Dithiocarbamation of spiro-aziridine oxindoles: a facile access to C3-functionalised 3-thiooxindoles as apoptosis inducing agents

Author(s):  
Shankaraiah Nagula ◽  
Akash P Sakla ◽  
Biswajit Panda ◽  
Kritika Laxmikeshav ◽  
Jay Prakash Soni ◽  
...  

Herein, we report the first dithiocarbamation of spiro-aziridine oxindoles involving regiospecific ring-opening by in situ generated nucleophilic dithiocarbamates as an instant source of sulfur. This approach afforded C3-functionalised-3-thiooxindoles in good...

Author(s):  
Wei-Cheng Yuan ◽  
Jian Zuo ◽  
Shu-Pei Yuan ◽  
Jian-Qiang Zhao ◽  
Zhen-Hua Wang ◽  
...  
Keyword(s):  

The reaction of N-alkoxycarbonyl-O-tosylhydroxylamines with indol-2-ones in situ generated from 3-halooxindoles has been developed for divergently accessing 4-aminoquinolin-2-ones and N-Cbz-N’-arylureas in good to excellent yields.


2004 ◽  
Vol 856 ◽  
Author(s):  
Alexandru D. Asandei ◽  
Isaac W. Moran ◽  
Gobinda Saha ◽  
Yanhui Chen

ABSTRACTTi(III)Cp2Cl-catalyzed radical ring opening (RRO) of epoxides or single electron transfer (SET) reduction of aldehydes generates Ti alkoxides and carbon centered radicals which add to styrene, initiating a radical polymerization. This polymerization is mediate in a living fashion by the reversible termination of growing chains with the TiCp2Cl metalloradical. In addition, polymers or monomers containing pendant epoxide groups (glycidyl methacrylate) can be used as substrates for radical grafting or branching reactions by self condensing vinyl polymerization. In addition, Ti alkoxides generated in situ by both epoxide RRO and aldehyde SET initiate the living ring opening polymerization of ε-caprolactone. Thus, new initiators and catalysts are introduced for the synthesis of complex polymer architectures.


2011 ◽  
Vol 49 (19) ◽  
pp. 4213-4220 ◽  
Author(s):  
Kubra Dogan Demir ◽  
Mehmet Atilla Tasdelen ◽  
Tamer Uyar ◽  
Asei William Kawaguchi ◽  
Atsushi Sudo ◽  
...  

2008 ◽  
Vol 9 (2) ◽  
pp. 704-710 ◽  
Author(s):  
Mohamad Takwa ◽  
Yan Xiao ◽  
Neil Simpson ◽  
Eva Malmström ◽  
Karl Hult ◽  
...  

Author(s):  
Quinton J Meisner ◽  
Sisi Jiang ◽  
Pengfei Cao ◽  
Tobias Glossmann ◽  
Andreas Hintennach ◽  
...  

The use of solid polymer electrolytes has previously proven to be an effective approach to address the lithium polysulfide dissolution and high electrode interfacial impedance of Li-S batteries via an...


Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 969
Author(s):  
Sonia Bujok ◽  
Jiří Hodan ◽  
Hynek Beneš

The high capacity of calcinated layered double hydroxides (LDH) to immobilize various active molecules together with their inherent gas/vapor impermeability make these nanoparticles highly promising to be applied as nanofillers for biodegradable polyester packaging. Herein, trihexyl(tetradecyl)phosphonium decanoate ionic liquid (IL) was immobilized on the surface of calcinated LDH. Thus, the synthesized nanoparticles were used for the preparation of polycaprolactone (PCL)/LDH nanocomposites. Two different methods of nanocomposite preparation were used and compared: microwave-assisted in situ ring opening polymerization (ROP) of ε-caprolactone (εCL) and melt-blending. The in situ ROP of εCL in the presence of LDH nanoparticles with the immobilized IL led to homogenous nanofiller dispersion in the PCL matrix promoting formation of large PCL crystallites, which resulted in the improved mechanical, thermal and gas/water vapor barrier properties of the final nanocomposite. The surface-bonded IL thus acted as nanofiller surfactant, compatibilizer, as well as thermal stabilizer of the PCL/LDH nanocomposites. Contrary to that, the melt-blending caused a partial degradation of the immobilized IL and led to the production of PCL nanocomposites with a heterogenous nanofiller dispersion having inferior mechanical and gas/water vapor barrier properties.


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