Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Laurence Miesch"'
Autor:
Mohamed Hazman, Martin Sühnel, Sandra Schäfer, Julie Zumsteg, Agnès Lesot, Fréderic Beltran, Valentin Marquis, Laurence Herrgott, Laurence Miesch, Michael Riemann, Thierry Heitz
Publikováno v:
Rice, Vol 12, Iss 1, Pp 1-14 (2019)
Abstract Background Jasmonate (JA) signaling and functions have been established in rice development and response to a range of biotic or abiotic stress conditions. However, information on the molecular actors and mechanisms underlying turnover of th
Externí odkaz:
https://doaj.org/article/7901ecde6b7a4de4baf6c917ab8e1ece
Publikováno v:
Plants, Vol 5, Iss 1, p 4 (2016)
The jasmonic acid (JA) signaling pathway plays important roles in adaptation of plants to environmental cues and in specific steps of their development, particularly in reproduction. Recent advances in metabolic studies have highlighted intricate mec
Externí odkaz:
https://doaj.org/article/57906f2bbfcb4689be22861af9b49410
Autor:
Laurence Miesch, Maxime Hourtoule
Publikováno v:
Organic Letters. 25:1727-1731
Autor:
Suzanne Daignan Fornier, Alexandre de Saint Germain, Pascal Retailleau, Jean-Paul Pillot, Quentin Taulera, Lucile Andna, Laurence Miesch, Soizic Rochange, Jean-Bernard Pouvreau, François-Didier Boyer
Publikováno v:
Journal of Natural Products. 85:1976-1992
Autor:
Baptiste Moegle, Maxime Hourtoule, Clément Gommenginger, Asmaa Belabbes, Claire Villette, David Elser, Emmanuel Gaquerel, Nicolas Navrot, Laurence Miesch
Publikováno v:
The Journal of Organic Chemistry. 87:7229-7238
Autor:
Maxime Hourtoule, Yongxiang Zheng, Anna Perfetto, Davide Luise, Ilaria Ciofini, Laurence Miesch
Publikováno v:
The Journal of Organic Chemistry. 87:5404-5411
Autor:
Laurence Miesch, Maxime Hourtoule
Publikováno v:
Organic & Biomolecular Chemistry. 20:9069-9084
The review covers recent advances in the development of new methods involving amination and alkoxylation reactions on N-allenamides covering cycloaddition, carbofunctionalization, halogenofunctionalization as well as hydrofunctionalization reactions.
Autor:
Santanu Ghosh, Yongxiang Zheng, Daniele Maccarone, Feven-Alemu Korsaye, Ilaria Ciofini, Laurence Miesch
Publikováno v:
Organic Chemistry Frontiers. 9:4057-4062
Benzo-1,5 dioxocines have been synthesized via unique ynamides tethered to propargylic ethers. Triton B allowed a proximal enol addition on the N-allenamide creating shelf-stable 8-membered-O-heterocycles with a broad functional group tolerance.
Autor:
Maxime, Hourtoule, Laurence, Miesch
Publikováno v:
Organicbiomolecular chemistry. 20(46)
The two-faced reactivity of
Autor:
Laurence Miesch, Emmanuel Gaquerel, Baptiste MOEGLE, David Pflieger, Claire Villette, David Elser
Specialized metabolite (SM) diversification is a core process to plants’ adaptation to diverse ecological niches. Here we implemented a computational mass spectrometry (MS)-based metabolomics approach to explore SM diversification in tissues of 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51b004dda8818986b24f0932ea89ff36
https://doi.org/10.1101/2022.09.12.507566
https://doi.org/10.1101/2022.09.12.507566