On the public citation graph

Synthesis and Structure Revision of the C43–C67 Part of Amphidinol 3

https://doi.org/10.1021/ol401176a
0 signed · 86 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/anie.200602742openalex-snapshot
Synthesis of the C31–C67 Fragment of Amphidinol 3
inferredcites →https://doi.org/10.1002/anie.201000517openalex-snapshot
Beyond the Pummerer Reaction: Recent Developments in Thionium Ion Chemistry
inferredcites →https://doi.org/10.1002/cber.190904202126openalex-snapshot
Über Phenyl‐sulfoxyessigsäure
inferredcites →https://doi.org/10.1002/cber.19100430241openalex-snapshot
Über Phenylsulfoxy‐essigsäure. (II.)
inferredcites →https://doi.org/10.1002/ejoc.200801117openalex-snapshot
Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction
inferredcites →https://doi.org/10.1016/j.bbamem.2004.09.002openalex-snapshot
Membrane-permeabilizing activities of amphidinol 3, polyene-polyhydroxy antifungal from a marine dinoflagellate
inferredcites →https://doi.org/10.1016/j.bmc.2007.12.029openalex-snapshot
Effects of lipid constituents on membrane-permeabilizing activity of amphidinols
inferredcites →https://doi.org/10.1016/j.bmcl.2004.04.029openalex-snapshot
Lingshuiol, a novel polyhydroxyl compound with strongly cytotoxic activity from the marine dinoflagellate Amphidinium sp
inferredcites →https://doi.org/10.1016/j.bmcl.2010.02.025openalex-snapshot
Sterol effect on interaction between amphidinol 3 and liposomal membrane as evidenced by surface plasmon resonance
inferredcites →https://doi.org/10.1016/j.hal.2004.07.004openalex-snapshot
The structures of five new antifungal and hemolytic amphidinol analogs from Amphidinium carterae collected in New Zealand
inferredcites →https://doi.org/10.1016/j.tet.2005.01.069openalex-snapshot
Hairpin conformation of amphidinols possibly accounting for potent membrane permeabilizing activities
inferredcites →https://doi.org/10.1016/j.tet.2006.03.004openalex-snapshot
Modern Pummerer-type reactions
inferredcites →https://doi.org/10.1016/j.tetlet.2004.05.067openalex-snapshot
Lingshuiols A and B, two new polyhydroxy compounds from the Chinese marine dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1016/j.tetlet.2005.04.041openalex-snapshot
Synthesis of highly substituted 2,6-anti-configured tetrahydropyrans. First steps towards an efficient access to amphidinol 3 ring system
inferredcites →https://doi.org/10.1016/j.tetlet.2006.02.045openalex-snapshot
Karatungiols A and B, two novel antimicrobial polyol compounds, from the symbiotic marine dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1016/j.tetlet.2008.08.103openalex-snapshot
Isolation and characterization of karlotoxin 1, a new amphipathic toxin from Karlodinium veneficum
inferredcites →https://doi.org/10.1016/j.tetlet.2009.03.065openalex-snapshot
Carteraol E, a potent polyhydroxyl ichthyotoxin from the dinoflagellate Amphidinium carterae
inferredcites →https://doi.org/10.1016/s0040-4020(01)97596-9openalex-snapshot
Total synthesis of the L-hexoses
inferredcites →https://doi.org/10.1016/s0040-4020(98)00898-9openalex-snapshot
Luteophanols B and C, new polyhydroxyl compounds from marine dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1021/cr00032a009openalex-snapshot
Catalytic Asymmetric Dihydroxylation
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/ja00026a027openalex-snapshot
Amphidinol, a polyhydroxy-polyene antifungal agent with an unprecedented structure, from a marine dinoflagellate, Amphidinium klebsii
inferredcites →https://doi.org/10.1021/ja00253a032openalex-snapshot
Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization
inferredcites →https://doi.org/10.1021/ja00538a077openalex-snapshot
The first practical method for asymmetric epoxidation
inferredcites →https://doi.org/10.1021/ja00820a036openalex-snapshot
Organic synthesis gy the Pummerer reaction. I. Synthesis of .alpha.-hydroxyaldehydes from .beta.-hydroxy sulfoxides
inferredcites →https://doi.org/10.1021/ja983655xopenalex-snapshot
Absolute Configuration of Amphidinol 3, the First Complete Structure Determination from Amphidinol Homologues: Application of a New Configuration Analysis Based on Carbon−Hydrogen Spin-Coupling Constants
inferredcites →https://doi.org/10.1021/jo00036a003openalex-snapshot
The osmium-catalyzed asymmetric dihydroxylation: a new ligand class and a process improvement
inferredcites →https://doi.org/10.1021/jo00170a070openalex-snapshot
Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones
inferredcites →https://doi.org/10.1021/jo00350a050openalex-snapshot
Selective transformation of 2,3-epoxy alcohols and related derivatives. Strategies for nucleophilic attack at carbon-1
inferredcites →https://doi.org/10.1021/jo01058a015openalex-snapshot
Epoxide Migrations with α,β-Epoxy Alcohols
inferredcites →https://doi.org/10.1021/jo901793fopenalex-snapshot
Stereoselective Synthesis of the C31−C40/C43−C52 Unit of Amphidinol 3
inferredcites →https://doi.org/10.1021/jo970273lopenalex-snapshot
Luteophanol A, a New Polyhydroxyl Compound from Symbiotic Marine Dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.1021/jo981810kopenalex-snapshot
Stereochemical Determination of Acyclic Structures Based on Carbon−Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products
inferredcites →https://doi.org/10.1021/np300604wopenalex-snapshot
Confirmation of the Absolute Configuration at C45 of Amphidinol 3
inferredcites →https://doi.org/10.1021/np900616qopenalex-snapshot
Structure and Biosynthesis of Amphidinol 17, a Hemolytic Compound from Amphidinium carterae
inferredcites →https://doi.org/10.1021/ol0157095openalex-snapshot
Chemoselective Cross-Metathesis Reaction. Application to the Synthesis of the C1−C14 Fragment of Amphidinol 3
inferredcites →https://doi.org/10.1021/ol050250qopenalex-snapshot
Synthesis of the C(1)−C(25) Fragment of Amphidinol 3: Application of the Double-Allylboration Reaction for Synthesis of 1,5-Diols
inferredcites →https://doi.org/10.1021/ol050477lopenalex-snapshot
A C-Glycosidation Approach to the Central Core of Amphidinol 3: Synthesis of the C39−C52 Fragment
inferredcites →https://doi.org/10.1021/ol0511833openalex-snapshot
The Polyol Domain of Amphidinol 3. A Stereoselective Synthesis of the Entire C(1)−C(30) Sector
inferredcites →https://doi.org/10.1021/ol052322jopenalex-snapshot
Synthesis of the C(43)−C(67) Fragment of Amphidinol 3
inferredcites →https://doi.org/10.1021/ol062875+openalex-snapshot
Development of an Access Route to the C31−C52 Central Core of Amphidinol 3
inferredcites →https://doi.org/10.1021/ol1015898openalex-snapshot
Synthesis of the Bis-tetrahydropyran Core of Amphidinol 3
inferredcites →https://doi.org/10.1021/ol7020934openalex-snapshot
Synthesis of the C1−C52 Fragment of Amphidinol 3, Featuring a β-Alkoxy Alkyllithium Addition Reaction
inferredcites →https://doi.org/10.1021/ol703042qopenalex-snapshot
Synthesis of the C(26)−C(42) and C(43)−C(67) Pyran-Containing Fragments of Amphidinol 3 via a Common Pyran Intermediate
inferredcites →https://doi.org/10.1021/ol802168ropenalex-snapshot
Combinatorial Synthesis of the 1,5-Polyol System Based on Cross Metathesis: Structure Revision of Amphidinol 3
inferredcites →https://doi.org/10.1039/b208078hopenalex-snapshot
The modified Julia olefination: alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds
inferredcites →https://doi.org/10.1055/s-0029-1217754openalex-snapshot
Convergent Synthesis of the C18-C30 Fragment of Amphidinol 3
inferredcites →https://doi.org/10.1055/s-1998-1570openalex-snapshot
A Stereoselective Synthesis oftrans-1,2-Disubstituted Alkenes Based on the Condensation of Aldehydes with Metallated 1-Phenyl-1H-tetrazol-5-yl Sulfones
inferredcites →https://doi.org/10.1055/s-2007-984910openalex-snapshot
Efficient Syntheses of the Polyene Fragments Present in Amphidinols
inferredcites →https://doi.org/10.1055/s-2007-985601openalex-snapshot
Stereoselective Synthesis of the C(53)-C(67) Polyene Fragment of Amphidinol 3
inferredcites →https://doi.org/10.3390/md304113openalex-snapshot
Luteophanol D, New Polyhydroxyl Metabolite from Marine Dinoflagellate Amphidinium sp.
inferredcites →https://doi.org/10.3987/com-10-s(e)86openalex-snapshot
Structural Reevaluations of Amphidinol 3, a Potent Antifungal Compound from Dinoflagellate

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.4591155openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or095.01openalex-snapshot
The J ulia– K ocienski Olefination
inferred← citeshttps://doi.org/10.1002/ajoc.202000181openalex-snapshot
Synthesis and Stereochemistry of the C30−C63 Section of Karlotoxin 2
inferred← citeshttps://doi.org/10.1002/ange.201507418openalex-snapshot
Stereochemical Studies of the Karlotoxin Class Using NMR Spectroscopy and DP4 Chemical‐Shift Analysis: Insights into their Mechanism of Action
inferred← citeshttps://doi.org/10.1002/ange.201712167openalex-snapshot
Synthesis and Stereochemical Revision of the C31–C67 Fragment of Amphidinol 3
inferred← citeshttps://doi.org/10.1002/anie.201507418openalex-snapshot
Stereochemical Studies of the Karlotoxin Class Using NMR Spectroscopy and DP4 Chemical‐Shift Analysis: Insights into their Mechanism of Action
inferred← citeshttps://doi.org/10.1002/anie.201712167openalex-snapshot
Synthesis and Stereochemical Revision of the C31–C67 Fragment of Amphidinol 3
inferred← citeshttps://doi.org/10.1002/asia.70353openalex-snapshot
Synthesis and Structure–Activity Relationship Studies of Truncated Artificial Analogues of Amphidinol 3
inferred← citeshttps://doi.org/10.1007/978-981-97-1619-7_3openalex-snapshot
A Long Journey Toward Structure Revision and Total Synthesis of Amphidinol 3
inferred← citeshttps://doi.org/10.1007/978-981-97-6830-1_6openalex-snapshot
NMR Studies on Natural Product—Stereochemical Determination and Conformational Analysis in Solution and in Membrane
inferred← citeshttps://doi.org/10.1016/b978-0-444-63359-0.00007-0openalex-snapshot
Nuclear Magnetic Resonance Spectroscopy for Structural Characterization of Bioactive Compounds
inferred← citeshttps://doi.org/10.1016/j.bbrep.2021.100941openalex-snapshot
Amphidinol 3 preferentially binds to cholesterol in disordered domains and disrupts membrane phase separation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2023.129594openalex-snapshot
Truncated Derivatives of Amphidinol 3 Reveal the Functional Role of Polyol Chain in Sterol-Recognition and Pore Formation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.09.104openalex-snapshot
Karlotoxin synthetic studies: concise synthesis of a C(42–63) B-ring tetrahydropyran fragment
inferred← citeshttps://doi.org/10.1016/j.tetlet.2025.155586openalex-snapshot
Syntheses of C22–C29 and C20–C29 sections of amphidinol 3
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00345openalex-snapshot
Structures of the Largest Amphidinol Homologues from the Dinoflagellate Amphidinium carterae and Structure–Activity Relationships
inferred← citeshttps://doi.org/10.1021/bi5002932openalex-snapshot
Direct and Stereospecific Interaction of Amphidinol 3 with Sterol in Lipid Bilayers
inferred← citeshttps://doi.org/10.1021/jacs.9b11789openalex-snapshot
Total Synthesis of Amphidinol 3: A General Strategy for Synthesizing Amphidinol Analogues and Structure–Activity Relationship Study
inferred← citeshttps://doi.org/10.1021/jo502322mopenalex-snapshot
Stereoselective Synthesis of the C1–C29 Part of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/np500275xopenalex-snapshot
Antifungal Amphidinol 18 and Its 7-Sulfate Derivative from the Marine Dinoflagellate Amphidinium carterae
inferred← citeshttps://doi.org/10.1038/s41598-017-11135-xopenalex-snapshot
Channel Formation and Membrane Deformation via Sterol-Aided Polymorphism of Amphidinol 3
inferred← citeshttps://doi.org/10.1039/c3np70062copenalex-snapshot
Isolation, structural determination and synthetic approaches toward amphidinol 3
inferred← citeshttps://doi.org/10.1039/c3ob41569dopenalex-snapshot
Diastereoselective synthesis of the C14–C29 fragment of amphidinol 3
inferred← citeshttps://doi.org/10.1039/c4np00144copenalex-snapshot
Marine natural products
inferred← citeshttps://doi.org/10.1039/c5sc00814jopenalex-snapshot
A highly convergent synthesis of the C1–C31 polyol domain of amphidinol 3 featuring a TST-RCM reaction: confirmation of the revised relative stereochemistry
inferred← citeshttps://doi.org/10.1039/d2np00023gopenalex-snapshot
Pitfalls in the structural elucidation of small molecules. A critical analysis of a decade of structural misassignments of marine natural products
inferred← citeshttps://doi.org/10.1246/bcsj.20200151openalex-snapshot
Structure Determination, Chemical Synthesis, and Evaluation of Biological Activity of Super Carbon Chain Natural Products
inferred← citeshttps://doi.org/10.1246/bcsj.20220273openalex-snapshot
Formation of a Tight Complex between Amphidinol 3 and Sterols in Lipid Bilayers Revealed by Short-Range Energy Transfer
inferred← citeshttps://doi.org/10.1246/cl.170050openalex-snapshot
Synthesis of a Truncated Analog of Amphidinol 3 Corresponding to the C21–C39/C52–C67 Section
inferred← citeshttps://doi.org/10.1246/cl.180475openalex-snapshot
Flow Synthesis of (3R)- and (3S)-(E)-1-Iodohexa-1,5-dien-3-ol: Chiral Building Blocks for Natural Product Synthesis
inferred← citeshttps://doi.org/10.2183/pjab.101.016openalex-snapshot
Conformational dynamics and molecular interactions of natural products: unveiling functional structures in biological membranes
inferred← citeshttps://doi.org/10.3987/com-18-13927openalex-snapshot
Synthesis of an Analog of Amphidinol 3 Corresponding to the C31–C67 Section
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.79.664openalex-snapshot
Total Synthesis of Amphidinol 3
inferred← citeshttps://doi.org/10.70675/72bda085zc395z4d80z9e55z7fd0d63cf1a9openalex-snapshot
Développement de nouvelles méthodes d'insertion du groupement trifluorométhyléther
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.