- In
organic chemistry, a
thial or
thioaldehyde is a
functional group which is
similar to an aldehyde, RC(O)H, in
which a
sulfur (S) atom
replaces the oxygen...
-
Names 2013. IUPAC–RSC. ISBN 978-0-85404-182-4. Zwanenburg, B. (2004). "
Thioaldehyde and
Thioketone S-Oxides and S-Imides (Sulfines and Derivatives)". In...
-
Wisconsin Colleges,
accessed on line
August 4, 2007. §R-5.6.1, Aldehydes,
thioaldehydes, and
their analogues, A
Guide to
IUPAC Nomenclature of
Organic Compounds:...
-
uncommon with
alkyl substituents, but one
example is thiobenzophenone.
Thioaldehydes are
rarer still,
reflecting their lack of
steric protection ("thioformaldehyde"...
- the
organosulfur compound with the
formula CH2S. It is the
simplest thioaldehyde. This
compound is not
observed in the
condensed state (solid or liquid)...
-
remarquable que je
nomme stilbène." (On
submitting this
sulfide [i.e.,
phenyl thioaldehyde, C6H5(CS)H] to [dry] distillation, it
gives several products, and among...
- .29..265K. doi:10.1016/0009-2614(74)85029-3. Cooper, N.J. (2005). "
Thioaldehydes and Thioketones".
Comprehensive Organic Functional Group Transformations...
- from
thiation of
ketones and aldehydes. The
incipient thioketones and
thioaldehydes undergo trimerization. One
example is 2,2,4,4,6,6-hexamethyl-1,3,5-trithiane...
-
Isocyanides −CN −NC cyano- isocyano- -nitrile*
isocyanide 5
Aldehydes Thioaldehydes −CHO −CHS formyl- thioformyl- -al* -thial* 6
Ketones Thioketones Selones...
- of the
substrate and
after hetero-analogous β-elimination of H2O, a
thioaldehyde is formed. This
compound is very
reactive and
easily hydrolyzed, releasing...
