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Concise Synthesis of PM-94128 and Y-05460M-A
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.200804571openalex-snapshot
Total Synthesis of Bacilosarcins A and B
inferredcites →https://doi.org/10.1016/0040-4020(95)00776-5openalex-snapshot
A Total Synthesis of the Natural Enantiomer of the Gastroprotective Natural Products AI-77-B and Amicoumacin C Hydrochloride
inferredcites →https://doi.org/10.1016/0957-4166(96)00291-1openalex-snapshot
An improved procedure to homochiral cyclic statines
inferredcites →https://doi.org/10.1016/j.tet.2008.04.076openalex-snapshot
Bacilosarcins A and B, novel bioactive isocoumarins with unusual heterocyclic cores from the marine-derived bacterium Bacillus subtilis
inferredcites →https://doi.org/10.1016/j.tetlet.2007.10.125openalex-snapshot
Total synthesis of (−)-2-epi-lentiginosine by use of chiral 5-hydroxy-1,5-dihydropyrrol-2-one as a building block
inferredcites →https://doi.org/10.1016/s0378-1097(02)01065-0openalex-snapshot
Screening for biologically active metabolites with endosymbiotic bacilli isolated from arthropods
inferredcites →https://doi.org/10.1016/s0923-2508(02)01320-7openalex-snapshot
Amicoumacin antibiotic production and genetic diversity of Bacillus subtilis strains isolated from different habitats
inferredcites →https://doi.org/10.1021/jm00379a002openalex-snapshot
1H-2-Benzopyran-1-one derivatives, microbial products with pharmacological activity. Conversion into orally active derivatives with antiinflammatory and antiulcer activities
inferredcites →https://doi.org/10.1021/np50075a006openalex-snapshot
Biologically Active Metabolites from Xenorhabdus Spp., Part 2. Benzopyran-1-one Derivatives with Gastroprotective Activity
inferredcites →https://doi.org/10.1021/ol035470nopenalex-snapshot
Asymmetric Total Synthesis and Stereochemical Elucidation of the Antitumor Agent PM-94128
inferredcites →https://doi.org/10.1038/ja.2006.50openalex-snapshot
Sg17-1-4, a Novel Isocoumarin from a Marine Fungus Alternaria tenuis Sg17-1
inferredcites →https://doi.org/10.1039/p19870001177openalex-snapshot
Stereospecific synthesis of N-protected statine and its analogues via chiral tetramic acid
inferredcites →https://doi.org/10.1055/s-1993-25834openalex-snapshot
Enantioselective and Diastereoselective Formation ofsyn-3-Hydroxy-4-amino Acids (syn-Statines) via Tetramic Acids
inferredcites →https://doi.org/10.1128/aac.45.11.3156-3161.2001openalex-snapshot
In Vitro Anti- Helicobacter pylori Activity of the Probiotic Strain Bacillus subtilis 3 Is Due to Secretion of Antibiotics
inferredcites →https://doi.org/10.7164/antibiotics.28.717openalex-snapshot
A new antibiotic, baciphelacin.
inferredcites →https://doi.org/10.7164/antibiotics.34.611openalex-snapshot
Amicoumacin-A,a new antibiotic with strong antiinflammatory and antiulcer activity.
inferredcites →https://doi.org/10.7164/antibiotics.45.1949openalex-snapshot
A new isocoumarin antibiotic, Y-05460M-A.
inferredcites →https://doi.org/10.7164/antibiotics.50.175openalex-snapshot
PM-94128, a New Isocoumarin Antitumor Agent Produced by a Marine Bacterium.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/adsc.70739openalex-snapshot
Isocoumarins a Privileged Scaffold: Isolation, Biosynthesis and Recent Progress in the Total Synthesis of Naturally Occurring Isocoumarins and Dihydroisocoumarins
inferred← citeshttps://doi.org/10.1002/cjoc.70266openalex-snapshot
Electrochemical Iodination‐Triggered Skeletal Rearrangement of Acryl Imides via Cascade Substitutions to Access α,β‐Dihydroxyl Amides
inferred← citeshttps://doi.org/10.1002/ejoc.201901114openalex-snapshot
Unified Total Synthesis of Hetiamacins A–D
inferred← citeshttps://doi.org/10.1007/7081_2021_55openalex-snapshot
Total Synthesis of the Amicoumacin Family of Natural Products
inferred← citeshttps://doi.org/10.1007/s10600-021-03323-zopenalex-snapshot
Progress in the Chemistry of Amino-Acid Derivatives of Isocoumarins and 3,4-Dihydroisocoumarins
inferred← citeshttps://doi.org/10.1007/s11596-024-2922-yopenalex-snapshot
Michael Acceptor Pyrrolidone Derivatives and Their Activity against Diffuse Large B-cell Lymphoma
inferred← citeshttps://doi.org/10.1016/b978-0-444-64068-0.00012-7openalex-snapshot
Amicoumacins and Related Compounds: Chemistry and Biology
inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.001openalex-snapshot
De Novo Synthesis of 3-Pyrrolin-2-Ones
inferred← citeshttps://doi.org/10.1016/bs.aihch.2018.10.004openalex-snapshot
Reactions of 3-pyrrolin-2-ones
inferred← citeshttps://doi.org/10.1016/j.ejmech.2016.03.025openalex-snapshot
Isocoumarins, miraculous natural products blessed with diverse pharmacological activities
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.117088openalex-snapshot
Exploring the anticancer potential and mechanisms of action of natural coumarins and isocoumarins
inferred← citeshttps://doi.org/10.1016/j.tet.2015.02.014openalex-snapshot
Stereoselective total synthesis of amicoumacin C
inferred← citeshttps://doi.org/10.1016/j.tetlet.2014.09.009openalex-snapshot
Total synthesis of AI-77-B
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.09.090openalex-snapshot
Synthesis of bacilosarcins B and C
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c02576openalex-snapshot
Application of Pd-Catalyzed C–H Alkylation Reaction in Total Syntheses of Twelve Amicoumacin-Type Natural Products
inferred← citeshttps://doi.org/10.1021/acsomega.0c06267openalex-snapshot
Asymmetric Total Synthesis of Hetiamacins A–F
inferred← citeshttps://doi.org/10.1021/cg3001619openalex-snapshot
Hydrogen-Bonded Helical Self-Assembly of Sterically-Hindered Benzyl Alcohols: Rare Isostructurality and Synthon Equivalence Between Alcohols and Acids
inferred← citeshttps://doi.org/10.1021/jo101757kopenalex-snapshot
Regioselective Inversion of the Hydroxyl Group in d -ribo-Phytosphingosine via a Cyclic Sulfate and Bis-Sulfonate Intermediate
inferred← citeshttps://doi.org/10.1093/bbb/zbac182openalex-snapshot
Concise synthesis of amino acid component of amicoumacins via dihydrooxazine formation through intramolecular conjugate addition
inferred← citeshttps://doi.org/10.1271/bbb.100646openalex-snapshot
Partial Racemization Occurring in the Hydroxylactonization of a δ,ε-Epoxy Amide
inferred← citeshttps://doi.org/10.3390/molecules15042771openalex-snapshot
A General and Simple Diastereoselective Reduction by L-Selectride: Efficient Synthesis of Protected (4S,5S)-Dihydroxy Amides
inferred← citeshttps://doi.org/10.3390/molecules25194446openalex-snapshot
Hetiamacin E and F, New Amicoumacin Antibiotics from Bacillus subtilis PJS Using MS/MS-Based Molecular Networking
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.68.387openalex-snapshot
Synthetic Studies on Bacilosarcins A and B, and Related Natural Products
inferred← citeshttps://doi.org/10.70675/7446be9ezdae6z4f84z818ezd04f35d7f193openalex-snapshot
Dihydropyridinones et Pyrrolones : précurseurs potentiels de gamma aminoacides cyclobutaniques
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