Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Gwénaëlle Hervé"'
Publikováno v:
RSC Adv.. 4:46218-46223
A facile and efficient methodology to obtain various 5-aryluracil derivatives was developed through a two steps sequence: a ligand-free Suzuki-Miyaura cross-coupling reaction starting from totally deprotected 5-iodo-(2′-deoxy)uridine followed by a
Publikováno v:
Tetrahedron Letters. 54:3374-3377
A new and efficient ligandless cross-coupling reaction of 6-iodouridine with various boronic acids in the presence of Na 2 PdCl 4 was performed at room temperature in aerobic water. The target 6-aryl analogues were obtained in moderate to good yields
Publikováno v:
Synthesis. 45:330-333
A series of 5-aryl-2′-deoxyuridines was prepared, using ligandless Suzuki–Miyaura cross-coupling reactions in neat water, starting from 5-iodo-2′-deoxyuridine as totally deprotected starting material. This ligand-free process gave good to high
Autor:
Gwénaëlle Hervé, Christophe Len
Publikováno v:
ChemInform. 46
Publikováno v:
ChemInform. 46
A facile and efficient methodology to obtain various 5-aryluracil derivatives was developed through a two steps sequence: a ligand-free Suzuki-Miyaura cross-coupling reaction starting from totally deprotected 5-iodo-(2′-deoxy)uridine followed by a
Autor:
Christophe Len, Gwénaëlle Hervé
Publikováno v:
Frontiers in Chemistry
Frontiers in Chemistry, Vol 3 (2015)
Frontiers in Chemistry, Vol 3 (2015)
Nucleoside analogues have attracted much attention due to their potential biological activities. Amongst all synthetic nucleosides, C5-modified pyrimidines and C7- or C8-modified purines have mostly been prepared using palladium cross-coupling reacti
Publikováno v:
ChemInform. 45
Nucleoside analogues have attracted much attention due to their potential biological activities. Amongst all synthetic nucleosides, C5-modified pyrimidines and C2- or C8-modified purines have been particularly studied. A large variety of palladium cr
Autor:
Gerald Enderlin, Pawan Kumar, Gwénaëlle Hervé, Poul Nielsen, Nicolai K. Andersen, Christophe Len, Lise Junker Nielsen, Mick Hornum, Guillaume Sartori
Publikováno v:
Kumar, P, Hornum, M, Nielsen, L J, Enderlin, G, Andersen, N K, Len, C, Hervé, G, Sartori, G & Nielsen, P 2014, ' High affinity RNA targeting by oligonucleotides displaying aromatic stacking and amino groups in the major groove. Comparison of triazoles and phenylsubstituents ', Journal of Organic Chemistry, vol. 79, no. 7, pp. 2854-2863 . https://doi.org/10.1021/jo4025896
Three 5-modified 2'-deoxyuridine nucleosides were synthesized and incorporated into oligonucleotides and compared with the previously published 5-(1-phenyl-1,2,3-triazol-4-yl)-2'-deoxyuridine monomer W. The introduction of an aminomethyl group on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::031ed8cd70ca8496c4a37fb66e7869a5
https://portal.findresearcher.sdu.dk/da/publications/374f59cc-1f24-4d0a-ae59-e926b88bfde3
https://portal.findresearcher.sdu.dk/da/publications/374f59cc-1f24-4d0a-ae59-e926b88bfde3
Publikováno v:
ChemInform. 44
A facile and efficient methodology for direct synthesis of 5-aryl-2′-deoxyuridines was developed through ligand-free Suzuki–Miyaura cross-coupling reactions starting from totally deprotected 5-iodo-2′-deoxyuridine and various boronic acids. Rea
Autor:
Henri Handel, Gwénaëlle Hervé, Hélène Bernard, Nathalie Le Bris, Jean-Jacques Yaouanc, Hervé des Abbayes
Publikováno v:
Journal of Organometallic Chemistry. 585:259-265
On reaction with Group 6 metal carbonyls M(CO)6, vic type bis-aminals L, issued from the condensation of an α-dicarbonyl compound on a linear tetraamine, give rise to mononuclear cis-M(CO)4L complexes.