snapshot
Syntheses and reactions of sulfinimines
inferredcites →https://doi.org/10.1021/ar020066uopenalex-snapshot
N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines
inferredcites →https://doi.org/10.1021/cr00013a008openalex-snapshot
Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines
inferredcites →https://doi.org/10.1021/ja00030a045openalex-snapshot
Chemistry of oxaziridines. 17. N-(Phenylsulfonyl)(3,3-dichlorocamphoryl)oxaziridine: a highly efficient reagent for the asymmetric oxidation of sulfides to sulfoxides
inferredcites →https://doi.org/10.1021/ja00083a066openalex-snapshot
First total synthesis of taxol. 1. Functionalization of the B ring
inferredcites →https://doi.org/10.1021/ja00117a050openalex-snapshot
Asymmetric Synthesis of 2H-Azirines: First Enantioselective Synthesis of the Cytotoxic Antibiotic (R)-(-)-Dysidazirine
inferredcites →https://doi.org/10.1021/ja00174a035openalex-snapshot
Chemistry of oxaziridines. 14. Asymmetric oxidation of ketone enolates using enantiomerically pure (camphorylsulfonyl)oxaziridine
inferredcites →https://doi.org/10.1021/ja00197a080openalex-snapshot
(-)-.alpha.,.alpha.-Dichlorocamphorsulfonyloxaziridine: a superior reagent for the asymmetric oxidation of sulfides to sulfoxides
inferredcites →https://doi.org/10.1021/ja00233a025openalex-snapshot
Chemistry of oxaziridines. 11. (Camphorylsulfonyl)oxaziridine: synthesis and properties
inferredcites →https://doi.org/10.1021/ja00300a054openalex-snapshot
Asymmetric oxygenation of chiral imide enolates. A general approach to the synthesis of enantiomerically pure .alpha.-hydroxy carboxylic acid synthons
inferredcites →https://doi.org/10.1021/ja00362a026openalex-snapshot
A stable sulfenic acid, 9-triptycenesulfenic acid: its isolation and characterization
inferredcites →https://doi.org/10.1021/ja00413a064openalex-snapshot
Chemistry of sulfenic acids. 4. The first direct evidence for the involvement of sulfenic acids in the oxidation of thiols
inferredcites →https://doi.org/10.1021/ja00417a084openalex-snapshot
Chemistry of the sulfur-nitrogen bond. X. Barriers to planar inversion in N-(4,4'-dimethylbenzophenylidene)arenesulfenamides and -selenenamides
inferredcites →https://doi.org/10.1021/ja00477a045openalex-snapshot
Chemistry of the sulfur-nitrogen bond. 14. Arenesulfenic acids from N-alkylidenearenesulfinamides (sulfinimines)
inferredcites →https://doi.org/10.1021/ja00526a040openalex-snapshot
Chemistry of oxaziridines. 1. Synthesis and structure of 2-arenesulfonyl-3-aryloxaziridines. A new class of oxaziridines
inferredcites →https://doi.org/10.1021/ja00822a055openalex-snapshot
Chemistry of the sulfur-nitrogen bond. VIII. N-Alkylidenesulfinamides
inferredcites →https://doi.org/10.1021/jo00002a056openalex-snapshot
Chemistry of oxaziridines. 15. Asymmetric oxidations using 3-substituted 1,2-benzisothiazole 1,1-dioxide oxides
inferredcites →https://doi.org/10.1021/jo00003a042openalex-snapshot
Chemistry of oxaziridines. 16. A short, highly enantioselective synthesis of the AB-ring segments of .gamma.-rhodomycionone and .alpha.-citromycinone using (+)-[(8,8-dimethoxycamphoryl)sulfonyl]oxaziridine
inferredcites →https://doi.org/10.1021/jo00035a014openalex-snapshot
Asymmetric oxidation of simple selenides to selenoxides in high enantiopurity. Stereochemical aspects of the allyl selenoxide/allyl selenenate rearrangement
inferredcites →https://doi.org/10.1021/jo00050a007openalex-snapshot
Asymmetric synthesis of sulfinimines: applications to the synthesis of nonracemic .beta.-amino acids and .alpha.-hydroxyl .beta.-amino acids
inferredcites →https://doi.org/10.1021/jo00120a014openalex-snapshot
Selective, Electrophilic Fluorinations Using N-Fluoro-o-benzenedisulfonimide
inferredcites →https://doi.org/10.1021/jo00126a070openalex-snapshot
Asymmetric Synthesis of (R)-(+)-.beta.-Phenylalanine from (S)-(+)-Benzylidene-p-toluenesulfinamide. Regeneration of the Sulfinimine Precursor
inferredcites →https://doi.org/10.1021/jo00166a028openalex-snapshot
Chemistry of sulfenic acids. 5. A novel rearrangement of 2,4,6-trineopentylbenzenesulfenic acid to 2-tert-butyl-4,6-dineopentylbenzo[b]thiete and 3,3-dimethyl-4,4-dihydro-6,8-dineopentylbenzo[b]thiopyran. Synthesis of thiete sulfoxides
inferredcites →https://doi.org/10.1021/jo00191a048openalex-snapshot
Synthesis of .alpha.-hydroxycarbonyl compounds (acyloins): direct oxidation of enolates using 2-sulfonyloxaziridines
inferredcites →https://doi.org/10.1021/jo00214a043openalex-snapshot
Chemistry of sulfenic acids. 6. Structure of simple sulfenic acids generated by flash vacuum pyrolysis
inferredcites →https://doi.org/10.1021/jo00231a030openalex-snapshot
Catalysis by cyclodextrins in nucleophilic aromatic substitution reactions. 2. Amines as nucleophiles
inferredcites →https://doi.org/10.1021/jo00256a018openalex-snapshot
Chemistry of oxaziridines. 10. Selective catalytic oxidation of sulfides to sulfoxides using N-sulfonyloxaziridines
inferredcites →https://doi.org/10.1021/jo00269a054openalex-snapshot
Asymmetric synthesis of the methyl and benzyl ethers of erythro-.alpha.,.beta.-diphenyl-.beta.-hydroxyethanol and erythro-.alpha.,.beta.-diphenyl-.beta.-hydroxyethylamine from (+)-(S)-benzoin
inferredcites →https://doi.org/10.1021/jo00297a062openalex-snapshot
The mechanism of oxygen transfer from an oxaziridine to a sulfide and a sulfoxide: a theoretical study
inferredcites →https://doi.org/10.1021/jo00299a007openalex-snapshot
Enantioselective synthesis of tertiary .alpha.-hydroxy carbonyl compounds using [(8,8-dichlorocamphoryl)sulfonyl]oxaziridine
inferredcites →https://doi.org/10.1021/jo00330a017openalex-snapshot
Chemistry of sulfenic acids. 3. Studies of sterically hindered sulfenic acids using flash vacuum pyrolysis
inferredcites →https://doi.org/10.1021/jo00348a039openalex-snapshot
Chemistry of oxaziridines. 2. Improved synthesis of 2-sulfonyloxaziridines
inferredcites →https://doi.org/10.1021/jo00357a017openalex-snapshot
Chemistry of sulfenic acids. 7. Reason for the high reactivity of sulfenic acids. Stabilization by intramolecular hydrogen bonding and electronegativity effects
inferredcites →https://doi.org/10.1021/jo00362a053openalex-snapshot
Asymmetric oxidation of ester and amide enolates using new (camphorylsulfonyl)oxaziridines
inferredcites →https://doi.org/10.1021/jo00371a038openalex-snapshot
Stereochemistry of the asymmetric oxidation of ketone enolates using (camphorylsulfonyl)oxaziridines
inferredcites →https://doi.org/10.1021/jo00372a025openalex-snapshot
Chemistry of oxaziridines. 7. Kinetics and mechanism of the oxidation of sulfoxides and alkenes by 2-sulfonyloxaziridines. Relationship to the oxygen-transfer reactions of metal peroxides
inferredcites →https://doi.org/10.1021/jo00381a051openalex-snapshot
Oxidation of silyl enol ethers using 2-sulfonyloxaziridines. Synthesis of .alpha.-siloxy epoxides and .alpha.-hydroxy carbonyl compounds
inferredcites →https://doi.org/10.1021/jo00403a038openalex-snapshot
Chemistry of the sulfur-nitrogen bond. 13. A new synthesis of N-alkylidenearenesulfenamides (sulfenimines): alkylation of sulfenamide enolate equivalents
inferredcites →https://doi.org/10.1021/jo00422a068openalex-snapshot
Synthesis of secondary and tertiary carbinamines from N-alkylidenearenesulfenamides and alkyl- and aryllithium reagents
inferredcites →https://doi.org/10.1021/jo00426a008openalex-snapshot
Chemistry of the sulfur-nitrogen bond. 12. Metal-assisted synthesis of sulfenamide derivatives from aliphatic and aromatic disulfides
inferredcites →https://doi.org/10.1021/jo00805a014openalex-snapshot
Chemistry of the sulfur--nitrogen bond. I. Thermal reactions of nitrobenzenesulfenanilides
inferredcites →https://doi.org/10.1021/jo00867a027openalex-snapshot
Isomeric ethylene selenodithiocarbonates
inferredcites →https://doi.org/10.1021/jo00944a017openalex-snapshot
Chemistry of the sulfur-nitrogen bond. V. Evidence for an intermolecular rearrangement in the rearrangement of arenesulfenanilides to o- and p-aminodiphenyl sulfides
inferredcites →https://doi.org/10.1021/jo00956a016openalex-snapshot
Chemistry of the sulfur-nitrogen bond. VI. Convenient one-step synthesis of sulfenimines (S-aryl thiooximes)
inferredcites →https://doi.org/10.1021/jo00971a009openalex-snapshot
Chemistry of the sulfur-nitrogen bond. II. Mechanistic study of the rearrangement of 2-nitrobenzenesulfenanilides to 2-aminobenzenesulfonanilides
inferredcites →https://doi.org/10.1021/jo01297a023openalex-snapshot
Chemistry of sulfenic acids. 1. Synthesis of trimethylsilyl arenesulfenates (arenesulfenic acids)
inferredcites →https://doi.org/10.1021/jo030081sopenalex-snapshot
Asymmetric Synthesis of cis-5-tert-Butylproline with Metal Carbenoid NH Insertion
inferredcites →https://doi.org/10.1021/jo030208dopenalex-snapshot
Asymmetric Synthesis of the Quinolizidine Alkaloid (−)-Epimyrtine with Intramolecular Mannich Cyclization and N-Sulfinyl δ-Amino β-Ketoesters
inferredcites →https://doi.org/10.1021/jo050373oopenalex-snapshot
Asymmetric Synthesis of 2,4,5-Trisubstituted Piperidines from Sulfinimine-Derived δ-Amino β-Ketoesters. Formal Synthesis of Pseudodistomin B Triacetate
inferredcites →https://doi.org/10.1021/jo9519928openalex-snapshot
Asymmetric Strecker Synthesis Using Enantiopure Sulfinimines and Diethylaluminum Cyanide: The Alcohol Effect
inferredcites →https://doi.org/10.1021/jo970077eopenalex-snapshot
Asymmetric Synthesis and Properties of Sulfinimines (Thiooxime S -Oxides)
inferredcites →https://doi.org/10.1021/jo9702610openalex-snapshot
Asymmetric Synthesis of β-Substituted α-Amino Acids Using 2H-Azirine-2-carboxylate Esters. Synthesis of 3,3-Disubstituted Aziridine-2-carboxylate Esters
inferredcites →https://doi.org/10.1021/jo972045xopenalex-snapshot
Asymmetric Fluorination of Enolates with Nonracemic N-Fluoro-2,10-Camphorsultams
inferredcites →https://doi.org/10.1021/jo9820622openalex-snapshot
Improved Synthesis of Enantiopure Sulfinimines (Thiooxime S -Oxides) from p -Toluenesulfinamide and Aldehydes and Ketones
inferredcites →https://doi.org/10.1021/jo991119xopenalex-snapshot
Asymmetric Synthesis of 4-Hydroxy-3-phenyltetrahydroisoquinoline Derivatives Using Enantiopure Sulfinimines (N-Sulfinyl Imines)
inferredcites →https://doi.org/10.1021/jo991389fopenalex-snapshot
Asymmetric Synthesis of 2H-Azirine 2-Carboxylate Esters
inferredcites →https://doi.org/10.1021/ol005580jopenalex-snapshot
δ-Amino β-Keto Esters, a Designed Polyfunctionalized Chiral Building Block for Alkaloid Synthesis. Asymmetric Synthesis of (R)-(+)-2-Phenylpiperidine and (−)-SS20846A
inferredcites →https://doi.org/10.1021/ol0061438openalex-snapshot
Alkaloid Synthesis Using Chiral δ-Amino β-Ketoesters: A Stereoselective Synthesis of (−)-Lasubine II
inferredcites →https://doi.org/10.1021/ol015945fopenalex-snapshot
Asymmetric Synthesis of Quaternary α-Amino Phosphonates Using Sulfinimines
inferredcites →https://doi.org/10.1021/ol0164839openalex-snapshot
Intramolecular Mannich Reaction in the Asymmetric Synthesis of Polysubstituted Piperidines: Concise Synthesis of the Dendrobate Alkaloid (+)-241D and Its C-4 Epimer
inferredcites →https://doi.org/10.1021/ol017289popenalex-snapshot
2H-Azirine 3-Phosphonates: A New Class of Chiral Iminodienophiles. Asymmetric Synthesis of Quaternary Piperidine Phosphonates
inferredcites →https://doi.org/10.1021/ol025831jopenalex-snapshot
Asymmetric Synthesis of Substituted Prolines from δ-Amino β-Ketoesters. Methyl (2S,5R)-(+)-5-Phenylpyrrolidine-2-carboxylate
inferredcites →https://doi.org/10.1021/ol034119zopenalex-snapshot
N-Sulfinyl β-Amino Weinreb Amides: Synthesis of Enantiopure β-Amino Carbonyl Compounds. Asymmetric Synthesis of (+)-Sedridine and (−)-Allosedridine
inferredcites →https://doi.org/10.1021/ol035390jopenalex-snapshot
Asymmetric Synthesis of Functionalized trans-2,6-Disubstituted Piperidines with N-Sulfinyl δ-Amino β-Ketoesters. Synthesis of (−)-Lasubine I
inferredcites →https://doi.org/10.1021/ol048157+openalex-snapshot
Asymmetric Synthesis of Cis-5-Substituted Pyrrolidine 2-Phosphonates Using Metal Carbenoid NH Insertion and δ-Amino β-Ketophosphonates
inferredcites →https://doi.org/10.1021/ol0485971openalex-snapshot
Asymmetric Synthesis of α-Amino 1,3-Dithioketals from Sulfinimines (N-Sulfinyl Imines). Synthesis of (2S,3R)-(−)-3-Hydroxy-3-methylproline
inferredcites →https://doi.org/10.1021/ol048981yopenalex-snapshot
Asymmetric Synthesis of syn-(2R,3S)- and anti-(2S,3S)-Ethyl Diamino-3-phenylpropanoates from N-(Benzylidene)-p-toluenesulfinamide and Glycine Enolates
inferredcites →https://doi.org/10.1021/ol049795vopenalex-snapshot
Asymmetric Synthesis of the Carbocyclic Nucleoside Building Block (R)-(+)-4-Aminocyclopentenone Using δ-Amino β-Ketophosphonates and Ring-Closing Metathesis (RCM)
inferredcites →https://doi.org/10.1021/ol060521copenalex-snapshot
Asymmetric Synthesis of Polyfunctionalized Pyrrolidines from Sulfinimine-Derived Pyrrolidine 2-Phosphonates. Synthesis of Pyrrolidine 225C
inferredcites →https://doi.org/10.1039/a827013zopenalex-snapshot
Asymmetric synthesis of amino acids using sulfinimines (thiooxime S-oxides)
inferredcites →https://doi.org/10.1039/c39770000025openalex-snapshot
2-Arylsulphonyl-3-phenyloxaziridines: a new class of stable oxaziridine derivatives
inferredcites →https://doi.org/10.1055/s-1987-27877openalex-snapshot
Improved Preparation of Optically Active Methylp-Tolyl Sulfoxide
inferredcites →https://doi.org/10.1055/s-2000-8710openalex-snapshot
Asymmetric Synthesis of the Four Stereoisomers of 4-Hydroxypipecolic Acid
inferredcites →https://doi.org/10.1080/00304949909355704openalex-snapshot
SYNTHESIS OF α-FLUORO ALDEHYDES AND KETONES. A REVIEW
inferredcites →https://doi.org/10.15227/orgsyn.069.0158openalex-snapshot
(+)-(2R,8aS)-10-(CAMPHORYLSULFONYL)OXAZIRIDINE
inferredcites →https://doi.org/10.3998/ark.5550190.0007.711openalex-snapshot
Asymmetric synthesis of heterocycles using sulfinimines (N-sulfinyl imines)
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.4773913openalex-extracted
Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
inferred← citeshttps://doi.org/10.2139/ssrn.4865942openalex-extracted
Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
inferred← citeshttps://doi.org/10.1002/0471264180.or099.01openalex-snapshot
Addition of Non‐Stabilized Carbon‐Based Nucleophilic Reagents to Chiral N ‐Sulfinyl Imines
inferred← citeshttps://doi.org/10.1002/9780470440124.ch1openalex-snapshot
Silver‐Mediated Oxidation Reactions: Recent Advances and New Prospects
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0425openalex-snapshot
Redox Chemistry and Electrochemistry of Metal Enolates
inferred← citeshttps://doi.org/10.1002/9780470682531.pat0930openalex-snapshot
Introduction to the Energetics and Thermochemical Aspects of Polynitrogen Species
inferred← citeshttps://doi.org/10.1002/9783527625505.ch5openalex-snapshot
Asymmetric Synthesis of Three‐ and Four‐Membered Ring Heterocycles with More than One Heteroatom
inferred← citeshttps://doi.org/10.1002/9783527823819.ch6openalex-snapshot
Polymers with Sulfur‐Nitrogen Bonds
inferred← citeshttps://doi.org/10.1002/adsc.200800500openalex-snapshot
Polymer‐Supported N‐Phenylsulfonyloxaziridine (Davis Reagent): A Versatile Oxidant
inferred← citeshttps://doi.org/10.1002/adsc.201400992openalex-snapshot
Highly Regio‐ and Diastereoselective Addition of Organolithium Reagents to Chiral Fluoroalkyl α,β‐Unsaturated N‐tert‐Butanesulfinyl Ketimines: A General and Efficient Access to α‐Tertiary Fluoroalkyl Allylic Amines and α‐Fluoroalkyl α‐Amino Acids
inferred← citeshttps://doi.org/10.1002/adsc.201700353openalex-snapshot
Stereoselective Mannich Reaction of N‐(tert‐Butylsulfinyl)imines with 3‐Fluorooxindoles and Fluoroacetamides
inferred← citeshttps://doi.org/10.1002/adsc.202500178openalex-snapshot
Titanium‐Free N‐Sulfinyl Ketimine Formation by Transimination
inferred← citeshttps://doi.org/10.1002/ajoc.202000160openalex-snapshot
Efficient Synthesis of Sulfenamides through Mitsunobu‐type Coupling Reaction of Thiols with Amines using Dibenzyl Azodicarboxylate
inferred← citeshttps://doi.org/10.1002/ajoc.202200554openalex-snapshot
An Expedient Iodine‐Catalyzed Synthesis of Unsymmetrical Thiosulfonates by Sulfonylation of Thiols using Sulfonyl hydrazides in the Presence of Oxone
inferred← citeshttps://doi.org/10.1002/ajoc.202300032openalex-snapshot
Iodine Catalysed Oxidative Cross‐Coupling of Thioureas and Amines without Desulfurization
inferred← citeshttps://doi.org/10.1002/ange.200901353openalex-snapshot
CH Hydroxylation Using a Heterocyclic Catalyst and Aqueous H2O2
inferred← citeshttps://doi.org/10.1002/ange.200905801openalex-snapshot
Carbonyl Imines from Oxaziridines: Generation and Cycloaddition of NOC Dipoles
inferred← citeshttps://doi.org/10.1002/ange.201702530openalex-snapshot
Total Synthesis of (−)‐Albocycline
inferred← citeshttps://doi.org/10.1002/ange.201706629openalex-snapshot
Totalsynthese von Naturstoffen und ein kreativer Weg zum Aufbau von quartären Stereozentren
inferred← citeshttps://doi.org/10.1002/anie.200901353openalex-snapshot
CH Hydroxylation Using a Heterocyclic Catalyst and Aqueous H 2 O 2
inferred← citeshttps://doi.org/10.1002/anie.200905801openalex-snapshot
Carbonyl Imines from Oxaziridines: Generation and Cycloaddition of NOC Dipoles
inferred← citeshttps://doi.org/10.1002/anie.201702530openalex-snapshot
Total Synthesis of (−)‐Albocycline
inferred← citeshttps://doi.org/10.1002/anie.201706629openalex-snapshot
Construction of Quaternary Stereogenic Centers in the Total Synthesis of Natural Products
inferred← citeshttps://doi.org/10.1002/asia.200800032openalex-snapshot
Total Synthesis of Siomycin A: Construction of Synthetic Segments
inferred← citeshttps://doi.org/10.1002/cbdv.201300009openalex-snapshot
Synthesis, Characterization, and Anti‐Amoebic Activity of N‐(Pyrimidin‐2‐yl)benzenesulfonamide Derivatives
inferred← citeshttps://doi.org/10.1002/chem.201000615openalex-snapshot
N‐Sulfinyl Amines as a Nitrogen Source in the Asymmetric Intramolecular Aza‐Michael Reaction: Total Synthesis of (−)‐Pinidinol
inferred← citeshttps://doi.org/10.1002/chem.201003222openalex-snapshot
Multicomponent Synthesis of Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1002/chem.201102426openalex-snapshot
A Versatile Ru Catalyst for the Asymmetric Transfer Hydrogenation of Both Aromatic and Aliphatic Sulfinylimines
inferred← citeshttps://doi.org/10.1002/chem.201404009openalex-snapshot
Double‐Addition Reaction of Aryl Methyl Sulfones with N‐tert‐Butylsulfinyl Imines: Diastereoselective and Concise Synthesis of 2‐Sulfonylated 1,3‐Diamines
inferred← citeshttps://doi.org/10.1002/chin.200712246openalex-snapshot
Adventures in Sulfur—Nitrogen Chemistry
inferred← citeshttps://doi.org/10.1002/chir.22283openalex-snapshot
Enantioselective Organocatalytic Oxaziridination of N‐Tosyl Aldimine Catalyzed by Cinchona Alkaloid‐Ester Derivatives
inferred← citeshttps://doi.org/10.1002/cjoc.201400419openalex-snapshot
Asymmetric Pudovik Reaction of Chiral Fluoroalkyl α,β‐Unsaturated Ketimines and Diphenyl Phosphite
inferred← citeshttps://doi.org/10.1002/cjoc.70708openalex-snapshot
Photoinduced‐Atom Transfer Radical Cyclization of 1,5‐Enenitriles with Thiosulfonates for the Synthesis of γ‐Lactams Bearing Sulfonyl and N‐ Sulfenyliminyl Groups
inferred← citeshttps://doi.org/10.1002/ejic.201201344openalex-snapshot
Organic‐Free Self‐Assembled Copper Sulfide Microflowers
inferred← citeshttps://doi.org/10.1002/ejoc.200901158openalex-snapshot
Enantiodivergent Approach to Trifluoromethylated Amines: A Concise Route to Both Enantiomeric Analogues of Calcimimetic NPS R‐568
inferred← citeshttps://doi.org/10.1002/ejoc.201000167openalex-snapshot
Copper‐Catalyzed Formation of Sulfur–Nitrogen Bonds by Dehydrocoupling of Thiols with Amines
inferred← citeshttps://doi.org/10.1002/ejoc.201100337openalex-snapshot
Sulfinamides as Highly Effective Amine Protecting Groups and Their Use in the Conversion of Amino Alcohols into Morpholines
inferred← citeshttps://doi.org/10.1002/ejoc.201201712openalex-snapshot
Chiral Aminated α‐Methylenebenzocycloalkenes from o‐Bromoaryl Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201402847openalex-snapshot
Copper‐Catalyzed Synthesis of Thiosulfonates by Oxidative Coupling of Thiols with Sodium Sulfinates
inferred← citeshttps://doi.org/10.1002/ejoc.201402884openalex-snapshot
Microwave‐Enhanced Asymmetric Transfer Hydrogenation of N‐(tert‐Butylsulfinyl)imines
inferred← citeshttps://doi.org/10.1002/ejoc.201403424openalex-snapshot
Metal‐Mediated Reformatsky Reaction of Bromodifluoromethyl Ketone and Imine
inferred← citeshttps://doi.org/10.1002/ejoc.201500134openalex-snapshot
Synthesis of Chiral β‐Aminomalonates from 2‐Chlorotetrafluoroethanesulfinyl Aldimines through the Mannich Reaction
inferred← citeshttps://doi.org/10.1002/ejoc.201500857openalex-snapshot
Copper‐Catalyzed Synthesis of N‐Formyl/Acylsulfenamides and ‐thiosulfonamides
inferred← citeshttps://doi.org/10.1002/ejoc.201600091openalex-snapshot
Copper‐Catalyzed Oxidative Synthesis of Sulfinamides Using Thiols or Disulfides with Amines
inferred← citeshttps://doi.org/10.1002/ejoc.201800838openalex-snapshot
Oxidative Coupling with S–N Bond Formation
inferred← citeshttps://doi.org/10.1002/ejoc.202500026openalex-snapshot
Advances in Sulfenamide Chemistry: Synthetic Strategies and Reactivity Profiles
inferred← citeshttps://doi.org/10.1002/hc.21130openalex-snapshot
Double Asymmetric Induction in the Synthesis of Enantiomeric α‐Aminophosphonic Acids Mediated by Sulfinimines
inferred← citeshttps://doi.org/10.1002/jhet.752openalex-snapshot
Novel sulfenamides as promising acetylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1002/marc.202000181openalex-snapshot
Making the Best of Polymers with Sulfur–Nitrogen Bonds: From Sources to Innovative Materials
inferred← citeshttps://doi.org/10.1002/marc.202100063openalex-snapshot
Synthesis and Post‐Polymerization Modification of Poly(N‐(4‐Vinylphenyl)Sulfonamide)s
inferred← citeshttps://doi.org/10.1002/slct.201600449openalex-snapshot
Cu(II)‐catalyzed Enantioselective α‐Hydroxylation and α‐Chlorination of β‐Ketoesters with N,N,O ‐Tridentate Chiral Phenanthroline Ligand
inferred← citeshttps://doi.org/10.1002/slct.202102857openalex-snapshot
Asymmetric Synthesis of α‐Amino Acids Bearing a 3‐Alkyloxindole Structural Motif
inferred← citeshttps://doi.org/10.1002/slct.202304204openalex-snapshot
Formal Synthesis of (+)‐Phomactin A via a Prins/Conia‐ene Cascade and γ‐Hydroxylation Strategy
inferred← citeshttps://doi.org/10.1002/slct.202404520openalex-snapshot
Base‐Promoted Diastereoselective Addition of 2‐Aryloxy‐2‐Fluoroketones to N‐(tert‐Butylsulfinyl)Imines
inferred← citeshttps://doi.org/10.1002/tcr.201600078openalex-snapshot
Renovation of Optically Active Phenanthrolines as Powerful Chiral Ligands for Versatile Asymmetric Metal Catalysis
inferred← citeshttps://doi.org/10.1002/tcr.70232openalex-snapshot
Oxaziridines: Versatile Reagents in Modern Organic Synthesis
inferred← citeshttps://doi.org/10.1007/s00706-018-2261-4openalex-snapshot
Comparison of conventional and microwave-assisted synthesis of some new sulfenamides under free catalyst and ligand
inferred← citeshttps://doi.org/10.1007/s11030-021-10235-1openalex-snapshot
Catalytic stereoselective Mannich-type reactions for construction of fluorinated compounds
inferred← citeshttps://doi.org/10.1007/s11172-018-2130-7openalex-snapshot
Synthesis and biological activity of fluorine-containing amino derivatives based on 4-caranethiol
inferred← citeshttps://doi.org/10.1007/s11434-010-3140-5openalex-snapshot
Diastereoselective addition of lithium enolate of γ-substituted α-diazoacetoacetate to N-sulfinyl imines
inferred← citeshttps://doi.org/10.1007/s11696-020-01362-4openalex-snapshot
Synthesis and antioxidant activity of monoterpene nitrobenzylidenesulfenimines
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00503-6openalex-snapshot
5.2 Oxidation: C–O Bond Formation by C–H Activation
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00048-5openalex-snapshot
Imines and Their N-Substituted Derivatives: Oximes and Their O-R Substituted Analogs
inferred← citeshttps://doi.org/10.1016/bs.alkal.2021.05.001openalex-snapshot
Aspidosperma and Strychnos alkaloids: Chemistry and biology
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.07.047openalex-snapshot
A sulfoximine-based inhibitor of human asparagine synthetase kills l-asparaginase-resistant leukemia cells
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.05.126openalex-snapshot
Synthesis and antitumor activity of substituted triazolo[4,3-a]pyrimidin-6-sulfonamide with an incorporated thiazolidinone moiety
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.11.103openalex-snapshot
Synthesis and evaluation of novel sulfenamides as novel anti Methicillin-resistant Staphylococcus aureus agents
inferred← citeshttps://doi.org/10.1016/j.chroma.2018.08.010openalex-snapshot
Chromatographic enantioseparation of chiral sulfinamide derivatives on polysaccharide-based chiral stationary phases
inferred← citeshttps://doi.org/10.1016/j.cjche.2023.03.001openalex-snapshot
Continuous, efficient and safe synthesis of 1-oxa-2-azaspiro [2.5] octane in a microreaction system
inferred← citeshttps://doi.org/10.1016/j.cplett.2018.07.007openalex-snapshot
Quantum chemical study on the role of water in the reaction of singlet methoxysulfonyl nitrene CH3OS(O)2N
inferred← citeshttps://doi.org/10.1016/j.molstruc.2013.05.044openalex-snapshot
Redox regulation of protein tyrosine phosphatase 1B (PTP1B): Importance of steric and electronic effects on the unusual cyclization of the sulfenic acid intermediate to a sulfenyl amide
inferred← citeshttps://doi.org/10.1016/j.tet.2008.02.102openalex-snapshot
Synthesis of polysubstituted pyrroles from sulfinimines (N-sulfinyl imines)
inferred← citeshttps://doi.org/10.1016/j.tet.2009.02.033openalex-snapshot
Synthesis of chiral sulfinamido-sulfonamides and their evaluation as ligands for the enantioselective ethylation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.tet.2009.12.013openalex-snapshot
Enantioselective synthesis of condensed and transannular ring skeletons containing pyrrolidine moiety
inferred← citeshttps://doi.org/10.1016/j.tet.2010.11.018openalex-snapshot
Beyond the chiral pool: a general approach to β-amino-α-keto amides
inferred← citeshttps://doi.org/10.1016/j.tet.2011.01.069openalex-snapshot
Stereoselective diversity-oriented syntheses of functionalized saccharides from bicyclic carbohydrate 1,2-lactones
inferred← citeshttps://doi.org/10.1016/j.tet.2011.07.019openalex-snapshot
Asymmetric synthesis of diverse α,α-diarylmethylamines via aryl Grignard additions to chiral N-2,4,6-triisopropylbenzenesulfinylimines
inferred← citeshttps://doi.org/10.1016/j.tet.2011.08.058openalex-snapshot
Oxidation reactions using polymer-supported 2-benzenesulfonyl-3-(4-nitrophenyl)oxaziridine
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.061openalex-snapshot
Asymmetric oxaziridination catalyzed by cinchona alkaloid derivatives containing sulfide
inferred← citeshttps://doi.org/10.1016/j.tet.2013.07.061openalex-snapshot
2-Pyridylsulfinamides as effective catalysts in the asymmetric alkylation of aldehydes with diethylzinc
inferred← citeshttps://doi.org/10.1016/j.tet.2013.12.071openalex-snapshot
2-Chlorotetrafluoroethanesulfinamide induced asymmetric vinylogous Mannich reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2014.07.052openalex-snapshot
Carbohydrate-derived iminium salt organocatalysts for the asymmetric epoxidation of alkenes
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.059openalex-snapshot
Asymmetric total synthesis of (−)-melotenine A
inferred← citeshttps://doi.org/10.1016/j.tet.2017.02.047openalex-snapshot
Unsymmetrical disulfide and sulfenamide synthesis via reactions of thiosulfonates with thiols or amines
inferred← citeshttps://doi.org/10.1016/j.tet.2018.02.029openalex-snapshot
Recent applications of N-sulfonyloxaziridines (Davis oxaziridines) in organic synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2018.10.005openalex-snapshot
Synthetic studies toward lindenane-type dimers via Diels-Alder reaction
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130496openalex-snapshot
Stereoselective addition of Grignard reagents to sulfinimines derived from tartrate diol (threitol): Generation of chiral building blocks for the collective total synthesis of lentiginosine, conhydrine and methyldihydropalustramate
inferred← citeshttps://doi.org/10.1016/j.tet.2024.134133openalex-snapshot
Synthesis of N-sulfenylimines via an electrochemical radical coupling of amines and thiols mediated by bromide ions
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.01.033openalex-snapshot
Total synthesis of (R)-(+)-salsolidine by hydride addition to (R)-N-tert-butanesulfinyl ketimine
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.08.132openalex-snapshot
Sulfinimine-derived 2,3-diamino esters in the asymmetric synthesis of piperidine (2S,3S)-(+)-CP-99,994
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.11.170openalex-snapshot
α-Amino 1,3-dithioketal mediated asymmetric synthesis of piperidines (L-733,060) and tetrahydrofuran glycines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.12.067openalex-snapshot
Convenient synthesis of chiral non-racemic S-mesityl sulfinimines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.01.028openalex-snapshot
Chiral N-phosphonyl imine chemistry: new reagents and their applications for asymmetric reactions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.02.076openalex-snapshot
Tandem enantioselective conjugate addition–Mannich reactions: efficient multicomponent assembly of dialkylzincs, cyclic enones and chiral N-sulfinimines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.04.038openalex-snapshot
Chiral N-phosphonyl imine chemistry: asymmetric 1,2-additions of allylmagnesium bromides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.06.125openalex-snapshot
Asymmetric synthesis of (2S,3R)-(−)-epi-CP-99,994 using sulfinimine-derived anti-2,3-diamino esters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.114openalex-snapshot
Photodesulfinylation of optically active N-sulfinyl amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.10.076openalex-snapshot
Total syntheses of (+)-monomorine I and (−)-indolizidine 195B from sulfinimine-derived 3-oxo pyrrolidine 2-phosphonates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.08.035openalex-snapshot
Direct synthesis of imines from primary alcohols and amines using an active ruthenium(II) NNN–pincer complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.045openalex-snapshot
Novel one-pot asymmetric cascade approach toward densely substituted enantioenriched α-methylene-γ-lactams
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.05.041openalex-snapshot
Stereoselective synthesis of mexiletine and structural analogs with chiral tert-butanesulfinamide
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.12.106openalex-snapshot
Asymmetric synthesis of homoallylic amines via 1,2-addition of Grignard reagent to aliphatic N-phosphonyl hemiaminal
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.063openalex-snapshot
Triisopropyl borate mediated N -sulfinyl imine formation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.04.051openalex-snapshot
A diastereoselective Mannich reaction of α-fluoroketones with ketimines: Construction of β-fluoroamine motifs with vicinal tetrasubstituted stereocenters
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152034openalex-snapshot
Highly stereoselective synthesis of non-racemic 3-substituted dihydro-benzo[de]isoquinolinones via an addition-cyclization-substitution method
inferred← citeshttps://doi.org/10.1016/j.tetlet.2021.152880openalex-snapshot
Reinventing the wheel for enabling the synthesis of hinckdentine A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.155243openalex-snapshot
Recent progress in the asymmetric construction of C N, C O, and C S bonds using chiral sulfinamide reagents
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80005-0openalex-snapshot
Chapter 3 Three-membered ring systems
inferred← citeshttps://doi.org/10.1016/s0959-6380(08)80014-1openalex-snapshot
Chapter 6.1 Six-membered ring systems: pyridine and benzo derivatives
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70030-3openalex-snapshot
Chapter 3: Three-Membered Ring Systems
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70039-xopenalex-snapshot
Chapter 6.1: Six-Membered Ring Systems: Pyridine and Benzo Derivatives
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00002openalex-snapshot
Modern Stereoselective Synthesis of Chiral Sulfinyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.0c00823openalex-snapshot
Asymmetric Induction with a Chiral Amine Catalyzed by a Ru-PNP Pincer Complex: Insight from Theoretical Investigation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b00357openalex-snapshot
Halide Influence on Molecular and Supramolecular Arrangements of Iron Complexes with a 3,5-Bis(2-Pyridyl)-1,2,4,6-Thiatriazine Ligand
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00938openalex-snapshot
Four-Step Total Synthesis of (+)-Euphococcinine and (±)-Adaline
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02227openalex-snapshot
Diastereoselective Synthesis of trans-β-Amino Cyclohexyl Ketones and trans-3-Amino-4-acyl-tetrahydropyrans from Intramolecular C-Alkylation of ω-Halo-Substituted β-Sulfinamido Ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02090openalex-snapshot
Electrochemical Direct Synthesis of N-Sulfenylimines from Amines in the Presence of Thiophenols
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01982openalex-snapshot
Diastereoselective Addition of Lithiated Allenyl Sulfones to Nonracemic Sulfinimines: Asymmetric Synthesis of Diverse Heterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01574openalex-snapshot
Diastereoselective Addition of Metal α-Fluoroenolates of Carboxylate Esters to N-tert-Butylsulfinyl Imines: Synthesis of α-Fluoro-β-amino Acids
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00463openalex-snapshot
Asymmetric Synthesis of Either Enantiomer of β-Butadienyl Amines by Isoprenylation of Davis–Ellman Imines
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01087openalex-snapshot
Dual Role of Sulfenamides in Iodine/Oxone-Catalyzed Three-Component Coupling of 2-Mercaptobenzoxazoles, Amines, and Ketones: Route toward α-Thioenamines and 2-Iminothiazolines
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00261openalex-snapshot
Aminoxidation of Arenethiols to N-Chloro-N-sulfonyl Sulfinamides
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01541openalex-snapshot
Synthesis of β-Amino-Substituted Enones by Addition of Substituted Methyl Enones to Sulfinimines: Application to the Total Synthesis of Alkaloids (+)-Lasubine II and (+)-241D and the Formal Total Synthesis of (−)-Lasubine I
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01979openalex-snapshot
Diastereoselective Mannich Reactions Using Fluorinated Ketones: Synthesis of Stereogenic Carbon–Fluorine Units
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02551openalex-snapshot
Development and Scope of the Arene-Fused Domino Michael/Mannich Reaction: Application to the Total Syntheses ofAspidospermaAlkaloids (−)-Aspidospermidine, (−)-Tabersonine, and (−)-Vincadifformine
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02611openalex-snapshot
Synthesis of β-Amino Ketones by Addition of Aryl Methyl Ketones to Sulfinimines: Application to the Total Synthesis of HPA-12, Norsedamine, and Sedamine
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01381openalex-snapshot
Addition of the Lithium Anion of Diphenylmethanol Methyl/Methoxymethyl Ether to Nonracemic Sulfinimines: Two-Step Asymmetric Synthesis of Diphenylprolinol Methyl Ether and Chiral (Diphenylmethoxymethyl)amines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02473openalex-snapshot
A Three-Component Derivatization Protocol for Determining the Enantiopurity of Sulfinamides by 1H and 19F NMR Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02938openalex-snapshot
Stereoselective Synthesis of β-Amino Ynones by the Addition of Alkynones to Nonracemic Sulfinimines: Formal Total Synthesis of l -Xylo and l -Arabino Phytosphingosines
inferred← citeshttps://doi.org/10.1021/acs.macromol.2c02507openalex-snapshot
Polymerization of Primary Amines with Sulfur Monochloride to Yield Red Polymers with a Conjugated SN Backbone
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00625openalex-snapshot
Stereocontrolled Addition of Scrambling ortho-Sulfinyl Carbanions: Easy Access to Homopropargylamines and α-Allenylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02608openalex-snapshot
Addition of Lithium Anion of (Acetylmethylene)triphenylphosphorane to Nonracemic Sulfinimines: Total Synthesis of (+)-241D and Formal Total Synthesis of (+)-Preussin
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02201openalex-snapshot
Domino Michael/Mannich Annulation Reaction of N-Sulfinyl Lithiodienamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03221openalex-snapshot
Kinetic Resolution of Sulfinamides via Asymmetric N-Allylic Alkylation
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c04122openalex-snapshot
Diarylamine Synthesis via Desulfinylative Smiles Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01738openalex-snapshot
Synthetic Approach toward Enantiopure Cyclic Sulfinamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02513openalex-snapshot
Diastereoselective Hydroxylation of N-tert-Butanesulfinyl Imines with 2-(Phenylsulfonyl)-3-phenyloxaziridine (Davis Oxaziridine)
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01969openalex-snapshot
Lithio Tris(methylthio)methane as Hydroxy/Thio/Aminocarbonyl Anion Equivalent: Asymmetric Synthesis of α-Amino Acid Esters, Thioesters, Amides, and Peptides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00110openalex-snapshot
Exploiting N-Centered Umpolung Reactivity of α-Iminomalonates for the Synthesis of N-Sulfenylimines and Sulfonamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00949openalex-snapshot
A General Method for Imine Formation Using B(OCH2CF3)3
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03564openalex-snapshot
Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey–Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02691openalex-snapshot
Asymmetric Synthesis of Axially Chiral Spiro Aziridines and Spiro Thiazolidinethiones from Sulfonyl Bicyclobutanes
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02074openalex-snapshot
Asymmetric Vinylogous Aza-Darzens Approach to Vinyl Aziridines
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02331openalex-snapshot
Umpolung Synthesis of Vicinal Diamines: Diastereoselective Addition of 2-Azaallyl Anions to Davis–Ellman’s Imines
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03242openalex-snapshot
Formal Synthesis of (+)-Phomactin A
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03309openalex-snapshot
Regiodivergent Ring-Opening Cross-Coupling of Vinyl Aziridines with Phosphorus Nucleophiles: Access to Phosphorus-Containing Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00564openalex-snapshot
Asymmetric Synthesis 1-Substituted 2,6-Diazaspiro[3.3]heptanes through Addition of 3-Azetidinecarboxylate Anions to Davis–Ellman Imines
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02545openalex-snapshot
Iodine/Manganese Dual Catalysis for Oxidative Dehydrogenation Coupling of Amines with Thiols
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03507openalex-snapshot
Stereoselective Addition of a Lithium Anion of 1,1-Diphenyl-2-aza-pentadiene to Sulfinimines: Application to the Synthesis of (−)-Epiquinamide
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03560openalex-snapshot
One-Step Diastereoselective Pyrrolidine Synthesis Using a Sulfinamide Annulating Reagent
inferred← citeshttps://doi.org/10.1021/ar4001839openalex-snapshot
Catalytic Access to α-Oxo Gold Carbenes by N–O Bond Oxidants
inferred← citeshttps://doi.org/10.1021/cr400611nopenalex-snapshot
Advances in the Chemistry of Oxaziridines
inferred← citeshttps://doi.org/10.1021/cr900382topenalex-snapshot
Synthesis and Applications of tert-Butanesulfinamide
inferred← citeshttps://doi.org/10.1021/cs500132mopenalex-snapshot
Asymmetric Catalytic Routes to Dialkyl Peroxides and Oxaziridines
inferred← citeshttps://doi.org/10.1021/ed500292qopenalex-snapshot
Diastereoselective Allylation of N-tert-Butanesulfinyl Imines: An Asymmetric Synthesis Experiment for the Undergraduate Organic Laboratory
inferred← citeshttps://doi.org/10.1021/ja204597kopenalex-snapshot
Concise Total Synthesis and Stereochemical Revision of all (−)-Trigonoliimines
inferred← citeshttps://doi.org/10.1021/ja2064457openalex-snapshot
Catalytic Enantioselective Oxaziridination
inferred← citeshttps://doi.org/10.1021/ja408114uopenalex-snapshot
Domino Michael/Mannich/N-Alkylation Route to the Tetrahydrocarbazole Framework of Aspidosperma Alkaloids: Concise Total Syntheses of (−)-Aspidospermidine, (−)-Tabersonine, and (−)-Vincadifformine
inferred← citeshttps://doi.org/10.1021/jacs.6b04072openalex-snapshot
Convergent and Biomimetic Enantioselective Total Synthesis of (−)-Communesin F
inferred← citeshttps://doi.org/10.1021/jacs.9b03438openalex-snapshot
Enantioselective Markovnikov Addition of Carbamates to Allylic Alcohols for the Construction of α-Secondary and α-Tertiary Amines
inferred← citeshttps://doi.org/10.1021/jo100680bopenalex-snapshot
Asymmetric Synthesis of Cyclic cis-β-Amino Acid Derivatives Using Sulfinimines and Prochiral Weinreb Amide Enolates
inferred← citeshttps://doi.org/10.1021/jo1024943openalex-snapshot
Asymmetric Synthesis of Ethoxydienamines in Superbasic Medium Mediated by Chiral Sulfinyl Group
inferred← citeshttps://doi.org/10.1021/jo200119xopenalex-snapshot
Optically Pure Polyfluoroalkanesulfinamides: Synthesis and Application as Promising and Monitorable Chiral Auxiliaries
inferred← citeshttps://doi.org/10.1021/jo2002352openalex-snapshot
Asymmetric Synthesis of anti-α-Substituted β-Amino Ketones from Sulfinimines
inferred← citeshttps://doi.org/10.1021/jo200715copenalex-snapshot
Enantioselective Synthesis of Diverse Sulfinamides and Sulfinylferrocenes from Phenylglycine-Derived Chiral Sulfinyl Transfer Agent
inferred← citeshttps://doi.org/10.1021/jo201849jopenalex-snapshot
One-Pot Synthesis of Chiral Nonracemic Amines
inferred← citeshttps://doi.org/10.1021/jo202144kopenalex-snapshot
An Approach to the Stereoselective Synthesis of Enantiopure Dihydropyrroles and Aziridines from a Common Sulfinyl-Sulfinamide Intermediate
inferred← citeshttps://doi.org/10.1021/jo202611vopenalex-snapshot
Synthesis of Enantiomerically Pure anti-1,2-Diaryl and syn-1,2-Alkylaryl vic-Selenoamines
inferred← citeshttps://doi.org/10.1021/jo202652fopenalex-snapshot
Enantioselective Synthesis of Cocaine C-1 Analogues using Sulfinimines (N-Sulfinyl Imines)
inferred← citeshttps://doi.org/10.1021/jo300110aopenalex-snapshot
Zinc-Mediated Diastereoselective Synthesis of 3-Amino Oxindoles by Addition of Methyl and Terminal Alkynes to N-tert-Butanesulfinyl Ketimines
inferred← citeshttps://doi.org/10.1021/jo300919xopenalex-snapshot
Microwave-Assisted Solvent-Free Synthesis of Enantiomerically Pure N -( tert -Butylsulfinyl)imines
inferred← citeshttps://doi.org/10.1021/jo400354ropenalex-snapshot
Design, Synthesis, and Applications of Chiral N-2-Phenyl-2-propyl Sulfinyl Imines for Group-Assisted Purification (GAP) Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1021/jo4020358openalex-snapshot
Total Synthesis, Stereochemical Assignment, and Biological Activity of All Known (−)-Trigonoliimines
inferred← citeshttps://doi.org/10.1021/jo500008eopenalex-snapshot
The Synthesis and Strecker Reaction of 2-Chlorotetrafluoroethanesulfinyl Ketimines
inferred← citeshttps://doi.org/10.1021/jo7018703openalex-snapshot
N-Isopropylsulfinylimines as Useful Intermediates in the Synthesis of Chiral Amines: Expeditive Asymmetric Synthesis of the Calcimimetic (+)-NPS R-568
inferred← citeshttps://doi.org/10.1021/jo701907dopenalex-snapshot
Stereocontrolled Synthesis of Methyl Silanediol Peptide Mimics
inferred← citeshttps://doi.org/10.1021/jo702130aopenalex-snapshot
An Efficient Method for the Synthesis of Nitropiperidones
inferred← citeshttps://doi.org/10.1021/jo801653copenalex-snapshot
Asymmetric Synthesis of Acyclic 1,3-Amino Alcohols by Reduction of N -Sulfinyl β-Amino Ketones. Formal Synthesis of (−)-Pinidinol and (+)- Epipinidinol
inferred← citeshttps://doi.org/10.1021/jo802812wopenalex-snapshot
Modular Stereocontrolled Assembly of R2Zn, Cyclic Enones and N-tert-Butanesulfinyl Imines
inferred← citeshttps://doi.org/10.1021/jo900046topenalex-snapshot
Asymmetric Synthesis of α-Alkylated N-Sulfinyl Imidates as New Chiral Building Blocks
inferred← citeshttps://doi.org/10.1021/jo900063nopenalex-snapshot
Computational Investigation of Rearrangements in Huisgen Cycloadducts of Azolium N-Dicyanomethanide 1,3-Dipoles with Alkynes: A Mechanistic Panoply
inferred← citeshttps://doi.org/10.1021/jo9001504openalex-snapshot
Vinylaluminum Addition to Sulfinimines (N-Sulfinyl Imines). Asymmetric Synthesis of anti-α-Alkyl β-Amino Esters
inferred← citeshttps://doi.org/10.1021/jp1035597openalex-snapshot
Kinetics and Mechanism ofS-Nitrosothiol Acid-Catalyzed Hydrolysis: Sulfur Activation Promotes Facile NO+Release
inferred← citeshttps://doi.org/10.1021/jp103616qopenalex-snapshot
Anomeric Effects in Sulfonyl Compounds: An Experimental and Computational Study of Fluorosulfonyl Azide, FSO2N3, and Trifluoromethylsulfonyl Azide, CF3SO2N3
inferred← citeshttps://doi.org/10.1021/ma4025174openalex-snapshot
UV–Vis Monitoring of Radical Polymerizations by Spin Trapping with Chromophoric Nitrones
inferred← citeshttps://doi.org/10.1021/ml2001483openalex-snapshot
Type 1 Phototherapeutic Agents, Part I: Preparation and Cancer Cell Viability Studies of Novel Photolabile Sulfenamides
inferred← citeshttps://doi.org/10.1021/ol063058copenalex-snapshot
Asymmetric Synthesis of anti- and syn-2,3-Diamino Esters Using Sulfinimines. Water and Concentration Effects
inferred← citeshttps://doi.org/10.1021/ol070365popenalex-snapshot
Asymmetric Synthesis of 2H-Azirine 3-Carboxylates
inferred← citeshttps://doi.org/10.1021/ol100211sopenalex-snapshot
Highly Diastereoselective α-Hydroxylation of Fox Chiral Auxiliary-Based Amide Enolates with Molecular Oxygen
inferred← citeshttps://doi.org/10.1021/ol100536eopenalex-snapshot
Highly Effective and Diastereoselective Synthesis of Axially Chiral Bis-sulfoxide Ligands via Oxidative Aryl Coupling
inferred← citeshttps://doi.org/10.1021/ol1017118openalex-snapshot
Asymmetric Total Synthesis of (S)-(+)-Cocaine and the First Synthesis of Cocaine C-1 Analogs from N-Sulfinyl β-Amino Ester Ketals
inferred← citeshttps://doi.org/10.1021/ol200263gopenalex-snapshot
Stereospecific Ring Expansion of Chiral Vinyl Aziridines
inferred← citeshttps://doi.org/10.1021/ol400720bopenalex-snapshot
Cycloaddition of Chiral tert -Butanesulfinimines with Trimethylenemethane
inferred← citeshttps://doi.org/10.1021/ol502463sopenalex-snapshot
Chemoselective Addition of Isocyanides to N-tert-Butanesulfinimines
inferred← citeshttps://doi.org/10.1021/ol502967xopenalex-snapshot
Asymmetric Synthesis of Trisubstituted Aziridines via Aza-Darzens Reaction of Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1021/ol503118vopenalex-snapshot
Formal Palladium-Catalyzed Asymmetric Hydrogenolysis of Racemic N-Sulfonyloxaziridines
showing the first 200 of 267 · page through all 267
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.