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Efficient Preparation of N-Phenylsulfenyl Ketimines from Oximes or Nitro Compounds without Racemization of α-Stereocenters
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200605054openalex-snapshot
Enesulfonamides as Nucleophiles in Catalytic Asymmetric Reactions
inferredcites →https://doi.org/10.1016/0957-4166(96)00195-4openalex-snapshot
Stereochemistry in the oxidation of primary amines to nitro compounds by dimethyldioxirane
inferredcites →https://doi.org/10.1016/j.tet.2006.06.107openalex-snapshot
Chiral non-racemic sulfinimines: versatile reagents for asymmetric synthesis
inferredcites →https://doi.org/10.1016/j.tetlet.2006.06.019openalex-snapshot
Synthesis and reactivity of 4″-phenylsulfinimine-avermectin B1 and 4′-phenylsulfinimine-avermectin B1 monosaccharide derivative
inferredcites →https://doi.org/10.1016/s0040-4020(01)01154-1openalex-snapshot
The reaction of oximes with tributylphosphine–phenyldisulfide: mechanistic insight and new synthetic possibilities
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/jo00043a047openalex-snapshot
A convenient and general preparation of N-sulfonylimines
inferredcites →https://doi.org/10.1021/jo061027popenalex-snapshot
Adventures in Sulfur−Nitrogen Chemistry
inferredcites →https://doi.org/10.1021/jo982059iopenalex-snapshot
Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones
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/ol048005eopenalex-snapshot
A General Method for the Preparation of N-Sulfonyl Aldimines and Ketimines
inferredcites →https://doi.org/10.1021/ol049979+openalex-snapshot
No-D NMR (No-Deuterium Proton NMR) Spectroscopy: A Simple Yet Powerful Method for Analyzing Reaction and Reagent Solutions
inferredcites →https://doi.org/10.1021/ol0708166openalex-snapshot
Asymmetric Synthesis of syn-α-Substituted β-Amino Ketones by Using Sulfinimines and Prochiral Weinreb Amide Enolates
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
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
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Synthesis of N-Sulfenylimines Via an Electrochemical Radical Coupling of Amines and Thiols Mediated by Bromide Ions
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub2openalex-snapshot
Trialkylphosphines
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Trialkylphosphines
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Trialkylphosphines
inferred← citeshttps://doi.org/10.1002/9780471264194.fos11442.pub5openalex-snapshot
Trialkylphosphines
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Electrochemical Cross‐Coupling Reactions
inferred← citeshttps://doi.org/10.1002/chem.201901537openalex-snapshot
Ditocopheryl Sulfides and Disulfides: Synthesis and Antioxidant Profile
inferred← citeshttps://doi.org/10.1002/chin.200814096openalex-snapshot
ChemInform Abstract: Efficient Preparation of N‐Phenylsulfenyl Ketimines from Oximes or Nitro Compounds Without Racemization of α‐Stereocenters.
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/ejoc.201201100openalex-snapshot
An Efficient Catalytic Method for Regioselective Sulfenylation of Electron‐Rich Aza‐Aromatics at Room Temperature
inferred← citeshttps://doi.org/10.1002/ejoc.201402894openalex-snapshot
A Base‐Mediated Mild Sulfenylation of Indoles and Pyrrole with α‐Acylthiones
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/j.tet.2013.02.070openalex-snapshot
Nitrogen-containing Lewis bases catalyzed highly regio- and stereoselective reactions of allenyl acetates with isatin-derived oximes
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.tetlet.2007.11.110openalex-snapshot
Catalytic, PMe3-mediated conversion of secondary nitroalkanes to ketones: a very mild Nef-type process
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.3c02090openalex-snapshot
Electrochemical Direct Synthesis of N-Sulfenylimines from Amines in the Presence of Thiophenols
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00270openalex-snapshot
Dearomative Indole Annulation with 2-Aminoaryldisulfide – an Approach for Accessing Polycyclic Indoline-Fused-Benzothiazine
inferred← citeshttps://doi.org/10.1021/ol203157sopenalex-snapshot
Relative Tendency of Carbonyl Compounds To Form Enamines
inferred← citeshttps://doi.org/10.1021/ol503760bopenalex-snapshot
Copper-Catalyzed Oxidative N–S Bond Formation for the Synthesis of N-Sulfenylimines
inferred← citeshttps://doi.org/10.1021/ol9017722openalex-snapshot
AuBr3-Catalyzed Thiooxime-to-Carbonyl Conversion: From Chiral Aliphatic Nitro Compounds to Ketones without Racemization
inferred← citeshttps://doi.org/10.1039/b717023hopenalex-snapshot
Synthetic methods : Part (iii) Heteroatom chemistry
inferred← citeshttps://doi.org/10.1039/c5ob01790dopenalex-snapshot
One pot oxidative N–S bond formation to access 2-sulfenylimine chromenes
inferred← citeshttps://doi.org/10.1039/c6ra01971dopenalex-snapshot
Direct synthesis of N-sulfenylimines through oxidative coupling of amines with disulfides/thiols over copper based metal–organic frameworks
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/10.1134/s2079978012010037openalex-snapshot
Stable synthetic equivalents of N-unsubstituted imines: Part 1. Synthesis
inferred← citeshttps://doi.org/10.3762/bjoc.19.106openalex-snapshot
N -Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations
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