| 1 | Author
| Anna Aiello, Ernesto Fattorusso, M. Arialuisa, M. Enna | Requires cookie* | | Title
| A New Antibiotic Chloro-Sesquiterpene from the Caribbean Sponge Smenospongia aurea  | | | Abstract
| A new sesquiterpene phenol, containing the rather uncommon chlorine atom, was isolated from a sample of Smenospongia aurea collected along Baham a's Islands. Its structure has been elucidated by spectroscopic analysis and confirmed via synthesis. This com pound exhibited antibacterial activity. | | |
Reference
| Z. Naturforsch. 48b, 209—212 (1993); received September 18. 1992 | | |
Published
| 1993 | | |
Keywords
| Spongidae, Smenospongia aurea, Sesquiterpene, Antibiotic, N M R Spectra | | |
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| default:Reihe_B/48/ZNB-1993-48b-0209.pdf | | | Identifier
| ZNB-1993-48b-0209 | | | Volume
| 48 | |
2 | Author
| JohannK. Lessmann, Helmut Rupa, Lackner, Karen Schmidt-Bäse, GeorgeM. Sheldrick | Requires cookie* | | Title
| Holger  | | | Abstract
| The isolation o f Juglorubin (2) from cultures o f Streptomyces spp., which produce a series o f other hydroxynaphthoquinones, is described. 2 is a unique, unusually condensed ionic color | | |
Reference
| Z. Naturforsch. 48b, 672 (1993); eingegangen am 21. Dezember 1992 | | |
Published
| 1993 | | |
Keywords
| Antibiotics, Juglomycins, X -Ray, N M R Spectra | | |
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| default:Reihe_B/48/ZNB-1993-48b-0672.pdf | | | Identifier
| ZNB-1993-48b-0672 | | | Volume
| 48 | |
3 | Author
| Lackner | Requires cookie* | | Title
| Octacidomycine, IV : Neue Totalsynthese von rac-Octacidomycin und strukturverwandten Oligocarbonsäuren Octacidom ycins, I V : A New Total Synthesis of rac-O ctacidom ycin and Structurally R elated O ligocarboxylic A cids A ndreas K rause, H elm ut  | | | Abstract
| a new strategy, an improved total synthesis of the unique antibiotic octacidomy-cin (1) and of structurally related oligocarboxylic acids was developed (Scheme 1,2). Starting from 3 and the tetraethylester of l,17-dibromo-6,6,12,12-heptadecane-tetracarboxylic acid (6) as a key compound, systematical fragment condensations lead to the nonatriacontane-pentadecacarboxylic acid 11 and hence to the 1,3,9,15,21,27,33,39-nonatriacontane-octacarbo-xylic acid 1. The synthetic pathway can easily be modified and generally be applied for the synthesis of a broad variety of hitherto unknown oligocarboxylic acids or their esters, respec tively, and even of cyclic analogues (Scheme 2). | | |
Reference
| Z. Naturforsch. 53b, 1043—1050 (1998); eingegangen am 22. Juni 1998 | | |
Published
| 1998 | | |
Keywords
| Antibiotics, Octacidomycins, Oligocarboxylic Acids, Synthesis, NMR Data Following | | |
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| default:Reihe_B/53/ZNB-1998-53b-1043.pdf | | | Identifier
| ZNB-1998-53b-1043 | | | Volume
| 53 | |
4 | Author
| Axel Lifferth3, IsabelB. Ahnera, Ut Helm, Lackner, M. Artina Schäferb | Requires cookie* | | Title
| Synthese und Struktur von Prolinring-modifizierten Actinomycinen des X-Typs Synthesis and Structure of Proline Ring Modified Actinomycins of the X-Type  | | | Abstract
| The first total synthesis o f actinomycins containing L-4-hydroxyproline (1) and the separa tion and NM R spectroscopic assignment o f the regioisomers X (V* and iso-X0/i (lc, le) are described. The synthetic X 0/j proves, that the oxidized proline ring of the natural actinomycins | | |
Reference
| Z. Naturforsch. 54b, 681—6 (1999); eingegangen am 15. Januar 1999 | | |
Published
| 1999 | | |
Keywords
| Antibiotics, Actinomycins, Synthesis, Crystal Structure, NM R Data | | |
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| default:Reihe_B/54/ZNB-1999-54b-0681.pdf | | | Identifier
| ZNB-1999-54b-0681 | | | Volume
| 54 | |
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