- Pictect-Spengler synthesis:
Intramolecular aza
Wittig reactions also
afford isoquinolines.
Isoquinolines find many applications, including: anesthetics; dimethisoquin...
- Calif.:
Transform Press (1997). ISBN 0963009699. The
Simple Plant Isoquinolines , with
Wendy Perry. Berkeley, Calif.:
Transform Press (2002). ISBN 0963009621...
-
synthesis of dihydroisoquinolines,
which can be
subsequently oxidized to
isoquinolines. Two
types of
mechanisms have
appeared in the
literature for the Bischler–Napieralski...
-
Isoquinoline alkaloids are
natural products of the
group of alkaloids,
which are
chemically derived from
isoquinoline. They form the
largest group among...
-
reaction has
general application in the
preparation of
isoquinoline derivatives.
Isoquinolines find many applications, including:
topical anesthetics...
- be
classified as
isoquinoline alkaloids and are
derived from benzylisoquinoline. They also
include the benzyl(tetrahydro)
isoquinoline alkaloids. Benzylisoquinoline...
- Brønsted acid. In this case, the
authors envision a
mechanism where the
isoquinoline is
alternately protonated in an
activating step, then
reduced by conjugate...
-
ester with a
strong base, such as an alkoxide, to form
substituted isoquinolines.
First described in 1900 by
chemists Siegmund Gabriel and
James Colman...
-
Biological Research. 90: 329–344. PMID 7202207., Myers, R. D. (1989). "
Isoquinolines, beta-carbolines and
alcohol drinking:
involvement of
opioid and dopaminergic...
- In enzymology, an
isoquinoline 1-oxidoreductase (EC 1.3.99.16) is an
enzyme that
catalyzes the
chemical reaction isoquinoline +
acceptor + H2O ⇌ {\displaystyle...
