On the public citation graph
Total Synthesis and Structural Elucidation of Azaspiracid-1. Final Assignment and Total Synthesis of the Correct Structure of Azaspiracid-1
0 signed · 121 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/1521-3773(20011105)40:21<4068::aid-anie4068>3.0.co;2-yopenalex-snapshot
Synthesis of the ABCD Ring System of Azaspiracid We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), The Skaggs Institute for Chemical Biology, a predoctoral…
inferredcites →https://doi.org/10.1002/anie.200351826openalex-snapshot
Total Synthesis of the Proposed Azaspiracid‐1 Structure, Part 2: Coupling of the C1–C20, C21–C27, and C28–C40 Fragments and Completion of the Synthesis
inferredcites →https://doi.org/10.1002/anie.200460695openalex-snapshot
Structural Revision and Total Synthesis of Azaspiracid‐1, Part 1: Intelligence Gathering and Tentative Proposal
inferredcites →https://doi.org/10.1002/anie.200460696openalex-snapshot
Structural Revision and Total Synthesis of Azaspiracid‐1, Part 2: Definition of the ABCD Domain and Total Synthesis
inferredcites →https://doi.org/10.1002/anie.200460864openalex-snapshot
Chasing Molecules That Were Never There: Misassigned Natural Products and the Role of Chemical Synthesis in Modern Structure Elucidation
inferredcites →https://doi.org/10.1016/0040-4039(94)88162-6openalex-snapshot
Selective deoxygenation of allylic alcohols and acetates by lithium perchlorate promoted triethylsilane reduction
inferredcites →https://doi.org/10.1016/s0040-4039(00)99477-2openalex-snapshot
Mild hydrogenolysis process by catalytic transfer hydrogenation
inferredcites →https://doi.org/10.1016/s0040-4039(96)02265-4openalex-snapshot
Lissoketal, a spiroketal from the Palauan ascidian Lissoclinum voeltzkowi
inferredcites →https://doi.org/10.1016/s0957-4166(02)00180-5openalex-snapshot
New total syntheses of (+)-macrosphelides C, F and G
inferredcites →https://doi.org/10.1021/ja001825bopenalex-snapshot
A New Method for the One-Step Synthesis of α,β-Unsaturated Carbonyl Systems from Saturated Alcohols and Carbonyl Compounds
inferredcites →https://doi.org/10.1021/ja00426a033openalex-snapshot
The ester enolate Claisen rearrangement. Stereochemical control through stereoselective enolate formation
inferredcites →https://doi.org/10.1021/ja00799a062openalex-snapshot
Electrophilic and nucleophilic organoselenium reagents. New routes to .alpha.,.beta.-unsaturated carbonyl compounds
inferredcites →https://doi.org/10.1021/ja981413ropenalex-snapshot
Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis
inferredcites →https://doi.org/10.1021/jo00399a052openalex-snapshot
Synthesis of .alpha.,.beta.-unsaturated carbonyl compounds by palladium(II)-catalyzed dehydrosilylation of silyl enol ethers
inferredcites →https://doi.org/10.1021/jo971046mopenalex-snapshot
A Versatile and Highly Selective Hypervalent Iodine (III)/2,2,6,6-Tetramethyl-1-piperidinyloxyl-Mediated Oxidation of Alcohols to Carbonyl Compounds
inferredcites →https://doi.org/10.1039/c39940000479openalex-snapshot
Stereoselective Favorskii rearrangement of carvone chlorohydrin; expedient synthesis of (+)-dihydronepetalactone and (+)-iridomyrmecin
inferredcites →https://doi.org/10.1039/p19750001574openalex-snapshot
A new method for the deoxygenation of secondary alcohols
inferredcites →https://doi.org/10.1246/cl.2000.1250openalex-snapshot
A New and One-Pot Synthesis of α,β-Unsaturated Ketones by Dehydrogenation of Various Ketones with N-tert-Butyl Phenylsulfinimidoyl Chloride
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471264180.or077.02openalex-snapshot
The Barton‐McCombie Reaction
inferred← citeshttps://doi.org/10.1002/0471264180.or098.01openalex-snapshot
The Saegusa Oxidation and Related Procedures
inferred← citeshttps://doi.org/10.1002/0471264229.os089.31openalex-snapshot
Discussion Addendum for: Oxidation of Nerol to Neral with Iodosobenzene and TEMPO
inferred← citeshttps://doi.org/10.1002/9780470053485.ch7openalex-snapshot
Protection for the Amino Group
inferred← citeshttps://doi.org/10.1002/9781118662083.cot01-001openalex-snapshot
Formation of Alkanes and Arenes by Reduction
inferred← citeshttps://doi.org/10.1002/9781118905074.ch07openalex-snapshot
Protection for the Amino Group
inferred← citeshttps://doi.org/10.1002/9783527634606.ch8openalex-snapshot
Biomimetic Syntheses of Alkaloids with a Non‐Amino Acid Origin
inferred← citeshttps://doi.org/10.1002/adsc.200800247openalex-snapshot
Studies toward the Synthesis of (−)‐Zampanolide: Preparation of the Macrocyclic Core
inferred← citeshttps://doi.org/10.1002/ajoc.201800074openalex-snapshot
Stereoselective Construction of Cisoidal Bisspiroacetal Frameworks through Magnesium Coordination of the Bilateral Acetal Oxygen Atoms
inferred← citeshttps://doi.org/10.1002/ange.200600295openalex-snapshot
Total Synthesis and Confirmation of the Revised Structures of Azaspiracid‐2 and Azaspiracid‐3
inferred← citeshttps://doi.org/10.1002/ange.200601872openalex-snapshot
Kaskadenreaktionen in der Totalsynthese
inferred← citeshttps://doi.org/10.1002/ange.200603353openalex-snapshot
Synthesis of the Southern FGHI Ring System of Azaspiracid‐1 and Investigation into the Controlling Elements of C28‐ and C36‐Ketalization
inferred← citeshttps://doi.org/10.1002/ange.200701515openalex-snapshot
Total Synthesis of (+)‐Azaspiracid‐1. Part I: Synthesis of the Fully Elaborated ABCD Aldehyde
inferred← citeshttps://doi.org/10.1002/ange.200701520openalex-snapshot
Total Synthesis of (+)‐Azaspiracid‐1. Part II: Synthesis of the EFGHI Sulfone and Completion of the Synthesis
inferred← citeshttps://doi.org/10.1002/ange.201711006openalex-snapshot
Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
inferred← citeshttps://doi.org/10.1002/ange.201711008openalex-snapshot
Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses
inferred← citeshttps://doi.org/10.1002/anie.200600295openalex-snapshot
Total Synthesis and Confirmation of the Revised Structures of Azaspiracid‐2 and Azaspiracid‐3
inferred← citeshttps://doi.org/10.1002/anie.200601872openalex-snapshot
Cascade Reactions in Total Synthesis
inferred← citeshttps://doi.org/10.1002/anie.200603353openalex-snapshot
Synthesis of the Southern FGHI Ring System of Azaspiracid‐1 and Investigation into the Controlling Elements of C28‐ and C36‐Ketalization
inferred← citeshttps://doi.org/10.1002/anie.200701515openalex-snapshot
Total Synthesis of (+)‐Azaspiracid‐1. Part I: Synthesis of the Fully Elaborated ABCD Aldehyde
inferred← citeshttps://doi.org/10.1002/anie.200701520openalex-snapshot
Total Synthesis of (+)‐Azaspiracid‐1. Part II: Synthesis of the EFGHI Sulfone and Completion of the Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201711006openalex-snapshot
Total Synthesis of (6R,10R,13R,14R,16R,17R,19S,20R,21R,24S, 25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product
inferred← citeshttps://doi.org/10.1002/anie.201711008openalex-snapshot
Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses
inferred← citeshttps://doi.org/10.1002/asia.200600059openalex-snapshot
Second‐Generation Total Synthesis of Azaspiracids‐1, ‐2, and ‐3
inferred← citeshttps://doi.org/10.1002/cbic.200900201openalex-snapshot
Monoclonal Antibodies with Orthogonal Azaspiracid Epitopes
inferred← citeshttps://doi.org/10.1002/ejoc.201300991openalex-snapshot
Marine Toxins in Italy: The More You Look, the More You Find
inferred← citeshttps://doi.org/10.1002/ejoc.201301293openalex-snapshot
Iridium‐Catalyzed Direct Dehydroxylation of Alcohols
inferred← citeshttps://doi.org/10.1002/ejoc.201901243openalex-snapshot
Stereocontrolled Synthesis as an Enabling Tool for the Configurational Assignment of Marine Polyketide Natural Products
inferred← citeshttps://doi.org/10.1002/jnr.21731openalex-snapshot
Cytotoxic effect of azaspiracid‐2 and azaspiracid‐2‐methyl ester in cultured neurons: Involvement of the c‐Jun N‐terminal kinase
inferred← citeshttps://doi.org/10.1007/978-94-007-6419-4_2openalex-snapshot
Toxins Produced by Marine Microorganisms: A Short Review
inferred← citeshttps://doi.org/10.1007/978-94-007-6419-4_20openalex-snapshot
Azaspiracid Toxins: Toxicological Profile
inferred← citeshttps://doi.org/10.1007/978-94-007-6650-1_2-1openalex-snapshot
Toxins Produced by Marine Microorganisms: A Mini Review
inferred← citeshttps://doi.org/10.1007/978-94-007-6650-1_20-1openalex-snapshot
Azaspiracid Toxins: Toxicological Profile
inferred← citeshttps://doi.org/10.1007/s00216-012-5849-2openalex-snapshot
Quantitative analysis of azaspiracids in Azadinium spinosum cultures
inferred← citeshttps://doi.org/10.1007/s11458-007-0046-0openalex-snapshot
A new era for organic synthesis—highlights of the recent progress
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00409-2openalex-snapshot
4.07 Electrophilic Cyclization
inferred← citeshttps://doi.org/10.1016/j.ab.2013.10.035openalex-snapshot
Microsphere-based immunoassay for the detection of azaspiracids
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.06.019openalex-snapshot
Azaspiracids modulate intracellular pH levels in human lymphocytes
inferred← citeshttps://doi.org/10.1016/j.bcp.2007.04.004openalex-snapshot
Irreversible cytoskeletal disarrangement is independent of caspase activation during in vitro azaspiracid toxicity in human neuroblastoma cells
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.089openalex-snapshot
From nature to the laboratory and into the clinic
inferred← citeshttps://doi.org/10.1016/j.bmc.2011.06.011openalex-snapshot
Survey of marine natural product structure revisions: A synergy of spectroscopy and chemical synthesis
inferred← citeshttps://doi.org/10.1016/j.carres.2006.07.005openalex-snapshot
C-Branched pyrrolidines from 2-C-acetylmethyl-glycosylazides. Reduction of imines formed by monosaccharide ring opening
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.12.012openalex-snapshot
The chemistry of the carbon–transition metal double and triple bond: Annual survey covering the year 2006☆
inferred← citeshttps://doi.org/10.1016/j.hal.2013.05.009openalex-snapshot
Effect of environmental and nutritional factors on growth and azaspiracid production of the dinoflagellate Azadinium spinosum
inferred← citeshttps://doi.org/10.1016/j.hal.2019.101629openalex-snapshot
Variability and profiles of lipophilic toxins in bivalves from Great Britain during five and a half years of monitoring: azaspiracids and yessotoxins
inferred← citeshttps://doi.org/10.1016/j.jchromb.2008.02.020openalex-snapshot
Purification of five azaspiracids from mussel samples contaminated with DSP toxins and azaspiracids
inferred← citeshttps://doi.org/10.1016/j.jchromb.2024.124065openalex-snapshot
New azaspiracid analogues detected as bi-charged ions in Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters
inferred← citeshttps://doi.org/10.1016/j.tet.2007.11.092openalex-snapshot
Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.05.049openalex-snapshot
Synthesis of oxa-aza spirobicycles by intramolecular hydrogen atom transfer promoted by N-radicals in carbohydrate systems
inferred← citeshttps://doi.org/10.1016/j.tet.2013.01.017openalex-snapshot
Selective deprotection of silyl ethers
inferred← citeshttps://doi.org/10.1016/j.tet.2017.04.063openalex-snapshot
Direct synthesis of oxazolidin-2-ones from tert -butyl allylcarbamate via halo-induced cyclisation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.05.021openalex-snapshot
Stereoselective synthesis of the ABCD ring framework of azaspiracids
inferred← citeshttps://doi.org/10.1016/j.toxicon.2009.09.001openalex-snapshot
Biosynthesis of toxic naturally-occurring seafood contaminants
inferred← citeshttps://doi.org/10.1016/j.toxicon.2021.06.010openalex-snapshot
Complex profiles of azaspiracid analogues in two culture strains of Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters determined by LC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.toxicon.2026.109148openalex-snapshot
Structure elucidation and in vitro toxicity of AZA-40, an azaspiracid isobaric to AZA-1
inferred← citeshttps://doi.org/10.1016/s0959-6380(09)70019-4openalex-snapshot
Chapter 6.4 (2006): Six-membered ring systems: with O and/or S atoms
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5b00712openalex-snapshot
Cutting-Edge and Time-Honored Strategies for Stereoselective Construction of C–N Bonds in Total Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02569openalex-snapshot
Total Synthesis of Jerangolid B via sp3–sp2 Stille Coupling
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00557openalex-snapshot
Synthesis of the C22–C40 Domain of the Azaspiracids
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03451openalex-snapshot
Synthesis of the C1–C19 Domain of Azaspiracid-34
inferred← citeshttps://doi.org/10.1021/cr9002402openalex-snapshot
Novel Syntheses of Bridge-Containing Organic Compounds
inferred← citeshttps://doi.org/10.1021/ja064948qopenalex-snapshot
Stereospecific Cross-Coupling of α-(Thiocarbamoyl)organostannanes with Alkenyl, Aryl, and Heteroaryl Iodides
inferred← citeshttps://doi.org/10.1021/ja804659nopenalex-snapshot
Total Synthesis of (+)-Azaspiracid-1. An Exhibition of the Intricacies of Complex Molecule Synthesis
inferred← citeshttps://doi.org/10.1021/jacs.5c11010openalex-snapshot
Divergent Total Syntheses of Elisapterane and Relevant Diterpenoids Assisted by In Silico Structure Reassignment
inferred← citeshttps://doi.org/10.1021/jacs.9b01537openalex-snapshot
Iterative Assembly of Polycyclic Saturated Heterocycles from Monomeric Building Blocks
inferred← citeshttps://doi.org/10.1021/jo102228jopenalex-snapshot
Synthesis-Guided Structure Revision of the Sarcodonin, Sarcoviolin, and Hydnellin Natural Product Family
inferred← citeshttps://doi.org/10.1021/jo500678kopenalex-snapshot
13C NMR Analysis of 3,6-Dihydro-2H-pyrans: Assignment of Remote Stereochemistry Using Axial Shielding Effects
inferred← citeshttps://doi.org/10.1021/jo802351bopenalex-snapshot
Inspirations, Discoveries, and Future Perspectives in Total Synthesis
inferred← citeshttps://doi.org/10.1021/ol501301wopenalex-snapshot
Singlet Oxygen-Mediated Synthesis of Bis-spiroketals Found in Azaspiracids
inferred← citeshttps://doi.org/10.1021/ol801673ropenalex-snapshot
TEMPO/NaIO4−SiO2: A Catalytic Oxidative Rearrangement of Tertiary Allylic Alcohols to β-Substituted α,β-Unsaturated Ketones
inferred← citeshttps://doi.org/10.1021/tx200553popenalex-snapshot
Comparative Effects of the Marine Algal Toxins Azaspiracid-1, -2, and -3 on Jurkat T Lymphocyte Cells
inferred← citeshttps://doi.org/10.1021/tx800165copenalex-snapshot
Azaspiracid Substituent at C1 Is Relevant to in Vitro Toxicity
inferred← citeshttps://doi.org/10.1038/s41557-025-01804-0openalex-snapshot
An enzymatic dual-oxa Diels–Alder reaction constructs the oxygen-bridged tricyclic acetal unit of (–)-anthrabenzoxocinone
inferred← citeshttps://doi.org/10.1039/b701533jopenalex-snapshot
Marine natural products: synthetic aspects
inferred← citeshttps://doi.org/10.1039/b705652bopenalex-snapshot
Recent advances in the total synthesis of pharmaceutically relevant diterpenes
inferred← citeshttps://doi.org/10.1039/b901578gopenalex-snapshot
Recent strategies for the preparation of C-1 glycals
inferred← citeshttps://doi.org/10.1039/c2cs35116aopenalex-snapshot
Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance
inferred← citeshttps://doi.org/10.1039/c2gc16397gopenalex-snapshot
Using water, light, air and spirulina to access a wide variety of polyoxygenated compounds
inferred← citeshttps://doi.org/10.1039/c5cc10518hopenalex-snapshot
Chemo- and regioselective reductive deoxygenation of 1-en-4-yn-ols into 1,4-enynes through FeF 3 and TfOH co-catalysis
inferred← citeshttps://doi.org/10.1039/c9sc06116aopenalex-snapshot
The enantioselective total synthesis of laurendecumallene B
inferred← citeshttps://doi.org/10.1093/toxsci/kfp246openalex-snapshot
Cell Volume Decrease as a Link between Azaspiracid-Induced Cytotoxicity and c-Jun-N-Terminal Kinase Activation in Cultured Neurons
inferred← citeshttps://doi.org/10.1093/toxsci/kfp312openalex-snapshot
Involvement of Caspase Activation in Azaspiracid-Induced Neurotoxicity in Neocortical Neurons
inferred← citeshttps://doi.org/10.1111/j.1574-6976.2011.00304.xopenalex-snapshot
Microalgae in the postgenomic era: a blooming reservoir for new natural products
inferred← citeshttps://doi.org/10.1159/000110456openalex-snapshot
The c-Jun-N-Terminal Kinase is Involved in the Neurotoxic Effect of Azaspiracid-1
inferred← citeshttps://doi.org/10.1177/1934578x0800301106openalex-snapshot
Synthetic and Computational Studies on the ABC Trioxadispiroketal Subunit of the Marine Biotoxin Azaspiracid-1
inferred← citeshttps://doi.org/10.1351/pac200880040727openalex-snapshot
Total synthesis of complex heterocyclic natural products
inferred← citeshttps://doi.org/10.2903/j.efsa.2008.723openalex-snapshot
Marine biotoxins in shellfish – Azaspiracid group ‐ Scientific Opinion of the Panel on Contaminants in the Food chain
inferred← citeshttps://doi.org/10.3390/md10061360openalex-snapshot
Production and Isolation of Azaspiracid-1 and -2 from Azadinium spinosum Culture in Pilot Scale Photobioreactors
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/md16060188openalex-snapshot
Phycotoxins in Marine Shellfish: Origin, Occurrence and Effects on Humans
inferred← citeshttps://doi.org/10.3390/md6020039openalex-snapshot
Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts
inferred← citeshttps://doi.org/10.4224/crm.2014.aza1-b.20131120openalex-snapshot
AZA1-b: Certified Calibration Solution for Azaspiracid-1
inferred← citeshttps://doi.org/10.4224/crm.2015.aza2-b.20131126openalex-snapshot
AZA2-b: Certified Calibration Solution for Azaspiracid-2
inferred← citeshttps://doi.org/10.4224/crm.2016.aza123.20040422openalex-snapshot
AZA123: Calibration Solution for Azaspiracid-1, -2, and -3
inferred← citeshttps://doi.org/10.4224/crm.2016.aza3-b.20150527openalex-snapshot
AZA3-b: Certified Calibration Solution for Azaspiracid-3
inferred← citeshttps://doi.org/10.70675/5d09f84fz6ea1z4415z9147z9e3269a4dc5dopenalex-snapshot
Synthèse totale de molécules marines biologiquement actives et d’analogues structuraux par application des réactions de métathèse et de la photochimie
inferred← citeshttps://doi.org/10.70675/748de27bza31bz44e5za456z9c315bf21112openalex-snapshot
Nouvelles approches pour la préparation de composés hétérocycliques saturés
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.