463298-67-1Relevant academic research and scientific papers
The direct synthesis of thioesters using an intermolecular radical reaction of aldehydes with dipentafluorophenyl disulfide in water
Nambu, Hisanori,Hata, Kayoko,Matsugi, Masato,Kita, Yasuyuki
, p. 1082 - 1083 (2002)
The combination of the water-soluble radical initiator, 2,2′-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (VA-044), and surfactant, cetyltrimethylammonium bromide (CTAB), was found to be the most suitable condition for the effective direct synthes
Efficient synthesis of thioesters and amides from aldehydes by using an intermolecular radical reaction in water
Nambu, Hisanori,Hata, Kayoko,Matsugi, Masato,Kita, Yasuyuki
, p. 719 - 727 (2007/10/03)
The combination of the water-soluble radical initiator, 2,2′-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride (VA-044) and the surfactant, cetyltrimethyl-ammonium bromide (CTAB), was found to be the most suitable condition for the effective and direct synthesis of useful active thioesters (pentafluorophenyl thioesters) in water. In addition, the direct amidation of aldehydes was achieved by the addition of the amines to the thioesterification reaction mixture in water.
