《Copper-Mediated Regioselective C-H Sulfenylation and Selenation of Phenols with Phenanthroline Bidentate Auxiliary》 was published in Organic Letters in 2020. These research results belong to Kajiwara, Rikuo; Takamatsu, Kazutaka; Hirano, Koji; Miura, Masahiro. Application of 882-33-7 The article mentions the following:
A copper-mediated,phenanthroline-directed highly ortho-selective C-H sulfenylation of phenols with diaryl disulfides proceeds to form the corresponding unsym. diaryl sulfides in good yield. He key to success is the introduction of a phenanthroline directing group of the bidentate-chelating nature, which is easily attachable,detachable, and even recyclable. Moreover, the same strategy is applicable to the C-H selenation, giving the diaryl selenides with high efficiency and regioselectivity.1,2-Diphenyldisulfane(cas: 882-33-7Application of 882-33-7) was used in this study.
1,2-Diphenyldisulfane(cas: 882-33-7) belongs to ethers.The C-O bonds that comprise simple ethers are strong. They are unreactive toward all but the strongest bases. Although generally of low chemical reactivity, they are more reactive than alkanes. Application of 882-33-7
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem