32362-99-5Relevant articles and documents
Facile Synthesis of Thiolacetates from Trichloromethyl Compounds
Romero-Ortega, Moises,Reyes, Horacio,Covarruvias-Zuniga, Adrian,Cruz, Raymundo,Avila-Zarraga, Jose Gustave
, p. 2765 - 2767 (2003)
A new method for the conversion of trichloromethyl compounds into the corresponding thiolacetates by treatment with sodium thiolacetate in the presence of thiolacetic acid is described. This transformation proceeds at room temperature in high yield when a strong electron-withdrawing substituent is attached to the trichloromethyl group.
Methanesulfonic anhydride-promoted sustainable synthesis of thioesters from feedstock acids and thiols
Singh, Pallavi,Peddinti, Rama Krishna
, (2021/02/22)
Abstract: An unprecedented metal-, halogen- and solvent-free, MSAA-promoted S-carbonylation of thiols with feedstock acids has been developed. This new transformation provides an efficient and atom-economic strategy for the synthesis of thioesters in a single operation from readily available and inexpensive starting materials. The reaction avoids the use of expensive and hazardous coupling reagents, bases and generates water as the only by-product, thus making this chemical synthetic process more viable, environment-friendly and contributing towards sustainable chemistry. Graphic abstract: [Figure not available: see fulltext.].
Naphthalimide derivatives containing benzyl-sulfur bond as cleavable photoinitiators for near-UV LED polymerization
Gao, Yanjing,Hu, Xiuyuan,Jiang, Shengling,Sun, Fang,Yu, Jia
, p. 1 - 19 (2020/07/28)
Three naphthalimide aryl benzyl sulfide derivatives (NABSs) cleavable photoinitiators (PIs) containing benzyl-sulfur bonds were designed and prepared. The effect of the benzyl-sulfur moiety and substituents located on benzene ring of the benzyl group on p
