Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marina Ionita"'
Autor:
Salim Ferdjani, Charles Tellier, Zeineddine Djeghaba, Bimalendu Roy, Claude Rabiller, Marina Ionita, Michel Dion
Publikováno v:
Biotechnology Letters. 33:1215-1219
The activity and stability of a β-glycosidase (Thermus thermophilus) and two α-galactosidases (Thermotoga maritima and Bacillus stearothermophilus) were studied in different hydrophilic ionic liquid (IL)/water ratios. For the ILs used, the glycosid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::205e2d876e6873e630954792867e21f3
https://doi.org/10.1007/s10529-011-0560-5
https://doi.org/10.1007/s10529-011-0560-5
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:4934-4937
All- O -undec-en-10-yl derivatives of d -glucose have been prepared and their affinities for the Plasmodium falciparum hexose transporter (PfHT) determined; the O -2 derivative displays a good apparent affinity for PfHT ( K I = 2 μM) with no signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52b151baa43788e678bc6782a959574e
https://doi.org/10.1016/j.bmcl.2007.06.021
https://doi.org/10.1016/j.bmcl.2007.06.021
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:1267-1271
A series of 3-O-substituted glucose derivatives was prepared with alkyl, alkenyl, aromatic and ferrocenic substituents; to vary lipophilicity and hydrogen bonding ethylenedioxy and perfluorinated fragments were also introduced. Apparent affinities fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef258ac0a01e24d4f69cfe48c1b8e639
https://doi.org/10.1016/j.bmcl.2005.11.068
https://doi.org/10.1016/j.bmcl.2005.11.068
Publikováno v:
ChemInform. 43
The regioselectivity of the reaction strongly depends on the substituent at the thiophene substrate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dca442940b7c07798769675c9b25947f
https://doi.org/10.1002/chin.201210102
https://doi.org/10.1002/chin.201210102
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2011, 21, pp.3530-3546. ⟨10.1055/s-0030-1260213⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2011, 21, pp.3530-3546. ⟨10.1055/s-0030-1260213⟩
SYNTHESIS, Georg Thieme Verlag, 2011, 21, pp.3530-3546. ⟨10.1055/s-0030-1260213⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2011, 21, pp.3530-3546. ⟨10.1055/s-0030-1260213⟩
International audience; The Pd(OAc)2/dppb system was found to be an efficient catalyst for the direct arylation of 3-substituted thiophene derivatives. The regioselectivity of the arylation strongly depends on the thiophene substituent and also on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eb1897a74de718fa3d7a1a07e033c9f
https://hal.archives-ouvertes.fr/hal-00652041
https://hal.archives-ouvertes.fr/hal-00652041
Publikováno v:
ChemSusChem
ChemSusChem, ChemPubSoc Europe/Wiley, 2010, 3 (3), pp.367-376. ⟨10.1002/cssc.200900258⟩
ChemSusChem, 2010, 3 (3), pp.367-376. ⟨10.1002/cssc.200900258⟩
ChemSusChem, ChemPubSoc Europe/Wiley, 2010, 3 (3), pp.367-376. ⟨10.1002/cssc.200900258⟩
ChemSusChem, 2010, 3 (3), pp.367-376. ⟨10.1002/cssc.200900258⟩
International audience; The palladium-catalyzed direct 3-arylation of benzofurans provides a cost-effective and environmentally attractive route for the preparation of 3-arylbenzofuran derivatives. The reactions were carried out using a wide variety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad376ca96b8c680a624733bb7f27c595
https://pubmed.ncbi.nlm.nih.gov/20039360
https://pubmed.ncbi.nlm.nih.gov/20039360