ILIV-3 Elucidation of conformation and configuration of natural compounds using residual dipolar couplings enhanced NMR(Spectroscopy in Natural Products Chemistry)
スポンサーリンク
概要
- 論文の詳細を見る
- 天然有機化合物討論会の論文
- 2006-07-23
著者
-
ZEECK Axel
Institut fur Organische Chemie, Universitat Gottingen
-
Zeeck Axel
Institue For Organic Chemistry University Of Gottingen
-
RADZOM Markus
Institut fur Organische und Bioorganische Chemie, Universitat Gottingen
-
Radzom Markus
Institue For Organic Chemistry University Of Gottingen
-
Haberz Peter
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Farjon Jonathan
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Reinscheid Uwe
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Junker Jochen
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Zweckstetter Markus
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Bermel Wolfgang
Bruker-Biospin
-
Blackledge Martin
Institut de Biologie Structurale
-
Griesinger Christian
Max-Planck Institute for Biophysical Chemistry, NMR-based Structural Biology
-
Haberz Peter
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
-
Junker Jochen
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
-
Reinscheid Uwe
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
-
Farjon Jonathan
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
-
Zweckstetter Markus
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
-
Griesinger Christian
Max-planck Institute For Biophysical Chemistry Nmr-based Structural Biology
関連論文
- Biosynthetic Capacities of Actinomycetes.Naphthgeranine F, a Minor Congener of the Naphthgeranine Group Produced by Streptomyces violaceus
- Structure and Biosynthesis of Cetoniacytone A, a Cytotoxic Aminocarba Suger Produced by an Endosymbiontic Actinomyces
- Metabolic Products of Microorganismen.270 The Structures of the Exfoliamycins
- Simocyclinones, Novel Cytostatic Angucyclinone Antibiotics Produced by Streptomyces antibioticus Tu 6040 : II. Structure Elucidation and Biosynthesis
- Simocyclinones, Novel Cytostatic Angucyclinone Antibiotics Produced by Streptomyces antibiotics Tu 6040 : I. Taxonomy, Fermentation, Isolation and Biological Activities
- Fogacin, a Novel Cyclic Octaketide Produced by Streptomyces Strain Tu 6319
- Retymicin, Galtamycin B, Saquayamycin Z and Ribofuranosyllumichrome, Novel Secondary Metabolites from Micromonospora sp. Tu 6368 : II. Structure Elucidation
- Retymicin, Galtamycin B, Saquayamycin Z and Ribofuranosyllumichrome, Novel Secondary Metabolites from Micromonospora sp. Tu 6368 : I. Taxonomy, Fermentation, Isolation and Biological Activities
- Aspochalamins A-D and Aspochalasin Z Produced by the Endosymbiotic Fungus Aspergillus niveus LU 9575 : II. Structure Elucidation
- Ripromycin and Other Polycyclie Macrolactams from Streptomyces sp. Tu6239: Taxonomy, Fermentation, Isolation and Biological Properties
- Endophenazines A-D, New Phenazine Antibiotics from the Athropod Associated Endosymbiont Streptomyces anulatus II. Structure Elucidation
- Endophenazines A-D, New Phenazine Antibiotics from the Arthropod Associated Endosymbiont Streptomyces anulatus I. Taxonomy, Fermentation, Isolation and Biological Activities
- ILIV-3 Elucidation of conformation and configuration of natural compounds using residual dipolar couplings enhanced NMR(Spectroscopy in Natural Products Chemistry)
- New Aminophenoxazinones from a Marine Halomonas sp. : Fermentation, Structure Elucidation, and Biological Activity
- Albocycline- and Carbomycin-type Macrolides, Inhibitors of Human Prolyl Endopeptidases
- New Albrassitriols from Aspergillus sp. (FH-A 6357)
- New Cineromycins and Musacins Obtained by Metabolite Pattern Analysis of Streptomyces griseoviridis (FH-S 1832) II. Structure Elucidation
- Bagremycin A and B, Novel Antibiotics from Streptomyces sp. Tu 4128
- Biosynthesis of Polyketomycin Produced by Streptomyces diastatochromogenes Tu 6028
- New Biologically Active Rubiginones from Streptomyces sp.
- Biosynthesis of Albocycline: Origin of the Carbon Skeleton
- Biosynthesis of Simocyclinone D8 in an ^O_2-rich Atmosphere
- Phenalinolactones A-D, terpenoglycoside antibiotics from Streptomyces sp. Tu 6071
- Biosynthesis of Cladospirone Bisepoxide, A Member of the Spirobisnaphthalene Family
- Cineromycins, γ-Butyrolactones and Ansamycins by Analysis of the Secondary Metabolite Pattern Created by a Single Strain of Streptomyces