A Simple Protocol for the Stereoselective Construction of Enaminyl Sulfonyl Fluorides was written by Leng, Jing;Tang, Wenjian;Fang, Wan-Yin;Zhao, Chuang;Qin, Hua-Li. And the article was included in Organic Letters in 2020.Related Products of 103-16-2 The following contents are mentioned in the article:
A clickable connective hub 1-bromo-2-triazolethane-1-sulfonyl fluoride (BTESF) was developed and successfully applied for the fluorosulfonylvinylation of a host of primary and secondary cyclic or acyclic amines including amino acids and pharmaceuticals. Further antimicrobial experiments revealed that vinyl sulfonyl fluoride functionalized norfloxacin, ciprofloxacin, and lomefloxacin exhibited 4-fold improved antimicrobial activity against Gram-pos. bacteria compared to their parent drugs. This study involved multiple reactions and reactants, such as 4-Benzyloxyphenol (cas: 103-16-2Related Products 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. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Related Products of 103-16-2
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem