-
isolated carbon centers,
often described as "C4−", in the
methanides or
methides; two-atom units, "C2−2", in the acetylides; and three-atom units, "C4−3"...
-
There are some
examples of
transient synthetic meta
quinone methides.
Quinone methides are cross-conjugated
rather than aromatic.
Nucleophilic addition...
-
Dimethylmercury is an
extremely toxic organomercury compound with the
formula (CH3)2Hg. A volatile, flammable,
dense and
colorless liquid, dimethylmercury...
-
These compounds are
related to the
corresponding quinones and
quinone methides by
replacement of the
oxygen atoms by CH2 groups. ortho- and para-xylylene...
- "1,4,5,8-naphthodiquinone") or
after it ("anthra-1,4-quinone").
Quinone methide –
where one O is
replaced by C Xylylene –
where both O's are
replaced by...
- radicals. Not all
inhibitors are
radicals however, with
quinones and
quinone methides being important examples.
Certain hydroxylamines and p-phenylenediamines...
- Samanta,
Sampak (17 July 2020). "1,6-Aza-Michael
addition of para-quinone
methides with N-heterocycles
catalyzed by Zn(OTf)2: A
regioselective approach to...
- "The role of
quinone methides in
thermostabilization of
hydrocarbon polymers—I.
Formation and
reactivity of
quinone methides".
Polymer Degradation and...
-
pentacyclic nortriterpen quinone and
belongs to the
family of
quinone methides. It has been used for
centuries as a
traditional Chinese medicine. In recent...
- pm and a
fifth Al atom at 221 pm.
Other carbides (IUPAC nomenclature:
methides) also
exhibit complex structures.
Aluminium carbide hydrolyses with evolution...
