66860-71-7Relevant academic research and scientific papers
Iron-Catalyzed Thiolation and Selenylation of Cycloalkyl Hydroperoxides via C-C Bond Cleavage
Sun, Qing-Xin,Chen, He,Liu, Shuai,Wang, Xiao-Qiang,Duan, Xin-Hua,Guo, Li-Na
, p. 11987 - 11997 (2021/09/02)
A cheap iron-catalyzed C-C bond cleavage/thiolation and selenylation of cycloalkyl hydroperoxides are presented. This redox-neutral protocol provides efficient access to diverse distal keto-functionalized thioethers and selenium compounds. Remarkably, only some amounts of disulfides are required for this transformation.
Intramolecular Charge-Transfer Interactions in Triplet Keto Sulfides
Wagner, Peter J.,Lindstrom, Michael J.
, p. 3057 - 3062 (2007/10/02)
The photochemistry of β-,γ-and δ-phenacyl sulfides, sulfoxides, and sulfones has been studied.The first group undergoes no irreversible reaction.The other two undergo type II photoelimination but in low quantum efficiency.Analysis of triplet lifetimes and product quantum yields indicates that all undergo rapid internal quenching, which is ascribed to a charge-transfer (CT) process.The positional dependence of rate constants for this CT reaction is β > γ > α >> δ > ε .Some rate constants (units of 1E8 s-1) for PhCO(CH2)nSBu are as follows: n = 1, 16; n = 2, 55; n = 3, 29; n = 4 ,1.7; n = 5, PhS BuS(O) >> BuS, BuSO2, CH3CO-S and range from 1E9-3*1E5 s-1.Rate constants for triplet state γ-hydrogen abstraction were found to correlate well with the ?1 values of the various sulfur groups, except for δ-sulfinyl, which apparently participates in the reaction.
