54146-76-8Relevant academic research and scientific papers
CATALYTIC AND IONIC REDUCTION OF THE DOUBLE BONDS IN 4H-CYCLOPENTATHIOPYRANS. ISOMERIC 2-THIABICYCLONONANES
Klimenko, S. K.,Tyrina, T. I.,Sorokin, N. N.
, p. 342 - 345 (2007/10/02)
The stereochemical direction in the reduction of the double bonds of monoaryl- and diaryl-substituted 4H-cyclopentathiopyrans during hydrogenation at platinum and during acid-catalyzed disproportionation in trifluoroacetic acid was studied.The structur
REACTIONS OF "SEMICYCLIC" 1,5-DIKETONES WITH HYDROGEN SULFIDE AND TRIFLUOROACETIC ACID
Stolbova, T. V.,Klimenko, S. K.,Kharchenko, V. G.
, p. 170 - 173 (2007/10/02)
The reactions of known and new "semicyclic" 1,5-diketones with hydrogen sulfide and with trifluoroacetic acid were studied.It was shown that under the investigated conditions both 1-aryl- and 1,3-diaryl-substituted diketones form 3R-5R-2-thiabicycloalkane
