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Synthesis and Phytotoxicity of Structural Analogues of Thaxtomin Natural Products
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s00425-005-0016-zopenalex-snapshot
Thaxtomin A induces programmed cell death in Arabidopsis thaliana suspension-cultured cells
inferredcites →https://doi.org/10.1016/0040-4020(96)00408-5openalex-snapshot
Synthèse d'analogues structuraux de thaxtomines, phytotoxines responsables de la gale de la pomme de terre
inferredcites →https://doi.org/10.1016/j.tet.2006.05.010openalex-snapshot
Efficient synthesis of 2,5-diketopiperazines using microwave assisted heating
inferredcites →https://doi.org/10.1016/s0968-0896(99)00059-0openalex-snapshot
Synthesis and biological activities of phenylahistin derivatives
inferredcites →https://doi.org/10.1021/ja00784a041openalex-snapshot
Total synthesis of a monocyclic peptide lactone antibiotic, etamycin
inferredcites →https://doi.org/10.1021/jo00065a001openalex-snapshot
Synthetic studies on thaxtomins A and B, phytotoxins associated with Streptomyces scabies, the causal organism of potato common scab
inferredcites →https://doi.org/10.1021/jo0012905openalex-snapshot
Total Synthesis of Anti-microtubule Diketopiperazine Derivatives: Phenylahistin and Aurantiamine
inferredcites →https://doi.org/10.1021/jo01266a091openalex-snapshot
Simple route to sterically pure diketopiperazines
inferredcites →https://doi.org/10.1055/s-1998-2184openalex-snapshot
Synthesis of Mukonine and Seven Further 1-Oxygenated Carbazole Alkaloids
inferredcites →https://doi.org/10.1071/ch9841791openalex-snapshot
Pyrazine chemistry. II. Reduction of 3,6-Dibenzylidenepiperazine-2,5-diones
inferredcites →https://doi.org/10.1081/scc-120030746openalex-snapshot
Improvements in Aldol Reactions with Diketopiperazines
inferredcites →https://doi.org/10.1093/jxb/ern344openalex-snapshot
Thaxtomin A affects CESA-complex density, expression of cell wall genes, cell wall composition, and causes ectopic lignification in Arabidopsis thaliana seedlings
inferredcites →https://doi.org/10.1105/tpc.013342openalex-snapshot
An Arabidopsis Mutant Resistant to Thaxtomin A, a Cellulose Synthesis Inhibitor from Streptomyces Species[W]
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04461.xopenalex-snapshot
A large, mobile pathogenicity island confers plant pathogenicity on Streptomyces species
inferredcites →https://doi.org/10.3390/molecules14082836openalex-snapshot
Efficient Microwave Assisted Syntheses of 2,5-Diketopiperazines in Aqueous Media
inferredcites →https://doi.org/10.3998/ark.5550190.0003.807openalex-snapshot
Synthesis of the diketopiperazine dipodazine
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ange.201801525openalex-snapshot
De novo Biosynthesis of “Non‐Natural” Thaxtomin Phytotoxins
inferred← citeshttps://doi.org/10.1002/anie.201801525openalex-snapshot
De novo Biosynthesis of “Non‐Natural” Thaxtomin Phytotoxins
inferred← citeshttps://doi.org/10.1007/s00044-012-0438-7openalex-snapshot
Efficient synthesis of piperazine-2,6-dione and 4-(1H-indole-2-carbonyl)piperazine-2,6-dione derivatives and their evaluation for anticancer activity
inferred← citeshttps://doi.org/10.1007/s00044-014-0969-1openalex-snapshot
Efficient synthesis of heterocyclic compounds derived from 2,6-dioxopiperazine derivatives and their evaluation for anti-inflammatory and anticancer activities
inferred← citeshttps://doi.org/10.1007/s00299-015-1888-4openalex-snapshot
Mechanisms of thaxtomin A-induced root toxicity revealed by a thaxtomin A sensitive Arabidopsis mutant (ucu2-2/gi-2)
inferred← citeshttps://doi.org/10.1016/b978-0-12-819962-6.00002-6openalex-snapshot
Synthesis and Reactions of Nitroindoles
inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.11.024openalex-snapshot
Heterocyclic cellular lipid peroxidation inhibitors inspired by the marine antioxidant barettin
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2013.11.001openalex-snapshot
Threats and opportunities of plant pathogenic bacteria
inferred← citeshttps://doi.org/10.1016/j.engmic.2022.100067openalex-snapshot
Natural and engineered cyclodipeptides: Biosynthesis, chemical diversity, and engineering strategies for diversification and high-yield bioproduction.
inferred← citeshttps://doi.org/10.1016/j.tet.2024.133838openalex-snapshot
Synthesis and spectroscopic investigation of substituted piperazine-2,5-dione derivatives
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c02616openalex-snapshot
Structure Simplification of Natural Products as a Lead Generation Approach in Agrochemical Discovery
inferred← citeshttps://doi.org/10.1021/cr200398yopenalex-snapshot
2,5-Diketopiperazines: Synthesis, Reactions, Medicinal Chemistry, and Bioactive Natural Products
inferred← citeshttps://doi.org/10.1021/jf506153topenalex-snapshot
Synthesis and Biological Evaluations of a Series of Thaxtomin Analogues
inferred← citeshttps://doi.org/10.1039/c4ob01148aopenalex-snapshot
A one-pot multicomponent coupling/cyclization for natural product herbicide (±)-thaxtomin A
inferred← citeshttps://doi.org/10.1039/c7ob02297bopenalex-snapshot
Synthesis of monoalkylidene diketopiperazines and application to the synthesis of barettin
inferred← citeshttps://doi.org/10.1039/c8np00025eopenalex-snapshot
A genomics perspective on natural product biosynthesis in plant pathogenic bacteria
inferred← citeshttps://doi.org/10.1071/ch10182openalex-snapshot
Highlights of the 2009 New South Wales Southern Highlands Conference on Heterocyclic Chemistry
inferred← citeshttps://doi.org/10.1111/nph.16334openalex-snapshot
Suberin deposition in potato periderm: a novel resistance mechanism against tuber greening
inferred← citeshttps://doi.org/10.1128/aem.00164-18openalex-snapshot
High-Yield Production of Herbicidal Thaxtomins and Thaxtomin Analogs in a Nonpathogenic Streptomyces Strain
inferred← citeshttps://doi.org/10.11606/d.11.2019.tde-17072019-091002openalex-snapshot
Potencial da taxtomina parcialmente purificada no controle de >i /i< e reação de cultivar de soja ao patógeno
inferred← citeshttps://doi.org/10.3389/fmicb.2015.00785openalex-snapshot
Rational and combinatorial tailoring of bioactive cyclic dipeptides
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