Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Didier Zurwerra"'
Autor:
Emmanuelle Villedieu-Percheron, Mathilde Lachia, Pierre M. J. Jung, Claudio Screpanti, Raymonde Fonné-Pfister, Sebastian Wendeborn, Didier Zurwerra, Alain De Mesmaeker
Publikováno v:
CHIMIA, Vol 68, Iss 9 (2014)
Seed germination and early seedling development are essential events in the plant life cycle that are controlled largely by the interplay and cross-talk between several plant hormones. Recently, major progress has been achieved in the elucidation at
Externí odkaz:
https://doaj.org/article/5e4b1cb1ffd24dfd8ddea96b760380c1
Autor:
Danielle Sayer, Alain De Mesmaeker, Claudio Screpanti, Hanno Christian Wolf, Stefano Rendine, Andreas Beck, Didier Zurwerra, Laure Castelli, Alexandre Lumbroso, Pierre-Yves Dakas, Raymonde Fonné-Pfister, Mathilde Lachia, Verity Laura Paul, Emmanuelle Villedieu-Percheron
Publikováno v:
Pest Management Science. 72:2054-2068
Background Strigolactones play an important role in the rhizosphere as signalling molecules stimulating the seed germination of parasitic weed seeds and hyphal branching of arbuscular micorrhiza, and also act as hormones in plant roots and shoots. St
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce00cd2bb9859aad106f5ac5241dbdcf
https://doi.org/10.1002/ps.4268
https://doi.org/10.1002/ps.4268
Autor:
Emmanuelle Villedieu-Percheron, Roman Staiger, Mathilde Lachia, Didier Zurwerra, Alain De Mesmaeker, Saron Catak
Publikováno v:
Tetrahedron Letters. 55:2446-2449
An intramolecular 6π/10π-electrocyclization from ketene-iminium salts was developed for the preparation of naphthylamines. Various substituents on the nitrogen, on the aromatic ring, and on the olefin were studied. Tricyclic skeletons were obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aa8c29571abbdaa5005576422eebc90
https://doi.org/10.1016/j.tetlet.2014.02.135
https://doi.org/10.1016/j.tetlet.2014.02.135
Autor:
Alexandre, Lumbroso, Emmanuelle, Villedieu-Percheron, Didier, Zurwerra, Claudio, Screpanti, Mathilde, Lachia, Pierre-Yves, Dakas, Laure, Castelli, Verity, Paul, Hanno Christian, Wolf, Danielle, Sayer, Andreas, Beck, Stefano, Rendine, Raymonde, Fonné-Pfister, Alain, De Mesmaeker
Publikováno v:
Pest management science. 72(11)
Strigolactones play an important role in the rhizosphere as signalling molecules stimulating the seed germination of parasitic weed seeds and hyphal branching of arbuscular micorrhiza, and also act as hormones in plant roots and shoots. Strigolactone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1524d2d2ba478899b59c58725fc65d40
https://pubmed.ncbi.nlm.nih.gov/26940902
https://pubmed.ncbi.nlm.nih.gov/26940902
Autor:
Didier Zurwerra, Leo Betschart, Florian Glaus, Jürg Gertsch, Walter Ganci, Julia K. Schuster, Karl-Heinz Altmann
Publikováno v:
Chemistry - A European Journal. 18:16868-16883
A new total synthesis of the marine macrolide (-)-zampanolide (1) and the structurally and stereochemically related non-natural levorotatory enantiomer of (+)-dactylolide (2), that is, ent-2, has been developed. The synthesis features a high-yielding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::411ec21deff71471aade324af2bd9028
https://doi.org/10.1002/chem.201202553
https://doi.org/10.1002/chem.201202553
Publikováno v:
ChemInform. 46
The condensation reaction of amidrazone and different arylboronic acids to gain access to boratriazaroles is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f099ac353dda015019842d9761d6d7bd
https://doi.org/10.1002/chin.201521208
https://doi.org/10.1002/chin.201521208
Publikováno v:
Organic letters. 17(1)
We describe the synthesis and stability analysis of novel boratriazaroles that can be viewed as bioisosteres of imidazoles or pyrazoles. These heterocycles could conveniently be obtained by condensing a boronic acid and amidrazone 1 in various solven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd052da0e128204d23d2d6e286e7a25
https://pubmed.ncbi.nlm.nih.gov/25514579
https://pubmed.ncbi.nlm.nih.gov/25514579
Autor:
Saron Catak, Didier Zurwerra, Roman Staiger, Emmanuelle Villedieu-Percheron, Alain De Mesmaeker, Mathilde Lachia
Publikováno v:
ChemInform. 45
An intramolecular 6π/10π-electrocyclization from ketene-iminium salts was developed for the preparation of naphthylamines. Various substituents on the nitrogen, on the aromatic ring, and on the olefin were studied. Tricyclic skeletons were obtained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c25050185197073a0ad3aecf1913638
https://doi.org/10.1002/chin.201438092
https://doi.org/10.1002/chin.201438092
Publikováno v:
Angewandte Chemie International Edition. 49:6936-6938
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3cef6468d74110bfe3ed0b4066a49b9
https://doi.org/10.1002/anie.201002788
https://doi.org/10.1002/anie.201002788
Publikováno v:
Angewandte Chemie. 122:7090-7092
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49778c5b9ca7e83a8b17c8a02461b55f
https://doi.org/10.1002/ange.201002788
https://doi.org/10.1002/ange.201002788