Design, synthesis, and biochemical evaluation of novel cruzain inhibitors with potential application in the treatment of Chagas’ disease
摘要:
A series of compounds bearing tetrahydronaphthalene, benzophenone, propiophenone, and related rigid molecular skeletons functionalized with thiosemicarbazone or unsaturated carbonyl moieties were prepared by chemical synthesis and evaluated for their ability to inhibit the enzyme cruzain. As potential treatment agents for Chagas' disease, three compounds from the group demonstrate potent inhibition of cruzain with IC50 values of 17, 24, and 80 nM, respectively. (c) 2006 Elsevier Ltd. All rights reserved.
Mild and Efficient Nickel-Catalyzed Heck Reactions with Electron-Rich Olefins
作者:Thomas M. Gøgsig、Jonatan Kleimark、Sten O. Nilsson Lill、Signe Korsager、Anders T. Lindhardt、Per-Ola Norrby、Troels Skrydstrup
DOI:10.1021/ja2084509
日期:2012.1.11
A new efficient protocol for the nickel-catalyzed Heckreaction of aryl triflates with vinyl ethers is presented. Mild reaction conditions that equal those of the corresponding palladium-catalyzed Heckreaction are applied, representing a practical and more sustainable alternative to the conventional regioselective arylation of vinyl ethers. A catalytic system comprised of Ni(COD)(2) and 1,1'-bis(
INHIBITORS OF CYSTEINE PROTEASES AND METHODS OF USE THEREOF
申请人:Siles Rogelio
公开号:US20090076076A1
公开(公告)日:2009-03-19
The present invention relates to semicarbazone or thiosemicarbazone inhibitors of cysteine proteases and methods of using such compounds to prevent and treat protozoan infections such as trypanosomiasis, malaria and leishmaniasis. The compounds also find use in inhibiting cysteine proteases associated with carcinogenesis, including cathepsins B and L.
Mild conversion of propargylic alcohols to α,β-unsaturated enones in ionic liquids (ILs); a new ‘metal free’ life for the Rupe rearrangement
作者:Ganesh C. Nandi、Benjamin M. Rathman、Kenneth K. Laali
DOI:10.1016/j.tetlet.2013.09.028
日期:2013.11
free protocol for the conversion of propargylic alcohols to cyclic and acyclic α,β-unsaturated enones via the Rupe rearrangement is reported. The method utilizes the Brønsted acidic ionic liquid [BMIM-SO3H][OTf] as catalyst and [BMIM][PF6] as solvent and offers the potential for recycling and reuse of the IL solvent. The feasibility to synthesize bicyclic fused cyclopentenone derivatives via a Rupe → Aldol → Nazarov
Azasteroids. Synthesis by Diels-Alder Reaction between Maleimides, Citraconimide, and Triazolindiones and 1-(1-Trialkylsiloxyvinyl)-3,4-dihydronaphthalene Derivatives
作者:Adnan Sultani、Harald Dietrich、Friedrich Richter、Hans-Hartwig Otto
DOI:10.1007/s00706-005-0344-5
日期:2005.9
3-Hydroxy derivatives, finally were synthesized by cleavage of the 3-methoxy group with BBr3. During these transformations the stereochemistry of the steroidal skeleton was not changed. The stereochemistry of these “unnatural” steroids was elucidated by spectroscopic methods, and compared with results from calculations, and with the configuration of natural estrane derivatives. Finally, an improved method
This process is a process for production of a vinyl chloride polymer by suspension polymerization or emulsion polymerization of vinyl chloride monomer or a mixture of vinyl chloride monomer with a vinyl monomer copolymerizable with said vinyl chloride monomer in an aqueous medium, characterized in that the polymerization is carried out in a polymerizer, the inner wall surface and portions of the auxiliary equipment thereof which may come into contact with the monomer during polymerization being previously coated with a scaling preventive comprising at least one selected from dyes, pigments and aromatic or heterocyclic compounds having at least 5 conjugated π bonds, while controlling the chloride ion concentration in the reaction mixture to not higher than 100 ppm. According to said process, scaling onto the inner wall surface of a polymerizer, etc. during polymerization can be prevented effectively and surely.