نتایج جستجو برای: 5 bromo 24 dichloro 6 methylpyrimidine

تعداد نتایج: 2036117  

2014
Tomasz Janeczko Monika Dymarska Edyta Kostrzewa-Susłow

Biotransformation of ten α-haloacetophenones in the growing culture of the strain Rhodotorula rubra KCh 82 has been carried out. Nine of the substrates underwent an effective enantioselective reduction to the respective (R)-alcohols according to Prelog's rule, with the exception of 2-chloro-1,2-diphenylethan-1-one that was not transformed by this strain. The expected reduction proceeded without...

Journal: :Chemical & pharmaceutical bulletin 2002
Chi-Tsan Liu Tsu-Chiang Tu Ling-Yih Hsu

Novel synthetic approach to mono-O-protected anti-conformationally constrained pyrimidine acyclic nucleoside was attained from the coupling of lithiated 2,4-dimethoxy-6-methylpyrimidine with 1-benzyloxy-3-(tert-butyldiphenylsilyloxy)propan-2-one, followed by the sequential reactions of methylthiomethylation, cyclization, hydroxylation, and dealkylation.

2008
Hai-Lian Liu Zhi-Qiang Du

The title compound, C(7)H(3)Cl(2)NO(4), was prepared by the reaction of 2,4-dichloro-6-nitro-toluene with 20% HNO(3) solution at 430 K. The carboxyl and nitro groups are twisted by 82.82 (12) and 11.9 (2)°, respectively, with respect to the benzene ring. The crystal structure is stabilized by O-H⋯O hydrogen bonding between carboxyl groups and weak C-H⋯O hydrogen bonding between the nitro group ...

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

Journal: :Chemical communications 2015
Bjarke S Donslund Alicia Monleón Jesper Larsen Lise Ibsen Karl Anker Jørgensen

The highly enantioselective dienamine-mediated formation of 5-bromo-6-(trifluoromethyl)-3,4-dihydro-2H-pyrans from α,β-unsaturated aldehydes and α-bromo-(trifluoromethyl)-enones employing a C2-symmetric aminocatalyst is described. The products are demonstrated to be applicable in coupling reactions directly onto the ring, thereby granting access to a broad scope of highly substituted 6-(trifluo...

Journal: :Molecules 2007
Ebru Mete Halise Inci Gul Cavit Kazaz

1-Aryl-3-phenethylamino-1-propanone hydrochlorides 1-10, which are potentialpotent cytotoxic agents, were synthesized via Mannich reactions using paraformaldehyde,phenethylamine hydrochloride as the amine component and acetophenone, 4'-methyl-, 4'-methoxy-, 4'-chloro-, 4'-fluoro-, 4'-bromo-, 2',4'-dichloro-, 4'-nitro-, 4'-hydroxyacetophenone or 2-acetylthiophene as the ketone component. Yields ...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

Journal: :The Biochemical journal 1977
G A Coetzee W Gevers

1. Treatment of hamster heart cells in primary culture with 5-bromo-2'-deoxyuridine resulted in the greatly increased activity of a particulate Ca2+- or Mg2+-dependent ATPase (adenosine triphosphatase). 2. 5-Bromo-2'-deoxyuridine exerted these effects only when it was incorporated into cellular DNA, and then in a concentration-dependent manner. 3. Serially replated cells contained less of the ...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

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