A compound (née frankiamide) isolated from Frankia was initially structurally elucidated on the basis of NMR and MS. However, X-ray analysis provided a structure that is in discord with this structure and in light of this the structure has now been revised and the compound renamed as demethyl (C-11) cezomycin.
Received: 2003-9-3
Published Online: 2014-6-2
Published in Print: 2003-12-1
© 1946 – 2014: Verlag der Zeitschrift für Naturforschung
You are currently not able to access this content.
You are currently not able to access this content.
Articles in the same Issue
- Atomvolumen, Packungsdichte undWertigkeit von Caesium unter Druck Atomic Volume, Packing Density and Valence of Cesium under Pressure
- Dinuclear Nickel(II) and Palladium(II) Complexes in Combination with Different Co-Catalysts as Highly Active Catalysts for the Vinyl/Addition Polymerization of Norbornene
- Synthesis and Characterization of N-Methyl-Substituted Germocanes. Crystal Structure of MeN(CH2CH2O)2GeBr2
- Molecular Structure and Thermal Analysis of Potassium Hydrogenphthalate Monohydrate
- Synthese flexibler difluorierter cyclopropanoider Nucleosidanaloga / Synthesis of Flexible Difluorinated Cyclopropanoid Nucleoside Analogues
- Electroreduction of Organic Compounds, 34 [1]. Cathodic Dehalogenation of Chloroarenes with Electron-Donating Substituents
- Kinetics of Oxidation of Benzaldehydes by Quinolinium Dichromate
- New Isoflavonoid from Dipterix odorata
- Frankiamide: A Structural Revision to Demethyl (C-11) Cezomycin
- Xyloccensin M and N, Two New B, D-seco Limonoids from Xylocarpus granatum
- Titanyl Acetylacetonate as an Efficient Catalyst for a Mild and Convenient Reduction of Carbonyl Compounds with NaBH4 under Aprotic Condition
- A Convenient Synthesis of New Pentaazacyclopentanaphthalene and Pentaazaphenanthrene Derivates
- A New Pyranoacridone Alkaloid from the Bark of Medicosma subsessilis (Rutaceae)
- Synthesis of Some New Furocoumarins and their Usage in Peptide Synthesis
- Isolation, Structure Elucidation and Activity of Anthracycline Acetates from a Terrestrial Streptomyces sp.
- Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants
Articles in the same Issue
- Atomvolumen, Packungsdichte undWertigkeit von Caesium unter Druck Atomic Volume, Packing Density and Valence of Cesium under Pressure
- Dinuclear Nickel(II) and Palladium(II) Complexes in Combination with Different Co-Catalysts as Highly Active Catalysts for the Vinyl/Addition Polymerization of Norbornene
- Synthesis and Characterization of N-Methyl-Substituted Germocanes. Crystal Structure of MeN(CH2CH2O)2GeBr2
- Molecular Structure and Thermal Analysis of Potassium Hydrogenphthalate Monohydrate
- Synthese flexibler difluorierter cyclopropanoider Nucleosidanaloga / Synthesis of Flexible Difluorinated Cyclopropanoid Nucleoside Analogues
- Electroreduction of Organic Compounds, 34 [1]. Cathodic Dehalogenation of Chloroarenes with Electron-Donating Substituents
- Kinetics of Oxidation of Benzaldehydes by Quinolinium Dichromate
- New Isoflavonoid from Dipterix odorata
- Frankiamide: A Structural Revision to Demethyl (C-11) Cezomycin
- Xyloccensin M and N, Two New B, D-seco Limonoids from Xylocarpus granatum
- Titanyl Acetylacetonate as an Efficient Catalyst for a Mild and Convenient Reduction of Carbonyl Compounds with NaBH4 under Aprotic Condition
- A Convenient Synthesis of New Pentaazacyclopentanaphthalene and Pentaazaphenanthrene Derivates
- A New Pyranoacridone Alkaloid from the Bark of Medicosma subsessilis (Rutaceae)
- Synthesis of Some New Furocoumarins and their Usage in Peptide Synthesis
- Isolation, Structure Elucidation and Activity of Anthracycline Acetates from a Terrestrial Streptomyces sp.
- Synthesis of Spacered Cyclopropanoid Muramyldipeptide Analogues as Potential Immunostimulants