- R2C=O,
thioketones have the
structure R2C=S,
which is
reflected by the
prefix "thio-" in the name of the
functional group. Thus the
simplest thioketone is...
-
Thioacetone is an
organosulfur compound belonging to the -thione
group called thioketones with a
chemical formula (CH3)2CS. It is an
unstable orange or
brown substance...
-
important compounds carbon disulfide,
carbonyl sulfide, and thiophosgene.
Thioketones (RC(=S)R′) are
uncommon with
alkyl substituents, but one
example is thiobenzophenone...
- Barton–Kellogg
reaction is a
coupling reaction between a
diazo compound and a
thioketone,
giving an
alkene by way of an
episulfide intermediate.[1][2][3] The Barton–Kellogg...
-
compound with the
formula (C6H5)2CS. It is the
prototypical thioketone.
Unlike other thioketones that tend to
dimerize to form
rings and polymers, thiobenzophenone...
- the
group of
compounds which are S,S-dioxides of
thioaldehydes and
thioketones, and have the
general formula R2C=SO2. The
first general method for preparation...
-
ylides to form a C2PS3 ring.
Thioketone Thioenol Organosulfur compounds Cooper, N.J. (2005). "Thioaldehydes and
Thioketones".
Comprehensive Organic Functional...
-
Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid
Sulfone Sulfonic acid
Thioketone Thial Thioester Thionoester Thioxanthate Xanthate Boron Boronic acid Borinic...
- "metaphysical stench".
There are also
thioketones, selenoketones, and telluroketones. Out of these,
thioketones are the most well-studied with 80% of...
-
methyl vinyl ketone with LD50 of 7 mg/kg (oral). ****tone
Ketone bodies Thioketone Triketone Ynone Ketosis Raymond,
Kenneth W. (2010).
General Organic and...
