87112-35-4Relevant academic research and scientific papers
A novel and facile synthesis of 3,5-Disubstituted isothiozoles under metal free conditions using acetophenones and dithioesters
Nagaraju, Chaithra,Ashok, Swarup Hassan,Shamanth, Sadashivamurthy,Nagarakere, Sandhya C.,Sunilkumar, Makanahalli P.,Subbegowda, Rangappa Kanchugarakoppal,Mantelingu, Kempegowda
, p. 2647 - 2654 (2020/08/05)
A facile and conveniently simple new protocol is devised for the synthesis of 3,5-disubstituted and annulated isothiozoles under transition metal and catalyst free conditions utilizing easily available acetophenones, dithioesters and NH4OAc. This strategy involves C=O and C=S functionalization via sequential imine formation followed by intra molecular cyclization and aerial oxidation forming consecutive C?N and S?N bonds respectively in one pot. This protocol offers a low cost, user friendly, straight forward and widely applicable approach to 3,5-disubstituted isothiazoles.
Fe(III), Co(II), Cu(II) and Ni(II) Derivatives of Some New Monothio-β-Diketones
Saini, S. K.,Gupta, V. D.,Mehrotra, R. C.
, p. 1424 - 1426 (2007/10/02)
A few new monothio-β-diketones, RCSCH2COR', where R=Ph; Me; R'= C6H4Cl(p), C6H4Br(p), C6H4Me(p), C6H4OCH3(p) have been synthesized and their metal complexes with Cu(II), Ni(II), Co(III) and Fe(III) were prepared.These were characterized by elemental anal
