- (C≡C−OH), the triple-bond
analogues to enols.
Ynols can
tautomerize to ketenes. The
deprotonated anions of
ynols are
known as ynolates, the triple-bond analogues...
- glycerol.
chemical compounds with one
hydroxyl group Alcohols Phenols Enols Ynols Polyols,
chemical compounds with
multiple hydroxyl groups Diols, chemical...
-
Ethynol (or hydroxyacetylene,
ethynyl alcohol) is an alkyne–alcohol (
ynol) with the
formula C2H2O. It is the much-less-stable
tautomer of ethenone. At...
- RR'HC−N+(=O)(O−) ⇌ RR'C=N+(O−)(OH)
nitroso – oxime: H−C−N=O ⇌ C=N−O−H
ketene –
ynol,
which involves a
triple bond: H−C=C=O ⇌ C≡C−O−H
amino acid –
ammonium carboxylate...
-
influence the enol-dione
equilibrium in acetylacetone.
Alkenal Enolase Ketone Ynol Geminal diol,
another form of
ketones and
aldehydes in
water solutions Regioselectivity...
-
under controlled cir****stances; this
method is
therefore used industrially.
Ynol Thioketene Miller R,
Abaecherli C, Said A,
Jackson B (2001). "Ketenes". Ullmann's...
- Acetylenediol, or ethynediol, is a
chemical substance with
formula HO−C≡C−OH (an
ynol). It is the diol of acetylene.
Acetylenediol is
unstable in the condensed...
-
cyclobutenone substrate using a hetero-[2+2]
cycloaddition between aryl
ynol ethers (aryl
ketene precursors), and the
following benzannulation enabled...
-
pilosa D****s, B.; Milet, A.; Philouze, C.; Greene, A. E.; Poisson, J.-F. o.,
Ynol Ethers from
Dichloroenol Ethers:
Mechanistic Elucidation Through 35Cl Labeling...
-
Kowalski ester homologation can also be used for the
preparation of
silyl ynol ethers.[citation needed]
Curtius rearrangement Kowalski, C. J.; Haque, M...
