Diphenyl Diselenide-Catalyzed Synthesis of Triaryl Phosphites and Triaryl Phosphates from White Phosphorus was written by Zhang, Yue;Cai, Ziman;Chi, Yangyang;Zeng, Xiangzhe;Chen, Shuanghui;Liu, Yan;Tang, Guo;Zhao, Yufen. And the article was included in Organic Letters in 2021.Product Details of 103-16-2 The following contents are mentioned in the article:
Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a di-Ph diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds Subsequent oxidation of triaryl phosphites produces triaryl phosphates and triaryl thiophosphates. Phosphorotrithioates are also prepared efficiently from aromatic thiols and aliphatic thiols. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Product Details of 103-16-2).
4-Benzyloxyphenol (cas: 103-16-2) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Product Details of 103-16-2
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem