On the public citation graph

New Conjugated Systems Derived from Piperazine-2,5-dione

https://doi.org/10.3390/50300629
0 signed · 15 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/bscb.19780870808openalex-snapshot
The cyclic dipeptides. Proper model compounds in peptide research.
inferredcites →https://doi.org/10.1007/978-3-7091-7083-0_2openalex-snapshot
Naturally Occurring 2,5-Dioxopiperazines and Related Compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)87270-6openalex-snapshot
Isolation of aspirochlorine (=antibiotic A30641) possessing a novel dithiodiketopiperazine structure from
inferredcites →https://doi.org/10.1021/jo01167a020openalex-snapshot
THE SYNTHESIS OF l(—)-LEUCYLGLYCYLGLYCINE1
inferredcites →https://doi.org/10.1021/jo01281a035openalex-snapshot
Synthesis of 3-isopropylidene-2,5-piperazinediones
inferredcites →https://doi.org/10.1039/jr9470001179openalex-snapshot
221. Pyrazine derivatives. Part III. Conversion of diketopiperazines into pyrazine derivatives. Synthesis of 2-hydroxy-3 : 6-di-sec.-butylpyrazine from isoLeucine
inferredcites →https://doi.org/10.1039/p19720002494openalex-snapshot
Pyrazine chemistry. Part IV. Thermal [1,4] eliminations from 3,6-di-hydropyrazines
inferredcites →https://doi.org/10.1039/p19730000404openalex-snapshot
Pyrazine chemistry. Part V. Diels-Alder reactions of some 2,5-dihydroxypyrazines
inferredcites →https://doi.org/10.1071/ch9841791openalex-snapshot
Pyrazine chemistry. II. Reduction of 3,6-Dibenzylidenepiperazine-2,5-diones
inferredcites →https://doi.org/10.1246/cl.1984.1301openalex-snapshot
FACILE SYNTHESIS AND CONVERSION OF MAIN SKELETON OF ASPIROCHLORIN TO 3-AMINOCOUMARIN DERIVATIVES
inferredcites →https://doi.org/10.3987/r-1983-07-1407openalex-snapshot
Stereoselective Synthesis of the Geometric and Optical Isomers of Unsaturated 3-Mono- and 3,6-Disubstituted 2,5-Piperazinediones

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.4651065openalex-extracted
inferred← citeshttps://doi.org/10.1002/ejoc.200800355openalex-snapshot
Differentiating Between Dipolarity and Polarizability Effects of Solvents Using the Solvatochromism of Barbiturate Dyes
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133838openalex-snapshot
Synthesis and spectroscopic investigation of substituted piperazine-2,5-dione derivatives
inferred← citeshttps://doi.org/10.1021/cr200398yopenalex-snapshot
2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products
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.