Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Gilles Quéléver"'
Publikováno v:
Tetrahedron Letters. 56:4043-4046
We report the successful combination of the convergent ‘click coupling’ of the divergently derived dendrons for synthesizing poly(aminoester) dendrimers. The concept of integrating ‘click’ chemistry into the combined convergent/divergent stra
Autor:
Mei Cong, Juan L. Iovanna, Laurence Borge, Yi Xia, Palma Rocchi, Ling Peng, Jingjie Tang, Gilles Quéléver
Publikováno v:
New Journal of Chemistry. 39:3889-3893
Synthetic nucleoside analogues with novel structural entities are of considerable importance in the search for new structural paradigms with biologically interesting activities. We report in this work that microwave promoted C–O coupling reaction i
Publikováno v:
Organic & Biomolecular Chemistry. 13:110-114
Various arylvinyltriazole nucleoside analogues were synthesized using Pd-catalyzed oxidative Heck reaction. This method affords the corresponding and otherwise difficult to achieve arylvinyltriazole nucleosides with good yields and large functional g
Autor:
Laurence Charles, Valérie Monnier, Rémi Giordanengo, Gilles Quéléver, Ling Peng, Camille Bouillon, Aura Tintaru
Publikováno v:
Rapid Communications in Mass Spectrometry. 24:2207-2216
An acid-terminated poly(amino)ester dendrimer was studied by electrospray ionization tandem mass spectrometry to establish its fragmentation pathways, with the aim of using them to investigate the structure of any defective molecules generated during
Publikováno v:
ChemInform. 46
Various arylvinyltriazole nucleoside analogues were synthesized using Pd-catalyzed oxidative Heck reaction. This method affords the corresponding and otherwise difficult to achieve arylvinyltriazole nucleosides with good yields and large functional g
Autor:
Jean-Chrétien Norreel, Jean-Louis Kraus, Gilles Quéléver, Younes Laras, Bernard Mallet, Amandine Rolland, Cédrik Garino, Vincent Moret, Nicolas Pietrancosta
Publikováno v:
HAL
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16, pp.3298-3301
Bioorganic and Medicinal Chemistry Letters, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2006, 16 (12), pp.3298-3301. ⟨10.1016/j.bmcl.2006.03.026⟩
Dysfunction of copper metabolism leading to its excess or deficiency results in severe ailments. Recently, neurodegenerative disorders such as Alzheimer’s disease have been associated with copper metabolism. Compounds having the ability to reduce c
Publikováno v:
Org. Biomol. Chem.. 1:1676-1683
In so much as bis-macrocyclic peptidomimetics have been recognized as high affinity substrates for HIV-1 protease, we were interested in the design and synthesis of new bis-macrocyclic bioisosteric analogues whose general structure is displayed on Fi
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1181-1189
Based on the specific PhePro proteolytic cleavage of the HIV-protease, we synthesized short pseudopeptides incorporating a 2-(phenylthio)pyrrolidin-3-one ring. We previously described various analogues based on this scaffold. We report herein a paral
Autor:
Xinjun Liu, Otmane Lamrabet, Yang Wang, Cheng-Cai Zhang, Fabio Ziarelli, Gilles Quéléver, Fanqi Qu, Amel Latifi, Zeinab Assaf, Ling Peng
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (33), pp.6470-6475. ⟨10.1039/c4ob01005a⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (33), pp.6470-6475. ⟨10.1039/c4ob01005a⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2014, 12 (33), pp.6470-6475. ⟨10.1039/c4ob01005a⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2014, 12 (33), pp.6470-6475. ⟨10.1039/c4ob01005a⟩
An ingenious and specific affinity resin designed to capture the 2-oxoglutaric acid (2-OG) binding proteins was constructed by appending a 2-OG tag to the solid resin via a Cu-catalyzed Huisgen "click" reaction. The so-obtained affinity resin was abl
Autor:
Fanqi Qu, Gilles Quéléver, Yuting Fan, Ling Peng, Yi Xia, Mei Cong, Yang Liu, Jean-Manuel Raimundo
Publikováno v:
ChemInform. 45
For the first time a mixed-ligand system, which can also activate C—Cl bonds in heteroaryl rings for C—S bond formation, is used in the title reaction.