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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
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Outgoing claims: the papers this work cites, builds on, or argues with.
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Structure elucidation of 21,22-dihydroxyonnamides A1–A4 from the marine sponge Theonella swinhoei: an empirical rule to assign the relative stereochemistry of linear 1,5-diols
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inferred← citeshttps://doi.org/10.1021/cr030733copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja010453jopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja9091853openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo102585kopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo500906vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo901793fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np000250topenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol049079topenalex-snapshot
Regioselective Cross-Metathesis Reaction Induced by Steric Hindrance
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1021/ol050477lopenalex-snapshot
A C-Glycosidation Approach to the Central Core of Amphidinol 3: Synthesis of the C39−C52 Fragment
inferred← citeshttps://doi.org/10.1021/ol0511833openalex-snapshot
The Polyol Domain of Amphidinol 3. A Stereoselective Synthesis of the Entire C(1)−C(30) Sector
inferred← citeshttps://doi.org/10.1021/ol052322jopenalex-snapshot
Synthesis of the C(43)−C(67) Fragment of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/ol062875+openalex-snapshot
Development of an Access Route to the C31−C52 Central Core of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/ol070042topenalex-snapshot
Relative and Absolute Configuration of Versipelostatin, a Down-Regulator of Molecular Chaperone GRP78 Expression
inferred← citeshttps://doi.org/10.1021/ol1005399openalex-snapshot
Direct Assignment of the Relative Configuration in 1,3,n-Methyl-Branched Carbon Chains by 1H NMR Spectroscopy
inferred← citeshttps://doi.org/10.1021/ol1015898openalex-snapshot
Synthesis of the Bis-tetrahydropyran Core of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/ol1021417openalex-snapshot
Versatile Configuration-Encoded Strategy for Rapid Synthesis of 1,5-Polyol Stereoisomers
inferred← citeshttps://doi.org/10.1021/ol2003836openalex-snapshot
Enantio- and Diastereoselective Synthesis of (E)-1,5-syn-Diols: Application to the Synthesis of the C(23)−C(40) Fragment of Tetrafibricin
inferred← citeshttps://doi.org/10.1021/ol401176aopenalex-snapshot
Synthesis and Structure Revision of the C43–C67 Part of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/ol7017856openalex-snapshot
Absolute Structure of Prunustatin A, a Novel GRP78 Molecular Chaperone Down-Regulator
inferred← citeshttps://doi.org/10.1021/ol7020934openalex-snapshot
Synthesis of the C1−C52 Fragment of Amphidinol 3, Featuring a β-Alkoxy Alkyllithium Addition Reaction
inferred← citeshttps://doi.org/10.1021/ol8016337openalex-snapshot
Structure of Membrane-Bound Amphidinol 3 in Isotropic Small Bicelles
inferred← citeshttps://doi.org/10.1021/ol802168ropenalex-snapshot
Combinatorial Synthesis of the 1,5-Polyol System Based on Cross Metathesis: Structure Revision of Amphidinol 3
inferred← citeshttps://doi.org/10.1021/ol900299xopenalex-snapshot
Symbiospirols: Novel Long Carbon-Chain Compounds Isolated from Symbiotic Marine Dinoflagellate Symbiodinium sp.
inferred← citeshttps://doi.org/10.1038/ja.2006.26openalex-snapshot
3-Normeridamycin: A Potent Non-Immunosuppressive Immunophilin Ligand is Neuroprotective in Dopaminergic Neurons
inferred← citeshttps://doi.org/10.1038/ja.2006.76openalex-snapshot
New Destruxins from the Marine-derived Fungus Beauveria felina
inferred← citeshttps://doi.org/10.1038/ja.2009.132openalex-snapshot
JBIR-69, a new metabolite from Streptomyces sp. OG05
inferred← citeshttps://doi.org/10.1038/s41429-020-0319-0openalex-snapshot
Identification, cloning and heterologous expression of biosynthetic gene cluster for desertomycin
inferred← citeshttps://doi.org/10.1038/s41429-021-00468-5openalex-snapshot
Marine natural products targeting the eukaryotic cell membrane
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/a901979kopenalex-snapshot
The structure elucidation and biological activities of high molecular weight algal toxins: maitotoxin, prymnesins and zooxanthellatoxins (1993 to 1999)
inferred← citeshttps://doi.org/10.1039/b108842dopenalex-snapshot
Determination of the absolute configurations of α-amino esters from the 19F NMR chemical shifts of their CFTA amide diastereomers
inferred← citeshttps://doi.org/10.1039/b310427nopenalex-snapshot
Amphidinolides, bioactive macrolides from symbiotic marine dinoflagellatesThe authors dedicate this review to the late Professor D. John Faulkner.
inferred← citeshttps://doi.org/10.1039/b809658aopenalex-snapshot
Structural revisions of natural products by total synthesis
inferred← citeshttps://doi.org/10.1039/b907649bopenalex-snapshot
Full relative stereochemistry assignment and conformational analysis of 13,19-didesmethyl spirolide C via NMR- and molecular modeling-based techniques. A step towards understanding spirolide’s mechanism of action
inferred← citeshttps://doi.org/10.1039/c0np00002gopenalex-snapshot
3D structures of membrane-associated small molecules as determined in isotropic bicelles
inferred← citeshttps://doi.org/10.1039/c0ob00685hopenalex-snapshot
Synthesis of 6-F-ergosterol and its influence on membrane-permeabilization of amphotericin B and amphidinol 3
inferred← citeshttps://doi.org/10.1039/c2ob26641eopenalex-snapshot
Diastereoselective synthesis of the C17–C30 fragment 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/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/c9np00059copenalex-snapshot
Chemical diversity and mode of action of natural products targeting lipids in the eukaryotic cell membrane
inferred← citeshttps://doi.org/10.1039/c9np00070dopenalex-snapshot
Inspirations from tetrafibricin and related polyketides: new methods and strategies for 1,5-polyol synthesis
inferred← citeshttps://doi.org/10.1039/d1sc02810copenalex-snapshot
Discovery of benthol A and its challenging stereochemical assignment: opening up a new window for skeletal diversity of super-carbon-chain compounds
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/10.1201/b13868-13openalex-snapshot
Bioactive Molecules from Symbiotic Marine Dinoflagellates
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/bcsj.20230166openalex-snapshot
NMR Studies on the Structure and Functions of Small Biomolecules with Highly Flexible Conformation
inferred← citeshttps://doi.org/10.1246/bcsj.81.307openalex-snapshot
Structural Features of Dinoflagellate Toxins Underlying Biological Activity as Viewed by NMR
inferred← citeshttps://doi.org/10.1246/cl.2008.1172openalex-snapshot
Accurate Measurement of Vicinal Carbon–Hydrogen Coupling Constants via Ammonium Nitrogen Based on HMBC Experiments
inferred← citeshttps://doi.org/10.1351/pac-con-11-09-32openalex-snapshot
Recent insights into natural venoms
inferred← citeshttps://doi.org/10.1515/znc-2016-0043openalex-snapshot
Membrane permeabilizing action of amphidinol 3 and theonellamide A in raft-forming lipid mixtures
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/10.3390/md15120393openalex-snapshot
Biotechnological and Pharmacological Applications of Biotoxins and Other Bioactive Molecules from Dinoflagellates
inferred← citeshttps://doi.org/10.3390/md18100497openalex-snapshot
LC-MS/MS Method Development for the Discovery and Identification of Amphidinols Produced by Amphidinium
inferred← citeshttps://doi.org/10.3390/md18120590openalex-snapshot
A Polyol-Polyol Super-Carbon-Chain Compound Containing Thirty-Six Carbon Stereocenters from the Dinoflagellate Amphidinium gibbosum: Absolute Configuration and Multi-Segment Modification
inferred← citeshttps://doi.org/10.3390/md20050333openalex-snapshot
Approaches to Configuration Determinations of Flexible Marine Natural Products: Advances and Prospects
inferred← citeshttps://doi.org/10.3390/md23090332openalex-snapshot
High Inter- and Intraspecific Variability in Amphidinol Content and Toxicity of Amphidinium Strains
inferred← citeshttps://doi.org/10.3987/com-03-s(p)33openalex-snapshot
A Unified Approach to the Enantioselective Synthesis of 2,6-cis and trans Disubstituted Tetrahydropyranones
inferred← citeshttps://doi.org/10.3987/com-10-s(e)86openalex-snapshot
Structural Reevaluations of Amphidinol 3, a Potent Antifungal Compound from Dinoflagellate
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
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