[EN] METHOD FOR TREATING FIBROSIS AND CANCER WITH IMIDAZOLIUM AND IMIDAZOLINIUM COMPOUNDS<br/>[FR] PROCÉDÉ DE TRAITEMENT DE LA FIBROSE ET DU CANCER AVEC DE L'IMIDAZOLIUM ET DES COMPOSÉS À BASE D'IMIDAZOLINIUM
申请人:AGENCY SCIENCE TECH & RES
公开号:WO2009096905A1
公开(公告)日:2009-08-06
There is presently provided methods for delivering an anti-fibrotic or anti-cancer agent to a cell. The methods comprise contacting a cell with an effective amount of imidazolium and imidazolinium compounds as described herein, including imidazolium and imidazolinium salts.
α-alkylated ketones has been disclosed via the reaction of primary alcohols with secondary alcohols and ketones by using [IrCl(COD)(NHC)] complexes as a catalyst. Various α-alkylated ketones were obtained in high yields from the alkylation of alcohol with alcohol and ketone with alcohol through a borrowing hydrogen reaction by using 0.05–0.5 mol % iridium(I) and a catalytic amount of KOH (5–10 mol %)
[EN] DISSOLUTION OF CELLULOSE IN IONIC LIQUIDS<br/>[FR] DISSOLUTION DE CELLULOSE DANS DES LIQUIDES IONIQUES
申请人:UNIV TEXAS TECH SYSTEM
公开号:WO2019143802A1
公开(公告)日:2019-07-25
The present invention includes a method for dissolving cellulose comprising dissolving cellulose in an ionic liquid and a co-solvent, wherein the ionic liquid is an imidazolium-based ionic liquid with, e.g., a halide or acetate as the anion.
METHOD FOR THE PRODUCTION OF DISUBSTITUTED IMIDAZOLIUM SALTS
申请人:Siemer Michael
公开号:US20100249432A1
公开(公告)日:2010-09-30
Process for preparing 1,3-disubstituted imidazolium salts of the formula I
where
R1 and R3 are each, independently of one another, an organic radical having from 1 to 20 carbon atoms,
R2, R4 and R5 are each, independently of one another, an H atom or an organic radical having from 1 to 20 carbon atoms,
X is the anion of a hydrogen acid having a pK
a
of at least 2 (measured at 25° C., 1 bar in water or dimethyl sulfoxide) and
n is 1, 2 or 3,
wherein
a) an α-dicarbonyl compound, an aldehyde, an amine and the hydrogen acid of the anion X
−
are reacted with one another and
b) the reaction is carried out in water, a solvent which is miscible with water or a mixture thereof.
PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
申请人:MAILLIET Patrick
公开号:US20110172199A1
公开(公告)日:2011-07-14
The invention relates to the platinum N-heterocycle derivatives of general formula (I)
in which—R
1
and/or R
2
are, independently of one another, an aryl or aralkyl group, each optionally substituted, a linear or branched C1-C6 alkyl group, a monocyclic C3-C7 cycloalkyl group or a linear or branched C2-C6 alkenyl group, or else R′ is a hydrogen atom and R is a group selected from the following groups: cycloalkyl or heterocycloalkyl, which is monocyclic or bicyclic and has from 3 to 8 carbon atoms, or benzyl, which is optionally substituted, or else R and R′ form, together with NH, a C3-C8 monocyclic or bicyclic heterocycloalkyl, V is a nitrogen atom or a C—R
4
radical, R
3
and/or R
4
are hydrogen or a phenyl group or R
3
and R
4
may also together form a C3-C6 alkylene radical or a C3-C6 heteroalkylene radical with one or more nitrogenous heteroatoms, it being possible for the carbon atoms of the heteroalkylene radical to be modified in the form of a carbonyl radical, and X is iodine, bromine, chlorine or a nitrato (—ONO
2
) group.