Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nathalie Chopin"'
Publikováno v:
ResearcherID
An efficient synthesis of the azetidinyl-thiazoline fragment of the antifungal and cytotoxic macrolides vioprolides A and C is reported. Key steps of the ynthesis include formation of the thiazoline by condensation of N-Alloc-trans (2S,4R)-4-methylaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f9e883973f03569b401f7ad2197a99e
https://doi.org/10.2174/157017810791514814
https://doi.org/10.2174/157017810791514814
Publikováno v:
The Journal of Organic Chemistry. 74:1237-1246
Dearomatization of electron-poor benzofurans is possible through involvement of the aromatic 2,3-carbon-carbon double bond as dienophile in normal electron demand [4 + 2] cycloadditions. The tricyclic heterocycles thereby produced bear a quaternary c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb18d2a5604d05f60d24b37b3f5b1372
https://doi.org/10.1021/jo802205d
https://doi.org/10.1021/jo802205d
Autor:
Stéphane Cérantola, Jean Le Bideau, Sylvia Colliec-Jouault, Corinne Sinquin, Agata Zykwinska, Jacqueline Ratiskol, Nathalie Chopin, Pierre Weiss
Publikováno v:
BioMed Research International, Vol 2015 (2015)
BioMed Research International
BioMed Research International, 2015, 2015, pp.1-9. ⟨10.1155/2015/508656⟩
BioMed Research International, Hindawi Publishing Corporation, 2015, 2015, pp.1-9. ⟨10.1155/2015/508656⟩
BioMed Research International
BioMed Research International, 2015, 2015, pp.1-9. ⟨10.1155/2015/508656⟩
BioMed Research International, Hindawi Publishing Corporation, 2015, 2015, pp.1-9. ⟨10.1155/2015/508656⟩
GY785 is an exopolysaccharide produced by a mesophilic bacterial strainAlteromonas infernusdiscovered in the deep-sea hydrothermal vents. GY785 highly sulfated derivative (GY785 DRS) was previously demonstrated to be a promising molecule driving the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::425198a9e1474e0c69a53289eb662449
https://doaj.org/article/6fa5e4e6509b4fe78f860f923c9c2c15
https://doaj.org/article/6fa5e4e6509b4fe78f860f923c9c2c15
Publikováno v:
ChemInform. 45
Polysaccharides are among the most abundant macromolecules on Earth. These polymers are easily obtained from various marine resources such as algae, microorganisms and crustacean shells. The structure of these natural carbohydrates is innovative and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59f6abf1ed3fcf7e4ba0cdc42ae4d7b9
https://doi.org/10.1002/chin.201432258
https://doi.org/10.1002/chin.201432258
Autor:
Ludger Johannes, Thomas Arnold, Jean-Claude Florent, Nathalie Chopin, Haifei Gao, Bernd Struth, Erik B. Watkins, Andrew J. C. Dennison
Publikováno v:
Biophysical journal 107(5), 1146-1155 (2014). doi:10.1016/j.bpj.2014.07.023
Globotriaosylceramide (Gb3), a glycosphingolipid found in the plasma membrane of animal cells, is the endocytic receptor of the bacterial Shiga toxin. Using x-ray reflectivity (XR) and grazing incidence x-ray diffraction (GIXD), lipid monolayers cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37efc3da635af78e0e904ec5ad74254b
https://pubmed.ncbi.nlm.nih.gov/25185550
https://pubmed.ncbi.nlm.nih.gov/25185550
Publikováno v:
Current Organic Chemistry (1385-2728) (Bentham Science Publ Ltd), 2014, Vol. 18, N. 7, P. 867-895
Current Organic Chemistry
Current Organic Chemistry, Bentham Science Publishers, 2014, 18 (7), pp.867-895. ⟨10.2174/138527281807140515152334⟩
Current Organic Chemistry, 2014, 18 (7), pp.867-895. ⟨10.2174/138527281807140515152334⟩
Current Organic Chemistry
Current Organic Chemistry, Bentham Science Publishers, 2014, 18 (7), pp.867-895. ⟨10.2174/138527281807140515152334⟩
Current Organic Chemistry, 2014, 18 (7), pp.867-895. ⟨10.2174/138527281807140515152334⟩
International audience; Polysaccharides are among the most abundant macromolecules on Earth. These polymers are easily obtained from various marine resources such as algae, microorganisms and crustacean shells. The structure of these natural carbohyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::896b0c881b9172ba87ee1c1428f434ff
https://archimer.ifremer.fr/doc/00199/31027/
https://archimer.ifremer.fr/doc/00199/31027/
Publikováno v:
ChemInform. 41
Key steps of the synthetic approach include formation of the four-membered ring by intramolecular alkylation of suitable protected precursor(III) followed by ring closure with L-cysteine (V) affording the title thiazoline fragment (VI).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a85ebff9c84f344ff3538ebfb61cadf9
https://doi.org/10.1002/chin.201047187
https://doi.org/10.1002/chin.201047187
Autor:
François Couty, Nicolas Rabasso, Hans Bräuner-Osborne, Birgitte Nielsen, Nathalie Chopin, Anders A. Jensen, Mie Kusk, Lennart Bunch, Gwilherm Evano
Publikováno v:
Organic & Biomolecular Chemistry. 3:3926
A set of ten azetidinic amino acids, that can be envisioned as C-4 alkyl substituted analogues of trans-2-carboxyazetidine-3-acetic acid (t-CAA) and/or conformationally constrained analogues of (R)- or (S)-glutamic acid (Glu) have been synthesized in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ebc78d5b32d2a010495aa418573a625
https://doi.org/10.1039/b509514j
https://doi.org/10.1039/b509514j