Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jean Francois Bonfanti"'
Autor:
Kenneth Simmen, Pierre Raboisson, Frederic Delouvroy, Maxwell D. Cummings, Wendy Mostmans, Tania Ivens, Pascale Dehertogh, Liesbet van der Helm, Geneviève Vandercruyssen, Origène Nyanguile, Walter Van den Broeck, Carlo Boutton, Jean Francois Bonfanti, Frederik Pauwels, Ludo Maria Marcel Quirynen
Publikováno v:
Antimicrobial Agents and Chemotherapy. 52:4420-4431
The exogenous control of hepatitis C virus (HCV) replication can be mediated through the inhibition of the RNA-dependent RNA polymerase (RdRp) activity of NS5B. Small-molecule inhibitors of NS5B include nucleoside and nonnucleoside analogs. Here, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02bd3cdba00a3b0ff19a49c2c9c34293
https://doi.org/10.1128/aac.00669-08
https://doi.org/10.1128/aac.00669-08
Publikováno v:
Synthetic Communications. 30:4213-4219
Pure mixed triglycerides can be prepared from diglycerides and by acylolysis of glycerolformal tosylate without isomerization. The last fatty chain, with or without a functional group, can be introduced on any position of glycerol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70d2b1b97178ef9996721a1af2de887e
https://doi.org/10.1080/00397910008087042
https://doi.org/10.1080/00397910008087042
Autor:
Jean‐Francois Bonfanti, Vincent Levacher, Christophe Hoarau, Philippe Jubault, Vincent Gembus, Olivier Querolle
Publikováno v:
ChemInform. 44
The present new functionalization method of imidazo[1,2-a]pyrazines proceeds selectively at C3 and C6 positions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eaa6721a209f13e59caad4d8c9795c7f
https://doi.org/10.1002/chin.201319183
https://doi.org/10.1002/chin.201319183
Autor:
Philippe Jubault, Jean‐Francois Bonfanti, Christophe Hoarau, Vincent Gembus, Olivier Querolle, Vincent Levacher
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2012, 14 (23), pp.6012-6015. ⟨10.1021/ol3029059⟩
Organic Letters, American Chemical Society, 2012, 14 (23), pp.6012-6015. ⟨10.1021/ol3029059⟩
An efficient “one-pot” selective functionalization at C3/C6 of imidazo[1,2-a]pyrazines has been developed via a palladium-catalyzed sequential Suzuki–Miyaura cross-coupling/direct C–H arylation, vinylation, and benzylation. The procedure rema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd4c52efa0dd37f4d79cf056e26a0dc7
https://pubmed.ncbi.nlm.nih.gov/23151283
https://pubmed.ncbi.nlm.nih.gov/23151283
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67733bbb9027fd29815cced8a5d6c0d9
https://doi.org/10.1002/chin.200005091
https://doi.org/10.1002/chin.200005091
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16d862e38b52051ccde512731de2e721
https://doi.org/10.1002/chin.200019071
https://doi.org/10.1002/chin.200019071
Publikováno v:
Synlett. 2000:248-250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::853ebe70dbaef18e008784a3721ba8a3
https://doi.org/10.1055/s-2000-6484
https://doi.org/10.1055/s-2000-6484
Publikováno v:
Synlett. 1999:1835-1837
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3c009459fc02297c1c94b863377e204
https://doi.org/10.1055/s-1999-2936
https://doi.org/10.1055/s-1999-2936
Publikováno v:
ChemInform. 32
Pure mixed triglycerides can be prepared from diglycerides and by acylolysis of glycerolformal tosylate without isomerization. The last fatty chain, with or without a functional group, can be introduced on any position of glycerol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6979f383e59259e331603321c3b88f37
https://doi.org/10.1002/chin.200108217
https://doi.org/10.1002/chin.200108217
Autor:
Wieslaw M. Kazmierski
This book focuses on new small molecule approaches to combat viral infections. The chapters describe the discovery and development from bench through the clinic of relatively recently-approved antiviral drugs and compounds in advanced clinical develo
