- In
organosulfur chemistry,
thioacetals are the
sulfur (thio-)
analogues of
acetals (R−CH(−OR)2).
There are two classes: the less-common monothioacetals...
- reduction.
Thioacetal Liu, Bin; Thayumanavan, S. (December 2020). "Mechanistic
Investigation on
Oxidative Degradation of ROS-Responsive
Thioacetal/Thioketal...
- S-acetal
refers to
compounds of type R1R2C(SR)(SR') (R,R' ≠ H, also
known as
thioacetal and thioketals.
Hemiaminal Orthoformate IUPAC,
Compendium of Chemical...
-
ylides in the
Wittig reaction to give the
alkenes With
thiols to give the
thioacetal With
hydrazine or 1-disubstituted
derivatives of
hydrazine to give hydrazones...
-
Example of
desulfurization of
thioacetals using Raney nickel...
- Wolfrom, M. L.; Karabinos, J. V. (June 1944). "Carbonyl
Reduction by
Thioacetal Hydrogenolysis".
Journal of the
American Chemical Society. 66 (6): 909–911...
- chromop**** that is
attached to the
dimerized cyclic peptide core and a
thioacetal bridge. It
intercalates into DNA at two
specific sites,
thereby blocking...
- atoms).
Examples include acetylenes (H−CC−R),
methyl sulfides (H−CH2SR),
thioacetals (H−CH(SR)2, e.g. dithiane),
methylphosphines (H−CH2PR2), furans, thiophenes...
-
nickel is used in
organic synthesis for desulfurization. For example,
thioacetals will be
reduced to
hydrocarbons in the last step of the
Mozingo reduction:...
- be
reversed when the
carbonyl group is
converted into a
dithiane or a
thioacetal. In
synthon terminology the
ordinary carbonyl group is an acyl cation...
