-
isomeric forms of
thiocarbamates: O-
thiocarbamates, ROC(=S)NR2 (esters), and S-
thiocarbamates, RSC(=O)NR2 (thioesters).
Thiocarbamates can be synthesised...
-
types of
thiocarbamate: O-
thiocarbamates (2), ROC(=S)NR2,
where the
carbonyl group (C=O) is
replaced with a
thiocarbonyl group (C=S) S-
thiocarbamates (3),...
- The
Riemschneider thiocarbamate synthesis converts alkyl or aryl
thiocyanates to
thiocarbamates under acidic conditions,
followed by
hydrolysis with ice...
- M.; Renny, J. S. (2009). "The Newman–Kwart
Rearrangement of O-Aryl
Thiocarbamates:
Substantial Reduction in
Reaction Temperatures through Palladium Catalysis"...
- (INN), sold
under the
brand name TAGRID,
among others, is a
synthetic thiocarbamate used as an anti-fungal
agent that may be sold
without medical prescription...
-
include benzoxaborole antifungals,
ciclopirox olamine antifungals,
thiocarbamate antifungals and
undecylenic alkanolamide antifungals.
Topical antifungal...
-
monoxide is very unstable.
Important compound classes are thiocarbonates,
thiocarbamates,
dithiocarbamates and trithiocarbonates.
Small inorganic carbon–nitrogen...
-
polymerization uses
thiocarbonylthio compounds, such as dithioesters,
thiocarbamates, and xanthates, to
mediate the
polymerization via a
reversible chain-transfer...
- Barton–McCombie deoxygenation.
Other uses
include the
synthesis of
thioamides and
thiocarbamates. Like the
analogous CDI, it may be used for
peptide coupling. Adrian...
-
Inhibits very long
chain fatty acid
synthesis Prosulfocarb,
Ethofumesate Thiocarbamates,
Benzofurans J -
Unknown Bensulide,
Delapon Chlorocarbonic acids K K3...
