1,2,4-Tris(trifluoromethyl)benzene: selective lithiation and subsequent electrophilic substitution
Related publications (35)
Graph Chatbot
Chat with Graph Search
Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
Carbon dioxide and the carbonates, the available natural C-1 sources, can be easily hydrogenated into formic acid and formates in water; the rate of this reduction strongly depends on the pH of the solution. This reaction is catalysed by ruthenium(II) pre- ...
A review. Strategies to functionalize simple, though structurally challenging, compds. in regiodivergent manner are outlined. The starting materials are inexpensive (5-500 e/mol) arenes or heterocycles bearing heterosubstituents such as Cl, F, CF3, OCF3, a ...
Periodic operation was applied to CO2 hydrogenation to CH4 at 383 K on 2% Ru/TiO2. A continuous feed recycle reactor combined with a diffuse reflectance IR cell and a mass spectrometer was used to follow simultaneously the gas phase CO2 and CH4 as well as ...
Complex hydrides such as LiBH4 and LiNH2 exceed the gravimetric hydrogen density of transition metal hydrides by one order of magnitude. However, hydrogen in complex hydrides is covalently bound and arranged in subunits e.g. [NH2]- and [BH4] - with a fixed ...
N-Protected o- and p-anisidines (2- and 4-methoxyanilines) undergo a hydrogen/metal exchange at the position adjacent to either the oxygen or nitrogen atom depending on what organometallic base is employed. These synthetically useful findings support previ ...
The acid-catalyzed cyclization-condensation between anilines and Et 4,4,4-trifluoroacetoacetate affords 1,4-dihydro-2-trifluoromethyl-4H-4-quinolinones, which can easily be converted into 4-bromo-2-(trifluoromethyl)quinolines. These undergo halogen/metal e ...
(Z)-(3,3-dimethylbicyclo[2.2.1]hept-2-ylidene)methyllithium can be readily generated by treatment of (Z)-3-bromomethylene-2,2-dimethylbicyclo[2.2.1]heptane with Me3CLi. At -75 Deg, the organometallic intermediate is configurationally stable and reacts with ...
A review with 62 refs. The appropriate choice of a metalating reagent is the key to the optional deprotonation of benzylamine derivs. at a position adjacent to the substituent or the nitrogen bearing side chain or even at the benzylic a-position of the lat ...
At -75 Deg, the superbasic mixt. of BuLi and KOCMe3 metalates 2-, 3-, and 4-FC6H4Me exclusively at an arom. position adjacent to the halogen, as demonstrated by quenching with CO2 to give the corresponding benzoic acids. In contrast, a mixt. of LiN(CHMe2)2 ...
Methanol dehydrogenation to formaldehyde was conducted in a fixed-bed flow reactor with sodium carbonate catalyst mixed with active carbons or transition metals. The additives promoted the reaction rate at 880-970 K without modifying formaldehyde selectivi ...
