- It is a
polar functional group.
Sulfoxides are
oxidized derivatives of sulfides.
Examples of
important sulfoxides are alliin, a
precursor to the compound...
-
Pierce Chemical. p. 145. Roy, Kathrin-Maria (15 June 2000), "Sulfones and
Sulfoxides", Ullmann's
Encyclopedia of
Industrial Chemistry, Weinheim, Germany: Wiley-VCH...
-
referred to as sulfides.
Sulfoxides are
intermediates in this route. For example,
dimethyl sulfide oxidizes to
dimethyl sulfoxide and then to
dimethyl sulfone...
-
inventory is large. The most
common sulfoxide ligand is
dimethyl sulfoxide (dmso). Many
sulfoxides are
known because an
enormous range of
organic substituents...
-
Methionine sulfoxide is the
organic compound with the
formula CH3S(O)CH2CH2CH(NH2)CO2H. It is an
amino acid that
occurs naturally although it is formed...
-
acetates are arenes, alkenes, amides, and phenols. The
usage of α-acyl
sulfoxides and
Lewis acids, such as TiCl4 and SnCl4,
allow the
reaction to proceed...
-
common double bonds are
found in azo
compounds (N=N),
imines (C=N), and
sulfoxides (S=O). In a
skeletal formula, a
double bond is
drawn as two
parallel lines...
- (September 2009). "Enantiomeric
behaviour of
albendazole and
fenbendazole sulfoxides in
domestic animals:
pharmacological implications".
Veterinary Journal...
- developments. The
reaction allows the
formation of
allylic alcohols from
allylic sulfoxides in a 2,3-sigmatropic rearrangement. The
reaction is a
powerful way to...
-
Methyl phenyl sulfoxide is the
organosulfur compound with the
formula CH3S(O)C6H5. A low-melting
white solid, it is an
oxidized derivative of thioanisole...
