Nature's inventory of halogenation catalysts: oxidative strategies predominate.
about
Characterization of the Conus bullatus genome and its venom-duct transcriptome.The halogenated metabolism of brown algae (Phaeophyta), its biological importance and its environmental significanceDiscovery and characterization of a marine bacterial SAM-dependent chlorinaseWhat's new in enzymatic halogenationsInsights into enzymatic halogenation from computational studiesFlavoenzymes: versatile catalysts in biosynthetic pathwaysMechanism of Enzymatic Fluorination in Streptomyces c attleyaStructural basis for halogenation by iron- and 2-oxo-glutarate-dependent enzyme WelO5Characterization of a Cyanobacterial Haloperoxidase and Evaluation of its Biocatalytic Halogenation PotentialStructure and biocatalytic scope of thermophilic flavin-dependent halogenase and flavin reductase enzymesCatalytic Mechanisms of Fe(II)- and 2-Oxoglutarate-dependent OxygenasesHalogenase-Inspired Oxidative Chlorination Using Flavin PhotocatalysisA new family of iron-dependent halogenases acts on freestanding substrates.4-chloroprolines: synthesis, conformational analysis, and effect on the collagen triple helixChemical and biological studies of nakiterpiosin and nakiterpiosinone.A flavin-dependent halogenase catalyzes the chlorination step in the biosynthesis of Dictyostelium differentiation-inducing factor 1.Direct nitration and azidation of aliphatic carbons by an iron-dependent halogenaseElucidation of the Fe(IV)=O intermediate in the catalytic cycle of the halogenase SyrB2.Metamorphic enzyme assembly in polyketide diversification.Credneramides A and B: neuromodulatory phenethylamine and isopentylamine derivatives of a vinyl chloride-containing fatty acid from cf. Trichodesmium sp. nov.Regioselective arene halogenation using the FAD-dependent halogenase RebH.A multitasking vanadium-dependent chloroperoxidase as an inspiration for the chemical synthesis of the merochlorins.Non-heme Fe(IV)-oxo intermediates.Characterization of biosynthetic genes of ascamycin/dealanylascamycin featuring a 5'-O-sulfonamide moiety in Streptomyces sp. JCM9888.Enzymatic functionalization of carbon-hydrogen bonds.A stereoselective vanadium-dependent chloroperoxidase in bacterial antibiotic biosynthesisConcise total synthesis of sintokamides A, B, and E by a unified, protecting-group-free strategy.Exploring the chemistry and biology of vanadium-dependent haloperoxidasesA sea of biosynthesis: marine natural products meet the molecular age.Nontargeted biomonitoring of halogenated organic compounds in two ecotypes of bottlenose dolphins (Tursiops truncatus) from the Southern California Bight.Expanding the enzyme universe: accessing non-natural reactions by mechanism-guided directed evolution.Independent Evolution of Six Families of Halogenating Enzymes.A metagenomic-based survey of microbial (de)halogenation potential in a German forest soil.Nonproteinogenic amino acid building blocks for nonribosomal peptide and hybrid polyketide scaffolds.The Chemistry and Biology of Nakiterpiosin - C-nor-D-Homosteroids.Specific chlorination of isoquinolines by a fungal flavin-dependent halogenase.Genomes to natural products PRediction Informatics for Secondary Metabolomes (PRISM)Substrate placement influences reactivity in non-heme Fe(II) halogenases and hydroxylases.Halogenase genes in nonribosomal peptide synthetase gene clusters of Microcystis (cyanobacteria): sporadic distribution and evolution.Copper(I)-alpha-ketocarboxylate complexes: characterization and O2 reactions that yield copper-oxygen intermediates capable of hydroxylating arenes
P2860
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P2860
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
description
2006 nî lūn-bûn
@nan
2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@ast
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@en
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@nl
type
label
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@ast
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@en
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@nl
prefLabel
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@ast
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@en
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@nl
P2093
P356
P1433
P1476
Nature's inventory of halogenation catalysts: oxidative strategies predominate.
@en
P2093
Christopher T Walsh
David A Vosburg
Frédéric H Vaillancourt
P304
P356
10.1021/CR050313I
P577
2006-08-01T00:00:00Z