Water-Promoted Reaction of C60Ar5Cl Compounds with Thiophenes Delivers a Family of Multifunctional Fullerene Derivatives with Selective Antiviral Properties was written by Kraevaya, Olga A.;Bolshakova, Valeriya S.;Peregudov, Alexander S.;Chernyak, Alexander V.;Slesarenko, Nikita A.;Markov, Vitaliy Yu.;Lukonina, Natalia S.;Martynenko, Vyacheslav M.;Sinegubova, Ekaterina O.;Shestakov, Alexander F.;Zarubaev, Vladimir V.;Schols, Dominique;Troshin, Pavel A.. And the article was included in Organic Letters in 2021.Category: esters-buliding-blocks This article mentions the following:
A reaction of the fullerene derivatives C60Ar5Cl was reported, which enabled the substitution of Cl with thiophene residues and the formation of the family of C1-sym. C60 fullerene derivatives with six functional addends C60Ar5Th. The discovered reaction provided a straightforward approach to the synthesis of previously inaccessible multifunctional water-soluble fullerene derivatives, including the compounds with antiviral activity against human immunodeficiency and influenza viruses. In the experiment, the researchers used many compounds, for example, Methyl 2-thienylacetate (cas: 19432-68-9Category: esters-buliding-blocks).
Methyl 2-thienylacetate (cas: 19432-68-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Esters contain a carbonyl center, which gives rise to 120鎺?C閳ユ弲閳ユ彊 and O閳ユ弲閳ユ彊 angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C閳ユ彊閳ユ弲 bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Category: esters-buliding-blocks
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics