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Asymmetric Synthesis and Properties of Sulfinimines (Thiooxime S -Oxides)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0040-4039(96)00707-1openalex-snapshot
Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate
inferredcites →https://doi.org/10.1016/0040-4039(96)00827-1openalex-snapshot
Aziridine-2-carboxylic acid mediated asymmetric synthesis of D-erythro- and L-threo-sphingosine from a common precursor
inferredcites →https://doi.org/10.1016/0040-4039(96)01168-9openalex-snapshot
2-Methyl N-(p-toluenesulfinyl)aziridine-2-carboxylic acid: Asymmetric synthesis of α-methylphenylalanine and α-methyl-β-phenylserine
inferredcites →https://doi.org/10.1016/0040-4039(96)01176-8openalex-snapshot
Synthesis of chiral non-racemic 2-arylpyrrolines by a [3+2] cycloaddition route
inferredcites →https://doi.org/10.1016/0957-4166(94)80045-6openalex-snapshot
Synthesis of (2R, 3S)-methyl-2-fluoro-3-(n-benzoylamino)-3-phenylpropanoate: Modified side chain of taxol
inferredcites →https://doi.org/10.1016/0957-4166(95)00010-mopenalex-snapshot
Asymmetric synthesis of α-amino acids via chiral N-alkylidenesulfinamides
inferredcites →https://doi.org/10.1016/0957-4166(95)00185-ropenalex-snapshot
Addition of dimethyloxosulfonium methylide to enantiomerically pure sulfinimines: Asymmetric synthesis of 2-substituted aziridines
inferredcites →https://doi.org/10.1016/b978-0-08-052349-1.00012-3openalex-snapshot
Nucleophilic Addition to Imines and Imine Derivatives
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)76775-xopenalex-snapshot
Approaches toward the total syntheses of astins A, B, and C
inferredcites →https://doi.org/10.1016/s0040-4039(00)78334-1openalex-snapshot
Asymmetric synthesis of the antibiotic (+)-thiamphenicol using cis-N-(p-toluenesulfinyl)aziridine 2-carboxylic acids
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/ja00117a050openalex-snapshot
Asymmetric Synthesis of 2H-Azirines: First Enantioselective Synthesis of the Cytotoxic Antibiotic (R)-(-)-Dysidazirine
inferredcites →https://doi.org/10.1021/ja00338a030openalex-snapshot
An efficient asymmetric oxidation of sulfides to sulfoxides
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/ja00822a055openalex-snapshot
Chemistry of the sulfur-nitrogen bond. VIII. N-Alkylidenesulfinamides
inferredcites →https://doi.org/10.1021/ja01027a055openalex-snapshot
Synthesis of isomerically pure .alpha.,.beta.-unsaturated nitriles via hydroalumination of alkynes
inferredcites →https://doi.org/10.1021/ja01592a068openalex-snapshot
Derivatives of Aromatic Sulfinic Acids. II. The Reaction of Thionyl Chloride with Sulfinic Esters1,2
inferredcites →https://doi.org/10.1021/jo00001a003openalex-snapshot
Stereoselective addition reactions of chiral N-benzylidene-p-toluenesulfinamides. Asymmetric syntheses of .beta.- and .gamma.-amino acids
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/jo00036a005openalex-snapshot
Synthesis of putative intermediates in the biosynthesis of the kinamycin antibiotics: total synthesis of phenanthroviridin aglycon and related compounds
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/jo00083a037openalex-snapshot
Application of New Camphor-Derived Mercapto Chiral Auxiliaries to the Synthesis of Optically Active Primary Amines
inferredcites →https://doi.org/10.1021/jo00091a001openalex-snapshot
Asymmetric Synthesis and Reactions of cis-N-(p-Toluenesulfinyl)aziridine-2-carboxylic Acids
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/jo00151a002openalex-snapshot
Preparation of primary amines and 2-azetidinones via N-(trimethylsilyl)imines
inferredcites →https://doi.org/10.1021/jo00338a050openalex-snapshot
Direct conversion of nitriles to .alpha.-alkylated aldehydes
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/jo00956a016openalex-snapshot
Chemistry of the sulfur-nitrogen bond. VI. Convenient one-step synthesis of sulfenimines (S-aryl thiooximes)
inferredcites →https://doi.org/10.1021/jo01087a013openalex-snapshot
Reductions with Dialkylaluminum Hydrides
inferredcites →https://doi.org/10.1021/jo951917xopenalex-snapshot
An Efficient Synthesis of (S)-(+)-Ethyl β-Amino-3-pyridinepropanoate Using Enantiopure Sulfinimines
inferredcites →https://doi.org/10.1021/jo9519928openalex-snapshot
Asymmetric Strecker Synthesis Using Enantiopure Sulfinimines and Diethylaluminum Cyanide: The Alcohol Effect
inferredcites →https://doi.org/10.1039/c39850001584openalex-snapshot
A new synthetic method for sulphenimines. Fluoride-catalysed reaction of N,N-bis(trimethylsilyl)sulphenamides with aldehydes and ketones
inferredcites →https://doi.org/10.1039/cc9960001503openalex-snapshot
A highly efficient asymmetric synthesis of β-aminophosphonic acids, via addition of α-phosphonate carbanions to chiral, enantiopure sulfinimines
inferredcites →https://doi.org/10.1039/p19820000339openalex-snapshot
Asymmetric induction in the reduction of optically active N-alkylidenesulphinamides by metal hydrides. A new, efficient enantioselective route to chiral amines
inferredcites →https://doi.org/10.1039/p19940000779openalex-snapshot
Pinacol–pinacolone rearrangement induced by aminium salts
inferredcites →https://doi.org/10.1039/p19960000691openalex-snapshot
Asymmetric synthesis of amines using a chiral, non-racemic, benzylidene sulfinamide derived from a recoverable precursor
inferredcites →https://doi.org/10.1039/p29850000491openalex-snapshot
The ambident reactivity of triphenylmethyl radicals in hydrogen-abstraction reactions and the mechanism of the base-catalysed rearrangement of (diphenylmethylene)cyclohexadienes (a type of semibenzene) into triphenylmethane
inferredcites →https://doi.org/10.1055/s-1972-21858openalex-snapshot
Reduction of Organic Compounds by Alkoxyaluminohydrides
inferredcites →https://doi.org/10.1055/s-1981-29378openalex-snapshot
Asymmetric Synthesis Using Nucleophilic Reagents Containing a Chiral Sulfoxide Group
inferredcites →https://doi.org/10.1055/s-1983-30623openalex-snapshot
A Novel Synthesis of Arenesulfinamides fromS-4-NitrophenylS-Substituted-Phenyl Sulfoximides with Elemental Sulfur in Liquid Ammonia
inferredcites →https://doi.org/10.1055/s-1996-5550openalex-snapshot
A Versatile and Convenient Synthesis of N-(Tri-i-propylsilyl)- and N-(t-Butyldimethylsilyl)aldimines
inferredcites →https://doi.org/10.15227/orgsyn.064.0196openalex-snapshot
(S)-( + )-2-(p-TOLUENESULFINYL)-2-CYCLOPENTENONE: PRECURSOR FOR ENANTIOSELECTIVE SYNTHESIS OF 3-SUBSTITUTED CYCLOPENTANONES
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/(sici)1099-0690(200001)2000:1<1::aid-ejoc1>3.0.co;2-6openalex-snapshot
Preparation of Achiral and of Enantiopure Geminally Disubstituted β-Amino Acids for β-Peptide Synthesis
inferred← citeshttps://doi.org/10.1002/047084289x.rl117mopenalex-snapshot
Lithium Hexamethyldisilazide
inferred← citeshttps://doi.org/10.1002/047084289x.rl117m.pub2openalex-snapshot
Lithium Hexamethyldisilazide
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/10.1002/0471264180.os077.06openalex-snapshot
Sulfinimines (Thiooximine S‐Oxides): Asymmetric Synthesis of Methyl (R)‐(+)‐β‐Phenylalanate from (S)‐(+)‐N‐(Benzylidene)‐p‐Toluenesulfinamide
inferred← citeshttps://doi.org/10.1002/0471264229.os094.25openalex-snapshot
Preparation of N ‐Sulfinyl Aldimines Using Pyrrolidine as Catalyst via Iminium Ion Activation
inferred← citeshttps://doi.org/10.1002/1099-0690(200012)2000:24<3961::aid-ejoc3961>3.0.co;2-popenalex-snapshot
A Novel Approach to Dihydropyrrolones from Iron-Substituted α,β-Unsaturated Imines and Organolithium and Grignard Reagents: Developments, Mechanisms and Stereoselective Syntheses
inferred← citeshttps://doi.org/10.1002/1099-0690(200104)2001:8<1449::aid-ejoc1449>3.0.co;2-2openalex-snapshot
Synthesis of Nonracemic α-Trifluoromethyl α-Amino Acids from Sulfinimines of Trifluoropyruvate
inferred← citeshttps://doi.org/10.1002/9783527828166.ch3openalex-snapshot
Olefination, Metathesis, and Epoxidation Reactions
inferred← citeshttps://doi.org/10.1002/adsc.201701510openalex-snapshot
Direct Synthesis of Sulfinamides by the Copper‐Catalyzed Electrophilic Amidation of Sulfenate Anions
inferred← citeshttps://doi.org/10.1002/adsc.202200113openalex-snapshot
Diastereoselective Synthesis of Chiral Oxathiazine 2‐Oxide Scaffolds as Sulfinyl Transfer Agents
inferred← citeshttps://doi.org/10.1002/adsc.70329openalex-snapshot
An Asymmetric Aryne‐capture Cascade Process: Tunable and Regiodivergent Synthesis of Chiral 2‐Aminobenzylamines by a Three‐Component Reaction
inferred← citeshttps://doi.org/10.1002/ange.200503369openalex-snapshot
Formation of Cyclic Sulfinates and Sulfinamides through Homolytic Substitution at the Sulfur Atom
inferred← citeshttps://doi.org/10.1002/ange.202011138openalex-snapshot
Hydroxylamin‐abgeleitetes Reagenz als duales Oxidationsmittel und Aminogruppendonor für die eisenkatalysierte Herstellung von ungeschützten Sulfinamiden aus Thiolen
inferred← citeshttps://doi.org/10.1002/ange.202109566openalex-snapshot
O2‐Assisted Four‐Component Reaction of Vinyl Magnesium Bromide with Chiral N‐tert‐Butanesulfinyl Imines To Form syn‐1,3‐Amino Alcohols
inferred← citeshttps://doi.org/10.1002/anie.200503369openalex-snapshot
Formation of Cyclic Sulfinates and Sulfinamides through Homolytic Substitution at the Sulfur Atom
inferred← citeshttps://doi.org/10.1002/anie.202011138openalex-snapshot
Hydroxylamine‐Derived Reagent as a Dual Oxidant and Amino Group Donor for the Iron‐Catalyzed Preparation of Unprotected Sulfinamides from Thiols
inferred← citeshttps://doi.org/10.1002/anie.202109566openalex-snapshot
O2‐Assisted Four‐Component Reaction of Vinyl Magnesium Bromide with Chiral N‐tert‐Butanesulfinyl Imines To Form syn‐1,3‐Amino Alcohols
inferred← citeshttps://doi.org/10.1002/asia.200800032openalex-snapshot
Total Synthesis of Siomycin A: Construction of Synthetic Segments
inferred← citeshttps://doi.org/10.1002/asia.201300051openalex-snapshot
Total Synthesis of Tubulysin U and Its C‐4 Epimer
inferred← citeshttps://doi.org/10.1002/chem.200204674openalex-snapshot
Highly Diastereoselective [3+2] Cycloadditions between Nonracemic p‐Tolylsulfinimines and Iminoesters: An Efficient Entry to Enantiopure Imidazolidines and Vicinal Diaminoalcohols
inferred← citeshttps://doi.org/10.1002/chem.201000217openalex-snapshot
2‐(p‐Tolylsulfinyl)benzyl Halides as Efficient Precursors of Optically Pure trans‐2,3‐Disubstituted Aziridines
inferred← citeshttps://doi.org/10.1002/chem.201002885openalex-snapshot
Functionalization of Mesoporous Carbon with Superbasic MgO Nanoparticles for the Efficient Synthesis of Sulfinamides
inferred← citeshttps://doi.org/10.1002/chem.201003222openalex-snapshot
Multicomponent Synthesis of Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1002/chem.201003542openalex-snapshot
Lewis Acid/Base Catalyzed [2+2]‐Cycloaddition of Sulfenes and Aldehydes: A Versatile Entry to Chiral Sulfonyl and Sulfinyl Derivatives
inferred← citeshttps://doi.org/10.1002/chin.199738127openalex-snapshot
ChemInform Abstract: Asymmetric Synthesis and Properties of Sulfinimines (Thiooxime S‐ Oxides).
inferred← citeshttps://doi.org/10.1002/ejoc.201201589openalex-snapshot
Asymmetric Synthesis of Structurally Diverse Aminophosphonic Acids by Using Enantiopure N‐(p‐Tolylsulfinyl)cinnamaldimines as Reagents
inferred← citeshttps://doi.org/10.1002/ejoc.201400035openalex-snapshot
Design Strategies for Enhanced Hydrogen‐Bond Donor Catalysts
inferred← citeshttps://doi.org/10.1002/ejoc.201402673openalex-snapshot
DMAP‐Catalysed Sulfinylation of Diacetone‐ D ‐Glucose: Improved Method for the Synthesis of Enantiopure tert‐Butyl Sulfoxides and tert‐Butanesulfinamides
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/hc.21130openalex-snapshot
Double Asymmetric Induction in the Synthesis of Enantiomeric α‐Aminophosphonic Acids Mediated by Sulfinimines
inferred← citeshttps://doi.org/10.1002/qua.23020openalex-snapshot
Relative stabilities of transition states determine diastereocontrol in sulfur ylide additions onto chiral N‐sulfinyl imines
inferred← citeshttps://doi.org/10.1007/s11172-016-1483-zopenalex-snapshot
Synthesis of chiral 1-(imidazol-2-yl)alkanamines using neomenthanethiol as a chiral auxiliary
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/10.1016/b0-08-044655-8/00036-2openalex-snapshot
Vinyl and Aryl Chalcogenides: Sulfur-, Selenium-, and Tellurium-based Functional Groups
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00056-8openalex-snapshot
Imines and Their N-Substituted Derivatives: Oximes and Their O-R Substituted Analogs
inferred← citeshttps://doi.org/10.1016/b978-0-08-044860-2.00004-0openalex-snapshot
1,2- and 1,4-Additions to C=X Bonds
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00318-9openalex-snapshot
3.18 Synthetically Derived Auxiliaries: Sulfur Derivatives (including Sulfilamines and Sulfoximines)
inferred← citeshttps://doi.org/10.1016/b978-0-08-095167-6.00320-7openalex-snapshot
3.20 Stoichiometric Auxiliary Ligands for Metals and Main Group Elements: Ligands for Lithium
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00802-8openalex-snapshot
8.02 Reduction of CN to CH–NH by Metal Hydrides
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00137-xopenalex-snapshot
Reduction of C=N by Metal Hydrides
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00107-7openalex-snapshot
Vinyl- and Aryl Chalcogenides: Sulfur-, Selenium-, and Tellurium-Based Functional Groups
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00112-7openalex-snapshot
Oxaziridines and Oxazirines
inferred← citeshttps://doi.org/10.1016/bs.aihch.2016.10.002openalex-snapshot
Synthesis of Piperidines and Dehydropiperidines
inferred← citeshttps://doi.org/10.1016/j.gresc.2025.12.013openalex-snapshot
Photocatalyzed site-selective aryl C–H sulfinamidation via thianthracene salts
inferred← citeshttps://doi.org/10.1016/j.ica.2003.12.030openalex-snapshot
Asymmetric synthesis of β-amino alcohol by reductive cross-coupling of planar chiral ferrocenecarboxaldehyde with N-tosyl ferrocenylideneamine, and its application to asymmetric reaction
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2004.10.045openalex-snapshot
Acyclic and cyclic aminophosphonic acids: asymmetric syntheses mediated by chiral sulfinyl auxiliary
inferred← citeshttps://doi.org/10.1016/j.tet.2006.06.072openalex-snapshot
Optically pure trans-2,3-disubstituted N-sulfinyl aziridines. Regio- and stereoselective opening mediated by the sulfinyl group
inferred← citeshttps://doi.org/10.1016/j.tet.2006.06.107openalex-snapshot
Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/j.tet.2008.09.083openalex-snapshot
An overview of stereoselective synthesis of α-aminophosphonic acids and derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2008.10.082openalex-snapshot
Preparation of (1R,1′R)-1,1′-(anthracene-9,10-diyl)bis(2,2,2-trifluoroethanamine): a chiral diamine with low basicity
inferred← citeshttps://doi.org/10.1016/j.tet.2012.10.085openalex-snapshot
Asymmetric synthesis of conformationally constrained L-AP4 analogues using chiral sulfinyl auxiliary
inferred← citeshttps://doi.org/10.1016/j.tet.2019.02.051openalex-snapshot
A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates
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.2004.10.031openalex-snapshot
Indium-mediated diastereoselective addition of allyl bromides to enantiomerically pure N-tert-butylsulfinyl aldimines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2005.05.026openalex-snapshot
Stereoselective synthesis of optically active 1-substituted-1-pyridyl-methylamines
inferred← citeshttps://doi.org/10.1016/j.tetasy.2006.04.026openalex-snapshot
Aza Diels–Alder reactions of sulfinimines with the Rawal diene
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.01.032openalex-snapshot
Highly diastereoselective nucleophilic addition reactions of masked acyl cyanide reagents to tert-butanesulfiminides
inferred← citeshttps://doi.org/10.1016/j.tetasy.2007.10.015openalex-snapshot
A facile synthesis of N-sulfinylaldimines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2005.10.067openalex-snapshot
Asymmetric synthesis of dihydroquinazolinones via directed ortho metalation and addition to tert-butanesulfinyl imines
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.2017.01.107openalex-snapshot
Synthesis and functionalization of N-sulfinyl imines: Sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151229openalex-snapshot
A practical asymmetric synthesis of ortho-substituted 4-pyrazolyl-2-ethylamines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151260openalex-snapshot
Ni/NHC-catalyzed cross-coupling of methyl sulfinates and amines for direct access to sulfinamides
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)00478-2openalex-snapshot
Synthesis of optically active phenylglycine derivatives from Ss-(+)-N-(benzylidene)-p-toluenesulfinamide by using Lewis acids and tert-amines
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00500-2openalex-snapshot
Aziridine mediated asymmetric synthesis of α-benzylserine and α-n-butylserine
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)01250-4openalex-snapshot
Reversal of diastereofacial selectivity in the nucleophilic addition reaction to chiral N-sulfinimine and application to the synthesis of indrizidine 223AB
inferred← citeshttps://doi.org/10.1016/s0040-4020(99)00451-2openalex-snapshot
Asymmetric synthesis of chiral amines by highly diastereoselective 1,2-additions of organometallic reagents to N-tert-butanesulfinyl imines
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)01423-4openalex-snapshot
Synthesis of enantiopure pyrrolidine and piperidine derivatives via ring closing metathesis
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)00122-8openalex-snapshot
A facile three-step synthesis of 1,2-amino alcohols using the Ellman homochiral tert-butylsulfinamide
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)02090-1openalex-snapshot
Synthetic studies on the thiostrepton family of peptide antibiotics: synthesis of the tetrasubstituted dehydropiperidine and piperidine cores
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)02294-8openalex-snapshot
Asymmetric synthesis of cetirizine dihydrochloride
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)00021-7openalex-snapshot
The use of enantiomerically pure N-sulfinimines in asymmetric Baylis–Hillman reactions
inferred← citeshttps://doi.org/10.1016/s0040-4039(03)00903-1openalex-snapshot
Effective tuning of the arene and alkanesulfinamides for highly enantioselective synthesis of (S)-4-chlorophenylphenylmethylamine, a key intermediate for antihistamic (S)-cetirizine
inferred← citeshttps://doi.org/10.1016/s0040-4039(97)01095-2openalex-snapshot
Aziridine 2-carboxylate ester mediated asymmetric synthesis of α-alkyl β-amino acids
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)00506-1openalex-snapshot
Sulfinimine mediated asymmetric synthesis of 3-substituted-1(2H)-isoquinolones: (3R,4S)-(−)-4-hydroxy-3-phenyltetrahydroisoquinoline
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01223-4openalex-snapshot
Synthesis and applications of nonracemic β-amino aldehydes to the asymmetric synthesis of piperdines: (+)-dihydropinidine
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)01698-0openalex-snapshot
Sulfinimines of trifluoropyruvate: Novel intermediates for chiral non racemic α-trifluoromethyl α-amino acids
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02168-6openalex-snapshot
Enantiomerically pure 2-alkyl and 2,3-dialkylaziridines from 2-sulfinylimines
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00756-xopenalex-snapshot
Ytterbium(III) triflate-catalyzed asymmetric nucleophilic addition of functionalized lithium (α-carbalkoxyvinyl)cuprates to chiral p-toluenesulfinimines (thiooxime S-oxides)
inferred← citeshttps://doi.org/10.1016/s0957-4166(01)00186-0openalex-snapshot
Synthesis of (R)-(+)-methyl 3-amino-3-(5-hydroxy-2-pyridinyl)propanoate, an analog of l-azatyrosine
inferred← citeshttps://doi.org/10.1016/s0957-4166(01)00411-6openalex-snapshot
Asymmetric syntheses of N-acetyl-(R)-coniine and N-Boc-(2R,6R)-solenopsin A via ring-closing metathesis
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00033-2openalex-snapshot
Asymmetric synthesis of 1,4-dideoxy-1,4-imino-d-ribitol via stereoselective addition of allylphenylsulfone to an aryl N-sulfinylimine
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00141-6openalex-snapshot
Synthesis of non-racemic β-branched α-(aminoalkyl)-acrylates from naturally occurring amino acids
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00684-5openalex-snapshot
A new efficient procedure for asymmetric synthesis of α-aminophosphonic acids via addition of lithiated bis(diethylamino)phosphine borane complex to enantiopure sulfinimines
inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00225-0openalex-snapshot
Asymmetric synthesis of functionalized piperidine derivatives: synthesis of (S)-anatabine
inferred← citeshttps://doi.org/10.1016/s0957-4166(98)00429-7openalex-snapshot
A stereoselective synthesis of bis-β-amino acids
inferred← citeshttps://doi.org/10.1016/s0957-4166(99)00036-1openalex-snapshot
Asymmetric synthesis of β-monosubstituted and β,β-disubstituted N-(p-toluenesulfinyl)-α-(aminoalkyl)acrylates via anionic additions of (α-carbalkoxyvinyl)cuprates to thiooxime S-oxides
inferred← citeshttps://doi.org/10.1016/s1874-5296(00)80020-0openalex-snapshot
Syntheses and reactions of sulfinimines
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00002openalex-snapshot
Modern Stereoselective Synthesis of Chiral Sulfinyl Compounds
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01363openalex-snapshot
Triphenylethanamine Derivatives as Cholesteryl Ester Transfer Protein Inhibitors: Discovery of N-[(1R)-1-(3-Cyclopropoxy-4-fluorophenyl)-1-[3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl]-2-phenylethyl]-4-fluoro-3-(trifluoromethyl)benzamide (BMS-795311)
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00415openalex-snapshot
Synthesis of N-Sulfenylimines from Disulfides and Primary Methanamines
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01307openalex-snapshot
Synthesis of Enantiopure 3-Hydroxypiperidines from Sulfinyl Dienyl Amines by Diastereoselective Intramolecular Cyclization and [2,3]-Sigmatropic Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01023openalex-snapshot
Diastereoselective Synthesis of Silyl-Substituted Pyrrolidines
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.7b00988openalex-snapshot
C1′-Azacycloalkyl Hexahydrocannabinols
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.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.1c01106openalex-snapshot
Rare-Earth-Catalyzed Transsulfinamidation of Sulfinamides with Amines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00347openalex-snapshot
A Silyl Sulfinylamine Reagent Enables the Modular Synthesis of Sulfonimidamides via Primary Sulfinamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04648openalex-snapshot
Stereodivergent Synthesis of Complex N -Sulfonimidoyl Lactams via the Castagnoli–Cushman Reaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02635openalex-snapshot
Stereodivergent Synthesis of Pseudotabersonine Alkaloids
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/acscatal.2c05169openalex-snapshot
Photoredox Alkylation of Sulfinylamine Enables the Synthesis of Highly Functionalized Sulfinamides and S(VI) Derivatives
inferred← citeshttps://doi.org/10.1021/cr068409fopenalex-snapshot
Applications of Menthol in Synthetic Chemistry
inferred← citeshttps://doi.org/10.1021/cr400553copenalex-snapshot
Recent Advances in the Stereoselective Synthesis of Aziridines
inferred← citeshttps://doi.org/10.1021/cr900382topenalex-snapshot
Synthesis and Applications of tert-Butanesulfinamide
inferred← citeshttps://doi.org/10.1021/ja037223kopenalex-snapshot
Development of Chiral Nucleophilic Pyridine Catalysts: Applications in Asymmetric Quaternary Carbon Synthesis
inferred← citeshttps://doi.org/10.1021/ja0515203openalex-snapshot
Highly Stereoselective Benzylation of N-Sulfinylketimines
inferred← citeshttps://doi.org/10.1021/ja056150xopenalex-snapshot
Enantioselective TADMAP-Catalyzed Carboxyl Migration Reactions for the Synthesis of Stereogenic Quaternary Carbon
inferred← citeshttps://doi.org/10.1021/ja4111418openalex-snapshot
A General Aminocatalytic Method for the Synthesis of Aldimines
inferred← citeshttps://doi.org/10.1021/ja8016957openalex-snapshot
Structures of β-Amino Ester Enolates: New Strategies Using the Method of Continuous Variation
inferred← citeshttps://doi.org/10.1021/jacs.4c06726openalex-snapshot
Palladium-Catalyzed Addition of Aryl Halides to N-Sulfinylamines for the Synthesis of Sulfinamides
inferred← citeshttps://doi.org/10.1021/jo030142mopenalex-snapshot
Improved Asymmetric Synthesis of Aziridine 2-Phosphonates Using (S)-(+)-2,4,6-Trimethylphenylsulfinamide
inferred← citeshttps://doi.org/10.1021/jo034477fopenalex-snapshot
Highly Diastereoselective Strecker Reaction of Enolizable Aliphatic Sulfinimines
inferred← citeshttps://doi.org/10.1021/jo048597eopenalex-snapshot
Synthesis of Enantiopure Sulfinimines (Thiooxime S-Oxides) Catalyzed by Yb(OTf)3 from p-Toluenesulfinamide and Aldehydes in Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1021/jo049666sopenalex-snapshot
Stereoselective Addition of α-Sulfinyl Carbanions to N-p-tolylsulfinylketimines: Synthesis of Optically Pure 1,2,2‘-Trialkyl-2-aminoethanols
inferred← citeshttps://doi.org/10.1021/jo061027popenalex-snapshot
Adventures in Sulfur−Nitrogen Chemistry
inferred← citeshttps://doi.org/10.1021/jo062296iopenalex-snapshot
Expedient Synthesis of Sulfinamides from Sulfonyl Chlorides
inferred← citeshttps://doi.org/10.1021/jo0624795openalex-snapshot
Asymmetric Synthesis of Aziridines by Reduction of N-tert-Butanesulfinyl α-Chloro Imines
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/jo2023119openalex-snapshot
The Role of β-Bulky Substituents in Aldol Reactions of Boron Enolates of Methylketones with Aldehydes: Experimental and Theoretical Studies by DFT Analysis
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/jo402802jopenalex-snapshot
Mechanistic Insights on the Stereoselective Nucleophilic 1,2-Addition to Sulfinyl Imines
inferred← citeshttps://doi.org/10.1021/jo500013eopenalex-snapshot
Collective Asymmetric Synthesis of (−)-Antofine, (−)-Cryptopleurine, (−)-Tylophorine, and (−)-Tylocrebrine with tert- Butanesulfinamide as a Chiral Auxiliary
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/jo802049uopenalex-snapshot
Synthesis of Highly Functionalized Pyrrolidines via a Selective Iodide-Mediated Ring Expansion of Methylenecyclopropyl Amides
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/jo900381bopenalex-snapshot
Stereoselective Control of Planar α-Dimethylsulfonium Benzyl Carbanions. Synthesis of Optically Pure trans-Aziridines
inferred← citeshttps://doi.org/10.1021/jo902048topenalex-snapshot
Asymmetric Synthesis of the Potent HIV-Protease Inhibitor, Nelfinavir
inferred← citeshttps://doi.org/10.1021/jo9022638openalex-snapshot
An Efficient Stereoselective Synthesis of Penaresidin A from (E)-2-Protected Amino-3,4-unsaturated Sulfoxide
inferred← citeshttps://doi.org/10.1021/jo971394oopenalex-snapshot
Studies toward the Asymmetric Synthesis of α-Amino Phosphonic Acids via the Addition of Phosphites to Enantiopure Sulfinimines
inferred← citeshttps://doi.org/10.1021/jo972076sopenalex-snapshot
Sulfinimine-Mediated Asymmetric Synthesis of (R)-(4-Methoxy-3,5-dihydroxyphenyl)glycine: The Central Amino Acid of Vancomycin and Related Agents
inferred← citeshttps://doi.org/10.1021/jo972303qopenalex-snapshot
Enantiomerically Pure α-Alkylidene β-Amino Esters from Asymmetric Addition of Metal Dienolates to N-Sulfinylimines
inferred← citeshttps://doi.org/10.1021/jo980970topenalex-snapshot
1-Alkenesulfinyl Chlorides: Synthesis, Characterization, and Some Substitution Reactions
inferred← citeshttps://doi.org/10.1021/jo981976lopenalex-snapshot
Novel Asymmetric C−C Bond Formation Process Promoted by Et2AlCl and Its Application to the Stereoselective Synthesis of Unusual β-Branched Baylis−Hillman Adducts
inferred← citeshttps://doi.org/10.1021/jo9820622openalex-snapshot
Improved Synthesis of Enantiopure Sulfinimines (Thiooxime S -Oxides) from p -Toluenesulfinamide and Aldehydes and Ketones
inferred← citeshttps://doi.org/10.1021/jo9903858openalex-snapshot
Additions of Enantiopure α-Sulfinyl Carbanions to (S)-N-Sulfinimines: Asymmetric Synthesis of β-Amino Sulfoxides and β-Αmino Alcohols
inferred← citeshttps://doi.org/10.1021/jo990907jopenalex-snapshot
Aza-Darzens Asymmetric Synthesis of N-(p-Toluenesulfinyl)aziridine 2-Carboxylate Esters from Sulfinimines (N-Sulfinyl Imines)
inferred← citeshttps://doi.org/10.1021/jo991119xopenalex-snapshot
Asymmetric Synthesis of 4-Hydroxy-3-phenyltetrahydroisoquinoline Derivatives Using Enantiopure Sulfinimines (N-Sulfinyl Imines)
inferred← citeshttps://doi.org/10.1021/jo991389fopenalex-snapshot
Asymmetric Synthesis of 2H-Azirine 2-Carboxylate Esters
inferred← citeshttps://doi.org/10.1021/ol015520topenalex-snapshot
Masked Oxo Sulfinimines ( N -Sulfinyl Imines) in the Asymmetric Synthesis of Proline and Pipecolic Acid Derivatives
inferred← citeshttps://doi.org/10.1021/ol015945fopenalex-snapshot
Asymmetric Synthesis of Quaternary α-Amino Phosphonates Using Sulfinimines
inferred← citeshttps://doi.org/10.1021/ol027464hopenalex-snapshot
Facile Synthesis of Optically Pure 1,2-Diaryl (and 1-Alkyl-2-aryl) Ethyl and Propylamines
inferred← citeshttps://doi.org/10.1021/ol048005eopenalex-snapshot
A General Method for the Preparation of N-Sulfonyl Aldimines and Ketimines
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1021/ol0611245openalex-snapshot
Use of α-Chlorinated N-(tert-Butanesulfinyl)imines in the Synthesis of Chiral Aziridines
inferred← citeshttps://doi.org/10.1021/ol061863lopenalex-snapshot
Fragmentation of 2,2,2-Triphenylethoxychlorocarbene: Evidence for Ultrafast Fragmentation−Rearrangement in Excited Diazirines
inferred← citeshttps://doi.org/10.1021/ol070056zopenalex-snapshot
Enantioselective Organocatalytic Oxidation of Functionalized Sterically Hindered Disulfides
inferred← citeshttps://doi.org/10.1021/ol071382hopenalex-snapshot
More than a Protective Group: Synthesis and Applications of a New Chiral Silane
inferred← citeshttps://doi.org/10.1021/ol200509copenalex-snapshot
Activation of the Si−B Linkage: Copper-Catalyzed Addition of Nucleophilic Silicon to Imines
inferred← citeshttps://doi.org/10.1021/op050182nopenalex-snapshot
A New and Direct Asymmetric Synthesis of a Hindered Chiral Amine via a Novel Sulfinate Ketimine Derived from N-Tosyl-1,2,3-oxathiazolidine-2-oxide: Practical Asymmetric Synthesis of (R)-Sibutramine
inferred← citeshttps://doi.org/10.1021/op700259dopenalex-snapshot
Practical Asymmetric Synthesis of Trifluoromethyl-Containing Aminoester Using a Modified Davis Protocol
inferred← citeshttps://doi.org/10.1039/a827013zopenalex-snapshot
Asymmetric synthesis of amino acids using sulfinimines (thiooxime S-oxides)
inferred← citeshttps://doi.org/10.1039/a907865gopenalex-snapshot
Theoretical investigation on the conformational preferences of sulfinimines
inferred← citeshttps://doi.org/10.1039/b005201iopenalex-snapshot
Se–N interactions in selenohydroxylamine: a theoretical study
inferred← citeshttps://doi.org/10.1039/b100465oopenalex-snapshot
Interaction of sulfinimines with boron Lewis acids†
inferred← citeshttps://doi.org/10.1039/b601527aopenalex-snapshot
Direct synthesis of chiral aziridines from N-tert-butyl-sulfinylketimines
inferred← citeshttps://doi.org/10.1039/b809772kopenalex-snapshot
tert-Butanesulfinimines: structure, synthesis and synthetic applications
inferred← citeshttps://doi.org/10.1039/b917435dopenalex-snapshot
Asymmetric synthesis of 2-substituted pyrrolidines by addition of Grignard reagents to γ-chlorinated N-tert-butanesulfinyl imine
inferred← citeshttps://doi.org/10.1039/b925209fopenalex-snapshot
Asymmetric synthesis of 2-arylpyrrolidines starting from γ-chloro N-(tert-butanesulfinyl)ketimines
inferred← citeshttps://doi.org/10.1039/c001471kopenalex-snapshot
Asymmetric synthesis of new chiral N-sulfinyl 2,2-disubstituted aziridines by Grignard additions across α-chloro N-sulfinyl ketimines
inferred← citeshttps://doi.org/10.1039/c0ob00078gopenalex-snapshot
Chiral sulfur derivatives in the allylation of acyl hydrazones: C2-symmetric bis-sulfinamides as enhanced chiral organic promoters.
inferred← citeshttps://doi.org/10.1039/c1ob05971hopenalex-snapshot
Chiral N-tert-butanesulfinyl α,β-unsaturated ketimine: a simple and highly effective olefin/sulfinimide hybrid ligand for asymmetric 1,4-additions
inferred← citeshttps://doi.org/10.1039/c4cc05751aopenalex-snapshot
Isolation of stable non cyclic 1,2-disulfoxides. Revisiting the thermolysis of S-aryl sulfinimines
inferred← citeshttps://doi.org/10.1039/c4nj01894jopenalex-snapshot
Synthesis of enantiomerically pure δ-benzylproline derivatives
inferred← citeshttps://doi.org/10.1039/c6ra26490eopenalex-snapshot
Direct synthesis of N-sulfinyl- and N-sulfonylimines via copper/ l -proline-catalyzed aerobic oxidative cascade reaction of alcohols with sulfinamides or sulfonamides
inferred← citeshttps://doi.org/10.1039/d0ob00720jopenalex-snapshot
A Selectfluor-promoted oxidative reaction of disulfides and amines: access to sulfinamides
inferred← citeshttps://doi.org/10.1039/d2cc02431dopenalex-snapshot
The advent of electrophilic hydroxylamine-derived reagents for the direct preparation of unprotected amines
inferred← citeshttps://doi.org/10.1039/d3ob01782fopenalex-snapshot
Synthesis of sulfinamides via photocatalytic alkylation or arylation of sulfinylamine
inferred← citeshttps://doi.org/10.1039/d4cc06395copenalex-snapshot
Synthesis of chiral N -free sulfinamides by asymmetric condensation of stable sulfinates and ammonium salts
inferred← citeshttps://doi.org/10.1039/d5qo00573fopenalex-snapshot
Reagent-controlled selective synthesis of sulfinamides and sulfoximines from tert -butanesulfinamide
inferred← citeshttps://doi.org/10.1039/d5ra00158gopenalex-snapshot
Photoredox-catalyzed deoxygenative radical transformation of alcohols to sulfinamides
inferred← citeshttps://doi.org/10.1039/oc094051openalex-snapshot
Chapter 2. Synthetic methods . Part (iv) Heteroatom methods
inferred← citeshttps://doi.org/10.1055/a-1426-4744openalex-snapshot
Syntheses and Transformations of Sulfinamides
inferred← citeshttps://doi.org/10.1055/sos-sd-127-00155openalex-snapshot
27.25 Product Class 25: N-Sulfanyl-, N-Selanyl-, and N-Tellanylimines, and Their Oxidation Derivatives
inferred← citeshttps://doi.org/10.1080/00397910008087166openalex-snapshot
Stereoselective Synthesis of Ferrocenylamino Acids
inferred← citeshttps://doi.org/10.1080/00397910008087297openalex-snapshot
Asymmetric Synthesis of Aziridinyl Phosphonates Using Darzens-Type Reaction of Chloromethyl Phosphonate to Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1080/00397911.2010.543748openalex-snapshot
Fast and Efficient Synthesis of Sulfinamides by the Oxidation of Sulfenamides Using Potassium Fluoride and m -Chloroperoxybenzoic Acid
inferred← citeshttps://doi.org/10.1080/00397919908086426openalex-snapshot
Synthesis of Enantiomerically Pure Sulfenimines and Sulfinimines Derived from (+)-Camphor
inferred← citeshttps://doi.org/10.1080/01961779908047955openalex-snapshot
Asymmetric Synthesis of Biologically Interesting Compounds Utilizing Chiral Sulfoxides
inferred← citeshttps://doi.org/10.1080/10426507.2014.906426openalex-snapshot
Chiral Sulfinimines in Asymmetric Synthesis of Enantiomeric Aminophosphonic Acids
inferred← citeshttps://doi.org/10.1080/10426509908039580openalex-snapshot
Asymmetric Synthesis of α-Amino Phosphonic Acids Employing Versatile Sulfinimines and Sulfonimines
inferred← citeshttps://doi.org/10.1080/10426509908546206openalex-snapshot
Asymmetric Synthesis of Aminophosphonic Acids
inferred← citeshttps://doi.org/10.1177/095632020401500502openalex-snapshot
Recent Advances in the Synthesis of the Carbocyclic Nucleosides as Potential Antiviral Agents
inferred← citeshttps://doi.org/10.1246/bcsj.20170194openalex-snapshot
Stereoselective Synthesis of β-Amino Acid Derivatives by Asymmetric Mannich Reaction in Flow
inferred← citeshttps://doi.org/10.1246/cl.2005.468openalex-snapshot
Lewis Base-catalyzed Diastereoselective Mannich-type Reaction between Ketene Silyl Acetals and Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1246/cl.2005.604openalex-snapshot
Lewis Base-catalyzed Diastereoselective Strecker-type Reaction between Trimethylsilyl Cyanide and Chiral Sulfinimines
inferred← citeshttps://doi.org/10.1248/cpb.58.265openalex-snapshot
Stereoselective Radical Addition of an Acetal to Sterically Tuned Enantiomerically Pure N-Sulfinyl Imines
inferred← citeshttps://doi.org/10.3390/51201251openalex-snapshot
Facile and Stereoselective Synthesis of Non-Racemic 3,3,3-Trifluoroalanine
inferred← citeshttps://doi.org/10.3390/molecules29163939openalex-snapshot
Preparation and Preclinical Evaluation of 18F-Labeled Olutasidenib Derivatives for Non-Invasive Detection of Mutated Isocitrate Dehydrogenase 1 (mIDH1)
inferred← citeshttps://doi.org/10.5772/intechopen.68707openalex-snapshot
Stereoselective Synthesis of α‐Aminophosphonic Acids through Pudovik and Kabachnik‐Fields Reaction
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