maitotoxin formula

Ask for details ; Follow Report by Math1729 1 week ago Log in to add a comment What do you need to know? More... Molecular Weight: 842.1 g/mol. 4 Spectral Information Expand this section. Number of times cited according to CrossRef: 60. and you may need to create a new Wiley Online Library account.Enter your email address below and we will send you your username,If the address matches an existing account you will receive an email with instructions to retrieve your username,I have read and accept the Wiley Online Library Terms and Conditions of Use.Number of times cited according to CrossRef:Eight-Membered Rings With One Oxygen Atom.Reference Module in Chemistry, Molecular Sciences and Chemical Engineering.Perspectives from nearly five decades of total synthesis of natural products and their analogues for biology and medicine.Development of New Synthetic Methods Using Oxiranyl Anions and Application in the Syntheses of Polycyclic Ether Marine Natural Products.Total Synthesis Endeavors and Their Contributions to Science and Society:A Personal Account.Research Progress in the Biosynthetic Mechanisms of Marine Polyether Toxins.Structural Diversity of Microalgal Marine Toxins.Recent Advances in the Analysis of Marine Toxins.Dianionic Oxy‐Cope Rearrangement with Benzil Derivatives: meso‐Selective 3,3‐Coupling of Two Tetrahydrofuran Moieties.Maitotoxin-4, a Novel MTX Analog Produced by Gambierdiscus excentricus.Characterization of an epoxide hydrolase from the Florida red tide dinoflagellate, Karenia brevis.Cyclisation mechanisms in the biosynthesis of ribosomally synthesised and post-translationally modified peptides.Nature-inspired enzymatic cascades to build valuable compounds.Recent Advances and Applications of Experimental Technologies in Marine Natural Product Research.Current Understanding and Hypotheses on the Biosynthesis of Microalgal Polyether Toxins.Toxins and Biologically Active Compounds from Microalgae, Volume 1.Synthesis of a chiral building block for highly functionalized polycyclic ethers.Synthesis and Biological Evaluation of QRSTUVWXYZA′ Domains of Maitotoxin.Journal of the American Chemical Society.Polyketide biosynthesis in dinoflagellates: what makes it different?.Computed Spectral Properties and Structure Identification.Heronapyrrole D: A case of co-inspiration of natural product biosynthesis, total synthesis and biodiscovery.Intermediates in monensin biosynthesis: A late step in biosynthesis of the polyether ionophore monensin is crucial for the integrity of cation binding.The Failure of Epoxide Ring Opening and the Limits of Cascade Reactions.The Discovery and Synthesis of Brevisamide.Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis.Origins of Oxygen Atoms in a Marine Ladder-Frame Polyether: Evidence of Monooxygenation by A very straightforward model for the biosynthesis of all known polyether ladders, including maitotoxin (the largest and most toxic of this structural family; see formula) is described, but is the structure of this giant molecule really known? Maitotoxin 2 . Palytoxin is a polyhydroxylated and partially unsaturated compound with a long carbon chain. Unspecified. 5 points Maitotoxin formula? .Synthesis of the ABCDEFG Ring System of Maitotoxin.Total Synthesis of Structurally Complex Marine Oxacyclic Natural Products.Bulletin of the Chemical Society of Japan.Quantum Mechanical Calculation of NMR Parameters in the Stereostructural Determination of Natural Products.Synthesis of Marine Polycyclic Polyethers via Endo-Selective Epoxide-Opening Cascades.New synthetic strategies for the stereocontrolled synthesis of substituted ‘skipped’ diepoxides.The biosynthesis of polyketide-derived polycyclic ethers.Design and Synthesis of Ladder-Shaped Polyethers and Evaluation of the Interaction with Transmembrane Proteins.The development of endo-selective epoxide-opening cascades in water.Die biosynthetische Grundlage der Polyketid‐Vielfalt.Epoxidöffnungskaskaden zur Synthese polycyclischer Polyether‐Naturstoffe.The Biosynthetic Logic of Polyketide Diversity.Epoxide‐Opening Cascades in the Synthesis of Polycyclic Polyether Natural Products.Epoxide‐Hydrolase‐Initiated Hydrolysis/Rearrangement Cascade of a Methylene‐Interrupted Bis‐Epoxide Yields Chiral THF Moieties without Involvement of a “Cyclase”.Chiral recognition of ethers by NMR spectroscopy.Annual Reports Section "B" (Organic Chemistry).Maitotoxin induces two dose-dependent conductances in Xenopus oocytes. The marine natural product maitotoxin has a molecular formula C 164H 256O 68S 2Na 2.

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