Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Elsa Van Elslande"'
Autor:
Capucine Jourdain de Muizon, Céline Moriou, Marceau Levasseur, David Touboul, Bogdan I. Iorga, Hristo Nedev, Elsa Van Elslande, Pascal Retailleau, Sylvain Petek, Eric Folcher, Arnaud Bianchi, Mireille Thomas, Solène Viallon, Sylvie Peyroche, Sarah Nahle, Marthe Rousseau, Ali Al-Mourabit
Publikováno v:
Marine Drugs, Vol 22, Iss 5, p 196 (2024)
As a result of screening a panel of marine organisms to identify lead molecules for the stimulation of endochondral bone formation, the calcareous sponge Pericharax heteroraphis was identified to exhibit significant activity during endochondral diffe
Externí odkaz:
https://doaj.org/article/c2d11d0a54a749a3a5a2d69cd70a18a2
Publikováno v:
Metabolites, Vol 11, Iss 7, p 444 (2021)
Microorganisms associated with termites are an original resource for identifying new chemical scaffolds or active metabolites. A molecular network was generated from a collection of strain extracts analyzed by liquid chromatography coupled to tandem
Externí odkaz:
https://doaj.org/article/bb71630035254eedb85186630703564b
Publikováno v:
Molecules, Vol 25, Iss 16, p 3565 (2020)
With the occurrence of antibiotic-resistant Staphylococcus aureus strains, identification of new anti-staphylococcal drugs has become a necessity. It has long been demonstrated that plants are a large and diverse source of antibacterial compounds. Ps
Externí odkaz:
https://doaj.org/article/ef6a6b5196e6446e934fcec29b892bfc
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(56)
We report herein a convenient and scalable dearomative hydroacylation reaction of indoles. Employing readily available aldehydes as the acyl source and TBADT as an inexpensive direct HAT photocatalyst, a variety of indoles derivatives were converted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9074b9af35166d1471615a7e847ade6c
https://pubmed.ncbi.nlm.nih.gov/35809229
https://pubmed.ncbi.nlm.nih.gov/35809229
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (17), pp.6407-6412. ⟨10.1021/jacs.1c03872⟩
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (17), pp.6407-6412. ⟨10.1021/jacs.1c03872⟩
International audience; A catalytic intermolecular amination of non-activated tertiary C(sp 3)−H bonds (BDE of 96 kcal.mol-1) is reported for substrates displaying an activated benzylic site (BDE of 85 kcal.mol-1). The tertiary C(sp 3)−H bond is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723a6ab570fbe1e293792fd55ee77bad
https://doi.org/10.1021/jacs.1c03872
https://doi.org/10.1021/jacs.1c03872
Autor:
Thierry Argant, François Blondel, Amaury Gilles, Catherine Lavier, Olivier Lempereur, Sébastien Nieloud-Muller, Stéphanie Roussel, Jean-Michel Treffort, Elsa Van Elslande, Hortense Bougherara, Marc-Antoine Jeanniot
Publikováno v:
Un lieu de culte antique immergé ISBN: 9782916125183
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c50d3372c066ca2469068cd26cce6134
https://doi.org/10.4000/books.alpara.6698
https://doi.org/10.4000/books.alpara.6698
Publikováno v:
Metabolites, Vol 11, Iss 444, p 444 (2021)
Metabolites; Volume 11; Issue 7; Pages: 444
Metabolites
Metabolites, MDPI, 2021, 11 (7), pp.444. ⟨10.3390/metabo11070444⟩
Metabolites; Volume 11; Issue 7; Pages: 444
Metabolites
Metabolites, MDPI, 2021, 11 (7), pp.444. ⟨10.3390/metabo11070444⟩
Microorganisms associated with termites are an original resource for identifying new chemical scaffolds or active metabolites. A molecular network was generated from a collection of strain extracts analyzed by liquid chromatography coupled to tandem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::010099d5951ffd71b7facee1d372d608
https://www.mdpi.com/2218-1989/11/7/444
https://www.mdpi.com/2218-1989/11/7/444
Publikováno v:
Journal of the American Chemical Society. 143(17)
A catalytic intermolecular amination of nonactivated tertiary C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ecb3bea052750ece4231900cd93948d
https://pubmed.ncbi.nlm.nih.gov/33900759
https://pubmed.ncbi.nlm.nih.gov/33900759
Autor:
Xavier Guinchard, Elsa Van Elslande, Zhenhao Zhang, Nicolas Glinsky-Olivier, Pierre Milcendeau
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2021, 86 (9), pp.6406-6422. ⟨10.1021/acs.joc.1c00270⟩
Journal of Organic Chemistry, American Chemical Society, 2021, 86 (9), pp.6406-6422. ⟨10.1021/acs.joc.1c00270⟩
International audience; Au(I) complexes catalyze iso-Pictet-Spengler reactions. Ethylamine or methylamine chains were introduced at C2, C4 or at the nitrogen atom of the indole ring, and the corresponding substrates were reacted in the presence of al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4a40a133760a6a50f25531aeeaced3d
https://hal.archives-ouvertes.fr/hal-03267801/document
https://hal.archives-ouvertes.fr/hal-03267801/document
Autor:
Mateja Matišić, Géraldine Masson, Thomas Varlet, Luc Neuville, Vincent Gandon, Elsa Van Elslande
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (30), pp.11611-11619. ⟨10.1021/jacs.1c04648⟩
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (30), pp.11611-11619. ⟨10.1021/jacs.1c04648⟩
International audience; A diastereodivergent and enantioselective synthesis of chiral spirocyclohexyl-indolenines with four contiguous stereogenic centers is achieved by a chiral phosphoric acid-catalyzed cycloaddition of 2-susbtituted 3-indolylmetha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef575e1ecb2c5ae954f3ff1c83b7bb8c
https://hal.archives-ouvertes.fr/hal-03329179/document
https://hal.archives-ouvertes.fr/hal-03329179/document