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Synthesis and reactivity of 4″-phenylsulfinimine-avermectin B1 and 4′-phenylsulfinimine-avermectin B1 monosaccharide derivative

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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1099-0690(199904)1999:4<785::aid-ejoc785>3.0.co;2-#openalex-snapshot
Steric and Electronic Effects in the Diastereoselective Catalytic Epoxidation of Cyclic Allylic Alcohols with Methyltrioxorhenium (MTO)
inferredcites →https://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
inferredcites →https://doi.org/10.1007/978-1-4612-3626-9openalex-snapshot
Ivermectin and Abamectin
inferredcites →https://doi.org/10.1016/b0-44-451924-6/00065-xopenalex-snapshot
The Insecticidal Macrocyclic Lactones
inferredcites →https://doi.org/10.1016/j.bmcl.2003.09.003openalex-snapshot
Synthesis and biological activities of novel 4″-alkylidene avermectin derivatives
inferredcites →https://doi.org/10.1016/j.tetlet.2004.06.002openalex-snapshot
From ( E )- and ( Z )-ketoximes to N -sulfenylimines, ketimines or ketones at will. Application to erythromycin derivatives
inferredcites →https://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
inferredcites →https://doi.org/10.1016/s0040-4039(02)02514-5openalex-snapshot
New and efficient synthesis of 5′-amino-5′-(S)-methyl-2′,5′-dideoxynucleosides
inferredcites →https://doi.org/10.1016/s0040-4039(98)02319-3openalex-snapshot
Unexpected effect of protecting group and solvent on the stereoselectivity of m-CPBA epoxidation of diprotected cis-4,5-dihydroxycyclohexenes
inferredcites →https://doi.org/10.1016/s0957-4166(96)00541-1openalex-snapshot
Stereoselective addition reactions to chiral N-benzylidene-p-toluenesulfinamides. Application to the synthesis of optically active 1,2-diphenylethylamines
inferredcites →https://doi.org/10.1016/s0957-4166(97)00208-5openalex-snapshot
Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond
inferredcites →https://doi.org/10.1016/s0960-894x(01)81193-8openalex-snapshot
Synthesis of avermectin B1-4″,4″a-oxide: a precursor of potent anthelmintic agents
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/ja972012zopenalex-snapshot
Catalytic Asymmetric Synthesis of tert-Butanesulfinamide. Application to the Asymmetric Synthesis of Amines
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/jo00414a017openalex-snapshot
Carbon-13 nuclear magnetic resonance substituent-induced shieldings and conformational equilibriums in cyclohexanes
inferredcites →https://doi.org/10.1021/jo010285dopenalex-snapshot
Role of Hydrogen Bonding in the Oxidation of Thianthrene 5-Oxide with Peroxy Acids
inferredcites →https://doi.org/10.1021/jo990303fopenalex-snapshot
Concise Asymmetric Synthesis of α-Amino Acid Derivatives from N-Sulfinylimino Esters
inferredcites →https://doi.org/10.1039/np9860300087openalex-snapshot
Avermectins and milbemycins
inferredcites →https://doi.org/10.1039/p19860002243openalex-snapshot
Reduction of oximes and aliphatic nitro compounds to imines for further in situ reactions: a novel synthesis of pyrroles and pyrrolin-2-ones

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.4672977openalex-extracted
Comparative Analysis of the Rhizosphere Soil Environment between Meloidogyne Incognita Infested and Healthy Lycopersicon Esculentum Plants
inferred← citeshttps://doi.org/10.1002/ejoc.201601446openalex-snapshot
Rearrangement Reactions Leading to Optically Active α,α‐Disubstituted Primary Allylamines
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/b978-008044992-0.00112-7openalex-snapshot
Oxaziridines and Oxazirines
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.12.069openalex-snapshot
New ventures in the chemistry of avermectins
inferred← citeshttps://doi.org/10.1016/j.bmc.2018.12.040openalex-snapshot
Design, synthesis, insecticidal activity and molecular docking of doramectin derivatives
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.05.056openalex-snapshot
Synthesis, biological activities and structure−activity relationships for new avermectin analogues
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.089openalex-snapshot
First example of an Ugi type reaction on phenylsulfinimine-avermectin B1 derivatives
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151552openalex-snapshot
Magnesium ethoxide mediated lactone aminolysis with aminoheterocycles
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c05036openalex-snapshot
Azobenzene-Avermectin B1a Derivatives for Optical Modulation of Insect Behaviors
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b11157openalex-snapshot
Insights into the Photodecomposition of Azidomethyl Methyl Sulfide: A S2/S1 Conical Intersection on Nitrene Potential Energy Surfaces Leading to the Formation of S-Methyl-N-sulfenylmethanimine
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/ol702212nopenalex-snapshot
Efficient Preparation of N-Phenylsulfenyl Ketimines from Oximes or Nitro Compounds without Racemization of α-Stereocenters
inferred← citeshttps://doi.org/10.1070/rcr5051openalex-snapshot
Recent advances in avermectin chemistry
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