-
Examples of keto-
enol tautomerism In
organic chemistry,
enols are a type of
functional group or
intermediate in
organic chemistry containing a
group with...
-
important for
enol- and enolate-based
carbonyl chemistry as well.
Chemical transformations affected by the
conversion to
either an
enolate or an
enol, in general...
-
electrophile through either an
enol or
enolate ion intermediate.
Because their double bonds are
electron rich,
enols behave as
nucleophiles and react...
- In
organosilicon chemistry,
silyl enol ethers are a
class of
organic compounds that
share the
common functional group R3Si−O−CR=CR2,
composed of an enolate...
-
common compounds that
react well with
bromine water are phenols, alkenes,
enols, the
acetyl group, aniline, and glucose. In addition,
bromine water is commonly...
- alkynes. Such
processes occur via
enols and
require the
presence of an acid and mercury(II)
sulfate (HgSO4).
Subsequent enol–keto
tautomerization gives a ketone...
-
atoms composing the
triple bond (C≡C−OH), the triple-bond
analogues to
enols.
Ynols can
tautomerize to ketenes. The
deprotonated anions of
ynols are...
-
Thebaine (paramorphine), also
known as
codeine methyl enol ether, is an
opiate alkaloid, its name
coming from the Gr**** Θῆβαι, Thēbai (Thebes), an ancient...
- with
enol,
which is a
functional group containing both
alkene (en-) and
alcohol (-ol).
Enamines are
considered to be
nitrogen analogs of
enols. If one...
- additions.[citation needed]
Enols are also
carbon nucleophiles. The
formation of an
enol is
catalyzed by acid or base.
Enols are
ambident nucleophiles,...
