Sulfurization of nonenolizable diketones
A Ishii, J Nakayama, MX Ding, N Kotaka…
Index: Ishii, Akihiko; Nakayama, Juzo; Ding, Meng-xin; Kotaka, Noboru; Hoshino, Masamatsu Journal of Organic Chemistry, 1990 , vol. 55, # 8 p. 2421 - 2427
Full Text: HTML
Citation Number: 31
Abstract
Sulfurization of Diketones with Lawesson's Reagent (LR). The sulfurization of diketones 1 was carried out with excess LR in every case, though one molecule of LR can theoretically sulfurize two carbonyl^.^ The sulfurization of diketone la proceeded easily. Heating la with LR in refluxing benzene for 6 h resulted in the complete consumption of la. Chromatographic workup of the mixture gave disulfide 2 (80%) and trithiolane 3a (13%). The reaction ...
Related Articles:
[Otsuka,S. et al. Journal of Organic Chemistry, 1966 , vol. 31, p. 4170 - 4174]