72373-65-0Relevant academic research and scientific papers
Electrochemical synthesis of methyl sulfoxides from thiophenols/thiols and dimethyl sulfoxide
Du, Ke-Si,Huang, Jing-Mei
, p. 1405 - 1411 (2018)
A new route for a one-pot synthesis of methyl sulfoxides from thiophenols/thiols and dimethyl sulfoxide using an electrochemical technique was developed. This protocol proceeded smoothly by employing electrons and hydrogen peroxide as clean oxidants, and a wide range of aromatic and aliphatic sulfoxides were synthesized in moderate to good yields.
Extending aromatic acids on TiO2 for cooperative photocatalysis with triethylamine: Violet light-induced selective aerobic oxidation of sulfides
Lang, Xianjun,Li, Hui,Li, Xia,Sheng, Wenlong,Zhou, Jun
supporting information, (2022/01/11)
Designing visible light photocatalysts with a metal oxide semiconductor as the starting material could expand a new horizon for the conversion and storage of solar energy. Here, the benchmark photocatalyst TiO2 was used to pursue this goal by a
Mechanistic insight into oxygen atom transfer reactions by mononuclear manganese(iv)-oxo adducts
Singh, Priya,Stewart-Jones, Eleanor,Denler, Melissa C.,Jackson, Timothy A.
supporting information, p. 3577 - 3585 (2021/03/22)
High-valent metal-oxo intermediates are well known to facilitate oxygen-atom transfer (OAT) reactions both in biological and synthetic systems. These reactions can occur by a single-step OAT mechanism or by a stepwise process initiated by rate-limiting el
2D and 3D Porphyrinic Covalent Organic Frameworks: The Influence of Dimensionality on Functionality
Chen, Wei,Ding, Huimin,Lang, Xianjun,Luo, Yi,Meng, Yi,Shi, Ji-Long,Sun, Junliang,Wang, Cheng,Zheng, Anmin
supporting information, p. 3624 - 3629 (2020/02/04)
The construction of 2D and 3D covalent organic frameworks (COFs) from functional moieties for desired properties has gained much attention. However, the influence of COFs dimensionality on their functionalities, which can further assist in COF design, has
Sulfoxide-to-sulfilimine conversions: Use of modified Burgess-type reagents
Hendriks, Christine M. M.,Lamers, Philip,Engel, Julien,Bolm, Carsten
, p. 3363 - 3368 (2013/12/04)
Sulfoxides can directly be converted into N-cyanosulfilimines using a new Burgess-type reagent. By applying this strategy with a related reagent variant, synthetically valuable NH-sulfoximines have been prepared from sulfoxides via N-protected sulfilimines. The practical three-step reaction sequence is generally high yielding and applicable to a wide range of substrates. The sulfoxide-to-sulfilimine conversion can also be performed under solvent-reduced conditions in a ball mill. Copyright
