Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Alexandre Lumbroso"'
Autor:
Johannes Büchler, Sumire Honda Malca, David Patsch, Moritz Voss, Nicholas J. Turner, Uwe T. Bornscheuer, Oliver Allemann, Camille Le Chapelain, Alexandre Lumbroso, Olivier Loiseleur, Rebecca Buller
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
The late-stage functionalization of unactivated carbon–hydrogen bonds is a difficult but important task, which has been met with promising but limited success through synthetic organic chemistry. Here the authors use machine learning to engineer We
Externí odkaz:
https://doaj.org/article/b0080e192c1f4807837af8d63df4a6df
Autor:
Alain De Mesmaeker, Claudio Screpanti, Raymonde Fonné-Pfister, Mathilde Lachia, Alexandre Lumbroso, Harro Bouwmeester
Publikováno v:
CHIMIA, Vol 73, Iss 7-8 (2019)
Strigolactones have been known as signaling molecules in the rhizosphere of plants since more than 50 years. However, their roles as phytohormone have been only recognized since 2008. We describe here a very efficient synthetic access to representati
Externí odkaz:
https://doaj.org/article/37e6df3903be45f48689252a266992f9
Autor:
Pierre Quinodoz, Alexandre Lumbroso, Mathilde Lachia, Claudio Screpanti, Stefano Rendine, Beyza Horoz, Mert Bozoflu, Saron Catak, Raymonde Fonné‐Pfister, Katrin Hermann, Alain De Mesmaeker
Publikováno v:
Helvetica Chimica Acta. 106
Autor:
Christian Gübeli, Claudio Screpanti, Alain De Mesmaeker, Mathilde Lachia, Alexandre Lumbroso, Lorenzo Borghi
Publikováno v:
Plant and Soil. 465:109-123
PurposeArbuscular mycorrhizal fungi (AMF) play important roles in agriculture because of their ability to improve plant resilience against abiotic and biotic stresses. AMF as a technology to promote a more sustainable agriculture holds great potentia
Autor:
Zeynep Aktas, Gamze Tanriver, Pierre Quinodoz, Dylan Dagoneau, Amandine Kolleth, Alexandre Lumbroso, Sarah Sulzer-Mossé, Alain De Mesmaeker, Saron Catak
Keteniminium salts (KIs) are versatile intermediates in synthetic organic chemistry. Elucidation of the mechanistic aspects of KI formation reactions facilitates the design of KI intermediates that give access to complex compounds. In this study, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::860b6813b4c1e0866bc78bd74cbe053a
https://doi.org/10.26434/chemrxiv-2022-24jhd
https://doi.org/10.26434/chemrxiv-2022-24jhd
Autor:
Dylan Dagoneau, Pierre Quinodoz, Amandine Kolleth, Mert Bozoflu, Beyza Horoz, Saron Catak, Philippe‐Alexandre Poisson, Alexandre Lumbroso, Sarah Sulzer‐Mossé, Alain De Mesmaeker
Publikováno v:
Helvetica Chimica Acta. 105
Autor:
Alain De Mesmaeker, Sarah Sulzer-Mosse, Dylan Dagoneau, Saron Catak, Amandine Kolleth, Gamze Tanriver, Ulfet Karadeniz, Alexandre Lumbroso
Publikováno v:
The Journal of Organic Chemistry. 85:449-463
A predictive computational study was conducted in order to assess the efficiency of electrocyclization reactions of keteniminium salts, in an effort to form a variety of heterocyclic systems, namely, 3-amino(benzo)thiophenes, 3-amino(benzo)furans, 3-
Autor:
Claudio Screpanti, Raymonde Fonné-Pfister, Alain De Mesmaeker, Alexandre Lumbroso, Mathilde Lachia, Harro J. Bouwmeester
Publikováno v:
Chimia, 73(7-8), 549-560. Swiss Chemical Society
CHIMIA, Vol 73, Iss 7-8 (2019)
CHIMIA, Vol 73, Iss 7-8 (2019)
Strigolactones have been known as signaling molecules in the rhizosphere of plants since more than 50 years. However, their roles as phytohormone have been only recognized since 2008. We describe here a very efficient synthetic access to representati
Autor:
Alain De Mesmaeker, Amandine Kolleth, Dylan Dagoneau, Pierre Quinodoz, Alexandre Lumbroso, Saron Catak, Sarah Sulzer-Mosse, Beyza Horoz
Publikováno v:
Helvetica Chimica Acta. 104
Autor:
Erwan Le Grognec, Carmen Ortiz Mellet, Alexandre Lumbroso, M. Isabel García-Moreno, Clément Berthonneau, Aurélien Planchat, Isabelle Beaudet, Jean-Paul Quintard
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (5), pp.1083-1099. ⟨10.1039/d0ob02249g⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (5), pp.1083-1099. ⟨10.1039/d0ob02249g⟩
International audience; A highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydropiperidines has been previously achieved through Sn/Li transmetalation of the corresponding stannylated dehydropiperidines or of their precursors.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f7d08bfb233a3d16e4bf48692fb1e3
https://hal.archives-ouvertes.fr/hal-03388809/document
https://hal.archives-ouvertes.fr/hal-03388809/document