Title: | "Synthesis of methyl 4-dihydrotrisporate B and methyl trisporate B, morphogenetic factors of Zygomycetes fungi" |
Author(s): | Nakamura Y; Paetz C; Boland W; |
Address: | "Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Jena, Germany. Max Planck Institute for Chemical Ecology, Biosynthesis/NMR, Jena, Germany. Max Planck Institute for Chemical Ecology, Department of Bioorganic Chemistry, Hans-Knoll-Strasse 8, 07745 Jena, Germany" |
ISSN/ISBN: | 0939-5075 (Print) 0341-0382 (Linking) |
Abstract: | "(9Z)-Methyl 4-dihydrotrisporate B and (9Z)-methyl trisporate B, pheromones of Zygomycetes fungi, have been synthesized using Stille cross-coupling from previously described cyclohexenone precursors. Conducting the coupling without protection groups allowed for a short and stereospecific synthesis route of the late trisporoids. Stability studies for both the compounds revealed (9Z)-methyl trisporate B to be very unstable against UV irradiation" |
Keywords: | "Carotenoids/*chemical synthesis Cyclohexenes/*chemical synthesis Fatty Acids, Unsaturated/*chemical synthesis Fungi, Unclassified/*chemistry/metabolism Mating Factor/*chemical synthesis/radiation effects Terpenes/*chemical synthesis Ultraviolet Rays Still;" |
Notes: | "MedlineNakamura, Yoko Paetz, Christian Boland, Wilhelm eng Germany 2017/11/22 Z Naturforsch C J Biosci. 2018 Jan 26; 73(1-2):59-66. doi: 10.1515/znc-2017-0148" |