89818-46-2Relevant academic research and scientific papers
Synthesis and catalytic study of open metal site metal–organic frameworks of Cu3(BTC)2 microbelts in selective organic sulfide oxidation
Rostamnia, Sadegh,Alamgholiloo, Hassan,Jafari, Maryam,Rookhosh, Rezan,Abbasi, Amir Reza
, p. 954 - 958 (2016)
The synthesis of open metal site metal–organic frameworks of Cu3(BTC)2 with microbelt morphology and a study of the catalytic oxidation of organic sulfides are reported. This CuBTC was found to be an efficient, selective and waste-fr
2-Pyridyl Sulfoxide Directed Pd(II)-Catalyzed C-H Olefination of Arenes with Molecular Oxygen as the Sole Oxidant
Yadav, Mamta,Jat, Ram Singh,Sarma, Bibek,Bhanuchandra
, p. 2269 - 2276 (2021/03/03)
Pd(II)-catalyzed C-H olefination of aryl 2-pyridyl sulfoxides with unactivated and activated olefins has been demonstrated. We employed environmentally benign and inexpensive molecular oxygen as the sole oxidant. The versatile nature of the 2-pyridyl sulf
Sulfoxide and Sulfone Synthesis via Electrochemical Oxidation of Sulfides
Lee, Sunwoo,Park, Jin Kyu
, p. 13790 - 13799 (2021/10/12)
The oxidation of diaryl sulfides and aryl alkyl sulfides to the corresponding sulfoxides and sulfones under electrochemical conditions is reported. Sulfoxides are selectively obtained in good yield under a constant current of 5 mA for 10 h in DMF, while sulfones are formed as the major product under a constant current of 10 or 20 mA for 10 h in MeOH. The oxygen of both the sulfoxide and sulfone function is derived from water.
Transition-Metal-Free Arylations of In-Situ Generated Sulfenates with Diaryliodonium Salts
Yu, Hao,Li, Zhen,Bolm, Carsten
supporting information, p. 7104 - 7106 (2018/11/23)
A transition-metal-free arylation of sulfenate anions generated from β-sulfinyl esters with diaryliodonium salts was developed. In this process, a new C-S bond is formed under mild reaction conditions providing a wide range of S,S-diaryl and S-alkyl S-aryl sulfoxides.
Post-synthetically modified SBA-15 with NH2-coordinately immobilized iron-oxine: SBA-15/NH2-FeQ3 as a Fenton-like hybrid catalyst for the selective oxidation of organic sulfides
Golchin Hosseini, Habib,Rostamnia, Sadegh
, p. 619 - 627 (2017/12/28)
A new modified SBA-15 meso-material with NH2-coordinately immobilized "iron-oxine" was fabricated by stepwise covalent grafting of -NH2 and then NH2-coordinate immobilization of tris(8-quinolinolato)iron onto the channels of SBA-15. The structural properties and chemical nature of SBA-15/NH2-FeQ3 were characterized by FTIR, scanning electron microscopy (SEM), SEM-EDX/mapping, transmission electron microscopy (TEM), low angle X-ray diffraction (L-XRD), thermal gravimetric analysis (TGA), N2-adsorption-desorption isotherms (BET) and atomic absorption spectroscopy (AAS). A Fenton-like green and eco-friendly procedure for the catalytic oxidation of aromatic organic sulfides to sulfones using H2O2 was investigated for the synthesised Fe/SBA-15 catalyst. This porous catalyst was found to be reusable for ten runs without appreciable change in the activity, or the composition of the catalyst.
Access to N-cyanosulfoximines by transition metal-free iminations of sulfoxides
Dannenberg,Fritze,Krauskopf,Bolm
, p. 1086 - 1090 (2017/02/10)
A transition metal-free synthesis of N-cyanosulfoximines from sulfoxides using N-chlorosuccinimide (NCS) as oxidising agent and cyanamide as nucleophilic amine source is reported. The products are obtained in moderate to excellent yields. The protocol enables an easy access to N-cyanosulfoximines from readily available starting materials under inversion of configuration at a preexisting stereogenic center.
Palladium-Catalyzed Arylation of Aryl Sulfenate Anions with Aryl Bromides under Mild Conditions: Synthesis of Diaryl Sulfoxides
Jiang, Hui,Jia, Tiezheng,Zhang, Mengnan,Walsh, Patrick J.
supporting information, p. 972 - 975 (2016/03/15)
A palladium-catalyzed arylation of aryl sulfenate anions generated from aryl 2-(trimethylsilyl)ethyl sulfoxides and CsF has been developed. This protocol is effective for the synthesis of diaryl sulfoxides and heteroaryl aryl sulfoxides under mild conditions employing aryl bromides. Various functional groups, including those with acidic protons, are well tolerated.
An increase in the cooperative catalytic performance of SBA-15 and TFE in selective oxidation of organic sulfides
Rostamnia, Sadegh,Doustkhah, Esmail,Bahrami, Kiumars,Amini, Soraya
, p. 334 - 337 (2015/05/05)
In this paper, trifluoroethanol (TFE) was confined into SBA-15 and compared with its similar non-fluorous systems in the metal-free oxidation of sulfides to sulfoxides in the presence of H2O2. This catalytic system successfully perfo
Diaryl sulfoxides from aryl benzyl sulfoxides: A single palladium-catalyzed triple relay process
Jia, Tiezheng,Bellomo, Ana,Montel, Sonia,Zhang, Mengnan,El Baina, Kawtar,Zheng, Bing,Walsh, Patrick J.
, p. 260 - 264 (2014/01/17)
A novel approach to produce diaryl sulfoxides from aryl benzyl sulfoxides is reported. Optimization of the reaction conditions was performed using high-throughput experimentation techniques. The [Pd(dba)2]/NiXantPhos catalyst system successfully promotes a triple relay process involving sulfoxide α-arylation, C-S bond cleavage, and C-S bond formation. The byproduct benzophenone is formed by an additional palladium-catalyzed process. It is noteworthy that palladium-catalyzed benzylative C-S bond cleavage of sulfoxides is unprecedented. A wide range of aryl benzyl sulfoxides, as well as alkyl benzyl sulfoxides with various (hetero)aryl bromides were employed in the triple relay process in good to excellent yields (85-99 %). Moreover, aryl methyl sulfoxides, dibenzyl sulfoxides, and dimethylsulfoxide could be utilized to generate diaryl sulfoxides involving multiple catalytic cycles by a single catalyst. Three for one: The [Pd(dba)2]/NiXantPhos (dba=dibenzylideneacetone) catalyst system successfully promotes a triple relay process involving sulfoxide α-arylation, C-S bond cleavage, and C-S bond formation to give diaryl sulfoxides (see picture). Aryl benzyl sulfoxides, as well as alkyl benzyl sulfoxides reacted with various (hetero)aryl bromides. Copyright
Palladium-catalyzed regioselective arylation of arene C-H bond assisted by the removable 2-pyridylsulfinyl group
Zhang, Xunbin,Yu, Ming,Yao, Jinzhong,Zhang, Yuhong
, p. 463 - 467 (2012/03/11)
A palladium-catalyzed arylation of arene C-H bond assisted by a removable 2-pyridylsulfinyl group is described. The reaction employs aryltrifluoroborates as the arylation reagent, leading to the corresponding products in moderate to good yield with broad substrate scope. The directing group can be removed or converted to other useful functionalities, which showcases the potential synthetic application of the methodology. Georg Thieme Verlag Stuttgart · New York.
