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Spiro-annulation of barbituric acid derivatives and its analogs by ring-closing metathesis reaction

https://doi.org/10.1016/j.bmcl.2004.12.034
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34/34 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

7 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 34 checked references that resolve
resolves10.1016/S0143-7208(03)00104-9
Synthesis and properties of some polycyclic barbiturate pigments
resolves10.1016/S0731-7085(02)00168-1
Determination of barbituric acid, utilizing a rapid and simple colorimetric assay
resolves10.1021/ol0352005
Novel NLO-phores with Proaromatic Donor and Acceptor Groups
resolves10.1021/ja0372098
Facile Synthesis of a Fullerene-Barbituric Acid Derivative and Supramolecular Catalysis of Its Photoinduced Dimerization
resolves10.1021/jo020761f
The Aminobarbituric Acid−Hydantoin Rearrangement
resolves10.1016/S0040-4039(02)00073-4
Preparation of 5-(cyclohexylmethyl)barbituric acid derivatives by acid-catalyzed reductive cyclohexylmethylation of barbituric acids with p-hydroxy or p-methoxybenzaldehydes
resolves10.1016/S0040-4039(01)01830-5
Preparation of 5-formyl- and 5-acetylbarbituric acids, including the corresponding Schiff bases and phenylhydrazones
resolves10.1016/S0040-4039(01)00621-9
Reductive C-alkylation of barbituric acid derivatives with carbonyl compounds in the presence of platinum and palladium catalysts
resolves10.1016/S0040-4039(00)00852-2
Decarbonylation of tetrasubstituted barbituric acids as a versatile method for preparation of N,N′,2,2-tetrasubstituted malonamides
resolves10.1016/S0531-5131(02)00758-6
The intravenous barbiturates
resolves10.1021/ja9936262
Control of Structural Isomerism in Noncovalent Hydrogen-Bonded Assemblies Using Peripheral Chiral Information
resolves10.1021/ja005886l
Helical Rosette Nanotubes:  Design, Self-Assembly, and Characterization
resolves10.1021/cr0200872
Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis
resolves10.1021/cr020109k
Synthesis of Phosphorus and Sulfur Heterocycles via Ring-Closing Olefin Metathesis
resolves10.1002/anie.200300576
Molybdenum and Tungsten Imido Alkylidene Complexes as Efficient Olefin‐Metathesis Catalysts
resolves10.1021/ar000114f
The Development of L<sub>2</sub>X<sub>2</sub>RuCHR Olefin Metathesis Catalysts:  An Organometallic Success Story
resolves10.1016/S0040-4020(97)10427-6
Recent advances in olefin metathesis and its application in organic synthesis
resolves10.1039/a703881j
Ring closing diene metathesis in organic synthesis
resolves10.1016/S0040-4039(98)00251-2
Synthesis of constrained α-amino acid derivatives via enyne metathesis reaction
resolves10.1055/s-1999-2896
Spiro-Annulation <i>via</i> Ring Closing Metathesis Reaction
resolves10.1039/a910217p
A new synthetic approach to 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) derivatives via enyne metathesis and the Diels–Alder reaction
resolves10.1002/1099-0690(200102)2001:4<787::AID-EJOC787>3.0.CO;2-N
Constrained Phenylalanine Derivatives by Enyne Metathesis and Diels−Alder Reaction
resolves10.1016/S0040-4020(02)01178-X
Synthesis of highly functionalized phenylalanine derivatives via cross-enyne metathesis reactions
resolves10.3998/ark.5550190.0004.308
Synthesis of spiro-cyclics via ring-closing metathesis
resolves10.1016/j.tetlet.2004.01.149
A new protocol for benzoannulation by double Claisen rearrangement and ring-closing metathesis reactions as key steps
resolves10.1016/j.tetlet.2003.12.075
Metathetic approach to naphthoxepin and spirocyclic molecular frameworks
resolves10.1016/j.tetlet.2004.11.013
N-Alkylation of diethyl acetamidomalonate: synthesis of constrained amino acid derivatives by ring-closing metathesis
resolves10.1021/ja00140a015
Practical catalyst for cyclic metathesis. Synthesis of functional and/or enantiopure cycloalkenes.
resolves10.1016/j.tetlet.2003.09.165
Novel ruthenium-catalyzed cleavage of allyl protecting group in lactams
resolves10.1002/chem.200305236
Ruthenium‐Catalyzed Chemoselective N‐Allyl Cleavage: Novel Grubbs Carbene Mediated Deprotection of Allylic Amines
resolves10.1016/j.tetlet.2004.11.012
Microwave-assisted Claisen rearrangement on a silica gel support
resolves10.1016/S0006-8993(01)02863-3
The antiepileptic drug losigamone decreases the persistent Na+ current in rat hippocampal neurons
resolves10.1016/0920-1211(90)90053-X
Effects of the tetronic acid derivatives AO33 (losigamone) and AO78 on epileptiform activity and on stimulus-induced calcium concentration changes in rat hippocampal slices
The 7 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib4_2
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib7_2
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib9
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib10_4
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib10_7
no DOI — not checked10.1016/j.bmcl.2004.12.034_bib11_4
no DOI — not checkedSome pyrazolone derivatives are useful for hypoxic ischemic brain disorders, especially ones of newborns caused by labor. For details, see: Tomoaki, I.; Tsuyomu. PCT Int. Appl. 2003, 29; WO 2003078401
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

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