72167-95-4Relevant articles and documents
Enantioselective Synthesis of Diaryl Sulfoxides Enabled by Molecular Recognition
Burg, Finn,Buchelt, Christoph,Kreienborg, Nora M.,Merten, Christian,Bach, Thorsten
, p. 1829 - 1834 (2021)
The enantioselective sulfoxidation of diaryl-type sulfides was accomplished using a chiral manganese porphyrin complex equipped with a remote molecular recognition site. Despite the marginal size difference between the two substituents at the prostereogen
Efficient synthesis of 3-substituted coumarins
Mashraqui, Sabir H.,Vashi, Dhaval,Mistry, Hitesh D.
, p. 3129 - 3134 (2007/10/03)
The Mukaiyama's esterification protocol, using 2-chloro-1-methylpyridinium iodide-triethylamine reagent, has been successfully exploited to provide rapid access to a variety of 3-substituted coumarins in satisfactory yields.
Synthesis of 3-Coumaryl Phenyl Sulfones or Sulfoxides
Merchant, J.R.,,Shah, P.J.,
, p. 441 - 442 (2007/10/02)
An unambiguous synthesis of a number of 3-coumaryl phenyl sulfones or sulfoxides have been described which were obtained by the oxidation of the corresponding sulfides with hydrogen peroxide.The sulfides were prepared by the Perkin-Oglialore reaction of o-hydroxyaldehyde with the sodium salt of different S-phenyl thioacetic acids.The sulfones did not exhibit any appreciable antituberculous activity in the preliminary screening tests.
