80033-09-6Relevant articles and documents
An efficient nanocluster catalyst for Sonogashira reaction
Chen, Cheng,Chen, Li,Li, Man-Bo,Luo, Gen,Lv, Qi-Long,Wu, Zhikun,Xu, Guo-Yong,Yang, Jinlong,Yang, Ying,Ye, Sun-Feng,Yuan, Jinyun
, p. 206 - 213 (2021/08/16)
Pd together with CuI has been well known as the catalyst towards Sonogashira reaction, which provides an effective route to functional alkynes. However, the achievement of high activity and selectivity of this catalytic system is still challenging in some cases. Illustrative examples include their low activity for aryl chloride substrates, and switched selectivity to oxidative coupling products in air atmosphere. In this work, a Cu-incorporated Au13 nanocluster [Au13Cu2(PPh3)6(SC2H4Ph)6]+[NO3]- (Au13Cu2) was designed and prepared in high yield via rapid synthesis. This atomically precise nanocluster shows the potential to be a novel catalytic system for Sonogashira reaction, featuring high activity and selectivity, as well as good recyclability even in air atmosphere.
Fused Selenazolinium Salt Derivatives with a Se-N+ Bond: Preparation and Properties
Arsenyan, Pavel,Vasiljeva, Jelena,Belyakov, Sergey,Liepinsh, Edvards,Petrova, Marina
supporting information, p. 5842 - 5855 (2015/09/15)
Convenient methods for the preparation of stable, fused selenazolinium salt systems with a Se-N+ bond have been developed. The mechanism for the formation of the selenazole cycle was investigated in detail by conducting multinuclear NMR experiments. The ability of these compounds to form stable inner salts was demonstrated. We have shown the glutathione peroxidase (GPx) like properties of selenazolopyridinium salts by oxidizing sulfur-containing natural amino acids, as well as aromatic and heteroaromatic aldehydes. The molecular structures of most of the compounds were confirmed by X-ray diffraction studies.
Low temperature organocopper-mediated two-component cross coupling/cycloisomerization approach toward N-fused heterocycles
Chernyak, Dmitri,Gadamsetty, Surendra Babu,Gevorgyan, Vladimir
supporting information; experimental part, p. 2307 - 2310 (2009/05/11)
(Chemical Equation Presented) Organocopper reagents smoothly react with heterocyclic propargyl mesylates at low temperature to produce N-fused heterocycles. The copper reagent plays a "double duty" in this novel cascade transformation, which proceeds via an SN2′ substitution followed by a subsequent cycloisomerization step.
