Results 251 to 260 of about 15,069 (303)
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Lithiation of pyridones

Journal of the Chemical Society, Chemical Communications, 1985
Lithiation of 1-methyl-4-pyridone with n-butyl-lithium at -78 °C proceeds smoothly at the C-2 position and 2-substituted-4-pyridones (1c–j) are obtained by subsequent reaction with electorphiles; lithiation of 1-methyl-2-pyridone takes place predominantly at the N-methyl, the lithio-derivative reacting rapidly, even at -78 °C with starting pyridone to ...
Premji Patel, John A. Joule
openaire   +1 more source

Lithiated benzyllithiums from chlorobenzyl chlorides by a DTBB-catalysed lithiation

Tetrahedron Letters, 1997
Abstract The reaction of 2-, 3- or 4-chlorobenzyl chlorides ( 1a-c ) with an excess of lithium and a catalytic amount of DTBB (7 mol%) in the presence of different electrophiles [Pr i CHO, Bu t CHO, Et 2 CO, (CH 2 ) 5 CO, PhCOMe, Me 3 SiCl] in THF at −50°C leads after hydrolysis with water, to the expected dioles or disilylated compounds 2aa-2cf .
Cecilia Gómez   +2 more
openaire   +1 more source

Electrochemical lithiation and de-lithiation of MWNT–Sn/SnNi nanocomposites

Carbon, 2005
Abstract Nanocrystalline multi-walled carbon nanotube (MWNT)–Sn and MWNT–SnNi composite anode materials were prepared by chemical reduction of SnCl2 and NiCl2 precursors in the presence of MWNTs. SEM and TEM observations showed that the Sn and SnNi particles are homogeneously dispersed on the MWNT surface and in the MWNT matrix.
Dou, S X   +3 more
openaire   +2 more sources

Reversibility of the lithiation of η6-naphthalenetricarbonylchromium

Journal of Organometallic Chemistry, 1987
Abstract The lithiation of naphthalenetricarbonylchromium with n-BuLi or tetramethylpiperidyllithium is under kinetic control, and with the latter reagent is highly regioselective in the 2-position. Addition of isopropylamine renders the process reversible, and an approximately 1 1 equilibrium mixture of 1- and 2-substitution product is formed.
Kundig, Ernst Peter   +2 more
openaire   +1 more source

Lithiation of a Pyrrolo-Annulated Tetrathiafulvalene

Synthesis, 2004
Mono- and bis-lithiations of N-tosyl monopyrrolotetrathiafulvalene provide novel methods for the introduction of substituents, such as alkyl and halogens, into the 4- and 6-positions of monopyrrolotetrathiafulvalenes.
Petersen, Bo Møller   +2 more
openaire   +1 more source

Rearrangement Reactions of Lithiated Oxiranes

The Journal of Organic Chemistry, 2013
The first computational study of the rearrangement reactions of oxiranes initiated by lithium dialkylamides is presented. Aside from the well-known carbenoid insertion pathways, both β-elimination and α-lithiation have been suggested as the exclusive mechanism by which oxiranes react in the presence of organolithium bases.
B Ramu, Ramachandran   +2 more
openaire   +2 more sources

Obviating the need for nanocrystallites in the extended lithiation/de-lithiation of germanium

Journal of Materials Chemistry A, 2015
Micrometer-sized germanium sub-telluride (Ge0.85Te0.15) particles show improved stability and capacity retention over similarly sized pure germanium particles when cycled at a rate of 1C over 500 cycles.
Emily J. Powell   +4 more
openaire   +1 more source

The Lithiation of 2‐Chloroglucal Derivatives.

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Boyd, Ewan   +6 more
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Mechanochemical lithiation of layered polysilane

Chem. Commun., 2014
Lithiated polysilane was synthesized by the mechanochemical reaction of layered polysilane with metallic lithium. The resulting dark green powder formed a Si–Li bond on the surface and demonstrated electroconductivity.
Masataka, Ohashi   +6 more
openaire   +2 more sources

By Lithiation

2004
N. Haider, W. Holzer
openaire   +2 more sources

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