Zobrazeno 1 - 10
of 39
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7982a4babcbedbc2ad37558813d436
https://doi.org/10.1016/j.tetlet.2011.10.096
https://doi.org/10.1016/j.tetlet.2011.10.096
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1e64b35c01f89ec5edeed6d33d7a8c
https://doi.org/10.1055/s-0029-1216905
https://doi.org/10.1055/s-0029-1216905
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bca5c2239364dabe680cc66aaa30344
https://doi.org/10.1002/chin.201303062
https://doi.org/10.1002/chin.201303062
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb1f11f3ef685bdcd444ffaea645735
https://doi.org/10.1002/chin.201006114
https://doi.org/10.1002/chin.201006114