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Merochlorins A–D, Cyclic Meroterpenoid Antibiotics Biosynthesized in Divergent Pathways with Vanadium-Dependent Chloroperoxidases
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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/cbic.200600338openalex-snapshot
A Gene Cluster for Prenylated Naphthoquinone and Prenylated Phenazine Biosynthesis in Streptomyces cinnamonensis DSM 1042
inferredcites →https://doi.org/10.1016/0031-9422(96)00284-1openalex-snapshot
Xanthones from Hypericum roeperanum
inferredcites →https://doi.org/10.1016/0378-1119(92)90627-2openalex-snapshot
Plasmid cloning vectors for the conjugal transfer of DNA from Escherichia coli to Streptomyces spp.
inferredcites →https://doi.org/10.1016/j.cbpa.2009.01.005openalex-snapshot
Opportunities for enzyme engineering in natural product biosynthesis
inferredcites →https://doi.org/10.1016/j.copbio.2010.09.010openalex-snapshot
Hybrid isoprenoid secondary metabolite production in terrestrial and marine actinomycetes
inferredcites →https://doi.org/10.1021/cr050313iopenalex-snapshot
Nature's Inventory of Halogenation Catalysts: Oxidative Strategies Predominate
inferredcites →https://doi.org/10.1021/ja109226sopenalex-snapshot
Structure and Biosynthesis of the Marine Streptomycete Ansamycin Ansalactam A and Its Distinctive Branched Chain Polyketide Extender Unit
inferredcites →https://doi.org/10.1021/ja201088kopenalex-snapshot
A Stereoselective Vanadium-Dependent Chloroperoxidase in Bacterial Antibiotic Biosynthesis
inferredcites →https://doi.org/10.1021/np058011zopenalex-snapshot
Antibiotic Terpenoid Chloro-Dihydroquinones from a New Marine Actinomycete
inferredcites →https://doi.org/10.1021/np800651mopenalex-snapshot
Biohalogenation: Nature’s Way to Synthesize Halogenated Metabolites
inferredcites →https://doi.org/10.1038/23748openalex-snapshot
A new pathway for polyketide synthesis in microorganisms
inferredcites →https://doi.org/10.1038/nature03668openalex-snapshot
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products
inferredcites →https://doi.org/10.1038/nature08303openalex-snapshot
Mechanistic considerations of halogenating enzymes
inferredcites →https://doi.org/10.1039/b302337kopenalex-snapshot
The role of vanadium bromoperoxidase in the biosynthesis of halogenated marine natural products
inferredcites →https://doi.org/10.1073/pnas.0337542100openalex-snapshot
PCR-targeted Streptomyces gene replacement identifies a protein domain needed for biosynthesis of the sesquiterpene soil odor geosmin
inferredcites →https://doi.org/10.1074/jbc.m406567200openalex-snapshot
Crystal Structure of a Bacterial Type III Polyketide Synthase and Enzymatic Control of Reactive Polyketide Intermediates
inferredcites →https://doi.org/10.1074/jbc.m500190200openalex-snapshot
A Novel Quinone-forming Monooxygenase Family Involved in Modification of Aromatic Polyketides
inferredcites →https://doi.org/10.1074/jbc.m611046200openalex-snapshot
Molecular Basis for Chloronium-mediated Meroterpene Cyclization
inferredcites →https://doi.org/10.1074/jbc.r109.001602openalex-snapshot
Exploring the Chemistry and Biology of Vanadium-dependent Haloperoxidases
inferredcites →https://doi.org/10.1111/j.1751-7915.2010.00219.xopenalex-snapshot
Engineering Streptomyces coelicolor for heterologous expression of secondary metabolite gene clusters
inferredcites →https://doi.org/10.1128/jb.182.15.4153-4157.2000openalex-snapshot
A Gene Cluster for the Mevalonate Pathway from Streptomyces sp. Strain CL190
inferredcites →https://doi.org/10.1128/jb.188.4.1236-1244.2006openalex-snapshot
Biosynthesis of a Natural Polyketide-Isoprenoid Hybrid Compound, Furaquinocin A: Identification and Heterologous Expression of the Gene Cluster
inferredcites →https://doi.org/10.1371/journal.pone.0029439openalex-snapshot
Novel Bacterial Metabolite Merochlorin A Demonstrates in vitro Activity against Multi-Drug Resistant Methicillin-Resistant Staphylococcus aureus
inferredcites →https://doi.org/10.7164/antibiotics.39.494openalex-snapshot
Structures of new antibiotics napyradiomycins.
inferredcites →https://doi.org/10.7164/antibiotics.40.740openalex-snapshot
Studies on new antibiotics SF2415. II. The structural elucidation.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113516zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/9783527681501.ch10openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201700833openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201900506openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201307200openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201405694openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201405696openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201407883openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201509573openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201611617openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201708474openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201710185openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201800343openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201804351openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201807844openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201813090openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202011171openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/anie.201307200openalex-snapshot
Biomimetic Total Synthesis of (±)‐Merochlorin A
inferred← citeshttps://doi.org/10.1002/anie.201405694openalex-snapshot
One‐Pot Enzymatic Synthesis of Merochlorin A and B
inferred← citeshttps://doi.org/10.1002/anie.201405696openalex-snapshot
A Multitasking Vanadium‐Dependent Chloroperoxidase as an Inspiration for the Chemical Synthesis of the Merochlorins
inferred← citeshttps://doi.org/10.1002/anie.201407883openalex-snapshot
Terpenoid Biosynthesis Off the Beaten Track: Unconventional Cyclases and Their Impact on Biomimetic Synthesis
inferred← citeshttps://doi.org/10.1002/anie.201509573openalex-snapshot
Specific Enzymatic Halogenation—From the Discovery of Halogenated Enzymes to Their Applications In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1002/anie.201611617openalex-snapshot
Cyanobacterial ent‐Sterol‐Like Natural Products from a Deviated Ubiquinone Pathway
inferred← citeshttps://doi.org/10.1002/anie.201708474openalex-snapshot
Structure and Mechanism of the Monoterpene Cyclolavandulyl Diphosphate Synthase that Catalyzes Consecutive Condensation and Cyclization
inferred← citeshttps://doi.org/10.1002/anie.201710185openalex-snapshot
“Head‐to‐Middle” and “Head‐to‐Tail” cis‐Prenyl Transferases: Structure of Isosesquilavandulyl Diphosphate Synthase
inferred← citeshttps://doi.org/10.1002/anie.201800343openalex-snapshot
Biocatalytic Oxidation Reactions: A Chemist's Perspective
inferred← citeshttps://doi.org/10.1002/anie.201804351openalex-snapshot
Total Synthesis Establishes the Biosynthetic Pathway to the Naphterpin and Marinone Natural Products
inferred← citeshttps://doi.org/10.1002/anie.201807844openalex-snapshot
Enzymatic Cascade Reactions in Biosynthesis
inferred← citeshttps://doi.org/10.1002/anie.201813090openalex-snapshot
Total Synthesis of (−)‐Merochlorin A
inferred← citeshttps://doi.org/10.1002/anie.202011171openalex-snapshot
Exploiting the Potential of Meroterpenoid Cyclases to Expand the Chemical Space of Fungal Meroterpenoids
inferred← citeshttps://doi.org/10.1002/anie.202415279openalex-snapshot
Modifications of Prenyl Side Chains in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/asia.201700420openalex-snapshot
Vanadium Chloroperoxidases: The Missing Link in the Formation of Chlorinated Compounds and Chloroform in the Terrestrial Environment?
inferred← citeshttps://doi.org/10.1002/asia.202200954openalex-snapshot
CuCl2‐Catalyzed α‐Chloroketonation of Aromatic Alkenes via Visible‐Light‐Induced LMCT
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Epoxomicin and Eponemycin Biosynthesis Involves gem ‐Dimethylation and an Acyl‐CoA Dehydrogenase‐Like Enzyme
inferred← citeshttps://doi.org/10.1002/cbic.201800116openalex-snapshot
Characterization of the Actinonin Biosynthetic Gene Cluster
inferred← citeshttps://doi.org/10.1002/cbic.201800225openalex-snapshot
Enzymatic Formation of Oxygen‐Containing Heterocycles in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1002/cbic.202500377openalex-snapshot
Functional Characterization of a Diazo‐Forming Enzyme in Meroterpenoid Biosynthesis
inferred← citeshttps://doi.org/10.1002/chem.201403953openalex-snapshot
A High‐Throughput Assay for Arylamine Halogenation Based on a Peroxidase‐Mediated Quinone–Amine Coupling with Applications in the Screening of Enzymatic Halogenations
inferred← citeshttps://doi.org/10.1002/chem.201902453openalex-snapshot
Organocatalytic Formal Intramolecular [3+2]‐Cycloaddition to Acquire Biologically Important Methanodibenzo[a,f]azulenes and Methanobenzo[f]azulenes
inferred← citeshttps://doi.org/10.1002/chem.202003741openalex-snapshot
The Total Synthesis of Diquinane‐Containing Natural Products
inferred← citeshttps://doi.org/10.1002/chem.202100985openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202101232openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202103254openalex-snapshot
Parts‐per‐Million‐Level, Catalytic [3+2]‐Annulations for the Asymmetric Synthesis of Methanobenzo[7]annulenes
inferred← citeshttps://doi.org/10.1002/chem.202303989openalex-snapshot
Strategies for the Construction of Benzobicyclo[3.2.1]octane in Natural Product Synthesis
inferred← citeshttps://doi.org/10.1002/cjoc.202200074openalex-snapshot
Development of Novel Phosphino‐Oxazoline Ligands and Their Application in Asymmetric Alkynlylation of Benzylic Halides
inferred← citeshttps://doi.org/10.1002/cjoc.202200129openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.202200521openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cjoc.70568openalex-snapshot
Enantioselective [4 + 2] Cycloaddition Enabled by Sequential Photoinduced [1,3]‐Silyl Migration and Isothiourea Catalysis
inferred← citeshttps://doi.org/10.1002/cmdc.201700451openalex-snapshot
Biosynthetically Guided Structure–Activity Relationship Studies of Merochlorin A, an Antibiotic Marine Natural Product
inferred← citeshttps://doi.org/10.1002/ejoc.202200143openalex-snapshot
A Single‐Step Synthesis of Stereodefined Skipped Trienes: Pd‐Catalyzed Cascade Reaction of Terminal Alkynes with Allylic Halides
inferred← citeshttps://doi.org/10.1002/iub.2418openalex-snapshot
Structure, catalysis, and inhibition mechanism of prenyltransferase
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
inferred← citeshttps://doi.org/10.1007/978-3-642-53971-8_27openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-007-7500-8_5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00253-019-10227-0openalex-snapshot
Exploration and genome mining of natural products from marine Streptomyces
inferred← citeshttps://doi.org/10.1007/s00253-021-11312-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00284-019-01698-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10295-013-1348-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10295-013-1389-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14676-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14711-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-804765-1.00008-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-816455-6.00014-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-95047-3.00005-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-18611-0.00002-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-444-63460-3.00001-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-444-64179-3.00004-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.mie.2018.01.037openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.mie.2018.02.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.mie.2018.02.026openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107699openalex-snapshot
The potential of marine natural Products: Recent Advances in the discovery of Anti-Tuberculosis agents
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2026.108797openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cbpa.2013.01.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2014.12.012openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2015.02.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ccr.2021.214404openalex-snapshot
Recent development of biomimetic halogenation inspired by vanadium dependent haloperoxidase
inferred← citeshttps://doi.org/10.1016/j.csbj.2021.12.024openalex-snapshot
The natural product biosynthesis potential of the microbiomes of Earth – Bioprospecting for novel anti-microbial agents in the meta-omics era
inferred← citeshttps://doi.org/10.1016/j.ejmech.2019.01.026openalex-snapshot
Marine natural products as potential anti-tubercular agents
inferred← citeshttps://doi.org/10.1016/j.ica.2016.06.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2018.04.110openalex-snapshot
Antibacterial macro molecules from marine organisms
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2015.08.009openalex-snapshot
Complete genome sequence of Streptomyces sp. CNQ-509, a prolific producer of meroterpenoid chemistry
inferred← citeshttps://doi.org/10.1016/j.pestbp.2017.12.005openalex-snapshot
Natural meroterpenoids isolated from the plant pathogenic fungus Verticillium albo-atrum with noteworthy modification action against voltage-gated sodium channels of central neurons of Helicoverpa armigera
inferred← citeshttps://doi.org/10.1016/j.sbi.2020.05.012openalex-snapshot
Halogenases: structures and functions
inferred← citeshttps://doi.org/10.1016/j.synbio.2016.09.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2017.02.054openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ymben.2018.03.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00019openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.biochem.2c00338openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c00245openalex-snapshot
Synergistic Dual Transition Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00478openalex-snapshot
Oxidative Cyclization in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00571openalex-snapshot
Enzymatic Halogenation and Dehalogenation Reactions: Pervasive and Mechanistically Diverse
inferred← citeshttps://doi.org/10.1021/acs.chemrev.7b00032openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jchemed.1c00267openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00926openalex-snapshot
Dryinones: Structure Elucidation of Red Colorants from Submerged Cultures of Pleurotus dryinus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01095openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00996openalex-snapshot
Naphthablins B and C, Meroterpenoids Identified from the Marine Sediment-Derived Streptomyces sp. CP26-58 Using HeLa Cell-Based Cytological Profiling
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00369openalex-snapshot
Diisoprenyl-cyclohexene/ane-Type Meroterpenoids from Biscogniauxia sp. and Their Anti-inflammatory Activities
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00502openalex-snapshot
Asymmetric Synthesis of Dihydronaphthoquinones Containing Adjacent Stereocenters via a Sulfa-Michael Addition Triggered Ring-Expansion Approach
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01400openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.9b00434openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02208openalex-snapshot
Guanahanolide A, a Meroterpenoid with a Sesterterpene Skeleton from Coral-Derived Streptomyces sp.
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01436openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02023openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00892openalex-snapshot
Ansalactams B–D Illustrate Further Biosynthetic Plasticity within the Ansamycin Pathway
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01078openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.6b03264openalex-snapshot
Dimericbiscognienyne A: A Meroterpenoid Dimer from Biscogniauxia sp. with New Skeleton and Its Activity
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00380openalex-snapshot
Total Synthesis of Sinensilactam A
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01019openalex-snapshot
Ni-Catalyzed Cross-Electrophile Coupling for the Synthesis of Skipped Polyenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01058openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01440openalex-snapshot
Meroindenon and Merochlorins E and F, Antibacterial Meroterpenoids from a Marine-Derived Sediment Bacterium of the Genus Streptomyces
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02840openalex-snapshot
(+/−)-Lucidumone, a COX-2 Inhibitory Caged Fungal Meroterpenoid from Ganoderma lucidum
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03095openalex-snapshot
Total Synthesis of Naphterpin and Marinone Natural Products
inferred← citeshttps://doi.org/10.1021/acscatal.0c00283openalex-snapshot
Versatile cis -isoprenyl Diphosphate Synthase Superfamily Members in Catalyzing Carbon–Carbon Bond Formation
inferred← citeshttps://doi.org/10.1021/acscatal.5c01239openalex-snapshot
Asymmetric Trapping of Siloxyketenes In Situ Generated from [1,3]-Silyl Migration of α-Ketoacylsilanes: A Visible-Light-Driven Palladium-Catalyzed [4 + 2] Cycloaddition
inferred← citeshttps://doi.org/10.1021/acscatal.7b01833openalex-snapshot
Synergistic Copper/Palladium Catalysis for the Regio- and Stereoselective Synthesis of Borylated Skipped Dienes
inferred← citeshttps://doi.org/10.1021/acschembio.5b00539openalex-snapshot
Mechanism-Based Post-Translational Modification and Inactivation in Terpene Synthases
inferred← citeshttps://doi.org/10.1021/cb400699popenalex-snapshot
Genetic Basis for the Biosynthesis of the Pharmaceutically Important Class of Epoxyketone Proteasome Inhibitors
inferred← citeshttps://doi.org/10.1021/ja409520vopenalex-snapshot
Flavin-Linked Oxidase Catalyzes Pyrrolizine Formation of Dichloropyrrole-Containing Polyketide Extender Unit in Chlorizidine A
inferred← citeshttps://doi.org/10.1021/ja500270mopenalex-snapshot
Cyclolavandulyl Skeleton Biosynthesis via Both Condensation and Cyclization Catalyzed by an Unprecedented Member of the cis-Isoprenyl Diphosphate Synthase Superfamily
inferred← citeshttps://doi.org/10.1021/jacs.1c13074openalex-snapshot
Cryptic Oxidative Transamination of Hydroxynaphthoquinone in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1021/jacs.5c01175openalex-snapshot
Intermolecular 1,2,4-Thiadiazole Synthesis Enabled by Enzymatic Halide Recycling with Vanadium-Dependent Haloperoxidases
inferred← citeshttps://doi.org/10.1021/jacs.5c17554openalex-snapshot
Chemoenzymatic Diazo Synthesis Enabled by Enzymatic Halide Recycling with Vanadium-Dependent Haloperoxidases
inferred← citeshttps://doi.org/10.1021/jacs.6c16767openalex-snapshot
A Substrate-Permissive Vanadium Haloperoxidase in Type II Polyketide Biosynthesis Unlocks Non-Native Halogenation across Diverse Substrate Scaffolds
inferred← citeshttps://doi.org/10.1021/jacs.8b10134openalex-snapshot
Total Enzyme Syntheses of Napyradiomycins A1 and B1
inferred← citeshttps://doi.org/10.1021/np400359yopenalex-snapshot
Highly Oxygenated Meroterpenoids from Fruiting Bodies of the Mushroom Tricholoma terreum
inferred← citeshttps://doi.org/10.1021/np5006136openalex-snapshot
Diterpene Alkaloids with an Aza-ent-kaurane Skeleton from Isodon rubescens
inferred← citeshttps://doi.org/10.1021/ol500800zopenalex-snapshot
Biomimetic Synthesis of (±)-Merochlorin B
inferred← citeshttps://doi.org/10.1021/sb3001062openalex-snapshot
Designed Biosynthesis of 36-Methyl-FK506 by Polyketide Precursor Pathway Engineering
inferred← citeshttps://doi.org/10.1038/ja.2012.74openalex-snapshot
The International Conference of Natural Product Biosynthesis (ICNPB, 8th US–Japan seminar on the Biosynthesis of Natural Products)
inferred← citeshttps://doi.org/10.1038/ja.2017.12openalex-snapshot
Biosynthetic studies on terpenoids produced by Streptomyces
inferred← citeshttps://doi.org/10.1038/ja.2017.52openalex-snapshot
New chlorinated xanthone and anthraquinone produced by a mangrove-derived fungus Penicillium citrinum HL-5126
inferred← citeshttps://doi.org/10.1038/nchem.2829openalex-snapshot
A unifying paradigm for naphthoquinone-based meroterpenoid (bio)synthesis
inferred← citeshttps://doi.org/10.1038/s41429-020-0330-5openalex-snapshot
Highlights of marine natural products having parallel scaffolds found from marine-derived bacteria, sponges, and tunicates
inferred← citeshttps://doi.org/10.1038/s41429-020-0331-4openalex-snapshot
Marine microbial natural products: the evolution of a new field of science
inferred← citeshttps://doi.org/10.1038/s41467-017-01975-6openalex-snapshot
Warhead biosynthesis and the origin of structural diversity in hydroxamate metalloproteinase inhibitors
inferred← citeshttps://doi.org/10.1038/s41467-025-57023-1openalex-snapshot
Unraveling the molecular basis of substrate specificity and halogen activation in vanadium-dependent haloperoxidases
inferred← citeshttps://doi.org/10.1038/s41598-017-13407-yopenalex-snapshot
Phyllomeroterpenoids A-C, Multi-biosynthetic Pathway Derived Meroterpenoids from the TCM Endophytic Fungus Phyllosticta sp. and their Antimicrobial Activities
inferred← citeshttps://doi.org/10.1039/9781837677436-00060openalex-snapshot
Chemoenzymatic Synthesis of Terpenoids
inferred← citeshttps://doi.org/10.1039/c3np70060gopenalex-snapshot
The role of transcription in heterologous expression of polyketides in bacterial hosts
inferred← citeshttps://doi.org/10.1039/c3np70077aopenalex-snapshot
Transition metal-promoted biomimetic steps in total syntheses
inferred← citeshttps://doi.org/10.1039/c5mt00324eopenalex-snapshot
Effects of trace metal ions on secondary metabolism and the morphological development of streptomycetes
inferred← citeshttps://doi.org/10.1039/c5np00090dopenalex-snapshot
Biosynthesis of fungal meroterpenoids
inferred← citeshttps://doi.org/10.1039/c5ob01946jopenalex-snapshot
Total synthesis and preliminary SAR study of (±)-merochlorins A and B
inferred← citeshttps://doi.org/10.1039/c6cc08126fopenalex-snapshot
Regioselective, cascade [3+2] annulation of β-naphthols (resorcinols) with Z-enoate propargylic alcohols: a novel entry for the synthesis of complex naphtho(benzo)furans
inferred← citeshttps://doi.org/10.1039/c6ob01733aopenalex-snapshot
Iron( iii ) chloride hexahydrate-promoted selective hydroxylation and chlorination of benzyl ketone derivatives for the construction of hetero-quaternary scaffolds
inferred← citeshttps://doi.org/10.1039/c8cc04285copenalex-snapshot
A catalytic allylic cation-induced intermolecular allylation-semipinacol rearrangement
inferred← citeshttps://doi.org/10.1039/c8ra07325bopenalex-snapshot
Applications of Friedel–Crafts reactions in total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/c8sc03697gopenalex-snapshot
Dalmanol biosyntheses require coupling of two separate polyketide gene clusters
inferred← citeshttps://doi.org/10.1039/c9np00025aopenalex-snapshot
Genetic platforms for heterologous expression of microbial natural products
inferred← citeshttps://doi.org/10.1039/c9np00051hopenalex-snapshot
Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases
inferred← citeshttps://doi.org/10.1039/c9ob01884kopenalex-snapshot
Haloperoxidases as catalysts in organic synthesis
inferred← citeshttps://doi.org/10.1039/c9ob01900fopenalex-snapshot
Synthesis of dibenzo[ a , d ]cycloheptanoids via aryne insertion into 2-arylidene-1,3-indandiones
inferred← citeshttps://doi.org/10.1039/d0np00005aopenalex-snapshot
An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study
inferred← citeshttps://doi.org/10.1039/d0np00018copenalex-snapshot
Meroterpenoid natural products from Streptomyces bacteria – the evolution of chemoenzymatic syntheses
inferred← citeshttps://doi.org/10.1039/d1np00010aopenalex-snapshot
Cryptic halogenation reactions in natural product biosynthesis
inferred← citeshttps://doi.org/10.1039/d2ob00370hopenalex-snapshot
Cephaloliverols A and B, two sterol-hybrid meroterpenoids from Cephalotaxus oliveri
inferred← citeshttps://doi.org/10.1039/d2ob02332fopenalex-snapshot
Resorculins: hybrid polyketide macrolides from Streptomyces sp. MST-91080
inferred← citeshttps://doi.org/10.1039/d2qo00792dopenalex-snapshot
Bio-inspired construction of a tetracyclic ring system with an avarane skeleton: total synthesis of dactyloquinone A
inferred← citeshttps://doi.org/10.1039/d3qo01510fopenalex-snapshot
Photo-hydroacylation: 1-tetralones from ortho -allylbenzaldehydes
inferred← citeshttps://doi.org/10.1039/d4np00048jopenalex-snapshot
The role and mechanisms of canonical and non-canonical tailoring enzymes in bacterial terpenoid biosynthesis
inferred← citeshttps://doi.org/10.1039/d5md01011jopenalex-snapshot
Empowering molecular complexity via biocatalysis: emerging blueprints in the total synthesis of medicinally relevant natural products
inferred← citeshttps://doi.org/10.1039/d5np00011dopenalex-snapshot
Prenylated bacterial natural products: occurrence, chemical diversity, biosynthesis and bioactivity
inferred← citeshttps://doi.org/10.1039/d5np00036jopenalex-snapshot
Streptomyces as a versatile host platform for heterologous production of microbial natural products
inferred← citeshttps://doi.org/10.1039/d5np00070jopenalex-snapshot
Diversity of enzymatic SAM-dependent C -methylation of aromatic compounds
inferred← citeshttps://doi.org/10.1039/d6qo00523copenalex-snapshot
Palladium-catalyzed [5 + 2] cycloaddition of vinyloxiranes with photogenerated siloxyketenes: access to seven-membered lactones
inferred← citeshttps://doi.org/10.1055/s-0036-1590919openalex-snapshot
Asymmetric Alkene and Arene Halofunctionalization Reactions in Meroterpenoid Biosynthesis
inferred← citeshttps://doi.org/10.1080/01614940.2020.1823788openalex-snapshot
Halogenases for biosynthetic pathway engineering: Toward new routes to naturals and non-naturals
inferred← citeshttps://doi.org/10.1080/14786419.2013.871546openalex-snapshot
A new prenylated indole derivative from endophytic actinobacteria Streptomyces sp. neau-D50
inferred← citeshttps://doi.org/10.1080/14786419.2025.2478528openalex-snapshot
Three new naphthoquinone-based meroterpenoids from Streptomyces sp. HBERC-16614 with antibacterial activities
inferred← citeshttps://doi.org/10.1128/aem.02430-14openalex-snapshot
The Vanadium Iodoperoxidase from the Marine Flavobacteriaceae Species Zobellia galactanivorans Reveals Novel Molecular and Evolutionary Features of Halide Specificity in the Vanadium Haloperoxidase Enzyme Family
inferred← citeshttps://doi.org/10.1128/genomea.01212-15openalex-snapshot
Draft Genome Sequence of Streptomyces sp. TP-A0890, a Producer of FR-900452 and A-74863a
inferred← citeshttps://doi.org/10.1128/mra.00035-24openalex-snapshot
Complete genome of Microbacterium plantarum CoE-159-22, isolated from traditionally produced Montenegrin cheese
inferred← citeshttps://doi.org/10.12677/amb.2020.94020openalex-snapshot
Research Progress in Microbial Halogenases and Their Industrial Applications
inferred← citeshttps://doi.org/10.1371/journal.pone.0143237openalex-snapshot
Diversity of ABBA Prenyltransferases in Marine Streptomyces sp. CNQ-509: Promiscuous Enzymes for the Biosynthesis of Mixed Terpenoid Compounds
inferred← citeshttps://doi.org/10.1534/g3.113.005967openalex-snapshot
PRICE: Software for the Targeted Assembly of Components of (Meta) Genomic Sequence Data
inferred← citeshttps://doi.org/10.18174/543999openalex-snapshot
Mapping natural product diversity through genomics
inferred← citeshttps://doi.org/10.2174/0122103155289998240611102259openalex-snapshot
Marine-derived Anti-tuberculosis Compounds
inferred← citeshttps://doi.org/10.31038/jppr.2020324openalex-snapshot
Cytotoxic Meroterpenes: A Review
inferred← citeshttps://doi.org/10.3184/174751918x15168821806597openalex-snapshot
Synthesis of New Oxido-Vanadium Complexes: Catalytic Properties and Cytotoxicity
inferred← citeshttps://doi.org/10.3389/fmicb.2017.00394openalex-snapshot
Cloning and Heterologous Expression of a Large-sized Natural Product Biosynthetic Gene Cluster in Streptomyces Species
inferred← citeshttps://doi.org/10.3390/biom10081187openalex-snapshot
Naphthoquinone-Based Meroterpenoids from Marine-Derived Streptomyces sp. B9173
inferred← citeshttps://doi.org/10.3390/biom9060225openalex-snapshot
Bioactivities of Halometabolites from Marine Actinobacteria
inferred← citeshttps://doi.org/10.3390/catal15070673openalex-snapshot
Recent Advances in Biocatalytic Dearomative Spirocyclization Reactions
inferred← citeshttps://doi.org/10.3390/md13074044openalex-snapshot
Biological Activity of Recently Discovered Halogenated Marine Natural Products
inferred← citeshttps://doi.org/10.3390/md16060177openalex-snapshot
Asperversins A and B, Two Novel Meroterpenoids with an Unusual 5/6/6/6 Ring from the Marine-Derived Fungus Aspergillus versicolor
inferred← citeshttps://doi.org/10.3390/md16090292openalex-snapshot
Bioactive Prenyl- and Terpenyl-Quinones/Hydroquinones of Marine Origin †
inferred← citeshttps://doi.org/10.3390/md18010022openalex-snapshot
New Napyradiomycin Analogues from Streptomyces sp. Strain CA-271078
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