38694-48-3Relevant articles and documents
Double prodrugs of a fosmidomycin surrogate as antimalarial and antitubercular agents
Courtens, Charlotte,Risseeuw, Martijn,Caljon, Guy,Maes, Louis,Cos, Paul,Martin, Anandi,Van Calenbergh, Serge
supporting information, p. 1232 - 1235 (2019/03/21)
A series of eleven double prodrug derivatives of a fosmidomycin surrogate were synthesized and investigated for their ability to inhibit in vitro growth of P. falciparum and M. tuberculosis. A pivaloyloxymethyl (POM) phosphonate prodrug modification was c
Pd-Catalyzed Highly Chemo- And Regioselective Hydrocarboxylation of Terminal Alkyl Olefins with Formic Acid
Ren, Wenlong,Chu, Jianxiao,Sun, Fei,Shi, Yian
supporting information, p. 5967 - 5970 (2019/08/26)
An efficient Pd-catalyzed hydrocarboxylation of alkenes with HCOOH is described. A wide variety of linear carboxylic acids bearing various functional groups can be obtained with excellent chemo- and regioselectivities under mild reaction conditions. The reaction process is operationally simple and requires no handling of toxic CO.
Synthetic method of terminal carboxylic acid
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Paragraph 0091-0094, (2019/11/21)
The invention discloses a synthetic method of a terminal carboxylic acid. The synthetic method is characterized by comprising the steps of adding an olefin represented by a formula (3) shown in the description, formic acid, acetic anhydride, Pd(OAc)2 and a monophosphorus ligand TFPP into an organic solvent in a proportion, carrying out hydrogen carbonylation reaction on the olefin represented by the formula (3) shown in the description, formic acid and acetic anhydride at 80-90 DEG C for 48h-72h under the catalysis of the metal palladium salt Pd(OAc)2 and the monophosphorus ligand TFPP so as to obtain the terminal carboxylic acid represented by a formula shown in the description, and separating a target product, namely the terminal carboxylic acid after the reaction is finished, wherein olefin represented by the formula (3) is selected from cycloolefins, or linear olefins of which the R1 is electron donating groups. By virtue of the method disclosed by the invention, corresponding terminal carboxylic acid and a derivative thereof can be prepared through the reaction under mild conditions of low temperature and no high pressure; and the steps of the synthetic method are simple and convenient, the operation is convenient, the yield is high, the energy source can be greatly saved, and the synthetic efficiency can be greatly improved.
AMINOALKYL-SUBSTITUTED N-THIENYL BENZAMIDE DERIVATIVE
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Paragraph 0130; 0162, (2014/09/17)
[Problem] To provide a compound that has an intestinal phosphate transporter (NPT-IIb) inhibitory action and is useful as an active ingredient of an agent for treating and/or preventing hyperphosphatemia. [Means for Solution] The present inventors conduct
NOVEL CYCLIC BENZIMIDAZOLE DERIVATIVES USEFUL ANTI-DIABETIC AGENTS
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Page/Page column 79-80, (2010/05/14)
Novel compounds of the structural formula (I) are activators of AMP-protein kinase and are useful in the treatment, prevention and suppression of diseases mediated by the AMPK- activated protein kinase. The compounds of the present invention are useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
Synthesis of new phosphonated tripod ligands as putative new therapeutic agents in the chelation treatment of metal intoxications
Burgada, Ramon,Bailly, Theodorine,Lecouvey, Marc,Larue, Valery,Leroux, Yves
, p. 349 - 352 (2007/10/03)
In a quest for new chelation therapy drugs for the treatment of intoxication by actinides, some new phosphonated chelating tripod ligands have been synthesized. They have been obtained by means of a coupling reaction between a diethylphosphonoalkanoic acid activated with N,N'-disuccinimidyl carbonate (DSC) and a series of polyamines, with subsequent deprotection of the phosphonate groups.
ACTIVATION ANIONIQUE DU PHOSPHITE DE DIETHYLE PAR LE FLUORURE DE POTASSIUM DEPOSE SUR ALUMINE, SYNTHESE DE PHOSPHONATES FONCTIONALISES
Villemin, Didier,Racha, Rassem
, p. 1789 - 1790 (2007/10/02)
Dry reactions of diethylphosphite on KF-AL2O3 with different electrophiles conduct to the synthesis of functionalized phosphonates.
Organophosphorus Chemistry. IV. Synthesis and Reactions of 2-Ethoxy-6-oxo-1,2-azaphosphinane 2-Oxide
Hewitt, David G.,Teese, Murray W.
, p. 1631 - 1642 (2007/10/02)
2-Ethoxy-6-oxo-1,2-azophosphinane 2-oxide (3) has been prepared by cyclocondensation of ethyl 4(R-amino-R-ethoxyphosphinoyl)butanoate (17).N-Alkylated derivatives of (3) were prepared by cyclocondensation of (17) in the presence of methyl iodide, allyl br