Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Laure Konnert"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1788-1795 (2017)
A lipase-catalyzed esterification of lignin model compounds in the ball mill was developed combining the advantages of enzyme catalysis and mechanochemistry. Under the described conditions, the primary aliphatic hydroxy groups present in the substrat
Externí odkaz:
https://doaj.org/article/38551420e10c46f29e89fed066a845bc
Autor:
Steve Reynaud, Suli-Anne Laurin, Justyna Ciolek, Peggy Barbe, Anne-Cécile Van Baelen, Michaël Susset, Florian Blondel, Marine Ghazarian, Julia Boeri, Margot Vanden Driessche, Grégory Upert, Gilles Mourier, Pascal Kessler, Laure Konnert, Rémy Beroud, Mathilde Keck, Denis Servent, Michel Bouvier, Nicolas Gilles
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, 2022, 65 (18), pp.12084-12094. ⟨10.1021/acs.jmedchem.2c00786⟩
Journal of Medicinal Chemistry, 2022, 65 (18), pp.12084-12094. ⟨10.1021/acs.jmedchem.2c00786⟩
International audience; The melanocortin 4 receptor (MC4R) plays a role in energy homeostasis and represents a target for treating energy balance disorders. For decades, synthetic ligands have been derived from MC4R endogenous agonists and antagonist
Publikováno v:
Chemical Reviews
Chemical Reviews, American Chemical Society, 2017, 117 (23), pp.13757-13809. ⟨10.1021/acs.chemrev.7b00067⟩
Chemical Reviews, American Chemical Society, 2017, 117 (23), pp.13757-13809. ⟨10.1021/acs.chemrev.7b00067⟩
International audience; The review highlights the hydantoin syntheses presented from the point of view of the preparation methods. Novel synthetic routes to various hydantoin structures, the advances brought to the classical methods in the aim of pro
Autor:
Ivan Halasz, Jean-Simon Suppo, Renata Marcia de Figueiredo, Jean-Marc Campagne, Evelina Colacino, Laure Konnert, Frédéric Lamaty, Lori Gonnet, Jean Martinez
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (20), pp.9802-9809. ⟨10.1021/acs.joc.6b01832⟩
Journal of Organic Chemistry, American Chemical Society, 2016, 81 (20), pp.9802-9809. ⟨10.1021/acs.joc.6b01832⟩
International audience; 5-Substituted-3-(alkoxycarbonyl)alkyl-hydantoin derivatives were prepared by mechanochemistry from amino esters or dipeptides, via a 1,1′-carbonyldiimidazole-mediated one-pot/two-step cyclization reaction involving amino aci
Publikováno v:
RSC Advances
RSC Advances, Royal Society of Chemistry, 2016, 6 (43), pp.36978-36986. ⟨10.1039/c6ra03222b⟩
RSC Advances, Royal Society of Chemistry, 2016, 6 (43), pp.36978-36986. ⟨10.1039/c6ra03222b⟩
International audience; Mechanochemistry was effective for the preparation of 3,5-disubstituted hydantoins from a-amino methyl esters, using either 1,1 0-carbonyldiimidazole (CDI) or alkyl isocyanates. The preparation of the antimicrobial additives,
Autor:
Laure Konnert, Jean-François Hernandez, Thibault Tintillier, Jean Martinez, Frédéric Lamaty, Lori Gonnet, Guillaume Laconde, Evelina Colacino, Natacha Venturini
Publikováno v:
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2017, 5 (4), pp.2936-2941. ⟨10.1021/acssuschemeng.6b02439⟩
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2017, 5 (4), pp.2936-2941. ⟨10.1021/acssuschemeng.6b02439⟩
International audience; An eco-friendly methodology for preparing Fmoc-, Z-, and Boc-Nprotected dipeptides and tripeptides is described, from the corresponding Nprotected-α-aminoacyl benzotriazoles and α-amino acid derivatives, with different Cterm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90ebf7b3ca15d6b4adc024dbba5dff58
https://hal.archives-ouvertes.fr/hal-03095301
https://hal.archives-ouvertes.fr/hal-03095301
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (9), pp.4008-4017. ⟨10.1021/jo500463y⟩
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (9), pp.4008-4017. ⟨10.1021/jo500463y⟩
International audience; Mechanochemical derivatizations of N- or Cprotected amino acids were performed in a ball mill under solvent-free conditions. A vibrational ball mill was used for the preparation of N-protected α- and β-amino esters starting
Publikováno v:
Chemical communications (Cambridge, England). 51(33)
A single-handed helical polymer ligand PQXphos afforded axially chiral biaryl esters with high enantioselectivities in asymmetric Suzuki–Miyaura cross-coupling. The use of naphthyl bromide bearing a 2,4-dimethyl-3-pentyl ester resulted in both high
Publikováno v:
ACS Sustainable Chemistry & Engineering
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2015, 3 (11), pp.2882-2889. ⟨10.1021/acssuschemeng.5b00819⟩
ACS Sustainable Chemistry & Engineering, American Chemical Society, 2015, 3 (11), pp.2882-2889. ⟨10.1021/acssuschemeng.5b00819⟩
International audience; 1,1′-Carbonyldiimidazole (CDI) was used as an eco-friendly acylation agent for the mechanochemical preparation of carbamates. The anticonvulsant N-methyl-O-benzyl carbamate was obtained in a vibrational ball-mill, while plan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25dcc0cfec811d5a0d4498053ef6e783
https://hal.archives-ouvertes.fr/hal-02370950/file/Hal-101.pdf
https://hal.archives-ouvertes.fr/hal-02370950/file/Hal-101.pdf
Publikováno v:
ChemInform. 45
Mechanochemical derivatizations of either N- or C-unprotected amino acids are performed in a vibrational or planetary ball mill under neat conditions.