ChemInform Abstract: Pd(0) Encapsulated Nanocatalysts as Superior Catalytic Systems for Pd-Catalyzed Organic Transformations

ChemInform ◽  
2016 ◽  
Vol 47 (46) ◽  
Author(s):  
S. Sadjadi ◽  
M. M. Heravi
RSC Advances ◽  
2016 ◽  
Vol 6 (91) ◽  
pp. 88588-88624 ◽  
Author(s):  
S. Sadjadi ◽  
M. M. Heravi

In the last decade, Pd(0) nanoparticles have attracted increasing attention due to their outstanding utility as nanocatalysts in a wide variety of key chemical reactions.


ChemInform ◽  
2004 ◽  
Vol 35 (20) ◽  
Author(s):  
Takahiro Nishimura ◽  
Sakae Uemura

2021 ◽  
Vol 25 ◽  
Author(s):  
Goutam Brahmachari ◽  
Nayana Nayek ◽  
Mullicka Mandal ◽  
Anindita Bhowmick ◽  
Indrajit Karmakar

: Ultrasonication, nowadays, is well-regarded as an effective green tool in implementing a plethora of organic transformations. The last decade has seen quite useful applications of ultrasound irradiation in synthetic organic chemistry. Ultrasound has already come out as a unique technique in green chemistry practice, for its inherent properties of minimizing wastes and reducing energy and time, thereby increasing the product yields with higher purities under milder reaction conditions. The present review summarizes ultrasound-promoted useful organic transformations involving both carbon-carbon and carbon-heteroatom (N, O, S) bond-forming reactions in the absence or presence of varying catalytic systems, reported during the period 2016-2020.


Synlett ◽  
2004 ◽  
pp. 0201-0216 ◽  
Author(s):  
Sakae Uemura ◽  
Takahiro Nishimura

RSC Advances ◽  
2020 ◽  
Vol 10 (42) ◽  
pp. 24893-24940 ◽  
Author(s):  
Majid M. Heravi ◽  
Bahareh Heidari ◽  
Vahideh Zadsirjan ◽  
Leila Mohammadi

In this review, the catalytic activity of encapsulated Cu-NPs in different important organic transformations is compared with those of a variety of organic, inorganic and hybrid porous materials bearing a traded metal ion.


2022 ◽  
Vol 0 (0) ◽  
Author(s):  
Abhijeet Singh ◽  
Pargat Singh ◽  
Mahendra Nath

Abstract Organic transformations using efficient, atom-economical, cost-effective and environmentally benign strategies for the construction of diversified molecules have attracted synthetic chemists worldwide in recent years. These processes often minimize the waste production and avoid the use of hazardous flammable organic solvents. Among various green protocols, the procedures using surfactant-based catalytic systems have received a considerable attention in organic synthesis. In this context, Bronsted acidic surfactants have emerged as efficient catalysts for various C–C, C–O, C–N and C–S bond forming reactions. Many of these reactions occur in water, as Bronsted acidic surfactants have a unique ability of creating hydrophobic pocket through micelle formation in aqueous medium and the substrate molecules react efficiently to afford the targeted products in good yields. In the past, Bronsted acidic surfactant combined catalysts successfully displayed their potential to accelerate the reaction rates of diverse organic transformations. This chapter presents a complete overview on Bronsted acidic surfactants catalyzed organic reactions to construct a variety of aromatic and heteroaromatic molecular frameworks.


RSC Advances ◽  
2016 ◽  
Vol 6 (116) ◽  
pp. 115364-115364
Author(s):  
S. Sadjadi ◽  
M. M. Heravi

Correction for ‘Pd(0) encapsulated nanocatalysts as superior catalytic systems for Pd-catalyzed organic transformations’ by S. Sadjadi and M. M. Heravi, RSC Adv., 2016, 6, 88588–88624.


Molecules ◽  
2022 ◽  
Vol 27 (2) ◽  
pp. 475
Author(s):  
Liang Nie ◽  
Xiangjun Peng ◽  
Haiping He ◽  
Jian Hu ◽  
Zhiyang Yao ◽  
...  

The development of graphene oxide–based heterogeneous materials with an economical and environmentally–friendly manner has the potential to facilitate many important organic transformations but proves to have few relevant reported reactions. Herein, we explore the synergistic role of catalytic systems driven by graphene oxide and visible light that form nucleophilic alkoxyl radical intermediates, which enable an anti-Markovnikov addition exclusively to the terminal alkenes, and then the produced benzyl radicals are subsequently added with N–methylquinoxalones. This photoinduced cascade radical difunctionalization of olefins offers a concise and applicable protocol for constructing alkoxyl–substituted N–methylquinoxalones.


2016 ◽  
Vol 10 (3) ◽  
pp. 259-270
Author(s):  
Ludmila Matienko ◽  
◽  
Larisa Mosolova ◽  
Vladimir Binyukov ◽  
Gennady Zaikov ◽  
...  

Mechanism of catalysis with binary and triple catalytic systems based on redox inactive metal (lithium) compound {LiSt+L2} and {LiSt+L2+PhOH} (L2=DMF or HMPA), in the selective ethylbenzene oxidation by dioxygen into -phenylethyl hydroperoxide is researched. The results are compared with catalysis by nickel-lithium triple system {NiII(acac)2+LiSt+PhOH} in selective ethylbenzene oxidation to PEH. The role of H-bonding in mechanism of catalysis is discussed. The possibility of the stable supramolecular nanostructures formation on the basis of triple systems, {LiSt+L2+PhOH}, due to intermolecular H-bonds, is researched with the AFM method.


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