On the public citation graph
Halogenated Helianane Derivatives from the Sponge Spirastrella hartmani
0 signed · 32 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf01945541openalex-snapshot
Insecticidal organophosphates: Nature made them first
inferredcites →https://doi.org/10.1016/0040-4020(78)80198-7openalex-snapshot
Structures and synthesis of some new antibacterial sesquiterpenoids from the gorgonian coral Pseudopterogorgia rigida
inferredcites →https://doi.org/10.1021/np50053a042openalex-snapshot
(+)-Curcuphenol and (+)-Curcudiol, Sesquiterpene Phenols from Shallow and Deep Water Collections of the Marine Sponge Didiscus flavus
inferredcites →https://doi.org/10.1021/np50074a048openalex-snapshot
Aromatic Disabolenes from an Australian Marine Sponge, Arenochalina sp.
inferredcites →https://doi.org/10.1093/jnci/82.13.1107openalex-snapshot
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
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.4666804openalex-extracted
Inverse Electron Demand Diels-Alder Reaction in Total Synthesis of Bioactive Natural Products
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod192openalex-snapshot
Porifera (Sponges)–2
inferred← citeshttps://doi.org/10.1002/9783527335855.marprod195openalex-snapshot
Porifera (Sponges)–5
inferred← citeshttps://doi.org/10.1002/adsc.70247openalex-snapshot
Harnessing the Excited‐State Reactivity of o ‐Nitrobenzyl Alcohols for the Rapid Synthesis of N ‐Substituted 2 H ‐Indazoles
inferred← citeshttps://doi.org/10.1002/ejoc.201100706openalex-snapshot
Total Synthesis of (+)‐7,11‐Helianane and (+)‐5‐Chloro‐7,11‐helianane through Stereoselective Aromatic Claisen Rearrangement
inferred← citeshttps://doi.org/10.1002/ejoc.201101393openalex-snapshot
Total Synthesis of (+)‐7,11‐Helianane and (+)‐5‐Chloro‐7,11‐helianane through Stereoselective Aromatic Claisen Rearrangement
inferred← citeshttps://doi.org/10.1002/tcr.202000086openalex-snapshot
Applications of Transition‐Metal‐Catalyzed Asymmetric Allylic Substitution in Total Synthesis of Natural Products: An Update
inferred← citeshttps://doi.org/10.1007/978-3-032-09901-3_1openalex-snapshot
The Diels–Alder Reaction as a Key Step in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1007/s11745-015-4028-6openalex-snapshot
Lysophospholipids from the Guangxi Sponge Spirastrella purpurea
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104420openalex-snapshot
Phenolic bisabolane and cuparene sesquiterpenoids with anti-inflammatory activities from the deep-sea-derived Aspergillus sydowii MCCC 3A00324 fungus
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100066openalex-snapshot
Inverse electron demand Diels-Alder reaction in total synthesis of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.003openalex-snapshot
The Claisen rearrangement in the syntheses of bioactive natural products
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.06.001openalex-snapshot
Expeditious synthesis of helianane and C-10 halogenated heliananes employing ring-closing metathesis
inferred← citeshttps://doi.org/10.1021/jacs.1c10927openalex-snapshot
Catalytic Synthesis of 1 H -2-Benzoxocins: Cobalt(III)-Carbene Radical Approach to 8-Membered Heterocyclic Enol Ethers
inferred← citeshttps://doi.org/10.1021/jacs.2c11310openalex-snapshot
Thermal and (Thermo-Reversible) Photochemical Cycloisomerization of 1 H -2-Benzo[ c ]oxocins: From Synthetic Applications to the Development of a New T-Type Molecular Photoswitch
inferred← citeshttps://doi.org/10.1021/ol2011117openalex-snapshot
Synthesis and Structural Revision of Phomopsin B, a Novel Polyketide Carrying a 10-Membered Cyclic-Ether Ring
inferred← citeshttps://doi.org/10.1021/ol2022214openalex-snapshot
Total Synthesis and Repudiation of the Helianane Family
inferred← citeshttps://doi.org/10.1021/ol2024778openalex-snapshot
Mollenyne A, a Long-Chain Chlorodibromohydrin Amide from the Sponge Spirastrella mollis
inferred← citeshttps://doi.org/10.1039/c6nj03825eopenalex-snapshot
Regioselective access of alkylidendibenzo[c,f]oxocine framework via cyclocarbopalladation/cross-coupling cascade reactions and reductive Heck strategy
inferred← citeshttps://doi.org/10.1039/c8sc05261aopenalex-snapshot
Tandem Peterson olefination and chemoselective asymmetric hydrogenation of β-hydroxy silanes
inferred← citeshttps://doi.org/10.1039/d0nj01396jopenalex-snapshot
Unraveling the helianane family: a complementary quantum mechanical study
inferred← citeshttps://doi.org/10.1039/d2qo00774fopenalex-snapshot
The synthesis of seven- and eight-membered rings by radical strategies
inferred← citeshttps://doi.org/10.3389/fmars.2022.950880openalex-snapshot
Anticancer potential of Spirastrella pachyspira (marine sponge) against SK-BR-3 human breast cancer cell line and in silico analysis of its bioactive molecule sphingosine
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.