- (from
Ancient Gr**** θεῖον (theion) 'sulfur'; also
known as
thiones or
thiocarbonyls) are
organosulfur compounds related to
conventional ketones in which...
- nasturtiums, and capers. The S-oxides of
thiocarbonyl compounds are
known as
thiocarbonyl S-oxides: (R2C=S=O, and
thiocarbonyl S,S-dioxides or sulfenes, R2C=SO2)...
- 6: 86. doi:10.15227/orgsyn.006.0086. K. T. Potts, C.
Sapino (1972). "
Thiocarbonyl halides". In S.
Patai (ed.). Acyl Halides. PATAI'S
Chemistry of Functional...
- An
ylide (/ˈɪlaɪd/) or ylid (/ˈɪlɪd/) is a
neutral dipolar molecule containing a
formally negatively charged atom (usually a carbanion)
directly attached...
- the
faster the
carbonyl group will be
converted into the
corresponding thiocarbonyl by Lawesson's reagent. The
chemistry of Lawesson's
reagent and related...
- (Z)-propanethial S-oxide), a
member of a
class of
organosulfur compounds known as
thiocarbonyl S-oxides (formerly "sulfines"), is a
volatile liquid that acts as a lachrymatory...
-
source material,
carbon monosulfide, is unstable. Thus, the
synthesis of
thiocarbonyl complexes requires indirect routes, such as the
reaction of disodium...
- XY=SO.
IUPAC considers the term 'sulfine' obsolete,
preferring instead thiocarbonyl S-oxide;
despite this, the use of the term
sulfine still predominates...
- Crich, D.; Quintero, L. (1989). "Radical
chemistry ****ociated with the
thiocarbonyl group". Chem. Rev. 89 (7): 1413–1432. doi:10.1021/cr00097a001. Forbes...
- (R2NCSS)2, are
disulfides but they
behave distinctly because of the
thiocarbonyl group.
Compounds with
three sulfur atoms, such as CH3S−S−SCH3, are called...
