On the public citation graph

An Efficient, One-Pot Synthesis of 3-Alkyl or Aryl Sydnoneimines

https://doi.org/10.1080/00397919208019267

0 signed · 25 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.

Claim with ORCID

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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/hlca.19620450713openalex-snapshot

Heilmittelchemische Studien In Der Heterocyclischen Reihe 35. Mitteilung. Über Sydnonimine. I. Herstellung und Eigenschaften von Sydnonimin‐Salzen

inferredcites →https://doi.org/10.1016/0040-4020(82)80186-5openalex-snapshot

Meso-ionic heterocycles (1976–1980)

inferredcites →https://doi.org/10.1021/cr60228a004openalex-snapshot

The Chemistry of the Sydnones

inferredcites →https://doi.org/10.1021/jm00292a042openalex-snapshot

Synthesis and pharmcological effects of some alkyl-, aryl, and aralkylsydnonimines

inferredcites →https://doi.org/10.1039/jr9570004409openalex-snapshot

889. Formation and properties of sydnone imines, a new class of meso-ionic compound, and some sydnones related to natural α-amino-acids

inferredcites →https://doi.org/10.1055/s-1988-27791openalex-snapshot

The Efficient Synthesis of 3-Arylsydnones Under Neutral Conditions

inferredcites →https://doi.org/10.1070/rc1980v049n01abeh002443openalex-snapshot

The Chemistry of Sydnone Imines

inferredcites →https://doi.org/10.1135/cccc19654257openalex-snapshot

Sydnones and sydnonimines XXVI. Reactivity of 3-arylsydnonimides

inferredcites →https://doi.org/10.1246/nikkashi1948.78.707openalex-snapshot

Studies on Mesoionic Compounds. V. Consideration on the Formation of Mesoionic Ring and a new Mode of Ring Formation.

inferredcites →https://doi.org/10.1248/cpb.18.128openalex-snapshot

Studies on Mesoionic Compounds. I. Synthesis of 3-Dialkylaminosydnonimines

inferredcites →https://doi.org/10.1254/jjp.20.23openalex-snapshot

CARDIOVASCULAR ACTION OF MESOIONIC COMPOUNDS, 3-SUBSTITUTED SYDNONIMINES

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.4608366openalex-extracted

N6 -Ferrocenylcarbonyl Derivatives of Sydnone Imines: Synthesis, Modification, Growth-Regulating and Antidote Against Herbicide "Zinger" Activities

inferred← citeshttps://doi.org/10.1002/chin.199232151openalex-snapshot

ChemInform Abstract: An Efficient, One‐Pot Synthesis of 3‐Alkyl‐ or Arylsydnonimines.

inferred← citeshttps://doi.org/10.1002/ejoc.202400387openalex-snapshot

Synthesis of Molsidomine and Mesocarb Analog via Mechanochemistry

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122975openalex-snapshot

N-ferrocenylcarbonyl derivatives of sydnone imines: synthesis, modification, growth-regulating and antidote against herbicide “Zinger” activities

inferred← citeshttps://doi.org/10.1016/j.tet.2025.134946openalex-snapshot

N6-α-azidoacetyl sydnone imines: Synthesis and reactivity in azide-alkyne cycloaddition reactions

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.01.019openalex-snapshot

N6 - tert -Butoxycarbonyl derivatives of sydnone imines: Preparation and synthetic use

inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00806openalex-snapshot

Click and Bio-Orthogonal Reactions with Mesoionic Compounds

inferred← citeshttps://doi.org/10.1021/jacs.2c09865openalex-snapshot

Fast and Bioorthogonal Release of Isocyanates in Living Cells from Iminosydnones and Cycloalkynes

inferred← citeshttps://doi.org/10.1039/c3ob41047aopenalex-snapshot

Novel amino acids: synthesis of furoxan and sydnonimine containing amino acids and peptides as potential nitric oxide releasing motifs

inferred← citeshttps://doi.org/10.1039/c8cc08533aopenalex-snapshot

Bioorthogonal release of sulfonamides and mutually orthogonal liberation of two drugs

inferred← citeshttps://doi.org/10.1055/a-2011-7264openalex-snapshot

NOBF4-Mediated Assembly of the Sydnone Imine Scaffold in the Synthesis of Double Nitric Oxide Donors

inferred← citeshttps://doi.org/10.3390/molecules26185705openalex-snapshot

Recent Advances in the Synthesis and Biomedical Applications of Heterocyclic NO-Donors

inferred← citeshttps://doi.org/10.70675/22dc8a53z7b3cz4b89z97b6zbc35ac5a2fe7openalex-snapshot

Les composés mésoioniques : de nouveaux outils pour la libération contrôlée de principes actifs

inferred← citeshttps://doi.org/10.70675/719fdcd4z34b2z4802z8e35z27bfba5f3205openalex-snapshot

Synthèses et applications d'iminosydnones en chemobiologie

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.