Xanthone dimers: a compound family which is both common and privileged.
about
Xanthones of Lichen Source: A 2016 UpdateUnusual dimeric tetrahydroxanthone derivatives from Aspergillus lentulus and the determination of their axial chiralitiesElucidation of cladofulvin biosynthesis reveals a cytochrome P450 monooxygenase required for anthraquinone dimerizationEnantioselective Total Synthesis of Secalonic Acid E.Syntheses of Dimeric Tetrahydroxanthones with Varied Linkages: Investigation of "Shapeshifting" Properties.Discovery, Characterization, and Analogue Synthesis of Bohemamine Dimers Generated by Non-enzymatic Biosynthesis.New chiral stationary phases based on xanthone derivatives for liquid chromatography.Two New Diphenylketones and a New Xanthone from Talaromyces islandicus EN-501, an Endophytic Fungus Derived from the Marine Red Alga Laurencia okamurai.Three xanthone dimers from the Thai mangrove endophytic fungus Phomopsis sp. xy21.New Insights into the Conversion of Versicolorin A in the Biosynthesis of Aflatoxin B1.Bifunctional CYP81AA proteins catalyse identical hydroxylations but alternative regioselective phenol couplings in plant xanthone biosynthesis.The antidepressant- and anxiolytic-like activities of new xanthone derivative with piperazine moiety in behavioral tests in mice.Lipid and Phenolic Constituents from Seeds of Hypericum perforatum L. and Hypericum tetrapterum Fr. and their Antioxidant Activity.Exodermis and endodermis are the sites of xanthone biosynthesis in Hypericum perforatum roots.Penicillixanthone A, a marine-derived dual-coreceptor antagonist as anti-HIV-1 agent.Expression in Pichia pastoris and characterization of two novel dirigent proteins for atropselective formation of gossypol.Formaldehyde-Extruding Homolytic Aromatic Substitution via C→O Transposition: Selective 'Traceless-Linker' access to Congested Biaryl Bonds.Biomimetic Total Synthesis of (±)-Griffipavixanthone via a Cationic Cycloaddition-Cyclization Cascade.Dirigent Proteins from Cotton (Gossypium sp.) for the Atropselective Synthesis of Gossypol.
P2860
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P2860
Xanthone dimers: a compound family which is both common and privileged.
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Xanthone dimers: a compound family which is both common and privileged.
@ast
Xanthone dimers: a compound family which is both common and privileged.
@en
Xanthone dimers: a compound family which is both common and privileged.
@nl
type
label
Xanthone dimers: a compound family which is both common and privileged.
@ast
Xanthone dimers: a compound family which is both common and privileged.
@en
Xanthone dimers: a compound family which is both common and privileged.
@nl
prefLabel
Xanthone dimers: a compound family which is both common and privileged.
@ast
Xanthone dimers: a compound family which is both common and privileged.
@en
Xanthone dimers: a compound family which is both common and privileged.
@nl
P2860
P356
P1476
Xanthone dimers: a compound family which is both common and privileged
@en
P2093
Kye-Simeon Masters
Stefan Bräse
P2860
P356
10.1039/C4NP00050A
P50
P577
2015-01-01T00:00:00Z