Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Michaela Engler-Lohr"'
Autor:
Bert Steffan, Timm Anke, Dörte Klostermeyer, Wolfgang Steglich, Veronika Hellwig, Stefan Kroiß, Sylvia Semar, Michaela Engler-Lohr, Peter Spiteller, Johannes Dasenbrock, Tilman Sindlinger
Publikováno v:
Tetrahedron. 55:10101-10118
The new antifungal strobilurins I (1) and K (19) are 3,4-dihydro-2H-benzo[b][1,4]dioxepin derivatives. Their structure and stereochemistry was determined by degradation to aldehyde 3. Both enantiomers of 3 were synthesised and the absolute configurat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8676758dd410aaac180f0273536f4aec
https://doi.org/10.1016/s0040-4020(99)00563-3
https://doi.org/10.1016/s0040-4020(99)00563-3
Publikováno v:
Zeitschrift für Naturforschung C. 54:163-168
A new antifungal (E)-β-methoxyacrylate, noroudemansin A (1), was isolated from cultures of Pterula sp. 82168. Its biological activities were investigated and compared with oudemansin A. The structure was elucidated by spectroscopic methods. Three se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29a96f34bf9a61286ddb948bbc42edfe
https://doi.org/10.1515/znc-1999-3-404
https://doi.org/10.1515/znc-1999-3-404
Publikováno v:
Journal of natural products. 63(9)
1(10),4-Germacradiene-2,6,12-triol (1), a new germacrane sesquiterpene, and 1,6-farnesadiene-3,10,11-triol (2), a known nerolidol derivative, were isolated from submerged cultures of the basidiomycete Resupinatus leightonii. Both compounds inhibited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5638c7502ec29ed690927f80c088bd4a
https://pubmed.ncbi.nlm.nih.gov/11000039
https://pubmed.ncbi.nlm.nih.gov/11000039