-
represents an
alkyl or aryl group).
Thioaldehydes are even more
reactive than thioketones.
Unhindered thioaldehydes are
generally too
reactive to be isolated...
-
uncommon with
alkyl substituents, but one
example is thiobenzophenone.
Thioaldehydes are
rarer still,
reflecting their lack of
steric protection ("thioformaldehyde"...
- .29..265K. doi:10.1016/0009-2614(74)85029-3. Cooper, N.J. (2005). "
Thioaldehydes and Thioketones".
Comprehensive Organic Functional Group Transformations...
-
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:...
- Bis(trimethylsilyl)sulfide: Part II.
Synthesis of
Aromatic and
Heteroaromatic o-Azido-
Thioaldehydes".
Chemistry Letters. 24 (2): 147. doi:10.1246/cl.1995.147. W. M. McGregor;...
-
Isocyanides −CN −NC cyano- isocyano- -nitrile*
isocyanide 5
Aldehydes Thioaldehydes −CHO −CHS formyl- thioformyl- -al* -thial* 6
Ketones Thioketones Selones...
-
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...
-
member of the sulfenes, the
group of
compounds which are S,S-dioxides of
thioaldehydes and thioketones, and have the
general formula R2C=SO2. The
first general...
- thioenolates.
These structures exhibit tautomerism to give
thioketones or
thioaldehydes,
analogous to keto–enol
tautomerism of
carbonyl structures. Chiang,...
- the
organosulfur compound with the
formula CH2S. It is the
simplest thioaldehyde. This
compound is not
observed in the
condensed state (solid or liquid)...
