- [(CH3)2N]2CH2 + H2O
Aminals are
encountered in, for instance, the
Fischer indole synthesis.
Several examples exist in nature.
Naturally occurring aminals Physostigmine...
- been
enough to earn
Funny Aminals the
total score of "9" I
begrudgingly bestowed upon it". "GCD :: Issue ::
Funny Aminals #1". www.comics.org. Retrieved...
- alkylimino-de-oxo-bisubstitution.
Hemiaminals can be
viewed as a
blend of
aminals and
geminal diol. They are a
special case of
amino alcohols. Hemiaminals...
-
Imidazolidines are
cyclic 5-membered
examples of the
general class of
aminals.
Imidazolidines are
traditionally prepared by
condensation reaction of...
- pentakis(dimethylamido)tantalum. It
reacts with many
carbonyl compounds.
Aldehydes give
aminals. For
example reaction of
dimethylamine and
formaldehyde gives bis(dimethylamino)methane:...
-
which can
react with a
second equivalent of the
secondary amine to form
aminals. At
increased temperatures,
pyridines including DMAP,
react with DCM to...
-
takes place between an
aldehyde or
ketone and a
primary amine. Similarly,
aminal formation takes place between an
aldehyde or
ketone and a
vicinal secondary...
- of type R1R2C(OR)(NR'2) (R,R' ≠ H) also
known as a
hemiaminal ether or
Aminal, a.k.a. aminoacetal. S,S-acetal
refers to
compounds of type R1R2C(SR)(SR')...
- (CH3)3COCH(N(CH3)2)2. The
compound is
classified as an
aminal ester, i.e. the tert-butyl
alcohol derivative of the
aminal bis(dimethylamino)methane. It is a colorless...
-
numeric names:
authors list (link) "O-Aminobenzaldehyde, Redox-Neutral
Aminal Formation and
Synthesis of Deoxyvasicinone".
Organic Syntheses. 89: 274...
