Iodine‐modified Pd catalysts promote the bifunctional catalytic synthesis of 2,5‐hexanedione from C6 furan aldehydes

ChemSusChem ◽  
2021 ◽  
Author(s):  
Zhikun Tong ◽  
Xiang Li ◽  
Jiawei Zhu ◽  
Shixia Chen ◽  
Guiping Dai ◽  
...  
2020 ◽  
Author(s):  
Shunya Ohuchi ◽  
Hiroki Koyama ◽  
Hiroki Shigehisa

A catalytic synthesis of cyclic guanidines, which are found in many biologically active compounds and natu-ral products, was developed, wherein transition-metal hydrogen atom transfer and radical-polar crossover were employed. This mild and functional-group tolerant process enabled the cyclization of alkenyl guanidines bearing common protective groups, such as Cbz and Boc. This powerful method not only provided the common 5- and 6-membered rings but also an unusual 7-membered ring. The derivatization of the products afforded various heterocycles. We also investigated the se-lective cyclization of mono-protected or hetero-protected (TFA and Boc) alkenyl guanidines and their further derivatiza-tions.


2021 ◽  
Vol 25 ◽  
Author(s):  
Réka Henyecz ◽  
György Keglevich

Abstract: Microwave (MW)-assistance may be a powerful tool also in the Hirao P–C coupling reactions of vinyl/aryl halides with dialkyl phosphites in the presence of Pd-catalysts/P-ligands elaborated forty years ago. This review surveys the development of this reaction by showing the expansion of the reagents and catalysts, as well as the information accumulated. The stress was laid on the “green” aspects, the simplification of the catalyst systems, and the reliable mechanistic details in order to be able to establish the optimum conditions. The best protocol involves the use of some excess of the >P(O)H reagent to ensure the PdII→Pd0 reduction and, via its trivalent tautomeric form (>POH) also the P-ligand. The overall rate is the result of two factors, the activity of the catalyst complex formed, and the reactivity of the reactants in the P–C coupling reactions. Both components are influenced by the nature of the aryl substituents in Ar2P(O)H. NiII salts may also be used as the catalyst precursor, however, despite the PdII→Pd0→PdII route, in this case, a NiII→NiIV→NiII sequence was proved.


2020 ◽  
Vol 24 ◽  
Author(s):  
Yanlin Zong ◽  
Qiankun Li ◽  
Hongliang Mu ◽  
Zhongbao Jian

Abstract:: The copolymers of carbon monoxide (CO) and olefins, namely polyketones, are a family of widely used materi-als. In the catalytic preparation of these materials, palladium(II) catalysts represent the most successful catalytic systems. The production of both alternating and non-alternating polyketones has been achieved, with great difference in their physical properties. Herein, a variety of palladium(II) catalysts employed for the copolymerization of CO with various olefinic mon-omers such as ethylene, α-olefins, styrene and polar vinyl monomers are fully summarized. The influence of important fac-tors such as solvents and counterions on specific copolymerization, is also discussed. This review aims to enlighten the de-sign of new Pd catalysts with improved properties, as well as the development of new polyketone materials.


2018 ◽  
Vol 16 (1) ◽  
pp. 59-65
Author(s):  
Sofiane Mekki ◽  
Lahcen Krabia ◽  
Saleh Mahmoud Saleh Mohamed ◽  
Salima Saidi-Besbes

An efficient catalytic synthesis of 4-aryl-3,4-dihydropyrimidine-2(1H)-one derivatives using copper (II), iron (III) and zinc (II) exchanged montmorillonite clays as a catalyst is described. The desired products were obtained in good yields.


2014 ◽  
Vol 11 (2) ◽  
pp. 288-294
Author(s):  
Hamidreza Barghi ◽  
Mikael Skrifvars ◽  
Mohammad Taherzadeh
Keyword(s):  

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