-
structure and is
responsible of the
linearity of
isocyanides,
although the
reactivity of
isocyanides reflects some
carbene character, at
least in a formal...
- the
smell of
methyl isocyanide, like that of
other simple volatile isocyanides, is
distinctly penetrating and vile.
Methyl isocyanide is
mainly used for...
- π-acceptor than CO and νNO is a
diagnostic tool in metal–nitrosyl chemistry.
Isocyanides, RNC, are
another class of
ligands that are
capable of π-backbonding...
-
Transition metal isocyanide complexes are
coordination compounds containing isocyanide ligands.
Several thousand isocyanides are known, but the coordination...
- CH3CH(O)CH2 + H2O + KCl The
carbylamine reaction for the
synthesis of
isocyanides from the
action of
chloroform on a
primary amine involves three dehydrohalogenations...
- as
defined by the
functional group C≡N-R. tert-Butyl
isocyanide, like most
alkyl isocyanides, is a
reactive colorless liquid with an
extremely unpleasant...
- [page needed][page needed]
Isocyanates should not be
confused with
cyanate esters and
isocyanides, very
different families of compounds. The
cyanate (cyanate ester) functional...
- (1977). "Chemistry of
sulfonylmethyl isocyanides. 12. Base-induced
cycloaddition of
sulfonylmethyl isocyanides to carbon,
nitrogen double bonds. Synthesis...
-
Isocyanide dichlorides are
organic compounds containing the RN=CCl2
functional group.
classically they are
obtained by
chlorination of
isocyanides. Phenylcarbylamine...
- reaction, by the
reaction of
various ketones (or aldehydes), amines,
isocyanides and
carboxylic acids.
These libraries can then be
tested with enzymes...
