Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Laura Zink"'
Publikováno v:
Molecules, Vol 16, Iss 8, Pp 6883-6893 (2011)
We report herein the synthesis of substituted 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)phenyl]-1-arylethanols, ethyl 3-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)-phenyl]-2-hydroxypropanoate and 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)benzyl]-2
Externí odkaz:
https://doaj.org/article/c95806b7b92d4f14815bc34e7cfd50bf
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2011, 52 (51), pp.6991--6996. ⟨10.1016/j.tetlet.2011.10.096⟩
Tetrahedron Letters, 2011, 52 (51), pp.6991--6996. ⟨10.1016/j.tetlet.2011.10.096⟩
Tetrahedron Letters, Elsevier, 2011, 52 (51), pp.6991--6996. ⟨10.1016/j.tetlet.2011.10.096⟩
Tetrahedron Letters, 2011, 52 (51), pp.6991--6996. ⟨10.1016/j.tetlet.2011.10.096⟩
International audience; New reductive alkylating agents in 4- and 5-nitroimidazole series produce exclusively O-alkylation with nitronate anions under classical S(RN)1 conditions at room temperature. Electron-transfer C-alkylation is observed under m
Autor:
Benjamin Noto, Wolfgang Roll, Laura Zinken, Robert Rischen, Laura Kerschke, Georg Evers, Walter Heindel, Michael Schäfers, Florian Büther
Publikováno v:
EJNMMI Research, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Backgrounds Elastic motion correction in PET has been shown to increase image quality and quantitative measurements of PET datasets affected by respiratory motion. However, little is known on the impact of respiratory motion correction on cl
Externí odkaz:
https://doaj.org/article/3bb751a9f6484b98948c5e07a4a58dc3
Publikováno v:
Synthesis. 2009:3150-3156
A new simple, rapid and high yielding synthesis (mean yield = 83%) of various 4-aryl, 4-heteroaryl, and 4-styryl-1,2-dimethyl-5-nitro-1H-imidazoles by palladium-catalyzed Suzuki― Miyaura cross-coupling reactions using microwave irradiation is descr
Publikováno v:
ChemInform. 44
The fluoro-substituted starting material (I) reacts with arylboronic acids under Suzuki—Miyaura conditions to give O-arylated products (III) instead of the expected C—C coupled compounds, required in pharmaceutical investigation.
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩
Tetrahedron Letters, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩
Tetrahedron Letters, Elsevier, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩
Tetrahedron Letters, 2012, 53 (40), pp.5393--5397. ⟨10.1016/j.tetlet.2012.07.107⟩
International audience; We describe herein a new unexpected palladium-catalyzed O-arylation reaction in fluorinated nitro(o-nitrophenyl)imidazole series involving arylboronic acids under Suzuki-Miyaura cross-coupling reaction conditions. (C) 2012 Els
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e60b7aca6ce9292d119aad678af62fe0
https://hal-amu.archives-ouvertes.fr/hal-01460457
https://hal-amu.archives-ouvertes.fr/hal-01460457
Publikováno v:
Molecules
Molecules, 2011, 16 (8), pp.6883--6893. ⟨10.3390/molecules16086883⟩
Molecules, Vol 16, Iss 8, Pp 6883-6893 (2011)
Molecules, MDPI, 2011, 16 (8), pp.6883--6893. ⟨10.3390/molecules16086883⟩
Molecules, 2011, 16 (8), pp.6883--6893. ⟨10.3390/molecules16086883⟩
Molecules, Vol 16, Iss 8, Pp 6883-6893 (2011)
Molecules, MDPI, 2011, 16 (8), pp.6883--6893. ⟨10.3390/molecules16086883⟩
International audience; We report herein the synthesis of substituted 2-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl) phenyl]-1-arylethanols, ethyl 3-[4-(1,2-dimethyl-5-nitro-1H-imidazol-4-yl)phenyl]-2-hydroxypropanoate and 2-[4-(1,2-dimethyl-5-nitro-1H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d44686070a85e87008169d426b2e2f15
https://hal.science/hal-01460323
https://hal.science/hal-01460323
Publikováno v:
ChemInform. 41
Autor:
Delphine Defforey, Benjamin J. Tully, Jason B. Sylvan, Barbara J. Cade-Menun, Brandi Kiel Reese, Laura Zinke, Adina Paytan
Publikováno v:
Frontiers in Marine Science, Vol 9 (2022)
Our understanding of phosphorus (P) dynamics in the deep subseafloor environment remains limited. Here we investigate potential microbial P uptake mechanisms in oligotrophic marine sediments beneath the North Atlantic Gyre and their effects on the re
Externí odkaz:
https://doaj.org/article/a4154ce5f3a546e7830e3d9d24db8b28
Autor:
Jordan T. Bird, Eric D. Tague, Laura Zinke, Jenna M. Schmidt, Andrew D. Steen, Brandi Reese, Ian P. G. Marshall, Gordon Webster, Andrew Weightman, Hector F. Castro, Shawn R. Campagna, Karen G. Lloyd
Publikováno v:
mBio, Vol 10, Iss 2 (2019)
ABSTRACT Energy-starved microbes in deep marine sediments subsist at near-zero growth for thousands of years, yet the mechanisms for their subsistence are unknown because no model strains have been cultivated from most of these groups. We investigate
Externí odkaz:
https://doaj.org/article/d423e7abca1c4ab1a265d684576e4603